Sunday, October 10, 2010

Tips & Secrets: How to Find a Good Pain Management Doctor

by Heather Grace

Living each day in pain is hard enough. Being diagnosed an Intractable Pain illness such as Central Pain Syndrome can be really scary. Obviously, you want to find a doctor quickly, and get the pain under control. That would be everyone's next logical step. However, as any persistent pain sufferer knows, it's really not that simple.

In this era of the Drug Enforcement Agency (DEA) and various state medical boards becoming watchdogs over prescription drugs, it can be hard--if not impossible--to get treatment for even those most serious diagnosis. If you've been diagnosed with any condition that causes severe, chronic pain, you've probably suffered far more than anyone should, in the system, just trying to get adequate pain management.

Conditions such as Central Pain Syndrome, Adhesive Arachnoiditis, Cauda Equina, Trigeminal Neuralgia, Interstitial Cystitis, Peripheral Neuropathy, etc., often go undiagnosed for long periods of time. They are ignored by family practitioners, chiropractors and even those claiming to be "pain management" physicians. I'm not saying they don't care about patient suffering. Most do care. However, the ugly truth is, far too many are unable to adequately care for such people. Worst still are the doctors who are--for various reasons--unwilling to treat these illnesses.



If you're suffering, afraid and know your pain is becoming harder and harder to cope with, what is the answer? Where can you find the best pain management physician in your area? Obviously, the answer isn't simple. With perseverance, however, you can find true pain management... just like I have. I am not going to pretend my story isn't a nightmare of both medical neglect and misdiagnoses. However, there is good news! Through my more than 10 years dealing with pain, I have learned a great deal about what works, and what doesn't.

How to Find a Good Pain Doctor:

  • Documentation. -- If You're In Pain, Be Ready To Prove It!

    Yes, it's a bit twisted. If you're dealing with serious pain, it doesn't seem fair that you should have to provide 'the facts' in order to get good treatment. You must get over this and just realize it's part of the process. Think of it from Dr. X's point-of-view. Most doctors, even the good ones who want to help you, are afraid they could be criminally prosecuted. Providing a prospective physician with documentation that backs up your pain will protect you. And, in doing so, it provides your potential new doctor with evidence necessary to feel safer taking you on, as a patient. This helps you to get the pain relief you are seeking.

    What will you need? First and foremost, keep everything that helps document your condition, in black and white! If you've had chronic pain for years, somewhere along the way, you must've received sort of written proof of your suffering. Keep a file of such information handy.

    Your files should include: all x-rays, MRIs, CAT scans, the accompanying reports, each physician's diagnostic information and any other hard facts about your condition. Be sure you also have a list of contact information for every physician you have ever seen, even those you only saw for tests, like an MRI. There are other hard facts you can compile, besides what you get from a doctor.

    For instance, you could keep a pain journal. Document each day's pain: a list of physical of your symptoms, describing how your pain feels and how long it lasts, including a rating from 0 to 10. Another good idea? Include your blood pressure and pulse rates, along with your pain rating. People in pain naturally have elavated blood pressure and pulse rates; generally far above the norm.



    Keep any other personal records you can. Take pictures of your scars, or pictures that show areas of your body that are visibly swollen/inflammed. Even if you don't think your pain areas are swollen, try taking a photo and seeing for yourself if there's any sign of swelling. My doctor took photos of my head, neck and upper back and the swelling was very apparent, even though I didn't realize it, before I saw the pictures!

  • HIPAA and Your Medical Records. -- Do I Need All My Records?

    The Health Insurance Portability and Accountability Act of 1996 (HIPAA) gives patients the right to access their own medical records. Post-HIPAA, most medical service providers require patient to sign a HIPAA authorization, formally requesting a copy of the medical record. Be aware that HIPAA prohibits charging the patient for the costs of locating and retrieving the medical record. While a "retrieval fee" cannot be charged, each establishment may elect to charge/not to charge patients for records, at their discretion. Laws may differ from state to state, so it's best to review your state's laws regarding fees.

    Things get really complicated when you try to get older records. Federal programs, such as Medicare and Medicaid, require records be kept at least 5 years from the date of the last patient contact. HMOs or other healthcare networks may require providers to maintain records for a certain period of time.

    What does all of this mean? Time is of the essence! It's important to try and retrieve your records as soon as possible, to ensure your information does not get destroyed! Review your state regulatory board’s requirements and/or your insurance provider's rules regarding record retention.

    Also, when a physician or other provider closes/relocates, rules may be different. Look into any special state provisions governing handling of the medical records. In these situations, it's always best to get your records, as soon as you are aware of the change. It's your duty to be your own advocate concerning your medical records. After all, no one else needs them as much as you do! Who should you ask for your records? Everyone!

  • Records: Hospitals, Physicians and More. -- Get Everything, Quick!

    If you've ever been in the emergency room and/or been hospitalized for any length of time due to your condition, you must follow up with these providers and get all documentation. Sadly, it may be the only way to prove you've been given morphine or similar stronger medications to treat your pain. If any of these visits included x-rays, MRIs or CAT scans, specifically ask for a copy of these films. (This may prove costly, if printed on actual film. If cost is an issue, when possible, get them on CD. This is generally cheaper and could even be free.)



    Be prepared to get all your files from every doctor you have seen, throughout your pain treatment. Always ask for x-rays, MRIs and CAT scans, on disc or printed on film. Realistically, it is best to have records dating back as far as you can, regarding any surgeries, illnesses, etc. That includes traditional doctors, previous pain doctors, holistic healers, support groups, everything!

  • A Complete Treatment History. -- What Do I Need?

    Having a complete treatment history is very helpful. You will find that pain doctors want a complete history of every remedy you have tried. This includes every medication you've taken for pain, every physical therapy modality, acupuncture, chiropractic care, etc. For example, if a prior doctor treated you with XYZ medication, then you will have proof of this.

    Believe it or not, this documentation can save you a lot of hassle, when dealing with insurers. Many insurers require patients to have what is called step therapy. Believing that it saves money, certain drugs must be tried first, before you can get coverage for a specific medicine that may be more costly. Records of the medicines you've taken can prevent unnecessary squabbles, getting the insurance to cover a new medication; especially when you can prove you've already tried the others! Even more importantly, this gives a doctor a picture of the hell you've already been through.

    The bottomline: If you have the documentation, then physicians will see how hard you've tried to get adequate pain relief. Even more than that, they will realize you are serious about pain management, and are not just a drug seeker, who hasn't tried any other treatments. It's an unfortunate label, but because of the fears doctors have, many wonder if the new patient they are seeing is just there for meds. Records validate your situation and help avoid misunderstanding about your motives. Tip: When trying to get a complete list of medications you've used, it may prove useful to request a report from your pharmacy regarding your past prescriptions.

  • How Do I Find The Best Fit For My Needs? -- The Hard Truth...

    If you are a patient with severe, chronic pain, chances are, you will need some sort of pain medication, i.e. opioids, as part of your treatment. This is just a fact of life for those of us with Intractable Pain, RSD, CRPS, Fibromyalgia, etc. It's easy to feel that this makes you bad or wrong or that you are somehow not as good a person as those who "tough it out" without meds. But, if you are suffering, remember this: Pain medicine was made for pain patients!

    Even though we know this, it's still NEARLY IMPOSSIBLE to find the right physician. Why? It's all about fear. Sadly, you can no longer just call up a physician's office, even those who specialize in pain, and get a straight answer regarding treatment protocol. Everyone is hyper-focused on what may happen if it's the DEA or the state medical board calling, not just Joe Pain Patient.

    So, here's the MOST IMPORTANT TIP I CAN GIVE YOU in this entire article: DO NOT CALL UP ANY DOCTOR'S OFFICE AND ASK IF THEY PRESCRIBE PAIN MEDICATION.

    I know that sounds completely ridiculous, but think about it... Most if not all physicians are now afraid they might lose their licenses, merely because they are prescribing pain medication to those who truly need it. If you were in that doctor's shoes, would you allow anyone in your office to admit you prescribe opioids to any random stranger, over the phone? Not likely.

    Even worse, anyone who asks such a question could easily be flagged as a drug-seeker, just for asking this question. The DEA has created a very real fear among even the best physicians out there. I have seen it with my own eyes! These are not easy times for the pain patient. So what else can be done? Think logically and use your best research skills... this may be a very tough process!

  • Your Prospective Physician's Views on Opioid Use. -- Investigate!

    Either you, or a friend who's good at using the Internet (and possibly your local university library's resources), will have to do some major research on pain management physicians in the area. This goes beyond using Google or Bing to find doctors in your area who call themselves a "pain management physician" -- that's just the first step. Once you have a list of at least a dozen doctors, go on to the real work.

    (Note: For the purposes of the article, I am referring to the doctor as a male, but we all know female doctors exist and treat pain as well. I just don't want to do that he/she and him/her thing throughout the article...ok?)

    You must find everything you can regarding this doctor:

    1. What do other patients say about him? Look for reviews throughout the internet, at sites like Yelp.com, and any others you can find, that don't charge a fee for the information. If a lot of people say he helped them, chances are, at least some of his patients are being prescribed pain medication. Some of them may say this, though you can never be sure, anymore.

    Look for hints that people are satisfied with his care and think he does a good job at providing some degree of pain relief. If a good percentage of the reviews are positive, this is a very good start! If the positive response is overwhelming, you may feel confident enough to make an appointment with this doctor. However, there are several other ways to check into the doctor more thoroughly...

