Fibromyalgia treatment research
Common Questions and Answers about Fibromyalgia treatment research
fibromyalgia
I am more hopeful than ever that soon there will be more answers for the cause and treatment of Fibromyalgia. Very informative article. Thank you.
Updates in Diagnosis and Treatment in Fibromyalgia and CFS videos:
http://www.offerutah.org/Dr.%20Lucinda%20Bateman%20-%202008%20Conference.htm ---------- “Updates in Diagnosis and Treatment of CFS” by Lucinda Batemen, MD, director of the Fatigue Consultation Clinic in Salt Lake City
http://www.offerutah.org/nleesmith.htm ----------“Updates in Diagnosis and Treatment of FM” by Dr.
http://www.medhelp.org/health_pages/Fibromyalgia/The-Latest-Research-on-Fibromyalgia/show/520?cid=39
Be sure to keep checking for more information.... some of the research is posted on a research website for mostly medical professionals. It is the best way to stay informed and make sure that your physician is informed.
IMO --- In my opinion = )
I'm not sure why my link was deleted. If you would like to check out my website, please check out my profile. I do post all of the latest fibro & CFS treatment plans (recommended by the experts). A lot of these treatment plans include supplements and that is something that many physicians do not prescribe for their patients.
widespread pain, disturbed sleep, and exhaustion from head to toe
shortness of breath, numbness and tingling sensations, muscle weakness
I get pain in my neck, like muscle stiffness and that comes and goes
leg cramping, fatigue, trembling nausea
I also had weakness in the left arm, pain and numbness as well
I was suffering from migraines and one had caused an anxiety attack
Fatigue, muscle weakness, trembling muscles, some muscle spasms, cramping in my right calf, tingling in hands feet and
i have fibromyalgia amongst other complaints.fro about 2 years i have had a swollen abdomen-lumpy and tender which progressed to sore and protruding ribs.have had ct and mri scans which gave no clues.doctors seem to ignore symptons,now i have a feeling of tightness around my ribs and am sore all around them.it feels like ribs are digging in me.
my heart goes out to people who have fibro not diagnosed correctly and in severe pain continously...is is too soon to hope time will change and fibromyalgia suffers will get the medical treatment they need....good post. thanks for sharing it...
I went thru 48 months of treatment developed fibromyalgia and worsened joint and bone pain. I have lost a lot of dexterity in my hands and fingers don't have a lot of feeling at the tips, but that's from the treatment. Pre-treatment I had a lot of winter arthritis-like pain in my joints and hands. Don't know if this helps, but I'm new to this forum. Wish I'd seen it when I was on treatment.
I work at a private research site that does multi-specialty research, and it would seem that people would be interested in participating in a study that offers a totally novel drug for fibromyalgia, in its last phases of research before it hits the market. however, we are having difficulty finding patients and I was wondering if this is partly due to fibro patients having negative experiences with doctors. anyone?
Since we have conditions that are relatively new and often misunderstood in the medical field, there are many members here who do their research and share that information with the other members.
You have been prescribed the standard treatment method for your situation; if there are newer treatment options your Oncologist would be the best source of this information. Treatment plans are formulated specifically for each patient based on the complete history and Pathology of their cancer. Regards ....
I research fibromyalgia because I have it and I am a site leader on another site constantly. My husband has Crohn's disease along with other things that go with it but he is allergic to Remicade. I have never seen anywhere that Remicade was used for fibromyalgia or CFS/ME.
I had only once tested my hbsag quantity since my diagnosis two years ago. The test was done a few weeks ago and came out about 17000iu/ml. In other words quite high, that should warrant treatment immediately, in my opinion, though my dumb doctors won't put me on treatment yet. But I'm going to fight them and insist that I need antiviral treatment.
At first she said I had RA, which would explain my joint pain and low white blood cell count, but now she says I have Fibromyalgia because the tests for RA came back negative and my hands don't look like RA hands. I tried to tell her from the research I've done I can have sero-negative RA which would mean that I would be less likely to have the nodules she is looking for but doctor's know best apparently.
I've been suffering from random pain AKA fibromyalgia since 2012 and after few years of research and dozens of tests & visits to doctors in 3 different countries I found the treatment that worked in my case and in several other cases. I now want to share my findings with you.
What/Symptoms: chronic random pain and odd sensations all over or throughout the body AKA fibromyalgia
More about these symptoms you may read in a previous post
https://www.medhelp.
Two years ago I came down with a mild flu which I passed onto my mother, at the end of it's duration we both ended up with Fibromyalgia, did my mother catch Fibro from me or is it just a co-incidence and seeing as we got it from a virus should we both get tested for the XMRV virus
I found this new research by Dr. Catherine M.Pittman - one of the foremost brain researchers in the country, to be interesting.
We are finding through both animal and human research that the medication class of benzodiazepines may actually prevent learning, both neuronal and cognitive and may prevent long term anxiety recovery. Our work has shown that the neuronal process for learning and also the process for unlearning (called extinction) is slowed or prevented by this class of medications.
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