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Hanging on
Remarkably mum is still hanging on through sheer grit we think.She's very weak and frail, had another couple of falls. Been in hospital with pneumonia before xmas and had pneumonia again 2 weeks ago. The care home are great but the frustration is the loss of speech for over 2 years now, no way to communicate
Remarkably mum is still hanging on through sheer grit we think.She's very weak and frail, had another couple of falls. Been in hospital with pneumonia before xmas and had pneumonia again 2 weeks ago. The care home are great but the frustration is the loss of speech for over 2 years now, no way to communicate
MRSYafffle
in
PSP Association
4 months ago
2nd short term Ginkgo trial underway
The 1st was around 10 days ago. 1 tablet taken evening of purchase, and 3 over the following day. The day after that T was not around in the afternoon for a few hours. I thought I had been cured (!) but did come back around 6pm. 3 tablets also taken over that day. The following day T was around and it
The 1st was around 10 days ago. 1 tablet taken evening of purchase, and 3 over the following day. The day after that T was not around in the afternoon for a few hours. I thought I had been cured (!) but did come back around 6pm. 3 tablets also taken over that day. The following day T was around and it
Ray200
in
Tinnitus UK
7 months ago
flu and covid vaccinations and back pain
Had both this morning - my flu arm is really sore, covid arm is fine, but my back is aching horribly. Could it be connected?
Had both this morning - my flu arm is really sore, covid arm is fine, but my back is aching horribly. Could it be connected?
Nuthatch
in
Bone Health and Osteoporosis UK
8 months ago
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covid
Hi I have Lupus plus another couple of auto immune disorders. My question is to anyone who has had Covid. I’m on my 14th day positive. How long has anyone else tested positive for. Thankyou
Hi I have Lupus plus another couple of auto immune disorders. My question is to anyone who has had Covid. I’m on my 14th day positive. How long has anyone else tested positive for. Thankyou
Tregarron
in
LUPUS UK
8 months ago
Is it Asthma COPD or Anxiety?
Hi first time posting and I apologise for the length of my question/information. In May hubby and me both came down with Covid, both had cold like symptoms cough, no smell or taste etc hubby slept a lot I didn’t. After 10 days hubby ok I wasn’t, breathing was difficult and cough horrendous Dr gave
Hi first time posting and I apologise for the length of my question/information. In May hubby and me both came down with Covid, both had cold like symptoms cough, no smell or taste etc hubby slept a lot I didn’t. After 10 days hubby ok I wasn’t, breathing was difficult and cough horrendous Dr gave
Grandmatoboys
in
Asthma Community Forum
8 months ago
Thoughts on Lignosus
Hello, I have just been in hospital for a week with a bad case of pneumonia, which came out of nowhere. I am only 44 and have no history of respiratory problems. The CT scan also showed mild bronchiectasis, which I am now finding out lots more about thanks to forums like this.I am now being bombarded
Hello, I have just been in hospital for a week with a bad case of pneumonia, which came out of nowhere. I am only 44 and have no history of respiratory problems. The CT scan also showed mild bronchiectasis, which I am now finding out lots more about thanks to forums like this.I am now being bombarded
PuzzlePuff
in
Lung Conditions Community Forum
4 months ago
Home now
Hi I would like to share what I've encountered the last 6 months and would love some feedback from anyone I fell ill back in late June 23 It seemed like a cold or flu coming on which turned into pneumonia in both lungs followed by a anti resistant bacterial infection baumanni that led to ards sepsis
Hi I would like to share what I've encountered the last 6 months and would love some feedback from anyone I fell ill back in late June 23 It seemed like a cold or flu coming on which turned into pneumonia in both lungs followed by a anti resistant bacterial infection baumanni that led to ards sepsis
Gl76
in
ICUsteps
4 months ago
Covid booster vaccination : Graves Disease
Any thoughts pl re having the covid booster vaccination when diagnosed with Graves Disease. I have at age 65 Graves Disease - diagnosed June 2023 - latest bloods - TSH/ T3/T4 in range - so improved, weight increasing ( I became under weight by far!) , and other aspects improving / energy a
Any thoughts pl re having the covid booster vaccination when diagnosed with Graves Disease. I have at age 65 Graves Disease - diagnosed June 2023 - latest bloods - TSH/ T3/T4 in range - so improved, weight increasing ( I became under weight by far!) , and other aspects improving / energy a
Littlefoot1thyroiduk
in
Thyroid UK
8 months ago
After covid flare up
after i got covid….just stuffy nose nothing more for 5,6 days…my arthritys flare up!! By back is coming back hurt a lot, even if i am in bio hyrimoz. Anybody have experience that? Suggestions? Tanks
after i got covid….just stuffy nose nothing more for 5,6 days…my arthritys flare up!! By back is coming back hurt a lot, even if i am in bio hyrimoz. Anybody have experience that? Suggestions? Tanks
Jack72
in
NRAS
8 months ago
mixing meds
if my husband and i have a cold--virus temperature we take lemsips xxx
if my husband and i have a cold--virus temperature we take lemsips xxx
Tut7iFru7i
in
AF Association
4 months ago
AIH links to Covid vaccine?
