God Bless Scientists who devote their Gifts to understanding and improving health!

I have fibromyalgia. This talk has helped me more than other doctors I have watched.

10 years still no help shame on this world!! Thanks so much for this ❤ bless all the loving kind souls X

I want Elliott on my team! Brilliant research

Dr. Frohman explains things so well; patients should know, he truly cares! Great video!

Good talk! Medical MS centers should have videos of this. Playing and sale or given

Excellent video

Because there isn't one yet for MS . I CAN'T HANDLE HEAT OR COLD.

Finest talk on MS I have watched to date. Tons of useful information if you want to understand what is going on in your body and take some action. Thanks for posting this.

Oh WOW!! Great Info!! I suffer terribly!!

Just great man. Thank you from belgium

Your video most helpful!

My heat intolerance vanished with a round of steroids. That was 7 yrs ago.

When I had MS-like symptoms, one of it was waking up (in some mornings) seeing blurred image with my left eye. I tried to put cold compress, warm compress, tea compress on my eye.. nothing worked. I tried to make eyes-exercises, massage the skin around the eye, take supplements (magnesium, calcium, vitamins, beta carotene) nothing worked. I thought that I have something in my eye.. but I didn't. Well.. since I feel better, I never had this again.. So.. it was really an MS-like symptom.

Interesting because im both heat and cold intolerant and have dysautonomia and thought that was my reason for having these symptoms. Lately with using my home furnace, im having horrible hot flushing surges, am beyond menopause and its becoming very bothersome. Also ive become heat intolerant during hot summers in the midwest. Odd stabbing nerve pains in my head and feet, and growing issues with the "hug" that is horribly uncomfortable. Beginning to think I need to be tested for MS to at least rule it out. Im a Sjogrens patient with Fibromyalgia, severe osteoarthritis, and like I said earlier dysautonomia recognized as Neuro Cardiogenic Syncope which in itself can be debilitating. You mention this loss of leg use in heat and I also experience this. Ive had the nerve conduction in my legs to test for MS but it was negative. Often Sjogrens patients do develop MS. I guess I need to see a neurologist again. Crossing my fingers that I dont have MS.

Someone can say that Stem cell treatment isn't good, but not in my case. In MS treatment clinic belgrade I find all what I was need. I am able to walk up and down stairs without a cane after treatment.

Core body temperature raises half a degree celsius and it causes all your MS symptoms to hit at once tenfold!! And even cause new symptoms!! Which aren't really knew they just weren't severe enough to notice!! 🤪💪

I am told I have Fibromyalgia. Yet the symptoms have progressed over the years. I have flares that keep me in bed for days. I have no choice but to push through. I have both heat and cold intolerance. I have Raynaud's in,both my hands and feet. This past winter I had frost bite. My muscles ache. I get cramps, aching, numbness and tingling that is rarely severe. Occipital headaches, swelling of hands and feet in the mornings with pain. Etc, etc...... I don't know that I have ever actually had an MRI of the brain. If so, it has been years. Is it possible that I have a "degree" of MS that hasn't been diagnosed? I do take Neurontin, Methotrexate, Baclofen, etc...... With sporadic treatment with Kenalog, Solumedrol, etc....usually these help for a while. This time, the treatment did not fully take away the pain, numbness and tingling. 😕

I'm very much into Holistic and encourage everyone with ms to get 2 books by Kathryn R Simpson called "The MS Solution", and an Adrenal Fatigue book. Well, I went to a very good Naturopath who has me on the very things (2 and they are cheap and natural) in the book. I am slowly starting to feel better and it's been 8 days. It's just common sense.

I use hyperbaric oxygen therapy and Isagenix for my M.S. and feel free to ask me about them. DX MS 2000 -- Christina

Where is this

Southwestern where

I'm researching reducing ms at home and found a great website at Denelle multi care (google it if you're interested)

This is not always true .I have been living with ms since 1976 . Matter of fact I do landscaping for a living ! And I can't stand to be in the house . I must be in the sun . I hurt in the cold and the heat makes my body feel better .

Thermal regulating is awful.....night times are the worst......

hyperbaric doesnt work,,talk about it as you get older,