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Disability Allowance - Any Advice Please
Hi everybody. At a recent trip to hospital for my usual check ups a question was posed by one of the medical staff. “Are you getting Disability Allowance”? No I answered! “Well you should have a look at that” they replied “especially if you have had to stop work” So that got me thinking. I am 62, I
Hi everybody. At a recent trip to hospital for my usual check ups a question was posed by one of the medical staff. “Are you getting Disability Allowance”? No I answered! “Well you should have a look at that” they replied “especially if you have had to stop work” So that got me thinking. I am 62, I
Investigator1
in
Vasculitis UK
10 months ago
Newbie - Should have wrapped up warm! Any tips? 😊
Hi all. I am new here so I thought I would say hi 👋. I started the C25K programme (again!) in Sept 23 and everything was going really well until I picked up a flu bug. I had to stop for a few weeks and I started the programme up again, only to the catch COVID 😭. I tried to start again after Christmas
Hi all. I am new here so I thought I would say hi 👋. I started the C25K programme (again!) in Sept 23 and everything was going really well until I picked up a flu bug. I had to stop for a few weeks and I started the programme up again, only to the catch COVID 😭. I tried to start again after Christmas
N3vrGiv3up
in
Couch to 5K
7 months ago
Constant lower Back/Left Bum cheek pain
Hi All,I have adenomyosis and I have been having constant and chronic lower back pain and pain on my left bum cheek for 9 months. Does anyone else with adenomyosis have this problem? I've had a laparoscopy and endo wasn't found but I wouldn't be surprised if I have it too. It's tormenting me and hugely
Hi All,I have adenomyosis and I have been having constant and chronic lower back pain and pain on my left bum cheek for 9 months. Does anyone else with adenomyosis have this problem? I've had a laparoscopy and endo wasn't found but I wouldn't be surprised if I have it too. It's tormenting me and hugely
ABFr23
in
Endometriosis UK
10 months ago
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Covid First Time
Well I have finally caught Covid, in fact it is the first time that I have noticeably caught anything since 2019. At the moment I have chills, vomiting and a headache=not happy. Just wondering if anyone has any tips or info. on how to stay as comfy as possible and anything to look out for Asthma wise
Well I have finally caught Covid, in fact it is the first time that I have noticeably caught anything since 2019. At the moment I have chills, vomiting and a headache=not happy. Just wondering if anyone has any tips or info. on how to stay as comfy as possible and anything to look out for Asthma wise
LittleZebra
in
Asthma Community Forum
10 months ago
Covid and AF
Apologies if I posted this earlier. Despite countless jabs against covid (I am 79 ) and escaping the virus the past three and a half years I succumbed to the latest variant last Sunday 10th Dec. At first I thought it was just a heavy cold with a cough. Also I was thinking that I was more susceptible
Apologies if I posted this earlier. Despite countless jabs against covid (I am 79 ) and escaping the virus the past three and a half years I succumbed to the latest variant last Sunday 10th Dec. At first I thought it was just a heavy cold with a cough. Also I was thinking that I was more susceptible
Camelia23
in
AF Association
10 months ago
COVID
Doea anyone have any advice. I had my ablation in September and a nurse told me not to have a flu jab or covid booster. I am now stuck at home with Covid. I am a little worried about it triggering AFib.
Doea anyone have any advice. I had my ablation in September and a nurse told me not to have a flu jab or covid booster. I am now stuck at home with Covid. I am a little worried about it triggering AFib.
