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Role of Luteolin in overcoming Parkinson's disease 2021
Role of Luteolin in overcoming Parkinson's disease 2021
https://sci-hub.ru/10.1002/biof.1706 "The incidence of life threating neurodegenerative diseases such as PD is increasing day by day. Sporadic as well as genetic causes are well documented. Due to the decline in the dopaminergic neurons,
Role of Luteolin in overcoming Parkinson's disease 2021
https://sci-hub.ru/10.1002/biof.1706 "The incidence of life threating neurodegenerative diseases such as PD is increasing day by day. Sporadic as well as genetic causes are well documented. Due to the decline in the dopaminergic neurons,
Bolt_Upright
in
Cure Parkinson's
8 months ago
New research
Did anyone listen to the piece on talk radio today about new lupus research? So exciting for all autoimmune diseases! Here is an article I found about it. https://lens.monash.edu/@medicine-health/2024/02/06/1386418/breakthrough-heralds-immune-personalised-medicine-for-lupus?amp=1
Did anyone listen to the piece on talk radio today about new lupus research? So exciting for all autoimmune diseases! Here is an article I found about it. https://lens.monash.edu/@medicine-health/2024/02/06/1386418/breakthrough-heralds-immune-personalised-medicine-for-lupus?amp=1
EllsBells591
in
LUPUS UK
6 months ago
Advice please?
Hi all. I just wanted to see if anybody has experienced the same as me. I am a 28 year old male. I used to drink very heavily for around 6-7 years. I drank vodka with lemonade and could get through a couple of litres a week following my dad's death (not an excuse but it is the reason I drank so much
Hi all. I just wanted to see if anybody has experienced the same as me. I am a 28 year old male. I used to drink very heavily for around 6-7 years. I drank vodka with lemonade and could get through a couple of litres a week following my dad's death (not an excuse but it is the reason I drank so much
Connorsw95
in
British Liver Trust
8 months ago
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Deuterium Depleted Water
OK guys, I've been looking at this for a while and thought I'd condense it down and share it with you guys.I'm really not interested in arguments with people. If you don't agree, get yourself a cup of coffee, chill out and move on. Water his made of hydrogen and oxygen. Deuterium is a hydrogen isotope
OK guys, I've been looking at this for a while and thought I'd condense it down and share it with you guys.I'm really not interested in arguments with people. If you don't agree, get yourself a cup of coffee, chill out and move on. Water his made of hydrogen and oxygen. Deuterium is a hydrogen isotope
MrG68
in
Advanced Prostate Cancer
8 months ago
Pain when breathing and short of breathe post ablation update
Thanks guys fir all your advice .I ended up at a n e after ringing 111 for advice. They red flagged me and did an immediate ecg to rule out a heart attack. Followed by bloods and a xray of my lungs .. All tests can back normal and they couldn't find and concerns . So I was sent hone and it's a mystery
Thanks guys fir all your advice .I ended up at a n e after ringing 111 for advice. They red flagged me and did an immediate ecg to rule out a heart attack. Followed by bloods and a xray of my lungs .. All tests can back normal and they couldn't find and concerns . So I was sent hone and it's a mystery
Sunnyann
in
Atrial Fibrillation Support
5 months ago
Help Needed! Have I got Pernicious Anaemia?
I hope this isn't too long and/or too boring. I suspect I have PA but as with a lot of people here, no-one seems to take B12 deficiency seriously. I also have hypothyroidism so as my symptoms got increasingly worse over the past few years, I blamed my thyroid - the two conditions have many symptoms
I hope this isn't too long and/or too boring. I suspect I have PA but as with a lot of people here, no-one seems to take B12 deficiency seriously. I also have hypothyroidism so as my symptoms got increasingly worse over the past few years, I blamed my thyroid - the two conditions have many symptoms
Grannypants
in
Pernicious Anaemia Society
6 months ago
PNT article on recent success in generating locus coeruleus (LC) norepinephrine (NE) neurons, to study their role in diseases such as PD.
