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balance issues
I have had glaucoma for years, last December 2023i had cataracts done to help with opening angles, then in March I had SLT & my pressures went down to 13&17 but since then my balance is not good, it hasn’t been good for long enough but worse now, could it be to do with when I am in shops with the light
I have had glaucoma for years, last December 2023i had cataracts done to help with opening angles, then in March I had SLT & my pressures went down to 13&17 but since then my balance is not good, it hasn’t been good for long enough but worse now, could it be to do with when I am in shops with the light
Hidden
in
Glaucoma UK
1 year 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
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
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Olaparib side effects - cough and breathlessness
Hi all. I've been taking Olaparib since May this year and have had a constant cough and breathlessness. It's getting me down a bit and I was wondering if anyone else has had this side effect and how long it lasted x
Hi all. I've been taking Olaparib since May this year and have had a constant cough and breathlessness. It's getting me down a bit and I was wondering if anyone else has had this side effect and how long it lasted x
Demelzatheseagull
in
My Ovacome
8 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
Loss of Sharpness after Eylea injection
Hello folks. My name is Michael. For years I was receiving shots of Eylea by a doctor that I trusted completely. About 3 years ago I moved and it was just too far to travel to continue seeing this great doctor. I then continued Eylea injections with a new Retina man. On about the 4th visit I noticed,
Hello folks. My name is Michael. For years I was receiving shots of Eylea by a doctor that I trusted completely. About 3 years ago I moved and it was just too far to travel to continue seeing this great doctor. I then continued Eylea injections with a new Retina man. On about the 4th visit I noticed,
shobud71
in
Macular Society
1 year ago
latanoprost and headaches
hi I’ve been using latanoprost eye drops for 7 weeks now, I have suspicious discs and a family history of glaucoma ( mother) and when prescribed my pressures were 22 in both eyes. For the last week I have woken with a headache, and I’m wondering if this could be related to the eye drops, as this is
hi I’ve been using latanoprost eye drops for 7 weeks now, I have suspicious discs and a family history of glaucoma ( mother) and when prescribed my pressures were 22 in both eyes. For the last week I have woken with a headache, and I’m wondering if this could be related to the eye drops, as this is
Popsicle57
in
Glaucoma UK
1 year 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
10 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
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
Dreading seeing the Rheumatologist
Hi everyone, I have an appointment coming up with my Rheumatologist which I’ve been under for the last 3 1/2 years (I’m in the UK, we don’t get a choice in who we see). It took him a couple of years to finally diagnose PMR. During that time I’d become almost housebound. He insisted I take the
Hi everyone, I have an appointment coming up with my Rheumatologist which I’ve been under for the last 3 1/2 years (I’m in the UK, we don’t get a choice in who we see). It took him a couple of years to finally diagnose PMR. During that time I’d become almost housebound. He insisted I take the
Bramble2000
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
8 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
8 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
Has anyone had more fertilised eggs 2nd time round with ICSI?
Hi everyone, I'm wondering if anyone undergoing ICSI had a more successful round of fertilised eggs 2nd time round and if there was anything you done differently? We had our first round in August and they managed to use 10 mature eggs after collecting 15 eggs, 24 hours later we were told that only
Hi everyone, I'm wondering if anyone undergoing ICSI had a more successful round of fertilised eggs 2nd time round and if there was anything you done differently? We had our first round in August and they managed to use 10 mature eggs after collecting 15 eggs, 24 hours later we were told that only
WMolly88
in
Fertility Network UK
5 months ago
Shingles vaccine
Just seen the BBC news health website. Shingles vaccines being offered to over 65’s ( was 70) and, even better, to vulnerable immune suppressed people over 55 from September 2023.
Just seen the BBC news health website. Shingles vaccines being offered to over 65’s ( was 70) and, even better, to vulnerable immune suppressed people over 55 from September 2023.
Amnesiac3637
in
NRAS
10 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
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
8 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
8 months ago
Flare and due COVID jab Friday
Hi all. I hope you are all well or as well as can be. 🙂 I'm booked for my spring COVID booster tomorrow but I'm starting to flare, sore hands and shoulders etc and they are starting me on hydroxychloroquine next week as well as the 3g if sulfasalazine I'm already on. Have any of you had the jab whilst
Hi all. I hope you are all well or as well as can be. 🙂 I'm booked for my spring COVID booster tomorrow but I'm starting to flare, sore hands and shoulders etc and they are starting me on hydroxychloroquine next week as well as the 3g if sulfasalazine I'm already on. Have any of you had the jab whilst
Haz58
in
NRAS
11 months ago
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