Treatments for ALS
🧐 Research Wanted 🤔
Hello frens. Seeking any advice regarding ALS treatments.
My friend was just diagnosed with ALS. I knew something was up, they hadn't been right, movements have been getting slower. Now, the onset has become rapid. I have little knowledge in regards to treatments. Are there things out there that doctors won't recommend or fall outside of the big pharma scope?
Everything I've read is that it's a death sentence and an awful progression. I feel terrible for them. 😔
I took care of someone with ALS for years and learned quite a bit. It is heartbreaking, no question. Person I cared for did not believe it mattered what he consumed. Moust be no diet soft drinks, no refined sugar, and do the parasite protocol w iver and fenben, 5 days with both, repeat in 3 weeks then again. Take when full moon is occuring. (Paradites are most active) This is very very important because there are indications that ALS and MS are parasitic involvements. Is your friend vaxxed? If so they need the full protocol. Including blocking spike protein with the nicotine 7mg patch worn daily for awhile. Listen to Dr. Ardis.
Thank you for the info. I'm not sure on the vaxxed part, but probably. I've already seen so many health issues with friends and co-workers after the vaxx. MS was one of them.
Nicotine is very addictive. I would be careful of Dr. Ardis and his claims of nicotine as a cure all of many diseases. Of note he is a chiropractor. Just my opinion.
Accidentally cured my lifelong chronic migraines when I started self-medicating my ADHD with 7mg nicotine patches every day
I wonder if that would work for my grandson. 11 years old ADHD affecting his school and behavior. He is small for his age, 60 pounds skinny.