Received mnd/als dx in dec/2015. Began in spring 2015 during tennis and bike ridingwith left foot drop and gait and balance problems and fatigue. After seeing multiple docs, went to neurologist, had EMG kand was told I had mnd. At that point was using cross country sticks to help with balance...
Hi,
Have anyone tried this machine to stimulate the muscles? I bought it couple weeks ago and have currently used it for my legs. I did some searches for a word "Stimulator" in this forum and found some old threads back in year 2012. According to PALS, these machines didn't help to keep the...
Hydroxytyrosol is a phenylethanoid, a type of phenolic phytochemical with antioxidant properties in vitro. In nature, hydroxytyrosol is found in olive leaf and olive oil, in the form of its elenolic acid ester oleuropein and, especially after degradation, in its plain form(***wiki)...
I got 3 month supply of Simplesa-Deanna Protocol from Simplesa company in june 2015. It expire 2018. I have to sell it bc my Father no longer needs it. He was diagnosed too late and died in July of 2015. It's never been used of opened. Brand new, price $307 for 1 month supply. Free shipping.
Hi All,
The latest I've read has tended to center around NO (Nitric Oxide) being bad for PALS. So when I see some of the ingredients in the DP several of them seem to promote the production of NO (AAKG, Arginine, etc...).
What am I missing here?
Or put another way, what would be the general...
Happy New Year everyone,
As some of you know my husband was diagnosed with ALS 3/2014 and given the standard 2-5 years to live. It is still unbelievable now even after 9 months. He is 32 years old. Now, not that this horrible disease has a specific mold, race, type, age or look...I would just...
I'm not sure about it and would like to know what you all think about it.
Here it is...
December 16, 2014
Dear ALS Fighters and Families:
There is an opportunity for us to expand WFND’S current therapy program for PALS (People with ALS) and to totally stop ALS progression. Although...
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Have not posted here previously, although I have been trolling. I was diagnosed with ALS officially on July 14th of this year. So......Hello.
It seems to me to be slow moving, I'm not taking any drugs at this time, although I'm using copious amounts of amino acids - L -Serene, coconut oil...