    2. What doctor have you heard people mention at other doctor's offices, hospitals, etc? Do people think the doctors on your list are good or bad? Can they recommend any other doctors, to add to your list?

    Speak to other patients who are like you--they can provide a wealth of information about the good doctors, and the not-so-good ones! Even more than that, ask some of the nurses and front office staff what they think about the doctors that their office refers patients to, for pain treatment.

    Or, ask your family doctor, when he refers you, for any information he has about the doctor he recommends. Chances are, someone will be able to provide you a good referral. If that doesn't work, there are advocacy groups out there. Look for one in your area, dedicated to pain patients. Or, visit the American Pain Foundation at www.painfoundation.org.

    3. What articles/groups/links does the doctor mention, on his web site? Do these provide any information about the types of doctor he is? If he lists/links to articles about prescription drug abuse or how to detox patients, obviously, this is probably a bad sign. Chances are, he's either against opioid use, or he might even be afraid to prescribe them to his patients.

    When looking for the best pain doctor, you really want one who is willing to use all the tools in his toolbox. If he's unwilling to use opioid pain medications, then his bias may get in the way of well-rounded treatment. As any patient knows, trying anything and everything, until you get the right treatment plan, is the mark of a good doctor. Good pain doctors are willing and able to prescribe whatever works.

    If the doctor's web site is openly in favor of pain medication (among other treatments), that's great! He's probably a good option. However, if it appears there's any degree of anti-opioid sentiment on his web site, it's important to look into the doctor further...

    4. What does his C.V. (curriculum vitae), a.k.a. his resume, say about him? More specifically, what did he focus on in his research? What papers has he written/co-written? What boards does he belong to? What groups is he a member of?

    This can be much more tricky. Here's a tip... if nothing on his C.V. mentions the word "opioid" or any known medications that pain patients use (generic names such as: codeine, hydrocodone, morphine, hydromorphone, fentanyl, etc.), then he probably isn't too keen on opioid pain medication.

    Sadly, many pain doctors are very procedure focused. They may try various injections in their offices, including nerve blocks, epidurals, etc. There are lots of non-opioid treatments available, and yes, these treatments have helped some, patients. However, from my experience, these treatments simply do not manage nearly enough of the people who are experiencing severe, chronic pain.

    A doctor with this sort of C.V. and no further "pro" pain medication evidence might be someone you consider a "backup" doctor. In other words, someone to visit only after others have not worked out. Remember, you want a doctor who treats his patients with all available methods of pain relief. A doctor who leaves opioids out of the equation has clearly taken a stand. And, it is most likely a stand against opioid use.

    Look at that C.V. in even greater detail. Does the research/writings mention use of pain medication to treat cancer pain? Or end of life care? What about post-operative pain? Sounds like a good sign, right? Maybe. But... maybe not.

    The sad fact is, some doctors do prescribe opioids to patients with cancer or those who are near death. Some will even prescribe these medications to patients after major surgery. However, this does not mean they will automatically prescribe to patients with chronic, severe pain. So, just because his C.V. mentions opioids, this might not mean he will treat someone with Intractable Pain, etc. You must take another step, in this case...

    Look even closer at that C.V. If the research/writings only mention chronic pain in relation to non-opioid therapy, then chances are, he's wary of utilizing opioids in patients with chronic pain. What non-opioid therapies does that include? There are many. Let's go over some of the common therapies, as well as their common side effects.

    Non-Opioid Treatments for Pain & Their Risks

    NSAIDs, Cox-2 Inhibitors or Acetaminophen also know as Tylenol, a.k.a Paracetamol/Propacetamol--all of these can cause severe stomach problems or bleeding. Transcutaneous electrical nerve stimulation (TENS), which many say have no side effects--in reality TENS can cause skin irritation/burns, headache or numbness and can kill anyone with a pacemaker. Nerve blocks with a "localized" anesthetic/corticosteroid, which can cause permanent muscle loss, weight gain and "moon-faced" appearance. Epidural steroid injections (spinal tap), which can puncture the spinal cord or cause nerve damage. Prialt (Ziconotide) via pump-based injection, known to cause cognitive impairment, unresponsiveness and even psychosis.

    These side effects might come as quite a shock. People tend to think that anything they can get without a prescription comes with little to no risk. Many also believe that non-opioid prescription medication is somehow better for you. Aren't these kinds of treatments "safer" than opioids? Not necessarily. Obviously, you must weigh the risks and benefits of all treatments when deciding what is right for you. Even vitamins and supplements have side effects. This is why all treatments for pain, including opioid pain medication, are overseen by your physician.

    So, if the doctor's research/writings include any of these treatments--but none regarding pain medication--this may mean he is against the use of opioids. It's important to weigh all the information you've uncovered, before deciding on the right choice for you.

    5. If all of the research thus far has not provided enough information to make an good decision regarding a doctor's stance on pain care, you may want to get access to one (or more) of the papers/research projects, mentioned on the C.V. Any university library should have access to the databases with this detailed information. Be aware that some may charge a fee for this service.

    If by this phase you haven't found any definitive answers, it might be best to go on to the next doctor on your list. Once you have selected the best doctor for your needs, you want to be prepared for interaction with the doctor. Trust is key. Thoughts of the DEA loom in most doctor's minds. So, what will help increase your chances of being treated like a true pain patient, and not a potential drug-seeker?

  • The Actual Office Visit: A Two-Way Interview. -- Be Prepared!

    When you visit a potential new pain doctor, you want to be organized, poised and as ready to talk as you are to listen. Think of this as an interview for both of you. He must earn your trust, but you must also earn his. Here are some important ways to make things go more smoothly.

    First, bring your best advocate with you, whether it is a loved one, or close friend. Be sure this person is willing to talk honestly and openly about how you have suffered--how pain has impacted you. This will help reinforce the seriousness of your situation. It demonstrates to the doctor that someone other that you, the patient, sees that you are in need of pain management. It may sound like an unnecessary inconvenience, but it truly helps the doctor feel more at ease about the reality of your condition. The more you can demonstrate your level of pain, as well as your desire to get back to a normal life, the better!

    Secondly, as hard as it is, remember that this visit is not just about ensuring the doctor can care for your medical needs. It's just as important to reassure the doctor regarding your intentions. You want the physician to see the extent of your illness, but also see you as a trustworthy person who just wants his help regarding pain relief.

    In addition to bringing someone with you, here are some important ways to show the doctor the urgency of your situation. Have the following documents with you:

    1. A list of all medications you are taking/have most recently taken to manage your pain.

    2. A list with all the prescription medications you have tried for pain relief. This should include pain medication, muscle relaxants, sleep medication, anti-inflammatories, etc.

    3. A list of all pain-related treatments you have tried. What holistic therapies, acupuncture, chiropractic care, physical therapy, over-the-counter medication, etc., have you tried?

    4. Complete contact information for your most recent doctor (be ready to tell him why it didn't work out, as well).

    * Note that you can put all of items 1-4 on the same sheet of paper, if they will fit.

    5. Recent x-ray/MRI/CAT scan films, especially from the last five years.

    6. A list of questions. You can show the list to the doctor, if necessary, to create an open dialogue--and TO ensure all your questions get answered! Additionally, if you have heard of any medications or treatments that you think might be beneficial to you, bring those along as well!

    7. Make copies of key documents you have, supporting your diagnosis and the reports/film that supports this diagnosis. This should be just a few pages, that you will give to your physician, to keep.

    8. It's not necessary to inundate the doctor with paperwork, but also have other important information from your files (as discussed above) in hand, at the initial visit. This doesn't mean your entire medical history, but key information that supports why you came to be in his office. Example: If you started with one bad disc in your low back, and now you have five, causing pain/numbness/difficulty walking, provide proof of all this. Bring physician reports which detail your diagnoses, as well as an overview of your treatment, what was prescribed, etc.

    It's not essential to bring any more than 25 pages. However, assure the doctor that you will provide copies of other pertinent data, on the next visit. It may help to ask him specifically what he would like to see, at a followup appointment.

    The more prepared you are for this visit, the better! Ensure that the visit includes a discussion of what does and does not work for you, from the lists you have provided. The goal is to leave the office with an idea of what the treatment plan will be, and hopefully with an initial prescription in hand--a starting point on your road to pain management.

    Keep in mind that even seeing the best pain doctor will not be a quick fix. Prepare for it to take a minimum of several months before you get the right treatment, to provide pain management and some degree of relief. This will likely include prescription medication, over-the-counter items such as amino acids, and even increased use of vitamins and minerals, including vitamin D3, calcium, magnesium, etc.

    Attention Readers: What do you think of the suggestions included here? Have anything to add? Any DO or DON'T to share? Please leave your comments below. Good luck and here's to better pain management for all of us!
  • Monday, August 30, 2010

    Make September 2010 Pain Awareness Month in YOUR State! Here's How....

    by Heather Grace

    It has never been more important for people to work together to fight the problems surrounding pain treatment. You can make a difference... How? Encourage your State Governor's Office to proclaim September 2010 as PAIN AWARENESS MONTH, (PAM) officially.

    What exactly is a Proclamation?
    A proclamation is an official public announcement of a celebration. State or local governments (governors or mayors) can issue proclamations. Proclamations can use dry, official language, or straightforward, simple language. The document is signed by a public official, such as the governor.

