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jackD
Perhaps processed form of Salajjit is safe for pwMS but commercial raw form needs to be taken with care http://health.indiamart.com/ayurveda/ay ... -herb.html

How has been your experience

Please see that Sillajit is high in iron content which may be bad for persons with CCSVI. Anybody with MS who has tried Sillajit, please comment.

Peanut3636 Great to hear a serviceman serving his nation with MS. I am also one of you but not in US. Since diagnosis, I am trying to cope up with demanding tasks of the service and by the Grace of God, I have disappointed none due to my stable state. I do want to ask about you especially once you a...

Hi Folks, any body taking Lisinopril or Hydrazaline for MS and has good results. Please share

Hello I have suffered from writers cramp (focal dystonia) for last fifteen years before my diagnosis of MS. I never knew that the writing difficulty, I was experiencing is actually a neurological condition. Lately I have come to know that many persons without MS also suffer from this disease. Is MS ...

MS and other autoimmune diseases including Hypothyroidism are said to be closely linked. Although no direct link between these two diseases has been established, I was just wondering how many pwMS are also diagnosed with Hypothyroidism. Your input would be greatly appreciated.

John My suggestions are 1. Immediately start taking LDN (Low Dose Neltrexone) 2. Check for CCSVI 3. Go for chiropractic treatment and check your spinal alignment especially Atlas since it all began after that minor accident 4. Get yourself checked again thru MRI after six months on LDN and after hav...

Imscared Tensions and anxieties can result in so many unexplained phenomenon. I think u need to relax first. If u see a problem, obviously you need to see a doc lol 8) . Please see that apart from MS, there could so many other things which could result into what u have said. I think simple blood inv...

Brad It looks like you do not have any symptoms related to MS right now which is a good news. Please see that as per my neuro, MS cannot be diagnosed on VEP and MRIs alone or even on one single episode of attack. The lesions which show on MRI show demylination which could be because of so many reaso...

rmanta I also suggest that you should consult a good doc and get your baseline levels checked which also include B-12 Level. Make sure, your doc must be in knowledge of all diseases which could mimic MS including Lyme. Get a list from net and show him, if necessary. If upper limbs are issues, I sugg...

Hi Laowai I am not in China but living close by in Pakistan. I had done some research on TCM treatment for MS and it indicated that Chinese medicine by the name of Ping Fu Tang had some success once given to 30 patients. Please see this link www.itmonline.org/arts/msalsmg.htm. From your post, it see...

My right hand started showing signs of heaviness and writing difficulties fifteen years before my diagnosis. During the MS attack in Dec 2008, I experienced heavy itching on the same hand to the point of bleeding due to scratching at night. My right hand feels better once I change my posture. I chec...

Interesting topic. Many of us still wonder why and how it happened. In my case, I found out that I have extended styloid passing near jugulars ( called Eagle Syndrome) plus I had an accident nearly 16 years before which caused compression in neck and possibly Upper Cervical misalignment (not diagnos...

Leonard Good Research. But have u ever thought why MS is most prevalent in some areas and not uniformly distributed around the globe. Then there is a gender difference also (more in women than men). Lately, people now disclose that even there minors have MS who do not get exposed to stress in life l...

I had numbness in feet once my herniated disc in lumber area was really bad. After physiotherapy and exercise, it got much better.collms did u get your lumber checked thru mri