Experiences with

Amyotrophic lateral sclerosis (ALS)

Written by Dr Matthew CL Phillips (clinical researcher on world’s first RCTs of low fat vs low carb diets in Parkinson’s and Alzheimer’s, and case studies in ALS and Huntington’s) and world’s leading mitochondria expert Dr Martin Picard.

usp=drive_link This campaign has the possibility to surpass the Ice Bucket Challenge for ALS, which created increased understanding and support so much so, that researchers have created two new drugs to treat ALS and believe there will be a cure in a few years time.

This "chicken and egg" question occurred to me while reading an interesting article [1] concerning Amyotrophic Lateral Sclerosis (ALS). I also saw parallels with some aspects of PD research.

Any experience with this would be greatly appreciated as it's probably the most annoying symptom out of them all, but als seems the most stubborn to leave :)

utm_source=PAR&utm_campaign=c732d6332f-Email_ENL_US_PAR&utm_medium=email&utm_term=0_62dd4fb5e3-c732d6332f-74556474 I have been trying to find out what is used to prepare Klotho gene therapy a therapy that supposedly could be used for Parkinson's, Alzheimers and ALS "Initial data suggest that maintaining

Hat jemand die Sanazon-Therapie als Teil ihrer OC-Behandlung ausprobiert? Ich habe es getan und es hat wirklich gut funktioniert. Ich bin auf der Suche nach Frauen, die das auch ausprobiert haben - ich kann nicht die Einzige sein! Du kannst mich ja auf Deutsch oder Englisch antworten.

Because I’ll soon die for ALS, which is no cure, no hope, I realize how PCa is so special and much more worrisome. Had I make the good choices, what a troublesome question! With ALS, one quickly dies, no questions, no hope, no disappointment.

Scroll down to the heading, "Vitamin B12 levels and MND/ALS". https://jmedicalcasereports.biomedcentral.com/articles/10.1186/1752-1947-4-298

After seeing 6 different (so called) nurologists who diagnosed me with ALS. I finally saw a 7th and 8th at Penn who understood my disease as MS. As of today, I am wheelchair bound and have lost most left side function. I get mild to severe vertigo.

Several neurodegenerative diseases (NDs), such as epilepsy, Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease (HD), and amyotrophic lateral sclerosis (ALS), which feature chronic progressive damage to the nervous system, have been proven to be tightly connected with nutrient availability

I AM ALS is initiating Cures for All, to unify the broader neurodegenerative community. I'm very happy to witness this paradigm shift. SE

[u][i]Alkaline phosphatase [/i][/u] It is an enzyme released as a response to injury to the bile ducts - not the liver itself. As more cells are injured, the more alk phos is released. Alk phos is not in itself harmful. Higher levels in the blood does not mean more tissue damage. Even lowering

How is everyone doing lately with their PBC? For some of us, the temps are cooler - maybe helping with less itching. Do you feel you are still living life as best you can despite any of the symptoms that may occur unexpectedly in your day? We all have PBC so differently, don't we? I hope you all try

[u][i]"upper limits of normal" [/i][/u] When we have any blood work done, there is always a 'normal' range given with our results. Hospitals or labs can somethings differ as to what their 'normal' is. Always look at what your results are according to that normal. According to Dr. Jones, in

The ambition is to supercharge human capabilities, treat neurological disorders like ALS or Parkinson’s, and maybe one day achieve a symbiotic relationship between humans and artificial intelligence.

Labs weren’t too bad, but will be curious to see what they say. Wbcs 1.9, hct 39.5, PLT 176, neutrophils 1.1, lymphocytes 0.6. Alk phos was a little high, but not near double, other liver enzymes were good. I figured it is because my thyroid needs adjusting as it was totally fine in June. But lipids

[i]For the most part physicians have given Urso up to a year to decide if you are a responder or not -- has the Urso decreased your numbers significantly in that time period.[/i] [i]According to Dr. Jones (world 's leading expert on PBC) the thinking may soon be that only a 6 month period

She had ALS, lost her voice sometime back... knew this was coming, still difficult. I know this is a lot... thanks.

[u][i]Urso responder........[/i][/u] Right now the criteria used is that the patients' alkaline phosphatase result is LESS than 1.67 times the upper limits of normal and the bilirubin results are less than one time the upper limits of normal. I know this can be very confusing. This is why

I have a history of mental health issues so FND sounds like the most likely culprit, as it seems to get worse after traumatic events or illness, but I can't shake ALS out of my mind, even though people on the ALS forum said this isn't how ALS manifests. Can someone offer insight? Thank you!