Link Between Multiple Sclerosis and Autism
If you google the two conditions together you will see an interesting trend of articles and studies. Those studies are mostly about parents with MS having children with autism. This suggests a link they are currently studying, but have no distinct answers on yet.
My own conditions have been getting progressively worse over the years. I fatigue faster, lose coordination a lot, have trouble forming words and speaking, and I have increasing random tremors that are more like lightning jolts. Autism isn’t particularly know for being a progressive condition. So what’s the difference?
I found this information about the nerve effects of the two conditions:
MS is a degeneration of protective layers around nerve endings, eventually leading to progressive nerve damage.
Autism is a developmental disorder of the nerves themselves.
So, from those two descriptions, it’s entirely possible to start out with Aspergers or some other form of autism and develop MS later on. Like Autism, MS can have profusely different effects on each person. It’s another broad spectrum with a hundred million combinations.
In any case, I am sitting on a possible MS diagnosis. That’s why I’m researching it to learn what the possibilities are and what I can do about it. No, I can’t stop it from happening, but knowledge is power. If I have to live with this condition, I want to know as much about it as possible. I see the neurologist this month.
I find the connection thought provoking to say the least. There are connections being drawn to Alzheimer’s and Parkinson’s as well. Is there a common root to link them all? If so, how do you find it? It must be like finding a specific needle in a stack of needles as big as the proverbial haystack.
I was living with MS for years before being officially diagnosed in 2021. I got annual MRIs, and I did not take any meds due to side effects. I had one flare up in 2021. My legs decided to a break, and I was numb from the waist down. I decided to try MS-4 from Uine Health Centre. The numbness and Muscle spasms went away after a couple of weeks, but it took almost 3 months to walk properly without a cane. In June, it will be four years without incident, and I am extremely happy that I made the decision to not take any meds and went for the MS-4 formula even though my neurologist got upset and one told me to quit my job because I will be disabled. Well, I am not disabled, I still refuse to take those meds, and I am doing just fine. Believe in yourself and go with your instincts. Doctors don’t know it all. I’m surprised a lot of people with MS haven’t heard of the MS-4 protocol, I got the treatment from uinehealth centre I am absolutely confident that this protocol offers a viable solution. I hope you find it helpful.
Sending you prayers, I was diagnosed in 2010 and seemed to go down hill quickly. In six years I could no longer work and had real problems with balance and joint pain. Brain fog was really bad sometimes. I took rebif and had a lot of problems and had to quit. I have been on techfadera (not spelled right) for a few years and have several side effects. I felt lost and decided to quit my meds due to side effects. Our care provider introduced me to Ayurvedic treatment. I had a total decline of all symptoms including vision problems, numbness and others. Sometimes, i totally forget i ever had MS. Visit Natural Herbs Centre web-site I am very pleased with this treatment. I eat well, sleep well and exercise regularly. God bless all MS Warriors
link between multiple sclerosis and autism
How about vaccines? Have you ever had the Hep B vaccine?