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COVID vaccination
I think all of these horrible symptoms we have are the results of COVID-19 vaccination. I’m so angry 😡
I think all of these horrible symptoms we have are the results of COVID-19 vaccination. I’m so angry 😡
Sissiotto
in
Pernicious Anaemia Society
2 months ago
Covid Vaccine help and advice please 😊
I have had a week of ill health (hellish) following every vaccine but my body seems to accept the Pfizer !! so this time round was hopeful. However there is none to be had . I have been offered the Moderna , has anyone else who has systemic lupus had this one ? And can you tell me how you were ? I just
I have had a week of ill health (hellish) following every vaccine but my body seems to accept the Pfizer !! so this time round was hopeful. However there is none to be had . I have been offered the Moderna , has anyone else who has systemic lupus had this one ? And can you tell me how you were ? I just
Maddymay65
in
LUPUS UK
2 months ago
Neuropathy worse after covid jab, anyone?
After my recent ninth Covid jab (second time with Moderna), I found I had reactions (have always had none before, lucky me). First I developed the grandly named"Covid arm" which was nothing much, just a faint, occasional itch around the jab area which disappeared after a week. Then, for about a week
After my recent ninth Covid jab (second time with Moderna), I found I had reactions (have always had none before, lucky me). First I developed the grandly named"Covid arm" which was nothing much, just a faint, occasional itch around the jab area which disappeared after a week. Then, for about a week
Trickysite
in
My Ovacome
2 months ago
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Covid Vax and age
I’m in the US and have lupus and many other disqualifying illnesses 😊. I just read a thread in which folks thought their PMR began with Covid jabs. After 3 Moderna, and 3 bouts of Covid I don’t think I want to get vaccinated again. But then there’s flirt. I have 2 grandchildren ages 5 and 4 with long
I’m in the US and have lupus and many other disqualifying illnesses 😊. I just read a thread in which folks thought their PMR began with Covid jabs. After 3 Moderna, and 3 bouts of Covid I don’t think I want to get vaccinated again. But then there’s flirt. I have 2 grandchildren ages 5 and 4 with long
MrsMarigold
in
PMRGCAuk
2 months ago
Protection from Coronaviruses That Haven’t Yet Emerged
To paraphrase Ozzy Osbourne, pandemics can spring up without warning. Although 101 years separated the most recent, truly global pandemics - the H1N1 virus killing tens of millions of people from 1918 to 1920 and SARS-COV2 killing an estimated 14.8 million people in 2020-21 alone https://www.ncbi.nlm.nih.gov
To paraphrase Ozzy Osbourne, pandemics can spring up without warning. Although 101 years separated the most recent, truly global pandemics - the H1N1 virus killing tens of millions of people from 1918 to 1920 and SARS-COV2 killing an estimated 14.8 million people in 2020-21 alone https://www.ncbi.nlm.nih.gov
bennevisplace
in
CLL Support
2 months ago
Osteoarthritis in knee
Hello I am new on this site and would like to thank admin for letting me on here. Going back about January 2024 time my left knee started to feel a little odd at the back (ham) think this is what it's name is, anyhow about 6/8 weeks ago plucked up enough courage to see a G.P at my local doctors, a
Hello I am new on this site and would like to thank admin for letting me on here. Going back about January 2024 time my left knee started to feel a little odd at the back (ham) think this is what it's name is, anyhow about 6/8 weeks ago plucked up enough courage to see a G.P at my local doctors, a
completely-zero654
in
Couch to 5K
3 months ago
Mouthwash
I am on 320 of alvesco a day at present along with fostair mart taken with my trusty aero chamber. I was on 640 of alvesco, however for the first time I was starting to get some irritations from this, mild oral thrush, joint pain, weight gain and some odd eye issues. So my consultant said to drop
I am on 320 of alvesco a day at present along with fostair mart taken with my trusty aero chamber. I was on 640 of alvesco, however for the first time I was starting to get some irritations from this, mild oral thrush, joint pain, weight gain and some odd eye issues. So my consultant said to drop
Homely2
Administrator
in
Asthma Community Forum
5 months ago
Update- Moderna Spikevax
Just to update. Received blood result and all within rang with the exception of Lymphocyte count which 3.1 only slightly over range. CPR 4 g/L, ESR 2. Which rules out PMR flare. So onwards and upwards, definitely downwards with Pred.-so pleased. I am now wondering whether the muscle paralysis I had
Just to update. Received blood result and all within rang with the exception of Lymphocyte count which 3.1 only slightly over range. CPR 4 g/L, ESR 2. Which rules out PMR flare. So onwards and upwards, definitely downwards with Pred.-so pleased. I am now wondering whether the muscle paralysis I had
Pebblegod
in
PMRGCAuk
2 months ago
From Prednisone to Morphine
I was wondering if anyone had been offered Morphine as an alternative to Prednisone? It’s been suggested to me by my new Rheumatologist recently. He’s questioning my diagnosis of PMR & suggests the pain is due to “wear & tear”. My pain is symmetrical, in all the usual places (knees, hips, shoulders,
I was wondering if anyone had been offered Morphine as an alternative to Prednisone? It’s been suggested to me by my new Rheumatologist recently. He’s questioning my diagnosis of PMR & suggests the pain is due to “wear & tear”. My pain is symmetrical, in all the usual places (knees, hips, shoulders,
Chelseadog
in
PMRGCAuk
3 months ago
what next?
