All these flare ups while LDN?

[Guest guest]

I have been watching this group for a while now and I see quite a few

posts... seems like at least one or more per week from people

experiencing exascerbations of their MS or minor flare ups of past

symptoms. The answer always seems to be poor diet or lack of

supplements. I have been considering LDN but seeing as how I am barely

mobile now. Need a wheelchair to go out, stairlifts to get around my

house and a walker around the house more often than I actually use it.

I am afraid that I cannot afford any set backs or worsening of my

symptoms. My MS has been stable ever since they figured out I was not

having exascerbations when I was ending up in the hospital but rather I

was having seizure problems from epilepsy that the doctors are saying

was caused by the lesions and scarring of my brain left behind from

past exascerbations of this wonderful disease.

Is there any hard facts from a medical research study of what

percentage of people with MS on LDN have setbacks when they first start

on LDN?