That’s wonderful. We’re so happy for you.God Bless!!NSMM
can you please text me what supplements you were on and how much of each you were taking.i dont know were to startmaybe his might help me along with the good Lord..thank you and God bless..
Hi, my name is Valeri Pavlov, I'm 39 and I was diagnosed with ALS in 2018, my symptoms started in 2017. Since then I keep fighting with these horrible disease. I may have lime and co-infections,and some viruses, bartonela and babesia. I have tried 24 months protocol with antibiotics and anti-virus drugs without success. Now I go every week on acupuncture, do some exercise and take supplements- parasite clean,Cat's claw, golden seal root,curcumin,vitamin C,vitamins B, Q10, magnesium, cistus tea,detox tea. Can you please send me an email what other supplements do you take and how (morning/evning, before/after meal), and any other advice that can help me to take care of my son.
hello I am recently diagnosed with AlS 01/20/22.it started with my left limb weakness, now It has moved to my right hand.does anyone know a good dictation app the one my computer is lousy. anyway, i am looking for a support group? i want to learn how to beat this disease
Hello, my husband 54 years old physically fit man was recently diagnosed (although we are told there is no Clinical Diagnosis) with PLS. Originally we thought his inability to walk was from a back issue to which he had surgery in 2020 after surgery he lost complete ability to walk with a walking device. Drs chalked it up to his spinal nerve just taking long to heal (which was never the case). I know this is an ALS site but according to everything I’m reading PLS is a form of ALS so I’m not sure why Drs wouldn’t treat both the same? A friend of ours told us about your story and it inspired me to reach out. My husband has been followed a Neurologist for Movement Disorders here in NYC and going for all the tests, & just this Monday we went to a top Dr in Columbia Presbyterian Medical center for PLS/Parkinson’s but after evaluating my husband & his test results he basically dismissed us apologized told us because PLS is not a Clinical Diagnosed Disease, there is no treatment or anything he can do for my husband other than taking the muscle stiffness medication he’s already taking. Please if there is anyway any suggestions or even lead us to a Dr that might be able to help or knows more we are willing to travel or try anything. At this point why not try what is helping treat with ALS.
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