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The way to access COVID-19 treatments has changed
The way to access COVID-19 treatments has changed, and is now different in the different nations of the UK. Check our article to find out what the process is for where you live: https://www.lupusuk.org.uk/accessing-covid-19-treatments/ These changes are particularly important for people in England and
The way to access COVID-19 treatments has changed, and is now different in the different nations of the UK. Check our article to find out what the process is for where you live: https://www.lupusuk.org.uk/accessing-covid-19-treatments/ These changes are particularly important for people in England and
Debbie_kinsey
Administrator
in
LUPUS UK
11 months ago
Scared
Hi there, I'm 38 year old active, fit woman. I've been diagnosed with severe cervical stenosis at c6-7 with radiculopathy. Have had symptoms for 20+ years not realising what it was. Then last summer after having an appendectomy and 3 weeks rest, the pain behind left shoulder blade and in neck flared
Hi there, I'm 38 year old active, fit woman. I've been diagnosed with severe cervical stenosis at c6-7 with radiculopathy. Have had symptoms for 20+ years not realising what it was. Then last summer after having an appendectomy and 3 weeks rest, the pain behind left shoulder blade and in neck flared
Rewe
in
Cervical Myelopathy
11 months ago
How often and duration of the Tass gloves?
Just completed the build. Wife used first time for 2 hrs with improved gait was able to walk in house without walker. Used walking sticks just due to fear of falling. Hand printing improved. However today after 2 hrs she said she felt very jittery, kind of like a residual feeling of vibratio So she
Just completed the build. Wife used first time for 2 hrs with improved gait was able to walk in house without walker. Used walking sticks just due to fear of falling. Hand printing improved. However today after 2 hrs she said she felt very jittery, kind of like a residual feeling of vibratio So she
Furch
in
Cure Parkinson's
7 months ago
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Hi all an update on my new rheumy
Hi everybody, yesterday evening I had an appointment with my new Rheumy. I was actually dreading it due to my last experience with the previous rheumatologist. Well I have to say he was brilliant listened to me, Then going on my symptoms and doing an ultrasound on my hands and looking at all my blood
Hi everybody, yesterday evening I had an appointment with my new Rheumy. I was actually dreading it due to my last experience with the previous rheumatologist. Well I have to say he was brilliant listened to me, Then going on my symptoms and doing an ultrasound on my hands and looking at all my blood
Wonderfullifeandmore
in
PMRGCAuk
11 months ago
A number of over the counter cold medicine in the USA in jeopardy
Here's the link to the artIcle https://www.wsj.com/health/healthcare/decongestant-cold-medicine-ineffective-f68df3f7?st=b0jipkx3rqa2o0a&reflink=article_copyURL_share
Here's the link to the artIcle https://www.wsj.com/health/healthcare/decongestant-cold-medicine-ineffective-f68df3f7?st=b0jipkx3rqa2o0a&reflink=article_copyURL_share
pdpatient
in
Cure Parkinson's
9 months ago
Immunocompromised people aged 50+ are now eligible for the shingles vaccine
Immunocompromised people aged 50 and over are now eligible for the shingles vaccine. The vaccine reduces your chances of getting shingles and reduces the risk of complications if you still develop it. Read more on our website, including answers to some commonly asked questions, here: https://www.lupusuk.org.uk
Immunocompromised people aged 50 and over are now eligible for the shingles vaccine. The vaccine reduces your chances of getting shingles and reduces the risk of complications if you still develop it. Read more on our website, including answers to some commonly asked questions, here: https://www.lupusuk.org.uk
Debbie_kinsey
Administrator
in
LUPUS UK
9 months ago
RLS and Covid vaccine
Just for everyones awareness, my RLS was way worsened by the covid vaccine and so far it seems to have been a permanent side effect. I had RLS since I was a kid but tyically lasted 10 to 30 minutes each night whereas after the vaccine (within days) it shot up to 2 to 3 hours. I wanted to make sure I
Just for everyones awareness, my RLS was way worsened by the covid vaccine and so far it seems to have been a permanent side effect. I had RLS since I was a kid but tyically lasted 10 to 30 minutes each night whereas after the vaccine (within days) it shot up to 2 to 3 hours. I wanted to make sure I
the7thsong
in
Restless Legs Syndrome
11 months ago
Rejected for anti virals
Hi everyone I tested positive for Covid on Tuesday and reported it to my GP surgery on Wednesday. I heard from Chelsea and Westminster Hospital on Thursday. They asked about how active my Lupus had been and I told them recently it had been pretty well controlled and they asked how it affected me and
Hi everyone I tested positive for Covid on Tuesday and reported it to my GP surgery on Wednesday. I heard from Chelsea and Westminster Hospital on Thursday. They asked about how active my Lupus had been and I told them recently it had been pretty well controlled and they asked how it affected me and
BookishVibes
in
LUPUS UK
11 months ago
Cold!
After doing the 20 min run on Saturday I rested Sunday. Haven't slept well for three nights now. Now I think I've got a cold. Headache, etc. Will rest with a short walk until Wednesday now. See how I feel then. Feeling very frustrated.
After doing the 20 min run on Saturday I rested Sunday. Haven't slept well for three nights now. Now I think I've got a cold. Headache, etc. Will rest with a short walk until Wednesday now. See how I feel then. Feeling very frustrated.
