Strange News Stories

Friday, May 22nd, 2009

Fibromyalgia Treatment

Fibromyalgia – One Out of Every 73 Americans is Affected. How to treat?

A short while ago I wrote about hope in treating fibromyalgia and that some physicians did not believe it a legitimate syndrome. I received a few unkind words about it as if it were my own private stance. Well, I am trying again. However, I advocate not to shooting the messenger. I just put together what I find and report it to you as impartial information. It is not a white paper on my position. With that said, I move ahead. However, I understand that is very difficult to be dispassionate when you are in pain and feel no one can help or cares.

There are many new treatments for fibromyalgia. Some work and some don’t. Not every treatment will help everyone, or do so in an equivalent manner. Some may not be helped at all. That is the nature of disease and medicine. Some people improve with time only.

This is a difficult disease to treat. As time has progressed, more physicians, therapists and patients are aware of its existence as a syndrome and its symptomtology. After all, one out of every 73 Americans is affected. The team approach for therapy is probably the most effective. A patient must be pro-active in her approach. Compliance must be high. The patient must be responsible in following the plan, taking the medications ordered and obtaining therapy as needed.

Although many general practitioners are becoming familiar with the problem, one should probably obtain a consultation in a pain management clinic where all the expertise is centralized. You need remember, this is the site where the physicians and therapist are who have the greatest experience in caring for patients with this disease.

The clinic will give each patients their own personal regimen. An active exercise program is desirable and can be very therapeutic. Resistance exercises are effective in increasing strength. Aerobic exercises also lead to improvement. But patient compliance can deteriorate quickly. If one can walk or garden or just get out and do something, one has a chance of improvement. This can start as a minimal program and increased in activity as the patient progresses. It is also important to use physical therapy with massage or skin cooling techniques. The use of ethyl chloride spray over trigger points is usually very effective. Other alternative therapies to consider are chiropractic and acupuncture.

Behavior modification is also suggested. Here, hypnosis can be used to induce relaxation, pain Free states and meditation. Stress avoidance skills and new coping activities may be learned. If one can avoid stress, a primary inciting factor, one can lessen the pain of the disease.

Multiple types of drugs have been used with varying degrees of success. In some low dose anti-depressants may help with pain and sleep. Combination therapy with Prozac and Elavil are more helpful than when used alone. Unfortunately, some experience more side effects or the symptoms become worse. Minor analgesics can be used successfully in some but are ineffective. One must consider chronic opioid treatment if pain is intractable. However, this has its own significant problems and side effects. Others suggest trying human growth hormone.

This summarizes current therapy. Hopefully, one of them can assist you in feeling better.

13 Responses to “Fibromyalgia Treatment”

Simply Ridiculous Says:

Yeah.. Resistance exercise is more effective than drugs..

Dear Simply Ridiculous, From an FM Sufferer: Says:

They didn’t indicate at any point that resistance exercise is more effective than drugs. They simply said that resistance exercise helps to increase strength, which is helpful because it causes the body to strain less, thus lowering the stress levels on your muscles.

dawn Says:

fibromyalgia was invented by doctors who don’t have the time to find the true diagnosis so instead of saying, “it’s just nerves” like they used to, they now say, “you have fibromyalgia” meanwhile sick people are walking around not knowing what they truly have & conversely how to treat it.

Melly Says:

I disagree with the figure of 1 out of every 73 people. Many people have it and are undiagnosed, and women get it more often then men. I have to take painkillers, or I couldn’t function. Marijuana works good too. It’s hard to exercise when your body feels like it got run over by a Mack truck.

dseesred Says:

another not so familiar therapy and possible underlying cause is hypothyroidism. Or at the very least, thyroid hormone not functioning in the body as it should (where thyroid levels are adequate but not getting to brain and/or muscle tissue for use.) There is alot of information about this treatment and therapy in the book, The Thyroid Solution. For those that struggle with this disease, just another piece of the very complicated puzzle.