    Checklist for Submitting & Securing a Pain Awareness Month Proclamation

    1. If you don’t have contact information for your Governor or are not sure of how to go about requesting a proclamation type the following phrase into a search engine (like Google) see what comes up. Phrase: “submitting a proclamation request to Governor [your Governor’s name] in [state name]”

    2. Once you have the contact information for state governor’s office, initiate contact and find out:
    • the protocol and timeline for requesting a proclamation
    • name and contact information for the administrative assistant in charge of proclamation requests
    • if any other group or organization has already submitted a request for a PAM proclamation
    • if there is a signing ceremony with the governor and, if so, the date and time
    • how to submit some draft language (fax, e-mail, snail mail)

    3. If another group or organization has already submitted a request for a PAM proclamation, ask the Governor’s office contact if your organization’s name or the American Pain Foundation can be added to the list of supporters in the proclamation language.

    4. If no other group or organization has submitted a request, you can either a) proceed with submitting your request OR b) let the Governor’s office contact know you will be submitting a request soon but first want to make some contacts with other groups whom might like to collaborate with you on the request.

    5. Other collaborators to consider:
    • Your state’s Power Over Pain Action Network – A leader directory can be found at:
    http://www.painfoundation.org/poweroverpain/default.asp?file=map.htm
    • Your State Pain Initiative – Contact list can be found at:
    http://www.aspi.wisc.edu/stcont.htm
    • American Cancer Society Chapter – e-mail ican@acscan.org to get contact info for your state
    • State Hospice Organization – try Googling “[state name] hospice and palliative care
    organization”
    • Local chapter of American Society for Pain Management Nursing – Chapter list can be
    found at: http://www.aspmn.org/Organization/chapter_list.htm
    • State nursing organization - try Googling “[state name] nurses association”
    • National Association of Social Workers state chapter – Contact list can be found at: http://www.socialworkers.org/chapters/default.asp.
    • Other self-help groups, i.e. Arthritis Foundation, MS Society, Lupus, Sjogrens, etc. Chapters can be found by Googling the organization’s name.

    6. Complete the proclamation template, including the sample letter and proclamation, below. Fill in the blanks with the needed information and then save as a Word file on your computer so you can print it, fax it, e-mail it or mail it, as needed. If
    some of your collaborators want to co-sign the letter, add their organizational name.

    7. Copy/paste the cover letter into Word. Fill in the blanks with the needed information and then save it as a Word file on your computer desktop. If some of your collaborators want to co-sign the letter, add their contact information and e-signatures.

    8. Even if you submitted it on-line using a template provided to you, consider sending a hard copy draft proclamation and cover letter to Governor’s office.

    9. After a week, check back with the Governor’s office contact to make sure the request was received. At that time also confirm the following:
    • When the final version on the proclamation will be ready
    • Date, time, and locale for signing ceremony - be sure to ask is there will be an official photographer present and, if so, how you can get order a copy of the official photo.
    • If there is no signing ceremony, request that the office send the finished proclamation directly to you as soon as it is finished. Be sure your contact information is included on all correspondence. And, it can’t hurt to ask if there is any possibility the Governor will pose for a photo with you (your group) at his/her convenience.

    10. Convey this information to any collaborators, and make needed travel plans (if needed).

    Tips for Leveraging Your Pain Awareness Month Proclamation

    1. Let the Governor’s office know how you intend to use the proclamation. For example, let them know that recognition of September as Pain Awareness Month is a way to raise awareness about the under treatment of pain and the barriers to effective pain management. Give them examples of the types of outreach you plan to do in the community to highlight the proclamation, such as media coverage of the proclamation or a community outreach event. Be sure to let the Governor’s office know of any events which occur as a result of the proclamation, this will improve your chances of getting their attention for another proclamation in following years.

    2. Ask them if they will issue a press release for PAM (see example at www.conqueringpaintogether.org) to the media and also on their official website.

    3. Issue your own press release mentioning proclamation and/or signing ceremony where appropriate.

    4. Ask any PAM collaborators who worked with you on submitting the proclamation request to issue their own PAM release, including an acknowledgment that the Governor issued a proclamation. Forward your press release and invite them to use any of the content they find helpful. Ask them to notify you if a release goes out.

    5. If you submit an op-ed piece or letter to the editor, mention that the Governor/city official declared September as Pain Awareness Month. Think about using an op-ed as a way to promote your PAM events.

    6. Use the proclamation as an opportunity to reach out to your elected officials and remind them of the important role they play in helping to remove the barriers to the adequate assessment and treatment of pain.

    7. Give copies of the proclamation to non-profit health organizations, support groups, etc. so, they, in turn, can promote awareness month and their services to persons in pain as well.

    GOOD LUCK! Together, we can make a difference!

    - - - - - -
    CA Sample Letter
    - - - - - -

    June 1, 2010

    Dear Governor,

    On behalf of the American Pain Foundation, Intractable Pain Patients United, For Grace, ThePainStore.com, as well as pain patients throughout the state of California, I am writing to you today to ask for your support in declaring September 2010, once again, as Pain Awareness Month in California.

    Pain is a national healthcare crisis--affecting tens of millions of Americans. It is the number one reason people seek medical care. Women and minorities suffer disproportionately. Undertreated pain has serious physiological, psychological, and social consequences. Pain weakens the immune system and slows recovery from disease or injury. Uncontrolled pain diminishes quality of life.

    Pain costs our economy $100 billion in medical costs and lost workdays. Undertreated pain drives up the cost of healthcare, because it extends lengths of stay in hospitals, increases emergency room visits, and leads to unplanned clinic visits.

    When pain is treated properly, many people can resume their lives. Treatments are available today to manage or greatly ease most pain, so people with pain should not suffer needlessly. People often mistakenly believe that pain is something they “just have to live with.” They are often made to feel that the pain is “just in their heads.”

    Unfortunately, many barriers prevent effective pain treatment. Limited access to health care systems, prescribed pain treatments, or sites of care is seriously impeding pain sufferers’ ability to get their pain appropriately assessed and treated. Furthermore, a dearth of trained pain specialists, overly restrictive regulatory policies, and the public’s negative stereotypes about pain are standing in the way of ensuring appropriate and effective pain care for all. THIS HAS GOT TO STOP. Now is the time to ensure appropriate pain treatment for patients everywhere!

    Congress declared the 10-year period that began January 1, 2001, as the Decade of Pain Control and Research. While progress has been made, much is left to do. We hope that we can count on your support to let your constituents know that having their pain taken seriously is a concern we jointly share.

    We hope you will find the enclosed draft language helpful in crafting a proclamation declaring September 2010 as Pain Awareness Month in California. Thank you for your attention to this very important issue. Please don’t hesitate to contact me, should you have any questions.

    Sincerely,
    Heather Grace
    Member, IPPU
    Founder, ThePainStore.com

    - - - - -
    Draft - September 2010: Pain Awareness Month
    - - - - -

    WHEREAS, physical pain affects tens of millions of Americans and untreated or inadequately treated pain can harm quality of life by diminishing the ability to function, socialize and be productive; and

    WHEREAS, despite this prevalence, access to appropriate and effective pain care remains a barrier for many Americans due to limited access to health care systems, appropriately trained pain specialists, prescribed pain treatments, or sites of care or pharmacies, as well as, negative stereotypes about pain, and

    WHEREAS, pain takes an economic toll on our country, costing billions of dollars each year in medical expenses, lost wages, reduced productivity, and other costs; and

    WHEREAS, improved pain management education and an effective multi-disciplinary treatment approach can help reduce suffering and remove barriers to pain-free living; and

    WHEREAS, the American Pain Foundation, Intractable Pain Patients United, For Grace, ThePainStore.com, and a variety of other professional and consumer organizations exist to advocate for people experiencing pain by increasing awareness and promoting access to appropriate pain treatment for all Californians,

    NOW THEREFORE, I, Arnold Schwarzenegger, GOVERNOR OF THE STATE OF California, do hereby proclaim September 2010 as:

    PAIN AWARENESS MONTH

    IN TESTIMONY WHEREOF, I have hereunto set my hand and caused to be affixed the Great Seal of the State of California, in the City of Sacramento, this 1st day of September, 2010.

    *** Signature of the Governor and Seal HERE ****

    Friday, July 9, 2010

    Now Is the Time to Get Involved! September 2010 is Pain Awareness Month

    by Heather Grace

    Are you experiencing chronic severe pain? Are you one of those suffering with an 'invisible illness' in silence? Are you a pain patient who feels alone, undertreated by doctors, ashamed to admit you have to take pain medication to survive? Pain can be an overwhelming condition--let's working together to conquer it... one patient at a time!

    Now is the time -- September 2010

    Outreach and advocacy activities are set to take place coast to coast. People will focus on raising awareness about the undertreatment of pain, advocating for change in governmental policies, and distributing educational resources to everyone who needs them: people with pain, their caregivers and health care practitioners.

    2010 marked an enormous victory for pain management. Provisions in the National Pain Care Policy Act passed with the Health Care Reform bill after 7 years in the making! We’ve garnered awareness and momentum around pain and the challenges it creates for millions of people, but there is still so much work to do. Most pain sufferers still do not receive the level of care they both need and deserve. Join the fight and make the difference!

