For about the past year, I've slowly developed debilitating symptoms in my hands, feet and face. I've seen 7 different doctors now (2 GPs, rheumatologist, neurologist, cardiologist, chiropractor, ENT) and have had a slew of tests performed, and I still haven't received any concrete diagnosis for my symptoms. Recently, I was diagnosed with Fibromyalgia, but my rheumatologist doesn't think that the numbness and constant lightheadedness I'm experiencing are normal symptoms. I also have been diagnosed with TMJ, very mild scoliosis, and a moderate misalignment in my lower back. The times I start to have these symptoms is if I am walking, driving, standing, exercising, or using the computer. If i'm lying in bed or sitting in a comfortable chair, I'm fine. I don't get tingling in my arms or complete numbness, but rather just a general lack of sensation. I also start to feel "separated" from my body; I'll feel very lightheaded and have severe spatial distortion, so my body feels detached from me, and I have a difficult time judging the distance of things. Sometimes the lightheadedness will get so bad that I'll start to develop "tunnel vision", where I have a hard time registering things peripherally, and I feel like I'm about to pass out. My right arm (and strangely, only my right arm) will start to feel "heavy", and if I look at it, it will feel like it's not my arm--even though I know it is. Despite all of these symptoms, I haven't developed any weakness in my limbs or lack of coordination. I've had 2 CT scans done, a slew of blood tests, and X-rays on my back and head, and everything has come back normal. The only thing I can think of at this point is that there is maybe some kind of nerve problem being caused by the misalignment in my lower back--but I would think my chiropractor would have seen that in the X-rays. Does anyone with back problems (or anyone at all) experience these symptoms, or have any idea what it could be?
It all started in my jaw. They said I had TMJ. I had arthroscopy done, had a mouth splint made, had my mouth stretched. It did not help.
I went to doctor after doctor, physical therapy, chiro, spent thousands of dollars. Quit going for awhile because I got so frustrated.
Decided to go to a well known ortho surgeon about 3 yrs ago. He performed anterior cervical disc fusion on C-5, C-6.
Once again it did not help! It only made matters worse.
Then I got right back on the treadmill, starting to get second opinions, therapy, etc. No diagnosis nor cure.
I recently went to a rheumotologist who diagnosed Fibromyalgia, Raynaud's. My GP says it's a combination of things...the above mentioned and RSD caused from the neck surgery.
The really sad part for me is I had to give up my job several years ago ( I had 30 yrs in!) because the pain is so debilitating. I cannot get Soc Sec Disability because as most people know in some medical profressional eyes these diagnosis are bogus.
All the doctor's want to do is try meds on me that absolutely make me sick! I cannot take Cymbalta, Lyrica, ect.
I decided if no medical proffesional could help me I would just try to help myself.
I started doing a low impact treadmill workout for 30 min every other day. I started taking (prescribed by rheumo) Magnesium 300mg and Vit D 15,000 untis 2x's a week.
I went for my first massage therapy. The therapist told me to take a bath in cider vinegar...today was my first experience with that.
Anyway I'm sorry this is so long...but I just wanted you to know you are not alone! (After a while everyone makes you think your psycho).
I haven't yet found anything that has helped me but I am still searching. I know that somewhere, someway there has to be a logical explanation. If not I'll have to learn to live with it and do the best I can.
Let me know how things turn out.
Best of health.
For me it seems that when I exercise things get worst and I get dizzy. Do any of you have the same thing after exercising?
I have been working at a computer for over 20 years. I think that my neck is very weak. I recently tried progesterone and it is helping.
If you can get testosterone it will also help heal. Then I work out and it builds muscle much quicker. You need that to keep your body in shape. I also tried prolotherapy in Chicago to tighten up my ligaments.
Don't give up..
Stretch - magnesium, maybe a good nerve pill for the times you need it most!
I also think it's due to too much estrogen in our bodies that loosens us up and causes all these goofy symptoms.
I found a solution for my condition though and today I am back to normal. There were 3 basic pieces to it.
-Avoid the things that were major contributors to the problem (for me, mouse and keyboard - I now only use a touchpad)
-Active Release techniques from a trained physical therapist
and the biggest part
-Changing my work chair to a zero-gravity recliner. Good ones are available for about $200.
Sitting in the zero gravity chair, I believe, allowed my body to correct the condition over time, on it's own. It took a few months.
Do we have anything in common? I am mostly vegetarian. I eat lots of nuts, beans, brown rice, quinoa, spinach, tomatoes, peppers, soy, some fish. Late 40's - no menopause yet. Really bad fibroids. Normal weight, bp and blood sugar, some arthritis in my joints. Gluten intolerant too. I have allergies and athsma and use inhaler sometimes. German, Scandanavian and Italian descent.
Maybe with so many of us having the same issues we can find some commonality between us - something we're eating, not eating. Something we're doing, something we all suffer from in addition to the funky symptoms. If anyone finds common ground with my post, please share, thanks!
Do we have anything in common? I am mostly vegetarian. I eat lots of nuts, beans, brown rice, quinoa, spinach, tomatoes, peppers, soy, some fish. Late 40's - no menopause yet. Really bad fibroids. Normal weight, bp and blood sugar, some arthritis in my joints. Gluten intolerant too. I have allergies and athsma and use inhaler sometimes. German, Scandanavian and Italian descent. Desk job - work at the computer most of the day.
Maybe with so many of us having the same issues we can find some commonality between us - something we're eating, not eating. Something we're doing, something we all suffer from in addition to the funky symptoms. If anyone finds common ground with my post, please share, thanks!