Cindy Says:

I spent 25 years of my life with debilitating Fibromyalgia and Chronic Fatigue, which my doctors said I would just have to learn to live with. That wasn’t good enough for me! Through much research on the internet and through medical journal articles, I was able to glean helpful knowledge that I have applied to my life. I have spent the last 25 years researching and have succeeded in overcoming 19 symptoms that had stolen my health for 25 years! I no longer struggle with ANY symptoms I had before and am currently training and preparing for an IRONGIRL TRIATHALON in July of 2010. How great it is to feel human again! I have become Certified in teaching low glycemic weight management and through my classes I help people to eat healthy (which is all part of a healthy lifestyle for anyone) and also how to apply principles of natural health in order to help them overcome
their health issues, too. It’s so exciting!

sharon Says:

I have severe CFIDS and FM. For pain nothing but Ultracet has worked for me. For my best friend with severe primary FM only heavy duty narcotics help reduce the pain to about an 8 on the scale of one to ten. She is now on Methadone and feeling much better. We both have tried everything suggested and really, only the meds have helped take the pain down. Down but never gone.
Also, although we are glad that FM is finally recognized as a real disease, it has also become a “garbage can” for doctors who can’t come up with other diagnoses. So, if you sort of fit the criteria for FM, that’s what they dump on you. I strongly suggest ruling everything out including the thyroid. Yes, FM is common but I think one out of 73 people is just a bit too high a number.

Lilian Says:

http://sacfs.asn.au/download/consensus_overview_fms.pdf

and

PROLOTHERAPY..

it works……………….!

Gwen Says:

I agree with Melly. Definately a lot more woman have FM and men also get it. I belive that the location as where you live in this country has a lot to do with higher numbers of folks with FM. I live on the east coast/ Cape Cod area and more woman than not have fibro. We have nasty cold winters that effect the pain Then we have rainy damp spring and half of the summer and that affects people with FM. When summer hits it comes on so hard that your body cannot adjust to the rapid change and we have more pain. I have been dealing with FM for over 30 years now and hydrotherapy, massage,acunture puncture helped for the first 15 years. Now it is so bad that i am lucky if I have 2 good days out of seven. If I were not on strong narcotics I would not be able to get out of bed, take a bath, and dress myself.

Linda Says:

I’am still trying to live with Fibro.It has cheated me and my love ones out of there Wife, Mother, Grandma. I’ve had it for some time now. and it is no fun.I’am taking Morphine twice aday. And it keeps alot of the pain away. I still can work, but there are day’s you don’t even want to get out of bed.

Linda Says:

i hope that soon they will come up with some kind of pill or a drink of some kind that will put our pain on hold. Or maybe get rid of the pain altogether. Excerise is great, but I found out that the next day or two was hell to pay. I do alot of walking and gardening.
I also found out that our location in Oregon, plays alot into my pain. We have alot of wet and cold weather.

Mike Brewer Says:

I spend most all my time as a Mentor to veterans with PTSD. The number of wives of vets who have been diagnosed with PTSD who have fibromyalgia is overwhelming. This is the stuff of epidemiology and the NIH. I think it is time for the Veterans Administration to conduct some research in their ranks.

Gwen Says:

I’m writing this in refrence to the person who said they were on morphine for Fibro. I was on morphinr for about 8 years, I was very miserable. I was on Kadian which is morphine in a time released capsul. Because I am on medicare and medicade I was told in January of this year that my perscription was no longer covered and I would have to change to the regular MS/morphine sulfate. Some folks with FM cannot tolarate a lot of meds. Due to the IBS I cannot break down the coating on the regular morphine. My Dr. changed me over to the Fetynal patch. It by passes your stomache all together.
This past week I read an artical on how Morphine has no effect on FM because folks with FM have CNS problems and it does not attach to the receptors in the brains pain signal system.
The article also stated that controlled tests on subjects with FM had great pain improvement with marijuana because it can attach it self to pain receptors in the brain.
As a 30 year FM/SLE patient most of my life sucks. I have more off days then days of acomplishment. I would be totally disabilitated without the Fetynal and marijuana. Marijuana works best in small doses so you do not build up a tollerance to it. I suggest 1 good joint smoked at 3 intervals a day, morning, midafternoon, and about 9PM.

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