    What will you do to make a difference in the treatment of pain this September? Last year's events were very successful. Here are some of the highlights:

  • Twenty-two “September is Pain Awareness Month” proclamations were declared by Governors and Mayors through the efforts of organizations working for better pain management practices.
  • Over 300 activities and events took place across the country with an thousands in attendance.

    I am certain this year, September 2010's Pain Awareness Month will have an even greater impact. Here are some of the projects in development:

    There are TWO events set up on FaceBook:
  • Women in Pain Awareness/Recognition - Over 100 People Attending/Maybe Attending
  • Women in Pain Awareness - Over 100 People Attending/Maybe Attending

    Join the American Pain Foundation's Virtual March:
    The VIRTUAL MARCH is an online event to unite, empower and rally! Whether you are in pain or you care about someone living in pain, help make a difference in policy and practice. Join the march! Help transform pain policy into improved pain management for all!

    There are many LIVE events being set-up nationwide, including:

    AZ:
  • Arizona Diamondbacks Helping Power of Pain Foundation Strike Out Chronic Pain - Sept 26. Fundraising Ticket/T-Shirt Sales by POP at Chase Field. The AZ Diamondbacks take on the LA Dodgers in the last home game of the season.

    CA:
  • For Grace's 3rd Annual Women in Pain Conference: Gender Matters - Sept 17. Register now! Women in pain, their caregivers and healthcare providers will gather in Los Angeles to educate, support and empower women to take responsibility for their own health and wellness.
  • Intractable Pain Patients United (IPPU) Pain Art Walk - Sept 25. Los Angeles/Orange County area artists will display their art, discussing their pain conditions, creating education/awareness.

    More information to come, soon! PLEASE -- send us information on your event and we will post it here! September 2010 is Pain Awareness Month -- It's OUR Month!

    :) Thanks everyone!
    Heather @ ThePainStore.com
  • Sunday, May 9, 2010

    Watch the Stossel Show Episode RE: Pain on Hulu -- Now!

    by Heather Grace

    John Stossel spoke out on behalf of pain patients everywhere, appearing on the O'Reilly Factor on February 23. Soon after, he took the topic on step further, discussing it on his show on the Fox Business Channel, "Stossel."

    On February 23, Bill O'Reilly spoke with John Stossel (briefly) about pain, doctors leaving the pain management field, patients not getting adequate care, etc. It was sort of a promo for the full show on the subject, Stossel Show, which aired February 25 on Fox Business. Get the scoop at: http://www.creators.com/opinion/john-stossel/whose-body-is-it-2010-02-24.html.

    It was a proud day--to see a member of the popular media coming to our defense. In the beginning of the segment on pain, Stossel remarked that he realizes many people fear death... that is their greatest fear. But, for him, being in severe pain the rest of his life is his greatest fear.

    As someone who has dealt with pain himself, Stossel knows all too well how serious an issue pain can be! Not only does he champion the plight of the pain patient, he recognizes the fear and trepidation created by the DEA for even the most dedicated, well-meaning GOOD pain doctor.

    His show delves deep into what the FDA does to patients, preventing them from getting the most effective care. He also discusses how the DEA has not just prosecuted doctors, causing good ones to use their life-savings defending themselves... but worse, how the DEA has also gone after patients! One patient discusses how he was personally jailed, because of the quantity of prescribed medication he had, for his own use. It's outrageous--a show that ALL PAIN SUFFERERS MUST SEE!

    Here's the link to Hulu... watch it now! Stossel asks: Who owns your body and why should the FDA control what you put in your body? The entire episode is great. However, if you want to just see the segment on pain, it's at 25:57. Check it out:
    http://www.hulu.com/watch/135096/stossel-thu-feb-25-2010#s-p4-so-i0

    But, don't just watch it! Let John Stossel know how much you appreciate what he did for all of us, as pain patients! Visit his web site: http://www.foxbusiness.com/on-air/stossel Or, email him: stossel@foxbusiness.com.

    Why? He is supporting our cause! It's a REALLY big deal that he recognizes how doctors are afraid to help pain patients. John Stossel is one of the few people IN THE MEDIA WHO IS IN OUR CORNER, so show your appreciation!

    Thanks all --- keep fighting the good fight and stay well!
    Love, Heather :)

    Wednesday, March 10, 2010

    Opioid Pain Relievers & Overdose - The Real Danger is Undertreated Pain

    by Heather Grace

    *** A New CALL TO ACTION - Read Chronic Noncancer Pain Management and Opioid Overdose: Time to Change Prescribing Practices & Share Your Feedback ***

    Attn All Pain Sufferers/Friends/Caregivers:

    ******************************************************************
    THIS IS A CALL TO ACTION, REQUESTING YOU:
    1. Read the article: http://www.annals.org/content/152/2/123.full.
    2. Share YOUR response on their site.
    3. Share YOUR response with the main author, the Deputy Director of the Office of National Drug Control Policy (the #2 Drug Czar under Pres. Obama).
    4. Share This With EVERYONE Who Understands Our Plight!
    ******************************************************************

    In short, Dr. A. Thomas McLellan and his co-author, have attacked the necessity of high-dose opioids in pain treatment. Sadly, this could have a huge impact on the future of everyone's access to medication. Important medication that is life-changing/life-saving!

    Here is my letter to the author. Please, take the time to share your thoughts as well!


    - - - - -

    Comments on Opioid Pain Relievers & Overdose Potential - The Real Danger is Untreated/Undertreated Pain

    by, Heather O. Grace

    I am writing in response to Dr. A. Thomas McLellan's editorial online at: www.annals.org/content/152/2/123.full.

    I hate having intractable pain, degenerative disc disease and neurological conditions that can prevent me from completing the simplest tasks. However, I can say with confidence that I am in no danger of overdose!

    No true pain patient is at risk of overdose when managed via regular visits to a competent doctor. Under 2% of people taking opioids ever overdose. In fact, the study Dr. McLellan references had even lower rates of overdose.

    It took me over five years of severe pain to find a doctor who would do anything and everything to help me. Unfortunately, I was at the end of my rope, suicidal, by that point.

    That doctor saved my life. Our system is broken--not serving severe chronic pain patients like me. If Dr. McLellan is truly concerned about pain patients dying, then I ask:

    What about the deaths of patients who don't get pain relief because the DEA restrictions have created a climate of fear among doctors? If you consider the deaths due to heart attack or stroke, in addition to those via suicide, the loss of life is far greater than the loss due to overdose.

    Access to medication is a constant concern (fear, really) for pain patients. Patients often have a medication that works, then it is suddenly no longer available. The DEA limits access to many opioids. Worse still, the DEA also routinely accesses confidential prescription records of individual patients--without warrants--in order to target doctors treating high-dose opioid patients.

    John Stossel, the famed journalist who was also treated for a serious pain condition, spoke on The O'Reilly Factor on Feb 23, and on his own show, Stossel, on Feb 25, 2010.

    He said: "The Drug Enforcement Agency's war on drug dealers has led them to watch pain-management doctors like hawks. Drugs like Vicodin and OxyContin provide wonderful pain relief. But because they are also taken by 'recreational' drug users, doctors go to jail for prescribing quantities that the DEA considers 'inappropriate.' As a result, pain specialists are scared into underprescribing painkillers. Sick people suffer horrible pain needlessly." Source: www.creators.com/opinion/john-stossel/whose-body-is-it-2010-02-24.htmlhttp://www.blogger.com/img/blank.gif

    "The system is broken, and patients are suffering," said Claudia Schlosberg, from the American Society of Consultant Pharmacists. "Law enforcement concern has to be compatible with meeting patients' needs. Right now it's not." Source: www.painreliefnetwork.org/page/2/

    And there are serious health implications: Dr. Forest Tennant, a founder of the American Society of Addiction Medicine has identified Cardiac Adrenal Pain Syndrome: "Severe pain is well-known to stimulate the cardiac and adrenal systems...The tachycardia and hypertension is caused by pain's over-stimulation of the nervous system. It's the root cause of cardiac and adrenal complications." Source: www.healthcentral.com/chronic-pain/c/3388/69308/information

    Treating severe pain patients is not the mystery many people might think it is. Doctors can use objective scales to diagnose patients: blood pressure/pulse, visible inspection, MRIs/CAT scans and bloodwork.

    If Dr. McLellan wants to truly help prevent deaths of pain patients, then there are 3 things I recommend the current administration focus its' efforts on:

    1. Revise DEA mandate that creates prescription fears even for doctors who treat legitimate pain patients. Don't restrict access to any of the FDA-approved opioids.

    2. Ensure pain treaters have access to appropriate documentation on HOW to objectively diagnose pain patients, such as the article written by Dr. Forest Tennant, who has treated pain patients for 25 years. Source: www.pain-topics.org/pdf/Tennant-PainSigns.pdf

    3. Create a nationwide Pain Patient's Bill of Rights, similar to the one in California. Include the CA patient rights, plus the objective diagnostic criteria, as noted in #2, above.

    By doing all three, a more comprehensive system of care will be in place, throughout the country. People are beginning to open their eyes to the truth about opioids. The Stossel Show is a wonderful step in the right direction. You, Dr. McLellan, as the Deputy Director of the Office of National Drug Control Policy, can be on the forefront of meaningful differences in the quality of care. Plus, with education comes less severe uncontrolled pain and, most certainly, less needless deaths.

