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Amyotrophic lateral sclerosis (ALS)
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If new ribosomes are created by existing ribosomes, how was the first ribosome created?
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.
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.
jeffreyn
in
Cure Parkinson's
3 months ago
ALS and B12
Scroll down to the heading, "Vitamin B12 levels and MND/
ALS
". https://jmedicalcasereports.biomedcentral.com/articles/10.1186/1752-1947-4-298
Scroll down to the heading, "Vitamin B12 levels and MND/
ALS
". https://jmedicalcasereports.biomedcentral.com/articles/10.1186/1752-1947-4-298
WiscGuy
in
Pernicious Anaemia Society
8 months ago
Are neurodegenerative diseases separate or do they represent a spectrum of disease?
I AM
ALS
is initiating Cures for All, to unify the broader neurodegenerative community. I'm very happy to witness this paradigm shift. SE
I AM
ALS
is initiating Cures for All, to unify the broader neurodegenerative community. I'm very happy to witness this paradigm shift. SE
SilentEchoes
in
Cure Parkinson's
9 months ago
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Sanazon therapy experiences/ Erfahrungen mit Sanazon
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.
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.
Hailun
in
My Ovacome
4 months ago
Effects of dietary intervention on human diseases: molecular mechanisms and therapeutic potential
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
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
Farooqji
in
Cure Parkinson's
4 months ago
Klotho gene therapy
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
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
Boscoejean
in
Cure Parkinson's
5 days ago
Elon Musk says Neuralink installs brain implant in first patient
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.
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.
Farooqji
in
Cure Parkinson's
6 months ago
I have PPMS.
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.
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.
MrB51
in
My MSAA Community
21 days ago
WHAT IS THIS?
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!
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!
anxious182
in
Functional Neurological Disorder - FND Hope
8 months ago
Health Anxiety
Since then, a variety of sensations and symptoms have caused me to believe I'm having heart attacks, various forms of cancer, diseases like
ALS
and MS, losing ability to breathe, etc. Only in the last week have I come to terms with the reality that it's all part of health anxiety.
Since then, a variety of sensations and symptoms have caused me to believe I'm having heart attacks, various forms of cancer, diseases like
ALS
and MS, losing ability to breathe, etc. Only in the last week have I come to terms with the reality that it's all part of health anxiety.
StringSlide
in
Anxiety and Depression Support
8 months ago
Carrying a lot - possible trigger warning.
She had
ALS
, lost her voice sometime back... knew this was coming, still difficult. I know this is a lot... thanks.
She had
ALS
, lost her voice sometime back... knew this was coming, still difficult. I know this is a lot... thanks.
melbrown
in
Anxiety and Depression Support
3 months ago
Don’t mean to be a downer but-
His brother did this for his
ALS
We were thinking about giving through Medcure as they claim to do everything for free but a few people recently had issues with them. Also they are a for profit type company.
His brother did this for his
ALS
We were thinking about giving through Medcure as they claim to do everything for free but a few people recently had issues with them. Also they are a for profit type company.
MouseAddams
in
Advanced Prostate Cancer
9 months ago
PLS ; primary lateral skcleosis
I was diagnosed in April 2014 with PLS ,a cousin of
ALS
, but not fatale, a slowly progressive disability illness causing hoarseness, balance problems, weakness, similarly to CMT. Now I'm wondering if I was misdiagnosed.
I was diagnosed in April 2014 with PLS ,a cousin of
ALS
, but not fatale, a slowly progressive disability illness causing hoarseness, balance problems, weakness, similarly to CMT. Now I'm wondering if I was misdiagnosed.
Countrygal2021
in
Thyroid UK
10 months ago
Hello 👋 CT scans
But I
ALS
found that Google shows that a lot of people say that it cannot. Can anyone shed some light on my broken soul at the moment??!!! I feel extremely doomed. I could spare a few pounds that's for sure Also.
But I
ALS
found that Google shows that a lot of people say that it cannot. Can anyone shed some light on my broken soul at the moment??!!! I feel extremely doomed. I could spare a few pounds that's for sure Also.
Hihihihihi72
in
British Liver Trust
8 months ago
Neurologist says he KNOWS why we get PD (and other neuro diseases) and has REVERSED ALS "Lou Gehrigs" in one patient! (an INCURABLE disease)
He interviews a neurologist/ researcher who has REVERSED "Lou Gehrigs"
ALS
in one patient! (That is a 100% INCURABLE disease.) Very revealing video.... -------------------------------------------------- https://youtu.be/ETKZS5e33VA
He interviews a neurologist/ researcher who has REVERSED "Lou Gehrigs"
ALS
in one patient! (That is a 100% INCURABLE disease.) Very revealing video.... -------------------------------------------------- https://youtu.be/ETKZS5e33VA
PDWarrior1900
in
Cure Parkinson's
1 year ago
Wednesday's Word
[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
[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
DonnaBoll
Administrator
in
PBC Foundation
1 month ago
Why would my Alk Phos go up after just starting urso?
Hi All, I have a question and wondered if anyone had an answer to if they had a similar experience. I just started taking Urso and have been on it now close to a month my recent blood work shows that my Alk Phos has increased rather than decreased. While I know it may take awhile for Urso to potentially
Hi All, I have a question and wondered if anyone had an answer to if they had a similar experience. I just started taking Urso and have been on it now close to a month my recent blood work shows that my Alk Phos has increased rather than decreased. While I know it may take awhile for Urso to potentially
Toddyboo
in
PBC Foundation
3 months ago
If your doctor worries that too much B12 is toxic, show them this study on ALS & B12
hl=en&as_sdt=0%2C5&q=
als
+methylcobalamin&btnG= And I'm pretty sure they aren't going by serum B12 levels 🤪
hl=en&as_sdt=0%2C5&q=
als
+methylcobalamin&btnG= And I'm pretty sure they aren't going by serum B12 levels 🤪
jade_s
in
Pernicious Anaemia Society
1 year ago
another pharma update
This is in regards to the pharma Ipsen... They are trialing a drug called Elafibranor. It is being used for treatment in PBC, biliary atresia (in children) , PSC, Alagille Syndrome, and Primary Familial Cholestasis. With patients taking Urso, often up to 40% do not see improvement. 3-5% of patients
This is in regards to the pharma Ipsen... They are trialing a drug called Elafibranor. It is being used for treatment in PBC, biliary atresia (in children) , PSC, Alagille Syndrome, and Primary Familial Cholestasis. With patients taking Urso, often up to 40% do not see improvement. 3-5% of patients
DonnaBoll
Administrator
in
PBC Foundation
3 months ago
milk thistle
has anyone taken milk thistle and alk phos or lft improve? are they any vitamins or supplements that have have been known to help PBC test results? thanks!
has anyone taken milk thistle and alk phos or lft improve? are they any vitamins or supplements that have have been known to help PBC test results? thanks!
Samanthaann
in
PBC Foundation
3 months ago
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