I have all of the MS symtoms even my brain mri states that there is a possibilty of demyliation however, I was recently diagnosed from one nerologist with demylation and from another fybramalgy(spelling). What seems to be the problem with being able to diagnose this disease it seems that the prolonging of not being able to get diagnose feels like I'm getting the wrong treatment.
Wow. This could be my story.
I have been diagnosed with everything you can imagine due to chronic muscle pain, spasms and weakness.
I have had brain MRI's, EMG's, Provoked visual, hearing and response test, spinal tap and blood work. My neuro is convinced I have MS but he says he cannot find anything to prove it. Sound like you?
I also worry about the fact that I am getting worse with time instead of better and if they could prove it is MS (if it is) I could be treated to delay the symptoms.
One of my diagnosis has been Fibromyalgia. I cannot believe Fibro can be this severe and painful. Maybe its my ignorance, I don't know.
What symptoms are you having? Do you have tender spots? I was tested at either 15/15 or 18/18 I can't remember which number they calculated it at. Even my scalp is sore to the touch. Do you have this too?
One thing I have discovered...I am seriously low on Vit D. I have been given a high dosage and while it doesn't help my pain so much it does make me feel better both mentally and physically.
I have been diagnosed with everything you can imagine due to chronic muscle pain, spasms and weakness.
I have had brain MRI's, EMG's, Provoked visual, hearing and response test, spinal tap and blood work. My neuro is convinced I have MS but he says he cannot find anything to prove it. Sound like you?
I also worry about the fact that I am getting worse with time instead of better and if they could prove it is MS (if it is) I could be treated to delay the symptoms.
One of my diagnosis has been Fibromyalgia. I cannot believe Fibro can be this severe and painful. Maybe its my ignorance, I don't know.
What symptoms are you having? Do you have tender spots? I was tested at either 15/15 or 18/18 I can't remember which number they calculated it at. Even my scalp is sore to the touch. Do you have this too?
One thing I have discovered...I am seriously low on Vit D. I have been given a high dosage and while it doesn't help my pain so much it does make me feel better both mentally and physically.
It feels good that I am not alone......my neuro said the same thing! I lost feelings of my left side and the dr. stated that I suffer from chronigical migrane with stroke like symptoms. I am in a wheel chair and have to use a walker and getting therapy to.....I am telling my family there is no such diagnose as that! I have also been diagnose with cluster headaches. I am so tired of being poked on and everthing.... 4 doctors stated that it look likd I have ms but that can't diagnose me either! I have cried, argue and prayed! It's has been a nightmare!