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I think I have fibromyalgia.I am not sure where to go to get diagnosed.My history: In 2000-diagnosed (ER) with a Migraine. In 2004-had a terrible headache(temporalForehead lift Temporal arteritis Temporal lobe seizure).Went to ER again. This time diagnosed with a sinus infection(ct scan).Was given high dose of antibiotics in ER for 10 days.1 week later, Tinnitus started-still have it. Also in 2004, diagnosed with depression. Psychiatrist put me on Lexapro.I thought the depression was d/t certain situations,loss of job and tinnitus.Also went to counseling. 2005- diagnosed with hypothyroidism. PrimaryPrimary amyloidosis Primary biliary cirrhosis Primary hyperparathyroidism Primary insomnia Primary lymphoma of the brain put me on low dose(0.5 mg)of synthroid. Early 2006-went off lexapro(got a job, still have tinnitus).In June, diagnosed with GERD, taking prilosecPrilosec Prilosec otc. Also been having off and neck pain in 2006.August-had terrible flu like symtoms with severe muscle weakness in my legs and tingling in my hands and feet.Was hospitalized for 5 days. Had an EMG(negative)a spinal tap(negative)and many blood tests(negative).I had an MRI of my head and neck. MRI showed a small nodule on my thyroid. Then,went for an ultrasound and a thyroid scan. My primary sent me to a Endo Dr.He diagnosed me with Hiroshimos disease and I am now taking 1 mg of synthroid daily since November.I am now experiencing terrible brain fog, neck pain off and on,sinus pressure and nasal drainage,middle and lower back pain off and on and I feel very depressed. My mother has fibromyalgia.I am not sure where to go next.I don't think going to my primary is the best bet.He minimizes things. I am afraid that he will just call it the flu or a virus.I need some advise on my next step-Thanks.
Well, your symp's definitely sound like FMS, also similar to CFS/CFIDS, Lyme, and other autoimmune diseases.
I highly recommend looking into the Marshall Protocol (MP), a curative therapy for people with autoimmune diseases/symptoms, you don't have to have an actual diagnosis, in fact the MP has hundreds of members who searched for years for help and always told they were fine. Here are some good links to check into for starters:
"What is the Marshall Protocol": http://www.marshallprotocol.com/forum2/4213.html
"Is the MP an applicable treatment for my disease?" http://www.marshallprotocol.com/forum32/1263.html
Then on their main page: marshallprotocol.com, look up the many different articles under the headings: "Essential Information about the MP" & "Marshall Protocol FAQ's"
This link is really interesting, check the list of symptoms of Th1 inflammation, "Hypervitaminosis-D Symptoms" http://www.marshallprotocol.com/forum2/2588.html
Here is a good website for Fibromyalgia: http://fmnetnews.com
But please check into the Marshall Protocol. And keep us posted!
See a RA for a diagnosis. That is a Rheumatoid Arthritis doctor. They also take care of other autoimmune disorders. Look up Rheumatolgy in your phone book yellow pages. Also check out what the last poster said.
Hi, I am from the Anxiety forum and I am just lurking around different sites and I read your post. I know that you said that you were once on Lexapro and was diagnosed with depression, but have gotten off the meds for that. However, a lot of your symptoms (tinnitis, tingling, pain in neck, fatigue, etc.) can also be symptoms of anxiety and depression. I suggest that you post your question on the Anxiety Forum and see what responses you get. There are many well-informed people who post on the sight who may be able to help you and give you some suggestions. Hope this helps.
this might sound kooky, but ... are you in your 30s or 40s? if so, you might have developed celiac disease. it is a digestive disease that can have symptoms including migraine, sinus, pain, fatigue, brain fog, GERD. it's often mistaken for fibro. just a thought. a gastroenterologist would dx it.
I highly recommend looking into the Marshall Protocol (MP), a curative therapy for people with autoimmune diseases/symptoms, you don't have to have an actual diagnosis, in fact the MP has hundreds of members who searched for years for help and always told they were fine. Here are some good links to check into for starters:
"What is the Marshall Protocol": http://www.marshallprotocol.com/forum2/4213.html
"Is the MP an applicable treatment for my disease?" http://www.marshallprotocol.com/forum32/1263.html
Then on their main page: marshallprotocol.com, look up the many different articles under the headings: "Essential Information about the MP" & "Marshall Protocol FAQ's"
This link is really interesting, check the list of symptoms of Th1 inflammation, "Hypervitaminosis-D Symptoms" http://www.marshallprotocol.com/forum2/2588.html
Here is a good website for Fibromyalgia: http://fmnetnews.com
But please check into the Marshall Protocol. And keep us posted!
Thank you