This Is MS Multiple Sclerosis Knowledge & Support Community

I use a non invasive medical device that increases blood flow to the entire body and brings oxygen to the cells through a engineered specific wave that stimulates the capillaries. It helps me a lot with fatigue and mobility and has helped my quality of life.

We have the technology now for better blood flow. Personally, I am using and helping people use a new non-invasive bio-energy mat for blood flow for home use. It looks like a mat with a computer. There is a multi-faceted energetic wave that stimulates the micro-vessels and brings oxygen to the entir...

I can only wear "keens" hiking boots. I like the Detroit Utility boot. It is not for drop foot, but has given me the most comfort and support.

Yes. Feet are freezing and only a hot bath will worm them. Usually happens at sunset.

Upper Cervical is definitely working for me. Totally effective. I can walk better and heat intolerance is better. I decided to go with it after CCSVI. I also have an MS physical therapist who it awesome. Trying to deal with MS from 3 fronts and it seems to be a working combo.

Yes. My feet are freezing. The only thing to get them back are hot baths and using my magnets helps.

Dear Cheerleader,

A very interesting and enlightening idea. I will look at the book maybe.

Thanks,

Kinora

Hello, I can not look at the computer for extended periods and can not reasearch the science, but has anyone made the connnection between CCSVI and Chlamydia Pneumonia? I see a relationship. http://www.CPn Help.org/thoughts_appertaining_ccs http://www.cdc.gov/ncidod/eid/vol4no4/campbell.htm http://w...

The first week I took Avonex, I felt psychotic. I have not taken CRABS for over 5 years. I can't say that I am doing great, but those injectables freaked me out. Copaxone left lumps in me, to this day and ate my tissue. Beware new users, they really do not tell you about the tissue wasting.