    I realize it is hard to understand our plight as someone on the outside of all this suffering. I didn't understand use of morphine or methadone until I was suffering and near my own demise. I urge you, Dr McLellan, to look at things from a fresh perspective, talking to pain patients and their doctors, to see what it is to live with pain. We take our opioids just as diabetics take insulin. There really is no difference.

    Please, Dr. McLellan, as the #2 Drug Czar working under Director, R. Gil Kerlikowske, you have the power to make positive changes to the way pain patients are treated. I urge you to take a stand in the right direction--to help pain patients--we are counting on you!

    Tuesday, February 23, 2010

    A CALL TO ACTION - JOHN STOSSEL SPEAKS OUT ON BEHALF OF PAIN PATIENTS WORLDWIDE

    *** A CALL TO ACTION - WATCH JOHN STOSSEL FEB 23 @ 8PM & FEB 25 @ 8PM + EMAIL REQUEST ***

    Attn All Pain Sufferers/Friends/Caregivers:

    ******************************************************************
    THIS IS A CALL TO ACTION, REQUESTING YOU
    1. Watch the O'Reilly Factor from Feb 23 at 8pm.
    2. Watch Stossel's Show on Fox Business from Feb 25 at 8pm.
    3. Email Bill O'Reilly AND John Stossel using the info below ASAP.
    4. Share This Blog With EVERYONE Who Understands Our Plight!
    ******************************************************************

    On February 23, on the O'Reilly Factor on Fox News at 8pm EST and PST, Bill O'Reilly spoke with John Stossel (briefly) about pain, doctors leaving the pain management field, patients not getting adequate care, etc. It was sort of a promo for the full show on the subject, Stossel Show, which aired February 25 on Fox Business. Get the scoop at: http://www.creators.com/opinion/john-stossel/whose-body-is-it-2010-02-24.html.

    IT IS VITALLY IMPORTANT TO SUPPORT PROGRAMMING THAT BENEFITS PAIN PATIENTS EVERYWHERE! Please let BOTH O'Reilly and Stossel know that you appreciate their coverage of this IMPORTANT topic!

    Get more info via The O'Reilly Factor web site at: http://www.foxnews.com/oreilly. Email him RE the Stossel episode Feb 23 on pain, SHOW YOUR SUPPORT. His email is: oreilly@foxnews.com. Also, you can call "The Radio Factor" live on the air at 1-877-9-NO-SPIN (877-966-7746) weekdays from noon to 2 p.m. ET.

    See John Stossel's show web site at: http://www.foxbusiness.com/on-air/stossel-- He is supporting our cause. It's a REALLY big deal that he recognizes how doctors are afraid to help pain patients. John Stossel is one of the few people IN THE MEDIA WHO IS IN OUR CORNER, so show you're appreciation. Let's talk to him too! Email him at stossel@foxbusiness.com.

    *** Below are sample emails you can use to send to both O'Reilly and Stossel. Feel free to send as is, with your name and info, or edit and send what you want to say, personally. But, the more mail they get, the better!!! ***

    Thanks all --- keep fighting the good fight and stay well!
    Love, Heather :)


    ------------ --------- ---------
    LETTER SAMPLES ARE BELOW
    ------------ --------- ---------


    Dear Mr. Bill O'Reilly,

    I was pleased to see the show with John Stossel discussing pain and the problems facing not only doctors, but pain patients in our health care system. I have Intractable Pain--a severe, constant pain that is not curable by any known means and which causes a bed or house-bound state and early death if not adequately treated. It causes adverse biologic affects on the body's cardiovascular, hormone, and neurologic systems.

    I would urge you, Mr. O'Reilly, as well as John Stossel, to pursue the issue of pain as a distinct, life-threatening illness. I agree with you wholeheartedly that the President's healthcare plan WILL NOT work. The plan is especially dangerous for people with severe illness, such as myself and many, many friends who suffer with nonstop (all day, every day) pain. Our voices are not heard often enough.

    WE NEED YOUR HELP -- PLEASE DISCUSS ISSUES OF PAIN MANAGEMENT AND HAVE PAIN PATIENTS REPRESENTED ON YOUR SHOW. We would all be very thankful! This is a growing problem worldwide that cannot be resolved until doctors are able to treat their pain patients without fear of prescribing the necessary medication.

    All of our lives are in jeopardy and we appreciate your show shining a light on the subject.

    Most Sincerely,
    YOUR NAME HERE
    Pain Sufferer

    Please visit these sites for reliable information on intractable pain:
    American Pain Foundation: www.painfoundation.org
    Intractable Pain Authority-Dr. Forest Tennant: www.foresttennant.com
    Intractable Pain Disease Site: www.intractablepaindisease.com

    - - - - - - - - - -


    Dear Mr. John Stossel,

    I was pleased to see you on the O'Reilly Factor discussing pain and the problems facing not only doctors, but pain patients in our health care system. I have Intractable Pain--a severe, constant pain that is not curable by any known means and which causes a bed or house-bound state and early death if not adequately treated. It causes adverse biologic affects on the body's cardiovascular, hormone, and neurologic systems.

    I would urge you, Mr. Stossel, as well as Mr. O'Reilly, to pursue the issue of pain as a distinct, life-threatening illness. I agree with you wholeheartedly that the President's healthcare plan WILL NOT work. The plan is especially dangerous for people with severe illness, such as myself and many, many friends who suffer with nonstop (all day, every day) pain. Our voices are not heard often enough.

    WE NEED YOUR HELP -- PLEASE DISCUSS ISSUES OF PAIN MANAGEMENT AND HAVE PAIN PATIENTS REPRESENTED ON YOUR SHOW. We would all be very thankful! This is a growing problem worldwide that cannot be resolved until doctors are able to treat their pain patients without fear of prescribing the necessary medication. All of our lives are in jeopardy and we appreciate you shining a light on the subject.

    Most Sincerely,
    YOUR NAME HERE
    Pain Sufferer

    Please visit these sites for reliable information on intractable pain:
    American Pain Foundation: www.painfoundation.org
    Intractable Pain Authority-Dr. Forest Tennant: www.foresttennant.com
    Intractable Pain Disease Site: www.intractablepaindisease.com

    Have YOUR letter to share? Include it below! Have a link to the videos? We'd love to see them too. :)

    Friday, February 19, 2010

    Pain Medication Accessibility for the Underinsured

    by Heather Grace

    Many people with chronic or intractable pain have a very hard time getting the medications they need for their very survival. It's a huge issue and though the government is trying to help the uninsured/underinsured, chances are, the very ill will not be helped by such a plan.

    Why? As most pain patients know, it's already happening under all current insurance plans. And, it happens frequently. Anyone who depends on large quantities of medication that are often quite costly is likely to have issues with ANY insurance plan.

    Insurers will delay or worse, deny coverage altogether. Many question the need for such medications, and it becomes a huge war between the insurer and the insured, with the doctors in the middle, trying desperately to ensure their patients survive.

    With all of this going on, ThePainStore.com is trying to do its part to help those in need. If you are currently having problems with your insurance company, or you don't have adequate coverage, there are several places you can look to for assistance.

    Please see our web site for the full details on the many programs available: Pain Patients: Access to Prescriptions.

    There are plans offered by specific pharmaceutical companies, as well as prescription assistance organizations. Additionally, there are prescription savings cards offered by many groups.

    Need to see someone right away? Visit the Free/Low-Cost Health Clinic Finder.

    If you are in California and have a serious illness, but cannot seem to get insurance through normal channels, there is a plan that may help. Get the details on the California Major Risk Medical Insurance Program.

    Also, we welcome you to share your experiences with us! Have experience with these plans? Tell us! Got recommendations for other plans we should add here? Please post them now! Have issues with getting the medication you need? Please share them with us -- right here on our blog. Thanks everyone!

    Thursday, December 17, 2009

    Keep Your Job or Find A New One: Surviving Pain While You Work!

    by Heather Grace

    Being in constant, severe pain while trying to keep a brave face is hard. Sometimes, it feels like Mission Impossible. The difficulty is multiplied exponentially when you are expected to perform as you normally do, throughout your daily routine. The big question is: When your pain is at its worst and you are forced to work your regular 40+ hour work week, how do you cope?

    My Story
    Coping isn't easy. Unless you have resources to help you survive, you just sort of muddle through. I've been there, on auto-pilot just trying to make it from one day to the next. I suffered in silence (well, mostly in silence), working in pain from late 1999 through July, 2004 when I was unceremoniously laid off.

    Despite excruciating headaches and the pain that raged from my spine to my extremities, I did my best at work, as I always did. Because I was my usual loyal self, I didn't want to let anyone down. I didn't want to disappoint anyone or appear weak. Being in a male-dominated field increased the pressure I put on myself. And when I was injured, I reasoned to myself as well as to others that sitting home wasn't going to change my condition. Even with the pain, I continued to be productive.

    When you are trying to keep it together and the pressure gets less and less tolerable, how do you know when to say 'when?' It's just not easy to know when to throw in the towel, even when working becomes completely overwhelming.

    Admittedly, part of the reason I continued to work was purely out of fear. I didn't know how I was going to survive without a job. The pressure only increased when I was awaiting two surgeries: a second nerve surgery on my arm and surgery on the severely bulging disc in my upper spine. As soon as I found out, I told my boss. Big mistake.

    It became obvious I was being looked at closely by upper management. We had recently been bought by a large multinational conglomerate. Gone was the family atmosphere that I had become accustomed to. Suddenly, there was an intense amount of pressure on me. I was accused of things I didn't do, and didn't even get an apology when the truth came out! It seemed they were waiting with bated breath for me to fail, even as I continued giving them my blood, sweat and tears. In the end, it didn't matter. They let me go, anyway.

