This Is MS Multiple Sclerosis Knowledge & Support Community

"Human upgrade device"

THX1138 - Thanks for the info re: Mg oil. Can you recommend a product available online? Jimmylegs - I don't know what his Mg serum status is. I was thinking of ordering an online micronutrient test ( https://www.spectracell.com/patients/patient-micronutrient-testing/) so as to determine if there are...

I am amazed that, it appears, I am the only one who has used Mg oil. Anyone use it ???? Does it help with spasticity? My old man has been having terrible spasticity at night lately (legs bending up seemingly from the hips so that the knees move toward the torso) and I am wondering if this might hel...

Does anyone use one?

Have any experience with them?

Asking on behalf of someone who is having a more and more difficult time getting from bed to scooter, scooter to toilet etc.

Why not post a You Tube or other similar internet video showing what the device is, how to make it and how to use it? Agreed. You have made multiple posts with basically this same description of your "device". Gristy - if your aim is to help other people with MS, why not make a video? Si ...

ElliotB wrote:I have asked before, can you please post instructions and/or a video on how to build a Multiiple Sclerosis 'Desatascador'.

I echo this sentiment.

Make a video!!!

https://www.ncbi.nlm.nih.gov/pubmed/27354653

Anyone have any thoughts on this study / this GcMAF substance?

Updates, anyone?

If you scroll down, there is a whole sub-forum for this protocol.

The answers you seek are probably therein.

I believe it's because a large amount of calcium can accumulate (hypercalcemia) in the body when taking high levels of Vitamin D.

I've heard some second hand accounts (from Brazil, seemingly) of people with "more aggressive MS (did not explicitly state SP or PP)" using this program. So what I'm wondering is whether you (persons with SPMS or PPMS) have personally used the protocol. Or if you have direct contact with a...

Let me rephrase: what form of MS were you diagnosed with?

Your diagnosis?

Does anyone find that remaining in a fasted state results in reduced symptom severity? And conversely, does anyone find that eating exacerbates symptoms (more weakness, difficulty in transferring)? I am simply trying to determine why this is the case for someone I know and which foods in particular ...

I am wondering whether anyone on here (specifically those with primary progressive MS) have experimented with any of the following for psychological benefits (i.e. coming to terms with death):

-LSD
-Psylocybin (magic mushrooms)
-DMT

Please, no lectures about legality.