Basil73
in
Couch to 5K
9 months ago
Positive update and jopefully helpful advice/suggestions..💗
Hey guys,I haven't been on here a while, but I've been busy trying new ways to manage and get better (and also had bad anxiety for a while which is the main reason I wasn't here😕) and I wanted to share in hopes that it could help someone else. So last year a had trouble walking, looking at people when
Hey guys,I haven't been on here a while, but I've been busy trying new ways to manage and get better (and also had bad anxiety for a while which is the main reason I wasn't here😕) and I wanted to share in hopes that it could help someone else. So last year a had trouble walking, looking at people when
Turquoisesummer
in
Fibromyalgia Action UK
11 months ago
Flu vaccine
Thank you for your replies and concerns regarding the flu vaccine. However I was querying if people with underactive thyroid/Hashimotos need to be more aware of taking it.
Thank you for your replies and concerns regarding the flu vaccine. However I was querying if people with underactive thyroid/Hashimotos need to be more aware of taking it.
292426
in
Thyroid UK
9 months ago
Gamma light and Alzheimers - free app
I know this is not specific to PD, but thought I'd share this article. You all have been so kind to share new advancements, thank you. This looks very interesting!!! https://www.cogentica.com/alzheimers-research-gamma/ Direct from the article: (also talks about bacteria and gamma light and sound
I know this is not specific to PD, but thought I'd share this article. You all have been so kind to share new advancements, thank you. This looks very interesting!!! https://www.cogentica.com/alzheimers-research-gamma/ Direct from the article: (also talks about bacteria and gamma light and sound
Kat343
in
Cure Parkinson's
10 months ago
Flu vaccine
Hi My flu vaccine is all booked. I’ve only ever had one before two years ago but occurred to me that maybe I should research if it’s ok to have it as I have Hashimotos/underactive thyroid. Appreciate any advice. 🌸
Hi My flu vaccine is all booked. I’ve only ever had one before two years ago but occurred to me that maybe I should research if it’s ok to have it as I have Hashimotos/underactive thyroid. Appreciate any advice. 🌸
292426
in
Thyroid UK
9 months ago
Paxlovid for Covid if you have PMR
hi all. Living in France for 5 months didn’t think I would get Covid here but I did. I think it came with our guests on the plane. But in any case I have Paxlovid with me but I keep seeing things that say don’t take it if you have autoimmune disorder. Is that us? My doctor gave it to me but…. I am down
hi all. Living in France for 5 months didn’t think I would get Covid here but I did. I think it came with our guests on the plane. But in any case I have Paxlovid with me but I keep seeing things that say don’t take it if you have autoimmune disorder. Is that us? My doctor gave it to me but…. I am down
bluegirl7
in
PMRGCAuk
11 months ago
Liver detox after chemo?
I am starting Taxotere next week and received some advice from a friend fighting serious colon cancer. He told me how he detoxed his liver after each cycle. He used TUDCA Bile salts and PectaSol from ECONugenics Company. https://econugenics.com/collections/pectasol?Wickedsource=Microsoft&Wickedid
I am starting Taxotere next week and received some advice from a friend fighting serious colon cancer. He told me how he detoxed his liver after each cycle. He used TUDCA Bile salts and PectaSol from ECONugenics Company. https://econugenics.com/collections/pectasol?Wickedsource=Microsoft&Wickedid
V10fanatic
in
Advanced Prostate Cancer
7 months ago
bronciectis
had bad bouts of weasin and verry sticky mucus in large amounts it woud carm dawn for a couple of hours then start again doctor as den me for X-ray she listend to my chest and said she coud hear fluid in bottom of. Lugs sent me for X-ray 2days later phone call saying for me to go back tomorrow I’m
had bad bouts of weasin and verry sticky mucus in large amounts it woud carm dawn for a couple of hours then start again doctor as den me for X-ray she listend to my chest and said she coud hear fluid in bottom of. Lugs sent me for X-ray 2days later phone call saying for me to go back tomorrow I’m
Redrum46
in
Lung Conditions Community Forum
9 months ago
Methylene Blue
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Trailing
in
Cure Parkinson's
1 year ago
Sensitive. Stopping Crinone Qn
hi everyone. Please don’t read if you’re not in the right headspace. I’ve very luckily had a BFP on my second fresh icsi cycle with NhS. I’m currently 15dp3dt of two embryos and have been told that I don’t need to use the Crinone gel anymore. I’ve a few more left from my previous private cycle and
hi everyone. Please don’t read if you’re not in the right headspace. I’ve very luckily had a BFP on my second fresh icsi cycle with NhS. I’m currently 15dp3dt of two embryos and have been told that I don’t need to use the Crinone gel anymore. I’ve a few more left from my previous private cycle and
Clayhugs
in
Fertility Network UK
6 months ago
the never ending hurdles
When we did our 2nd icsi cycle we were told there was a 2% chance of total fertilisation failure, well, we were the 2% and none of our eggs fertilised. Now when pgta testing following our 3rd cycle we were told there was a 2% chance our embryos wouldn’t survive the thaw…and guess what, our top graded
When we did our 2nd icsi cycle we were told there was a 2% chance of total fertilisation failure, well, we were the 2% and none of our eggs fertilised. Now when pgta testing following our 3rd cycle we were told there was a 2% chance our embryos wouldn’t survive the thaw…and guess what, our top graded
Hidden
in
Fertility Network UK
6 months ago
Flying with liquid medication
I go on holiday in a couple of weeks and need to take all my needles and lubion as well as Tinzaparin. Although they are less than 100ml in each vial/syringe, collectively they’ll be more than 100ml. Do I just need to take my prescription or do I have to declare the meds or get in touch with the airports
I go on holiday in a couple of weeks and need to take all my needles and lubion as well as Tinzaparin. Although they are less than 100ml in each vial/syringe, collectively they’ll be more than 100ml. Do I just need to take my prescription or do I have to declare the meds or get in touch with the airports
Alwaysbelieving
in
Fertility Network UK
10 months ago
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