    The day I was laid off seemed like the worst day of my life. How would I survive? Pay my way? Because of the pain and the uncertainty that came with it, the last few years of my life had already been a roller-coaster.

    The pain was bad enough--not only was it constant, but it seemed to be getting more intense. My emotions were so near the surface these days, crying came far too easily. This only increased when I realized everything I owned was probably going to have to be given up. It's amazing how attached I had become to having my own home, to having nice things. At the same time, I would've gladly given up everything if I could just be whole again. A big part of me wished, hoped, prayed...wanted an answer. A miracle. The cure.

    But, there wasn't one.

    Finally, in early 2007, I found a doctor that helped me see my future. I had thought for so long that I didn't have one. 'Pain management' never sounded good to me, but soon, I was living it

    It actually felt good to be able to manage my pain. I spent each day trying to minimize activities that hurt, and maximize things that bring me any degree of happiness. Laughter is a serious gift. Even smiles are! Being able to go back to work has been hard, but I am thankful every day that I am capable of doing so. It still amazes me--I had been so certain I would never again be able to work!

    Yes, it hurts. Yes, it is work just to keep my pain somewhat in check. I use amino acids, vitamins and supplements of all kinds, because they work!

    In addition, I've learned to monitor my body and accept my limitations. I watch my blood pressure and pulse, any numbness or other nerve issues. I know when to say when. I know my body better than I ever did before. And, it's a joy! Being productive; doing something other than sitting/laying around all day--that is a true gift. I have recently realized that working full-time is no longer an option. This is something I have had to wrestle with for SEVERAL years in order to accept it. However, I am finding ways to keep active despite the challenges I face.

    So, how can YOU make it work? There are many tools that you can use -- things that I have tried and have found helpful:

    #1: Slow and Steady
    Try to give yourself plenty of time to do things that make your daily routine easier. If you work outside the home, be sure to plan your day wisely. If you are less rushed, there is less reason to add stress to your day unnecessarily.

    For me, I find it very important to get up, then give myself time to relax in my favorite chair and plan out my day. I also use that time to take care of the things that need to get done at home. As I sit there, I go over what I need to accomplish before that day, where I need to go, what I will wear, what I will take with me, etc. Once I have gotten things all planned out, I act.

    Sometimes, when I am extra-stressed or maybe even over-tired, I spend that planning time in bed, making sure I press the 'snooze' button, as I lay there and plan, think, and maybe even drift back to sleep for a few more minutes. It's a relaxing way to start the day, and something I have come to rely on, in order to make it work.

    #2. Pain Management
    Managing the pain is my ever-present goal. For me, while I am planning out my day, I sometimes start to feel pain before it is time for my morning meds. So, I may find it necessary to take something for 'break-through pain' (BTP).

    Often, it is one of my prescription meds, combined with two non-prescription meds: ibuprofen and Excedrin, as well as amino acids like Taurine and GABA. Combining the prescription medication with these over-the-counter items allow the medication to work better. (If you read the handbook on finding a good pain doctor, you can learn more about this option, called a "potentiator.")

    Focusing on pain management throughout your day will help ensure a much easier experience at your job. It might take time to find the perfect regimen for you, but I promise, when you do, it will feel like a true miracle!

    #3. Eating Right: Protein and Fiber are Required
    Planning out proper meals is vitally important to anyone with chronic or intractable pain. In addition to a morning meal with lots of protein and a decent amount of fiber, you need to ensure high protein snacks are available, whether you are at home, on the job, or somewhere on-the-go.

    I always make sure I take my morning meds, then ensure I have my lunch as well as several snacks with me if I will be away from hom. Each of my meals and snacks (as often as possible) has an excellent balance of protein and fiber, along with other ingredients.

    Pain patients need lots of protein in order to reduce pain naturally. (Learn more about this in the handbook referenced above, as well as the Intractable Pain Patient's handbook.)

    You will also find, that most opioid-based pain relievers have a constipating effect. If you don't eat lots of fiber, believe me, you'll regret it later. Fresh fruit and vegetables are very good for you, when possible. Try an apple or perhaps some broccoli dipped in low-fat ranch dressing. Also, an easier snack is dried fruit and nuts (aka trail mix) and/or, certain energy bars, when it comes to fiber AND protein. Check your labels!

    In the summer months, I often try to start the day with a protein shake, complete with some nice frozen berries and other seasonal fruit (tasty and fiber-rich!). A cold smoothie-like shake, with soy or whey protein powder (my fave is vanilla whey protein by Body Fortress--1/2 scoop is 13 grams of protein), makes for an excellent breakfast drink! Use your choice of regular milk/soy milk, water, yogurt or any combo of those, to your desired smoothie consistency.

    Want to have another smoothie later in the day? Try freezing them. Then, put one in the fridge in the AM to use around lunchtime. Or, try a frozen alternative! If you use lots yogurt in your smoothies, they are actually not too frozen to eat like a freezer-based treat. But unlike your typical frozen yogurt or sorbet, you have a dessert packed with protein and fiber! YYUUUUMMM!

    #4: Coping with a Busy and/or Stressful Day - Your Arsenal of Options
    Today's world is so busy, even for people in pain. The world doesn't stop turning when you are having a hard day!

    On days when I am either too busy to take care of myself properly, or on days when I am rushing all over the place, doing lots of moving, it's important to have an arsenal of items to help reduce the incidence of pain.

    In addition to ensuring you have your meds with you (I've forgotten them before and am forced to go back and get them, ugh!) at ALL TIMES, make sure your fave pain relief items are at your disposal. ThePainStore.com has lots of great topical pain relief options.

    I have had wonderful success with pain sprays, which are now my absolute favorite choice. Not only does the smell dissipate quickly, there is less risk of any staining or mess to your clothing. Additionally, it's INSTANT relief to tense muscles. Yes! Try this: take your Biofreeze, StoPain Spray or My Omega and put a small amount in a travel-size spray bottle. Then pack it with your regular work stuff. It's EXCELLENT!

    What else is good for the pain? I like Tiger Balm and most of the OTC pain patches, such as Salon Pas and Tiger Balm's patches. They are great when you have pain in a specific area... the patches/gels/sprays go to work and relieve pain over a period of time. Definitely makes the work day easier.

    #5: Focus on Why It's a Good Day--Today!
    What else can be done? A huge part of coping is also just letting go of the negativity around you. Don't get caught up in the way life used to be, or in focusing on the bad things that have happened. Let go of all of that, and focus on the good in your life: right now, today. Be positive and live in the now--it makes dealing with the rough days that much easier!

    Believe me, I know how hard it can be... Yes, I used to have X, Y, or Z. But, I can say with conviction that I didn't appreciate those things as much as I should have. Now, I can appreciate the little things in life that I truly never even noticed before. The past should stay in the past, where it belongs, as much as possible.

    I also control any unnecessary negativity, preventing it from invading my daily life. For instance, I don't keep up with the local or national news, because I know it will only try to zero in on some invented reality--a new pseudo-crisis that I don't want to know about. Gangs, drugs, illness, poverty... yes, I know they exist and I am sad that they do. But, the way the media can put this hyper-focus on the BAD things that are going on isn't good for anyone! I focus on what is going on in MY reality, MY life.

    The hardship going on in other places, to other people, is really not a positive way to spend my time. Thinking of things like this that trigger negativity in you. Get rid of those things. You don't need them!

    Maybe the nightly news or CNN.com are just too much for you these days. Skip them. You are in control of your world.

    You decide what images come into you world and if you're like me, you choose to watch funny movies, inspiring true stories, creative unique independent films, etc. I am in control of my life in a way I never was before, and that is how I cope. I know what I need and what is best, and I try to live each day keeping my focus on the here and now--on MY here and now.

    There's no reason you can't do that, too. You'll never realize how depressing the news is until you free yourself from it! It's truly liberating and makes coping with the realities of YOUR life that much easier. And, a lot can be said for comic relief. Yes, pain is a SERIOUS condition. But, watching a good comedy--one that makes you really laugh--goes a long way in keeping you thinking positively!

    #6 Find Meaning, Because Work Doesn't Have to be a 4-Letter Word!
    Let's face it, work can be a real pain in the rear! Not every day is going to be easy, or fun. Many times, you will wish you were anywhere but there. (Even before you had pain, chances are, you felt this way!)

    So, what can you do to make your work day more enjoyable? Do something you enjoy doing! Work at a company you believe in, or work with people you like being around. It will do wonders for your pain if you can at least have some fun while you're at work. I have been trying my best to do something I believe in, with my whole heart and soul.

    Launching ThePainStore.com has been very meaningful to me, because it allows me to help others manage their pain. I also spend time assisting my favorite doctor in his office, with patients, assisting in both front and back office procedures. I file, copy, make phone calls, gather charts, ensure we have copies of test results, put together special pain creams made to the doctor's specs... whatever is needed for the patients that day.

    It makes me genuine happy to help people--especially new patients that were once like me. In pain, scared, not sure they could ever feel 'normal' again. Working in that office, knowing the good that is done there, it brings me incredible joy.

    So, think long and hard and make it a goal to find the right place for you... What can you do, that has meaning for you?