Be-still-my-heart
in
AF Association
10 months ago
Bands pulmonary fibrosis tomography
hello my story in short in 2022 I had covid 19 after recovery I did a lung X-ray which did not show anything suspicious now in September 2023 a year after covid19 I started having breathing difficulties I couldn't breathe deeply and I was falling into bed we can't I'm going to the end of the cascading
hello my story in short in 2022 I had covid 19 after recovery I did a lung X-ray which did not show anything suspicious now in September 2023 a year after covid19 I started having breathing difficulties I couldn't breathe deeply and I was falling into bed we can't I'm going to the end of the cascading
Petre84
in
Lung Conditions Community Forum
10 months ago
A Shingrix thank you
Hi, I just wanted to thank so many of you who have spoken of your side effects with the second Shingrix, yet being worth it. It was when I recently read here that being only half vaccinated was still being open to Shingles that spurred me into getting the second one today, after 2 1/2 years. After
Hi, I just wanted to thank so many of you who have spoken of your side effects with the second Shingrix, yet being worth it. It was when I recently read here that being only half vaccinated was still being open to Shingles that spurred me into getting the second one today, after 2 1/2 years. After
Schubert1870
in
CLL Support
7 months ago
Phone-call from receptionist today
Only just joined and not sure where to begin as I feel as if I’m in shock a little and desperately trying to find out information. I had a phone call from the drs receptionist this afternoon to tell me I have hypothyroidism after some blood tests and needed to pick up a prescription which I would need
Only just joined and not sure where to begin as I feel as if I’m in shock a little and desperately trying to find out information. I had a phone call from the drs receptionist this afternoon to tell me I have hypothyroidism after some blood tests and needed to pick up a prescription which I would need
Benjipuss
in
Thyroid UK
10 months ago
covid meds and prednisolne
Evening all I have PMR and currently tapering Pred down, I am on 3 mg per day. However yesterday I tested positive for Covid. Two questions 1. do I need to inform my GP as my immune system is compromised the NHS site is not clear. 2. What meds does anyone suggest for the hacking cough, runny nose
Evening all I have PMR and currently tapering Pred down, I am on 3 mg per day. However yesterday I tested positive for Covid. Two questions 1. do I need to inform my GP as my immune system is compromised the NHS site is not clear. 2. What meds does anyone suggest for the hacking cough, runny nose
JAC1947
in
PMRGCAuk
10 months ago
Acid Reflux - coughing
I have been suffering for the last 7 weeks with a constant cough. I take Gaviscon and 1 x 20mg omeprazole, I have not seen a doctor yet as I have been away. Does anyone else get a constant cough which may be related to GERD? I also now have a runny nose but can't be a cold as I've had it so long. Can
I have been suffering for the last 7 weeks with a constant cough. I take Gaviscon and 1 x 20mg omeprazole, I have not seen a doctor yet as I have been away. Does anyone else get a constant cough which may be related to GERD? I also now have a runny nose but can't be a cold as I've had it so long. Can
Gib90
in
Scleroderma & Raynaud's UK (SRUK)
7 months ago
A little, very quiet, thumbs up 👍
Well, I've been keeping quiet about returning (again!) to C25K but I have just managed Week 4, Run 3 without any problems so I am HOPING I can finally get back on the trotting pony regularly now. After literally a whole year of Covid, colds, sinus and chest infections, PVF/Long Covid, post-Covid cough
Well, I've been keeping quiet about returning (again!) to C25K but I have just managed Week 4, Run 3 without any problems so I am HOPING I can finally get back on the trotting pony regularly now. After literally a whole year of Covid, colds, sinus and chest infections, PVF/Long Covid, post-Covid cough
Over60sRunner
Graduate
in
Couch to 5K
10 months ago
Long Covid
Hi All Last week I was diagnosed with post covid viral syndrome (long Covid) I am feeling so unwell and fatigued, just wonder if anyone on here is coping with that too Thanks Annie
Hi All Last week I was diagnosed with post covid viral syndrome (long Covid) I am feeling so unwell and fatigued, just wonder if anyone on here is coping with that too Thanks Annie
Annieosb
in
Lung Conditions Community Forum
10 months ago
PMR and Pfizer Covid Vaccine
Within 5 days of my husband and I receiving the first Pfizer Covid jab, he started getting pains in his legs and shoulders. He took paracetamol & used Bio Freeze, similar to deep heat. He got progressively worse, a GP diagnosed Frozen Shoulder over the phone, prescribed Co-Codamol & Naproxen. Within
Within 5 days of my husband and I receiving the first Pfizer Covid jab, he started getting pains in his legs and shoulders. He took paracetamol & used Bio Freeze, similar to deep heat. He got progressively worse, a GP diagnosed Frozen Shoulder over the phone, prescribed Co-Codamol & Naproxen. Within
heartsonfire
in
PMRGCAuk
10 months ago
Pneumonia vaccination
Hi all. I have recently returned to Spain for the foreseeable future and managed to get my covid vaccination shortly after my arrival a few weeks ago. I had my flu vaccination in the UK just before we came out. I have to say that I have responded well to both vaccinations with no adverse side effects
Hi all. I have recently returned to Spain for the foreseeable future and managed to get my covid vaccination shortly after my arrival a few weeks ago. I had my flu vaccination in the UK just before we came out. I have to say that I have responded well to both vaccinations with no adverse side effects
Elispeth
in
PMRGCAuk
10 months ago
FLU SYMPTOMS
Has anyone ever had flu symptoms , eg; achy, with vague headache could this be a symptom of not enough medication of Levothyroxine any answer would be appreciated.
