Experiences with

Amyotrophic lateral sclerosis (ALS)

Ich habe sehr auf Mucuna gesetzt, um die Nebenwirkungen etwas rauszuschieben, da ich denke, dass das natürliche L-Dopa verträglicher ist als die vom Neurologen verschriebene Sinemet. Oder ist bei mir !/2 Sinemet zu wenig als Decarboxylasehemmer?

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.

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.

Neurological Disorders: Rett syndrome, Angelman syndrome, Friedreich's ataxia, ALS (amyotrophic lateral sclerosis), and Fibrodysplasia ossificans progressiva (FOP). Endocrine Disorders: Acromegaly, Gigantism, Dwarfism (e.g., achondroplasia), Hypothyroidism, and Hyperthyroidism.

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 :)

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.

good morning all The blood results from the test I went for after much indecision due to my cold are “sub optimal” shall we say… Kidney function which is always poor even worse than usual and even creatinine out of range. But I am more concerned that my Alk Phos liver enzyme which has crept up through

Good morning all! (Morning in the US. 24 degrees and freezing rain later today!), If you look at my posts you will see that I have had a "blip" on my PBC radar. My old doctor retired and I went to a new practice about 2.5 weeks ago. She did a lot of blood work I haven't had in a long time, and a

Trigger warning if you are easily pulled into depression or anxiety about your condition: Hello all. I posted on here a couple of days ago because I was going to get a Fibroscan yesterday to see where my liver is on the Fibrosis scale. I was diagnosed Stage 2 (PBC Stage) in 2014. Not sure

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

Just a few notes from what I saw so far: - This paper lists all the different metal ions and how their distribution in the brain varies in different neurological diseases (AD, PD, ALS, and HD). All of these have metal ion oddities but the oddities are different.

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.

I began taking Acalabrutinib on Oct 7, along with Co-Trimoxazole 160 mg twice a day on Monday, Wednesday and Friday and Aciclovir 200 mg 3 x day. I took Allopurinol for 4 weeks and then it was stopped. Initially, I seemed to have no side effects, not even the headaches that others have reported.

Hi, I’ve been really unwell this year with scleroderma/PBC/Sjögren’s syndrome and I also have hypothyroidism. I started methotrexate a few weeks ago and I’m trying to get used to that, and now I’ve been told after many years of dodging it, that I have to start urso as my alk phos has been elevated

[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

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.

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

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.

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