I have been doing research as you do for better or worse when you are newly diagnosed in my case AIH I came across Covid linked articles What are people’s thoughts
I have been doing research as you do for better or worse when you are newly diagnosed in my case AIH I came across Covid linked articles What are people’s thoughts
DebbyJ1
in
British Liver Trust
8 months ago
Sharing my experience of having the flu with Parkinson's...
Hi everyone. I just wanted to share my experience of combining a severe flu with my Parkinson's symptoms. I've had Parkinson's for six years and I'm generally doing relatively well. But recently, I caught a severe flu while traveling in Italy with my wife and it made my symptoms much worse, with massive
Hi everyone. I just wanted to share my experience of combining a severe flu with my Parkinson's symptoms. I've had Parkinson's for six years and I'm generally doing relatively well. But recently, I caught a severe flu while traveling in Italy with my wife and it made my symptoms much worse, with massive
Michel0220
in
Cure Parkinson's
4 months ago
chest infections ATM
Hope all my lung buddies are well atm. There are a-lot of respiratory bugs around at the moment. The hospitals are struggling. Please take extra care not to get near anyone with cold or flu symptoms.
Hope all my lung buddies are well atm. There are a-lot of respiratory bugs around at the moment. The hospitals are struggling. Please take extra care not to get near anyone with cold or flu symptoms.
Kristicats
in
Lung Conditions Community Forum
4 months ago
8th COVID JAB REACTION??
I had my latest Covid vaccine 5 days ago; no reaction for the rest of that day (usual sore arm) but each day since I’ve become gradually more breathless upon exertion and thus light headed. My symptoms have worsened considerably ((couldn’t dress this morning without have to rest after each item was
I had my latest Covid vaccine 5 days ago; no reaction for the rest of that day (usual sore arm) but each day since I’ve become gradually more breathless upon exertion and thus light headed. My symptoms have worsened considerably ((couldn’t dress this morning without have to rest after each item was
CallMeSunny
in
NRAS
8 months ago
Molnupiravir interactions with flecainide/tambocor
Hello everyone, On 9/24/23 i tested positive for covid for the first time. I discovered that Paxlovid is contraindicated for people taking flecainide. (I take 100mg, twice a day. ) My pharmacist noted that Molnupiravir (Lagevrio) was used as an alternative to Paxlovid for people in my situation. I
Hello everyone, On 9/24/23 i tested positive for covid for the first time. I discovered that Paxlovid is contraindicated for people taking flecainide. (I take 100mg, twice a day. ) My pharmacist noted that Molnupiravir (Lagevrio) was used as an alternative to Paxlovid for people in my situation. I
Wombat8
in
AF Association
8 months ago
Respite in South Bucks
HiI am new to this site. My lovely mum who is 78 lives with me after my healthy father passed away with covid in 2020. She was diagnosed with Parkinsons after a hip op severely damaged a nerve causing a drop foot. The neurologist just suggested she had it. So in 2019 I think she started these meds.
HiI am new to this site. My lovely mum who is 78 lives with me after my healthy father passed away with covid in 2020. She was diagnosed with Parkinsons after a hip op severely damaged a nerve causing a drop foot. The neurologist just suggested she had it. So in 2019 I think she started these meds.
MSACarer1000
in
Multiple System Atrophy Trust
8 months ago
Heads Up
Got this text message yesterday. High risk in this context not related to age - OH is older than me and hasn’t had one. Wasn’t categorised as ‘high risk’ in last outbreak. I’ve looked into this and it seems that the ‘high risk’ criteria have been revised and that some neurological and psychiatric
Got this text message yesterday. High risk in this context not related to age - OH is older than me and hasn’t had one. Wasn’t categorised as ‘high risk’ in last outbreak. I’ve looked into this and it seems that the ‘high risk’ criteria have been revised and that some neurological and psychiatric
Hidden
in
Thyroid UK
8 months ago
Covid and steroid increase
I’m sure this has been answered before so apologies. I have Covid and on 2.75mg of steroids. Should I increase for few days or should I see how it goes? Thanks
I’m sure this has been answered before so apologies. I have Covid and on 2.75mg of steroids. Should I increase for few days or should I see how it goes? Thanks
Rosina1871
in
PMRGCAuk
8 months ago
IVIG - how soon does it benefit?
My husband - CLL, on Calquence since April 2021 - has begun a schedule of monthly IVIG, mainly because he had 2 life threatening infections late spring/early summer (staph that went rogue, followed by c. Diff thanks to months of antibiotics). His ID doc has said that the IG may likely have Covid antibodies
My husband - CLL, on Calquence since April 2021 - has begun a schedule of monthly IVIG, mainly because he had 2 life threatening infections late spring/early summer (staph that went rogue, followed by c. Diff thanks to months of antibiotics). His ID doc has said that the IG may likely have Covid antibodies
OaktownA
in
CLL Support
8 months ago
Having a cold whilst stimming
Hi everyone, hope you're all well. I'm on day 10 of stims and just getting over a cold. Has anyone been ill during it and still gone on to have a good number of eggs collected and the quality being good too? Does being ill have an affect? Thanks.
Hi everyone, hope you're all well. I'm on day 10 of stims and just getting over a cold. Has anyone been ill during it and still gone on to have a good number of eggs collected and the quality being good too? Does being ill have an affect? Thanks.
Soapqueen87
in
Fertility Network UK
4 months ago
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