"Nerve cells originating in the locus coeruleus extend throughout the brain and spinal cord via an extensive branching system, where they release norepinephrine to regulate heartbeat, blood pressure, arousal, memory, and attention." "In Parkinson’s, the locus coeruleus is one of the first brain regions
"Nerve cells originating in the locus coeruleus extend throughout the brain and spinal cord via an extensive branching system, where they release norepinephrine to regulate heartbeat, blood pressure, arousal, memory, and attention." "In Parkinson’s, the locus coeruleus is one of the first brain regions
jeffreyn
in
Cure Parkinson's
8 months ago
help !
last couple days Iv had serve chest pains it’s right in the middle of my chest and now it’s round my back like ribs feels all tight! When I press down it hurts so much and I’m getting shortness of breathe but I don’t think it’s a heart attack but I’m panicking it is! When I google it says it could be
last couple days Iv had serve chest pains it’s right in the middle of my chest and now it’s round my back like ribs feels all tight! When I press down it hurts so much and I’m getting shortness of breathe but I don’t think it’s a heart attack but I’m panicking it is! When I google it says it could be
Kaaayla
in
Anxiety Support
5 months ago
Australian research - possible cure?
I don’t like raising false hope among our community about ‘cures’ toted in the media, but I found this article interesting. It’s about the T-cells, which many of us already know is involved in autoimmune activity: https://www.sbs.com.au/news/podcast-episode/australian-researchers-develop-world-first-method-of-treating-lupus
I don’t like raising false hope among our community about ‘cures’ toted in the media, but I found this article interesting. It’s about the T-cells, which many of us already know is involved in autoimmune activity: https://www.sbs.com.au/news/podcast-episode/australian-researchers-develop-world-first-method-of-treating-lupus
MusicalFurbaby
in
LUPUS UK
6 months ago
Bisoprolol and Mechanism of Action- Breathlessness
So I am on a tiny, baby dose of Bisporolol (1.25mg) after taking 2.5/made me dizzy and have pauses after PACs. I am getting this weird breathlessness. It is so hard to explain. I hiked a trail in our woods today with ko problem, but then sat on the couch and watched a movie and felt like I couldnt
So I am on a tiny, baby dose of Bisporolol (1.25mg) after taking 2.5/made me dizzy and have pauses after PACs. I am getting this weird breathlessness. It is so hard to explain. I hiked a trail in our woods today with ko problem, but then sat on the couch and watched a movie and felt like I couldnt
MeganMN
in
Atrial Fibrillation Support
5 months ago
Medication for Vasculitis
Hi. I have had Vasculitis for four years and my current medication is Prednisolone 5.5 mg daily and Methotextrate Injection 25mg weekly. Following the onset of my illness I now have to use a wheeled walker to get around and can no longer drive a motor vehicle.
Hi. I have had Vasculitis for four years and my current medication is Prednisolone 5.5 mg daily and Methotextrate Injection 25mg weekly. Following the onset of my illness I now have to use a wheeled walker to get around and can no longer drive a motor vehicle.
oscar294
in
Vasculitis UK
5 months ago
Update-Covid antiviral
This evening I finally got the call from a consultant from , Stoke Mandeville hospital.Booked in for liver and kidney blood test and infusion .... what a relief . Just want to feel better. Thank you all for your advice and care. 😊
This evening I finally got the call from a consultant from , Stoke Mandeville hospital.Booked in for liver and kidney blood test and infusion .... what a relief . Just want to feel better. Thank you all for your advice and care. 😊
Stavrou1
in
CLL Support
8 months ago
I am waiting to find out if I have Lupus but I haven’t got my ANA result back yet and I want to know if people think this could be lupus
Hi, I have been having concerns for over a year about me having Lupus. I had a blood test last year which everything came back normal and the ANA was negative however I am experiencing more symptoms this year and I have taken another blood test and so far the bloods again are normal but I have currently
Hi, I have been having concerns for over a year about me having Lupus. I had a blood test last year which everything came back normal and the ANA was negative however I am experiencing more symptoms this year and I have taken another blood test and so far the bloods again are normal but I have currently
katiepops2004
in
LUPUS UK
6 months ago
Declining psa #8