Has anyone ever had flu symptoms , eg; achy, with vague headache could this be a symptom of not enough medication of Levothyroxine any answer would be appreciated.
13vc
in
Thyroid UK
7 months ago
internal shingles
hi, I’ve been diagnosed with internal shingles and it’s the most painful thing I have ever experienced. I’m on my last day of Aciclovir, I’m taking paracetamol and codeine during the day and 3 amitriptyline at night, this has been going on for over a week. Is this normal? Any advice gladly accepted
hi, I’ve been diagnosed with internal shingles and it’s the most painful thing I have ever experienced. I’m on my last day of Aciclovir, I’m taking paracetamol and codeine during the day and 3 amitriptyline at night, this has been going on for over a week. Is this normal? Any advice gladly accepted
Mongoose123
in
PMRGCAuk
9 months ago
Finally got flu vax!
After 4+ months of waiting told 'on the list' many times, nurse from gp surgery came. Says don't know what district nurses are doing lately. 🤷♀️ Also gave me pneumonia vax- never had or been offered before🤔 No Covid as run out. Can I sue if I contract Covid or is it all forgotten about now? Yet I
After 4+ months of waiting told 'on the list' many times, nurse from gp surgery came. Says don't know what district nurses are doing lately. 🤷♀️ Also gave me pneumonia vax- never had or been offered before🤔 No Covid as run out. Can I sue if I contract Covid or is it all forgotten about now? Yet I
fraid
in
Asthma Community Forum
8 months ago
Off on all meds
ITS GOING TI BE 2 YEARS I AM OFF ALL TYPE OF MEDS FOR MY RA.DUE TO ALL KIND OF INFECTIONS.I MUST SAY I HAVE BEING COPING VERY WELL ONCE IN A WILE MY LEFT KNEE GETS SWOLLEN BUT U PUT ICE PADS AND OFF AGAIN.I AM 69 YEARS OLD AND HAVE RA AND SJOGRENS SINCE 40.I HAVE HAD BREAST CANCER LUNG FIBROSIS I SUFFER
ITS GOING TI BE 2 YEARS I AM OFF ALL TYPE OF MEDS FOR MY RA.DUE TO ALL KIND OF INFECTIONS.I MUST SAY I HAVE BEING COPING VERY WELL ONCE IN A WILE MY LEFT KNEE GETS SWOLLEN BUT U PUT ICE PADS AND OFF AGAIN.I AM 69 YEARS OLD AND HAVE RA AND SJOGRENS SINCE 40.I HAVE HAD BREAST CANCER LUNG FIBROSIS I SUFFER
Al1954
in
NRAS
10 months ago
Orphenadrine
My hwp had been using ophenadrine some time ago and stopped because of fears around using anticholinergics. However, his unrelenting battle with sciatica has me wondering if it might not be worth taking the risk. He is a well person in every other way, but the pain has him battling to do exercise. He
My hwp had been using ophenadrine some time ago and stopped because of fears around using anticholinergics. However, his unrelenting battle with sciatica has me wondering if it might not be worth taking the risk. He is a well person in every other way, but the pain has him battling to do exercise. He
ghoegap
in
Cure Parkinson's
10 months ago
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