I was diagnosed with PMR five years ago and my gp kept me on Prednisolone for two years which resulted in a catalogue of side effects including glaucoma and cataracts. My diagnosis was confirmed as RA shortly after. I have been taking methotrexate successfully since. However my condition has worsened
I was diagnosed with PMR five years ago and my gp kept me on Prednisolone for two years which resulted in a catalogue of side effects including glaucoma and cataracts. My diagnosis was confirmed as RA shortly after. I have been taking methotrexate successfully since. However my condition has worsened
Pange63
in
NRAS
7 months ago
COVID diagnosis
Just been on a 300 mile bike ride and returned with COVID. Don't feel too bad but should I contact consultant. I have had a vaccination about 3 weeks ago.
Just been on a 300 mile bike ride and returned with COVID. Don't feel too bad but should I contact consultant. I have had a vaccination about 3 weeks ago.
Guinness4822
in
CLL Support
2 months ago
COVID, FND, and Cymbalta Ruined My Life
This is a long story, and I apologize in advance for any, bitter angry undertones. I'll skip all of the grief I've had in life and the hard times that I've experienced. I'll try to keep it to the medical issues. It will feel good to tell a part of my story, arguably the hardest I've been through.***Trigger
This is a long story, and I apologize in advance for any, bitter angry undertones. I'll skip all of the grief I've had in life and the hard times that I've experienced. I'll try to keep it to the medical issues. It will feel good to tell a part of my story, arguably the hardest I've been through.***Trigger
LoverOfAllThings
in
Functional Neurological Disorder - FND Hope
2 months ago
Increase in Synthroid Dose Worse Before Feeling Better?
Hello, I'm a long time hypothyroid patient but the last few years after covid have been a wild ride finding the right dose again. I'm curious if anyone can offer insight as to why the first one to two weeks of a medication dose increase I feel amazing and then I tank horribly after. All the hypo symptoms
Hello, I'm a long time hypothyroid patient but the last few years after covid have been a wild ride finding the right dose again. I'm curious if anyone can offer insight as to why the first one to two weeks of a medication dose increase I feel amazing and then I tank horribly after. All the hypo symptoms
Clarabethk
in
Thyroid UK
2 months ago
Hello
Hello again Hi. Ive had to shut down and rejoin the group. HU was playing up. Here is my original post. Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse
Hello again Hi. Ive had to shut down and rejoin the group. HU was playing up. Here is my original post. Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse
Trish_PBG
in
FND Action
2 months ago
Hello again
Hi. Ive had to shut down and rejoin the group. HU was,playing up. I have such great comments and ideas,already from Lady4 and others, so thank you. Below was, my original post Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are
Hi. Ive had to shut down and rejoin the group. HU was,playing up. I have such great comments and ideas,already from Lady4 and others, so thank you. Below was, my original post Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are
Trish_PBG
in
Functional Neurological Disorder - FND Hope
2 months ago
covid booster (Maderna)
morning all!! I have RA and I’m booked in for my annual covid booster!my concern is that from day one I’ve always had Pfizer vaccine but apparently there not using it this time around and it’s been replaced with Maderna it just makes me feel uneasy as I never had any problems with Pfizer!!have any you
morning all!! I have RA and I’m booked in for my annual covid booster!my concern is that from day one I’ve always had Pfizer vaccine but apparently there not using it this time around and it’s been replaced with Maderna it just makes me feel uneasy as I never had any problems with Pfizer!!have any you
Mybirthday1975
in
NRAS
2 months ago
Omicron variant
Hi all I have bronchiectasis (since 2012) and have been super careful during the pandemic. However, I missed my last vaccine (having had 4 over the years as well as both flu and shingles jabs) as the nearest place the NHS website could offer me for the 5th Covid jab was 22 miles away! With no public
Hi all I have bronchiectasis (since 2012) and have been super careful during the pandemic. However, I missed my last vaccine (having had 4 over the years as well as both flu and shingles jabs) as the nearest place the NHS website could offer me for the 5th Covid jab was 22 miles away! With no public
swimmer
in
Lung Conditions Community Forum
3 months ago
Tinnitus and Meniere's
Has anyone ever received Intratympanic steroid injection in their ear(s) for Tinnitus or Meniere's? I was just curious if it was worth it and made matters better. Is the injection painful or create other issues? My ENT has recommended it for my left ear which has a variety of issues. Thanks.
Has anyone ever received Intratympanic steroid injection in their ear(s) for Tinnitus or Meniere's? I was just curious if it was worth it and made matters better. Is the injection painful or create other issues? My ENT has recommended it for my left ear which has a variety of issues. Thanks.
MrGC314
in
Tinnitus UK
3 months ago
Scared and lost
Hello, I am not too sure where to start, so much has happened. I am a 50 year-old female. A couple of years ago, I had a pain in my abdomen on the right side and my stools became orange. The GP sent me for an ultrasound where they saw I had polyps on my gallbladder. The GP phoned me on the 31st Dec to
Hello, I am not too sure where to start, so much has happened. I am a 50 year-old female. A couple of years ago, I had a pain in my abdomen on the right side and my stools became orange. The GP sent me for an ultrasound where they saw I had polyps on my gallbladder. The GP phoned me on the 31st Dec to
Foi24
in
British Liver Trust
3 months ago
Finally a little light!
Many of you have been kind in giving me advice and support over the last year, especially when I was 'wading through treacle'. A few weeks ago I had another steroid injection and leflunomide added to my MTX. I hardly dare say this but I'm actually starting to feel better. My joints have gone down so
Many of you have been kind in giving me advice and support over the last year, especially when I was 'wading through treacle'. A few weeks ago I had another steroid injection and leflunomide added to my MTX. I hardly dare say this but I'm actually starting to feel better. My joints have gone down so
HeadInASpin
in
NRAS
3 months ago
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