Gm folks, hope all is well during this Christmas season… I’ve just received my 8th psa test after getting off ADT, 9 months of using alternative meds ivermectin, cbd oil turmeric zinc ashwaganda n dim a natural estrogen blocker solely. Psa came in at .95 down from 1.29, 6 weeks ago and down from 1.95
Gm folks, hope all is well during this Christmas season… I’ve just received my 8th psa test after getting off ADT, 9 months of using alternative meds ivermectin, cbd oil turmeric zinc ashwaganda n dim a natural estrogen blocker solely. Psa came in at .95 down from 1.29, 6 weeks ago and down from 1.95
Nfler
in
Advanced Prostate Cancer
8 months ago
knocked sideways
Ive been reading all your posts but not actually written anything for a while because in my stupid head I thought we were plodding along even if it was at a plateau level. Kev was diagnosed with non alcoholic liver cirrhosis back in July. He also had sepsis twice and ended up in intensive care where
Ive been reading all your posts but not actually written anything for a while because in my stupid head I thought we were plodding along even if it was at a plateau level. Kev was diagnosed with non alcoholic liver cirrhosis back in July. He also had sepsis twice and ended up in intensive care where
Snips71
in
Liver4Life
8 months ago
combining standard PCA care with alternative care
In a three month period my PSA went from 58 to 70. Obviously my testosterone was producing more new cancer cells than my alternative treatment. I started the combination treatment on Dec 1 by taking 2 ORGOVYX. Dec 15 my PSA is 27.5 and I will take one more ORGOVYX today hoping to reduce PSA to 10
In a three month period my PSA went from 58 to 70. Obviously my testosterone was producing more new cancer cells than my alternative treatment. I started the combination treatment on Dec 1 by taking 2 ORGOVYX. Dec 15 my PSA is 27.5 and I will take one more ORGOVYX today hoping to reduce PSA to 10
agnut
in
Fight Prostate Cancer
8 months ago
FREE Arthritis Self-Management Event
I thought some of you may be interested in this event on Wed 6th March, 6.00pm (GMT); its aimed at young people or anyone supporting a young person with arthritis. Tickets can be booked here: https://www.eventbrite.co.uk/e/arthritis-me-tickets-811392285167 Ann Arthritis Action Comms Team,
I thought some of you may be interested in this event on Wed 6th March, 6.00pm (GMT); its aimed at young people or anyone supporting a young person with arthritis. Tickets can be booked here: https://www.eventbrite.co.uk/e/arthritis-me-tickets-811392285167 Ann Arthritis Action Comms Team,
arthritis_action
Partner
in
Arthritis Action
6 months ago
PSA on the rise
Good morning everyone, my PSA has been undectable, {<.01} since July 2022. Not real long, but it has been a good time. Felt good, no pain, can look on my profile for more details. I am on Xtandi and Lupron--(3 months). (I had taxetere in 2021) I get my PSA checked every three months right before
Good morning everyone, my PSA has been undectable, {<.01} since July 2022. Not real long, but it has been a good time. Felt good, no pain, can look on my profile for more details. I am on Xtandi and Lupron--(3 months). (I had taxetere in 2021) I get my PSA checked every three months right before
JD-guy
in
Advanced Prostate Cancer
8 months ago
National Bill to End Parkinson's
Hello, I'll keep it short and sweet. 55 yr male. Diagnosed at 42 yr. Fitness fanatic, which has kept this damn disease at bay......for the most part. Just wondering what everyone thinks of this new Bill to End Parkinson's Act. Should we be excited, worried, indifferent? Is it gonna just be all talk and
Hello, I'll keep it short and sweet. 55 yr male. Diagnosed at 42 yr. Fitness fanatic, which has kept this damn disease at bay......for the most part. Just wondering what everyone thinks of this new Bill to End Parkinson's Act. Should we be excited, worried, indifferent? Is it gonna just be all talk and
Metalovinshaker13
in
Cure Parkinson's
8 months ago
PSA post Salvage Radiation
Prior post: My husband, at diagnosis had 3+4 on a couple of samples and chose to have surgery. He had clean margins and reached undetectable PSA after Prostatectomy. Near the end of 5th year after surgery his PSA became detectable. He did salvage radiation at .09 PSA. His PSA went down to .08 after
Prior post: My husband, at diagnosis had 3+4 on a couple of samples and chose to have surgery. He had clean margins and reached undetectable PSA after Prostatectomy. Near the end of 5th year after surgery his PSA became detectable. He did salvage radiation at .09 PSA. His PSA went down to .08 after
Silverlings
in
Advanced Prostate Cancer
8 months ago
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