    And, I know what you might be thinking... Now is not exactly the best time to be changing jobs, so if you have something secure, why not find a way to look at it differently?

    I once heard the story of a gentleman who worked in the Maintenance Department at NASA. He essentially swept floors--keeping the place spotless for 25 years. Whenever someone would ask him what he did, he would say proudly, "I help Astronauts in the Space Program." He could've just as easily said, "I am 'just' a Janitor," but because he had a healthy, positive perspective, what he did had meaning for him. Even if he never took flight himself, he was a proud member of the team that made it happen.

    What can you do to put a healthy spin on your perspective?

    #7 Volunteerism - Meaningful Work for Others Also Helps You
    Many employers are working with charitable organizations these days. It not only boosts employee morale, but it provides a nice tax write-off for the organization as well.

    Even if your company isn't doing so now, find ways to incorporate charity into what you already do. Is there extra of your product that could be donated? Is there a service you might be able to provide to charitable groups? Almost every company has old or outdated equipment, such as computers, fax machines, cell phones, etc, that may be donated to a charity instead of being disposed of. Anything that is still has a useful life can be transformed from 'waste' to a donation. By integrating volunteerism into a company, it can be beneficial on many levels, and most companies are grateful for the tax incentives!

    Even if volunteerism through your employer isn't an option, it might be an option to consider in your off time. If you have the ability to help others, it brightens your day and somehow, you don't notice the pain as much.

    For those who can no longer work, volunteerism can bolster your self-esteem while you help someone less fortunate. No matter your circumstance, there are always those who have things harder, who need help that you can offer.

    Seek out people you can help, and get busy! :) Even if it's about sharing your support over the phone or Internet, you CAN and WILL make a difference, in a way that works for YOU!

    #8 Just Getting Back to Work? Where To Begin...
    Is there a specific 501c3 government-approved nonprofit group that you admire? Maybe they have a need for volunteer assistance, or even part-time help that pays you a little something.

    If you've been in so much pain thus far that you haven't been able to work, consider starting back at a nonprofit. There are lots of nonprofit jobs out there, just 'Google' it, and find one that suits you. It's a good place to start if you're not sure what you want to do.

    If you are doing something you are proud of, it makes you feel good, while helping others. And, the best part is the positive feeling you get--even in spite of whatever else you may be dealing with. I have always found things easier to do if they have meaning for me. As they say, "Do what you love and you will never 'work' a day in your life."

    I now live it, so I know it is true. I don't think of it as a job, but as an opportunity--to help others while I continue to reinforce what works for me. Not every day is easy, but the positive aspects definitely outweigh the pain.

    And, since I would be in pain no matter what I do, I might as well do something that makes me feel good in other ways, right?

    Give it a try, and you'll feel it too.

    #9 Share Your Story - Make Others Understand
    There is nothing worse in life than feeling alone and misunderstood. In order to have a decent experience at work, share your story with the people you know well and trust on the job.

    Let them know what you are going through, the emotions involved, why it is so hard. Tell them how it is different than a regular old 'boo-boo' -- print out information on your diagnosis from a trusted resource, if need be.

    Not only will they be understanding, they can offer you support and maybe even some advice. They will also feel better about stepping in if you have to take a day off, or are having a tough day and need a break. Keeping it all inside may seem like the best thing to do, especially in jobs where gossip is rampant, but if you have people on your side, that kind of thing won't matter so much, will it?

    And, as hard as it may be, it's definitely a good idea to work with your doctor on what to tell HR. I would recommend having your physician explain your condition in writing. Then, meet with the people you need to at work, clarifying with HR/your boss how your condition impacts you, that it is a disability, etc. That way it is on record, in case you need time off or certain accommodations. All of this helps protect you, under the law.

    Had I not been so afraid to tell someone in HR about what was going on, perhaps I wouldn't have dealt with so much obvious discrimination by upper management at my job. As illegal as it is, believe me, it happens more often than you would think. Protect yourself!

    #10 Never Give Up!
    I cannot stress this enough... Never give up. I think that's the most important thing I can tell anyone who is dealing with pain and having a very hard time with it. You may not have very decent pain management yet. You may be going through periods of anxiety, pain, anger, depression...the feeling of hopelessness that tends to coincide with your life being turned upside down.

    But I promise you, inner strength is what will get you through this. Find that inner strength, that resolve, the tenacity that's helped you deal with your pain thus far. Read everything you can get your hands on, find out what works for others. Use your common sense along with good old-fashioned 'trial and error' to come up with the best possible protocol for you. Working with a good doctor, of course, will make this easier.

    New options are coming available all the time. There are pharmaceuticals in development, centuries old options that are being studied/used/understood, items being imported from other countries and utilized, and even new tests to understand the genetics behind severe pain and thus, in time, what can be done about it.

    I found my miracle -- pain management. And, now I am back to work. No, it's not a regular 40-hour a week 'day job' but I am doing something positive, for myself. And, I have lots of ideas and plans for the future. I am not allowing my disease to take over... I struggle with it, but I am confident I can muddle through. Surviving 10+ years with pain has made me stronger than I ever thought possible!

    I never thought I'd be so happy about working, but believe me, I am thankful, every day. You can get there, too. :) Good luck!

    Sunday, August 2, 2009

    The Benefits of Pain Sprays For Persistent Pain - Treating Pain On-The-Go

    by Heather Grace

    As a long-time pain sufferer, any product that seems too good to be true leaves me skeptical... as it should. I have dealt with severe, chronic pain for over 10 years and was diagnosed two years ago with Intractable Pain (IP). For those of you who don't know what that means, I am in pain nearly all day, every day. I have neurological problems, headaches, and suffer a host of side effects that are not at all pleasant. (You can read more about IP here.)

    I have tried everything. Physical therapy, biofeedback, EMS/TENS, ultrasound, massage, chiropractic care, spinal injections/nerve blocks, accupuncture/accupressure, prescription medication and yes, even surgery. I have also fallen pray to the promises of many over-the-counter products that promise pain relief:

    A whole host of vitamins, supplements and nonprescription medication. Patches that either fall off mid-use OR stick too well thus hurting and/or leaving areas of redness/broken skin when you attempt to take them off. Hot packs, cold packs--combination hot/cold packs...packs that you can attach to here or there on your body. Then there's the creams: smelly creams, greasy creams, creams that stain, some that do all of the above! Ugh.

    When you don't know what you're looking for, not only do you spend a lot of money needlessly; you end up becoming a guinea pig, desperately searching for adequate pain management. Sure, some things work a little, help a little, make life a little easier. But most are a huge waste of money!

    Then, two years ago I found the answer... a pain clinic with a caring doctor that knows what works and what doesn't. Imagine that! Thanks to him, I have narrowed my search, using the nonprescription items that he has tested with his own patient population, to ensure effectiveness.

    He even put out a wonderful handbook earlier this year, called "What To Do While Looking For A GOOD Pain Doctor." Get your FREE copy here.

    Since then, I have found what works for me, and have had enough pain relief to go from sitting around/laying around, in such ercruitiating pain that I couldn't do much else -- to launching THIS VERY SITE in order to help others. It may not seem like much to you, but for me, it's been THE miracle of all miracles!

    Then, this past Christmas, I received a present from Dr. T--a pain spray. Sure, I was skeptical. But, after a few sprays, the headache I had melted away--I was SMILING. It was magical. RELIEF! Instantly! Like nothing I had ever tried. Sure, other things had worked for me. But not so quickly. Not like this!

    So, here in this blog, I will detail the three pain sprays I believe in most. I will tell you what makes each one special, which one I like most and why, and give you the links to purchase them, should you wish to try them for yourself. If not, please try to find them locally--it's worth the effort, because they are WONDERFUL!



    ThePainStore.com's OFFICIAL REVIEWS:
    The Absolute BEST Topical Pain Sprays




    My #2 Choice of 4 oz Pain Relievers: Biofreeze

    Having never tried a pain spray before, Biofreeze amazed me. I had a horrific headache, getting caught in traffic on the way to my doctor's office. He presented the bottle of Biofreeze to me as a Christmas present! It was by far the best present I got for Christmas 2008! My headache lessened, I instantly felt better. For a chronic pain sufferer, that's pretty powerful!

    Biofreeze is very popular, and because of it's use mainly in clinics, it's harder to get, and as such, is also one of the more expensive sprays. Is it worth the price? Absolutely! Are the other options? Sure, we carry two. Biofreeze is unique in that it contains Ilex and several herbal extracts not used in other products. I love it! Sprays at any angle and the relief lasts for up to two hours. It's wonderful!

    Gets 4.5 out of 5 stars, and is ThePainStore.com's #2 choice for 4 oz pain sprays. It would be PERFECTION if only it was easier to get, and was slightly less expensive!

    My #1 Choice of 4 oz Pain Sprays: StoPain

    StoPain is our top pick for 4 oz pain sprays! It's effective for instant relief of headaches with no medication needed, which is a true miracle for me! I cannot imagine life without pain sprays anymore.

    Compares to Biofreeze and I would say it's hard to distinguish between the two. Contains 8% menthol compared to Biofreeze's 10%. Definitely less expensive! Sprays at any angle and the relief lasts for up to two hours. It's wonderful!

    Because of it's price and the fact that it's much easier to use, StoPain is ThePainStore.com's official choice for #1 Pain Spray, 4 oz Size.

    Note that right now it's even less expensive: StoPain has graciously provided ThePainStore.com with a limited supply of $2 rebate forms. With purchase, you will receive this rebate, and get an even better deal on your first purchase of StoPain, thru Dec 31, 2009! (Limit one rebate per person or address.)

    DRUMROLL PLEASE...
    My #1 Choice of ALL Pain Sprays: MyOmega

    MyOmega gets voted #1 because it provides instant pain relief, but more than that, the relief lasts! MyOmega has time-released Ice Pearls that keep the menthol penetrating into your muscles, continuing your pain management for longer than any other pain spray I've used.

    The first pain spray I ever tried was Biofreeze, which was exceptional, however, I have been swayed by MyOmega. Not only do you get TWICE the amount (8 oz instead of Biofreeze's 4) for just a few dollars more, but you get more menthol and a more lasting relief!

    It's not just our #1 Best Pain Spray, it is by far our bestseller... our #1 Topical.

    So, get our most highly recommended pain relief spray today--you won't be disappointed! Treats muscle pain, headaches, even sprains or strains, and inflammation too! You will be pleasantly surprised by this product. It's true targeted pain relief in a spray. More than that, it's a 5-star product! You will feel better in seconds. It's a miracle in a can -- I keep pain spray with me wherever I go!

    The Best Topicals on ThePainStore.com -- Targeted Pain Relief Sprays:
  • MyOmega - #1 Pain Spray
  • StoPain - #1 Pain Spray, 4 oz Size
  • Biofreezze - #2 Pain Spray, 4 oz Size
  • Saturday, June 13, 2009

    The FDA is Trying to Regulate Opioids - Why We Must Fight It!

    by Heather Grace

    Here's my letter to the FDA regarding their new attempt to control opioids, with their 'Risk Evaluation and Mitigation Strategies.' Visit the site and make your own comments NOW: http://www.regulations.gov/fdmspublic/component/main?main=DocketDetail&d=FDA-2009-N-0143. Deadline: June 30, 2009.

    RE Docket No. FDA-2009-N-0143:

    While I choose to have some faith in the FDA, and believe that they are attempting to help people by setting up these REMS, the idea is ill-conceived. To develop Risk Evaluation and Mitigation Strategies for certain opioid drugs assumes that the FDA has better knowledge about the patient than their treating physician does. I am sure when the people who drafted the REMS got together, it sounded like a good idea, but really, it is not that simple.

    It is more than impractical--it is impossible to have the government control the dispensing of certain medications, and then truly make those medications available freely to those who need them.

    Anyone who knows even a little about pain management understands how complex it is. Any pain patient, any good pain management physician will state unequivocally, there is no recipe for success in treating pain. There is no black and white diagnostic standard.

    While some people suffer one short bout of chronic pain, lasting little over 90 days and then they get better, there are also many serious pain sufferers, with very serious diagnoses.

    A doctor may have certain preferences about what he tries with a patient, and what she/he feels works well. After the first line treatment, she/he may try other options, other combinations, until a patient is stabilized and the pain is being effectively managed. As we all know, the ultimate goal is to get the patient back to some semblance of a normal life, where daily activities are possible, without excruciating pain limiting one to a bed-bound or couch-bound state.

    Physicians are often limited by what a patient’s prescription plan will cover, so that, too, impacts what is prescribed. However, sometimes patients are faced with the issue of either getting proper pain management and going broke, paying out of pocket for things that aren’t covered, or accepting a lesser medication, that involves lesser pain relief.

    There are already so many stumbling blocks for patients trying to find relief. I would hate to see the government further regulate the process, thus making it more difficult for people who are plagued by pain, and already have a very hard life.

    There is a huge distinction between simple chronic pain and a diagnosis of Intractable Pain. Do you realize what Intractable Pain really means? Someone on the outside really doesn’t know what it looks like, or how it feels. It’s really impossible to understand the agony. If you have never experienced any sort of serious injury, count yourself lucky. Intractable Pain literally means pain that never goes away. Daily pain. Hourly pain. Minute-by-minute clock-watching, excruciating ‘will it ever end, dear God, please’ pain.

    The official definition, according to IntractablePainDisease.com: "A severe, constant pain that is not curable by any known means and which causes a bed or house-bound state... Intractable Pain (IP) has four outstanding characteristics: (1) constant, (2) severe, (3) disabling, and (4) causes detectable biologic impacts on the body's blood pressure, pulse rate, hormone levels, and neurologic systems. It should be considered a serious catastrophic condition that, inadequately treated, leads to premature death. Some of its complications include dementia, osteoporosis, muscle wasting, obesity, and cardiovascular disease."

    For people who live it, trust me, life is already plenty difficult. To make it any harder, would truly be an injustice. REMS would endanger the lives of anyone with IP or a similar diagnosis.

    I urge the FDA to first, get a better understanding of what Intractable Pain and its related diagnoses, means to the people dealing with it. Meet with an expert, someone like Forest Tennant, M.D., Dr.PH, who can accurately lead you through IP and its challenges. I am confident that patients with severe chronic pain/IP are in good hands with physicians like Dr. Tennant. Why?

    A physician with effective knowledge of pain management has many tools available, regarding assessment of one’s pain management. She/he can assess the patient’s overall affect, as well as their ability to function as they did prior to injury. The doctor may use simple in-office tests, such as blood pressure and pulse rates, their gait and speech, to gauge a patient’s current pain level. She/he may also rely on blood tests that show how well a patient metabolizes medication, thus further justifying a patient’s need for high-dose opioid therapy.

    Though some are new, there are many ways to understand why patients need the medications they need. There are clear-cut tests to show how effective their medications are. Therefore, I do not see a need for government intervention.

    The REMS states that it intends to ensure that the benefits of these drugs continue to outweigh certain risks. I believe there is a serious danger in trying to establish a need for medication within the concrete walls of an institution, instead of by the warm hands of the treating physician, where there is the full gambit of a patient’s history: their MRIs, CT scans, X-rays, blood work, physical examination, blood pressure and pulse rates.

    Death by overdose is a rare occurrence. It is not something that happens frequently when a patient is being accurately monitored and treated by a responsible physician who truly knows their history, knows their pain, and understands the patient's prescribing needs. Only a knowledgeable pain doctor can truly mitigate the risks of these drugs, on a case-by-case basis.

    To quote Dr. Forest Tennant, M.D., Dr.PH. in The Intractable Pain Patient's Handbook for Survival: “The biggest problem an Intractable Pain (IP) patient faces for survival is that a bona fide IP patient is a rarity among chronic pain patients... Control of IP requires the daily use of prescription medication. I estimate that one IP case occurs among about every thousand chronic pain patients. Due to IP's rarity, almost every doctor, insurance plan, hospital, or family member you encounter will initially assume you are just another, average, chronic pain patient who can get by with the standard firstline treatments such as exercise, positive mental attitude, acupuncture, massage, and non-prescription drugs. To survive, you will constantly have to fight this misconception, and you must educate most of the people you encounter.

    “IP patients all require a custom-made, one-of-a-kind treatment plan. Most physicians and other medical personnel you encounter may be bewildered and even fearful of your treatment, because they may not have encountered another patient with your pain severity.”

    Dr. Tennant’s handbook further cautions those with IP to understand that pain is their enemy: “Your IP is long-standing, constant, keeps you from sleeping, drives up your pulse rate and blood pressure, and alters your adrenal hormone levels. You must remember that your pain is your enemy. To cause it to worsen or flare for any reason may do further damage to nerves and other body tissues that are already permanently damaged.

    “Your attitude about pain must change. Increased pain hurts you. When the pain flares, your pulse rate increases, and hormones stored in your adrenal gland flood your system causing further body deterioration, rusting, and aging.

    “Therefore, you MUST do whatever it takes to suppress your pain and prevent flare-ups. You simply want to keep pain as far away and as controlled as possible. Never try to ‘work through it’ or ‘tough it out’ or believe that character and will power will solve your problem.”

    Dr. Tennant has extensively studied Cardiac Adrenal Pain Syndrome – a serious threat to IP patients. Pain control is vital to survival, and to have uncontrolled pain creates a serious risk of damage to the heart, and even death. DEATH.

    REMS is a serious threat to pain patients. Such regulation, ironically, could lead to death, due to uncontrolled pain. If the goal is to reduce deaths, then why on earth would you keep treatment from those who genuinely need it, for their very survival?

    I hope you will understand, based on the many concerned citizens who have reached out to you, that the REMS program is not going to work. It wasn’t well-conceived or thought through. It may work for certain patients, but it would prove a huge detriment to those who suffer with conditions like Intractable Pain. I wish there was an easy answer. Believe me, it would make so many lives easier. But, because there is not a quick fix, the FDA should not further involve themselves in the treatment of patients, because they simply have no business trying to ‘protect’ people when they don’t fully understand the treatment of pain.

    Like many others, I have done what I can to help the pain community. I have worked with many pain patients as well as pain management doctors. I offer products to help make lives easier.

    Like many of those utilizing my site, I suffer with Intractable Pain. Unless you know someone with IP, or you treat patients with IP, you cannot possibly understand the difficulty in treating these patients and finding a regimen that will work for them. We already live much shorter lives than the rest of the world. Why make the time we have here any harder?

    Please stop trying to regulate pain medication. It’s simply too complex for a government agency to control without seriously harming its citizens.

    Most Sincerely,
    Heather Grace
    ThePainStore.com
    & Intractable Pain ‘Survivor’