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Genital chlamydial infection
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Unexplained increase in mortality rates
I'd like to begin by saying I'm not a conspiracy theorist by any stretch of the imagination but having heard so many stories (mostly first hand and through personal experience) since the outbreak of Covid in Jan 2020 I am beginning to question what's going on. A recent publication in LANCET, no less
I'd like to begin by saying I'm not a conspiracy theorist by any stretch of the imagination but having heard so many stories (mostly first hand and through personal experience) since the outbreak of Covid in Jan 2020 I am beginning to question what's going on. A recent publication in LANCET, no less
SuperSanta
in
British Heart Foundation
6 months ago
covid 19 and Funcational Gait Disorder
Hi All I’ve had Funcational Gait disorder for 12 long years now, so cannot walk very far and rely on my mobility scooter and walking stick to get around. Last Sunday I came down with covid and it seems to have attacked my legs so I’m almost unable to stand let alone walk a few steps. Has anyone else
Hi All I’ve had Funcational Gait disorder for 12 long years now, so cannot walk very far and rely on my mobility scooter and walking stick to get around. Last Sunday I came down with covid and it seems to have attacked my legs so I’m almost unable to stand let alone walk a few steps. Has anyone else
lorettapalmer
in
Functional Neurological Disorder - FND Hope
6 months ago
Need advice on what to do next!
Recently diagnosed with Hashimotos following endocrinologist appt, which was actually to investigate causes for my hair loss (lost 60% of hair after covid vaccination, then Covid itself in early 2022). Also been suffering other symptoms for around 2 years - weight gain, tired all the time, joint pains
Recently diagnosed with Hashimotos following endocrinologist appt, which was actually to investigate causes for my hair loss (lost 60% of hair after covid vaccination, then Covid itself in early 2022). Also been suffering other symptoms for around 2 years - weight gain, tired all the time, joint pains
ErnieBear
in
Thyroid UK
6 months ago
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common cold lingers
back in April 2020 i had covid the first time (that was early before we knew anything) since then when i get a cold (head cold, sinus infection, common cold) i notice that i feel bad for like 3-5 days but i will have a lingering cough for like a 5-10 days afterwards. i was blaming it on covid and the
back in April 2020 i had covid the first time (that was early before we knew anything) since then when i get a cold (head cold, sinus infection, common cold) i notice that i feel bad for like 3-5 days but i will have a lingering cough for like a 5-10 days afterwards. i was blaming it on covid and the
pete-paz
in
CLL Support
6 days ago
post quadruple bypass
I first started having problems in my legs in 2010.I was sent to vascular specialist who stated there was nothing wrong and from that I was sent for heart tests and again I was told there was nothing wrong.The pain was increasing in my right calf and was then in my left calf.I explained I was scared
I first started having problems in my legs in 2010.I was sent to vascular specialist who stated there was nothing wrong and from that I was sent for heart tests and again I was told there was nothing wrong.The pain was increasing in my right calf and was then in my left calf.I explained I was scared
wardywill
in
British Heart Foundation
6 months ago
Pegasys side effects
I was switched from 500 Hydroxyurea/day to 90mg Pegasys every two weeks. The pain in hips and thighs is substantial - headache also, but not as bothersome as the muscle pain. Has anyone else experience this on Pegasys. Also, has anyone tried CoQ10 for muscle pain and has it work? Thanks
I was switched from 500 Hydroxyurea/day to 90mg Pegasys every two weeks. The pain in hips and thighs is substantial - headache also, but not as bothersome as the muscle pain. Has anyone else experience this on Pegasys. Also, has anyone tried CoQ10 for muscle pain and has it work? Thanks
Dusty777
in
MPN Voice
4 months ago
Covid
Two members of my family have Covid.. My mum is suffering from ET. She bever got vaccinated cos she got scared at that time due to many cases of thrombosis and sudden deaths we had in my country.. Anyone else who hasn't got the vaccine and went through Covid. We were maked and kept distance and all but
Two members of my family have Covid.. My mum is suffering from ET. She bever got vaccinated cos she got scared at that time due to many cases of thrombosis and sudden deaths we had in my country.. Anyone else who hasn't got the vaccine and went through Covid. We were maked and kept distance and all but
PHGR
in
MPN Voice
6 months ago
Efficacy of Trihexyphenidyl on Apraxia of Eyelid Opening in Parkinsonism: A Case Report
Apraxia of eyelid opening (AEO) is occasionally seen in Parkinson’s disease (PD) or related diseases. However, many clinicians have trouble with the management of AEO by Parkinsonism. The following link mentions a case of apraxia of eyelids opening in PD patient which was successfully treated with the
Apraxia of eyelid opening (AEO) is occasionally seen in Parkinson’s disease (PD) or related diseases. However, many clinicians have trouble with the management of AEO by Parkinsonism. The following link mentions a case of apraxia of eyelids opening in PD patient which was successfully treated with the
Farooqji
in
Cure Parkinson's
4 months ago
Free Covid Rapid Lateral Flow Test
Does anyone know how to obtain Covid Rapid Lateral Flow Tests free-of-charge in the U.K.? The Gov U.K. site says they are not available direct but are available via your local Pharmacy. None of my local pharmacy stores issue these tests free-of-charge under the NHS but are happy to charge £13 each, even
Does anyone know how to obtain Covid Rapid Lateral Flow Tests free-of-charge in the U.K.? The Gov U.K. site says they are not available direct but are available via your local Pharmacy. None of my local pharmacy stores issue these tests free-of-charge under the NHS but are happy to charge £13 each, even
Richardmint
in
CLL Support
6 months ago
My rheumy tele-consultation due to Covid.
HAPPY NEW YEAR. Hope you all enjoy much better health in 2024. An update. A couple of weeks back I had a tele-consultation with my rheumy as I had Covid. This was my 1st encounter with Covid after 3 years and 8 months! On the tele-consult app I was able to upload a brief resumé of my last
HAPPY NEW YEAR. Hope you all enjoy much better health in 2024. An update. A couple of weeks back I had a tele-consultation with my rheumy as I had Covid. This was my 1st encounter with Covid after 3 years and 8 months! On the tele-consult app I was able to upload a brief resumé of my last
IdasMum
in
PMRGCAuk
6 months ago
Pelvic pain and sex
Hi , sorry sounds like a stupid question - Does sex hurt with reoccurring pelvic pain ? Can it trigger the pain to come back or an infection to start if someone has abscess in pelvic area such as fallopian tubes or near ovaries?
Hi , sorry sounds like a stupid question - Does sex hurt with reoccurring pelvic pain ? Can it trigger the pain to come back or an infection to start if someone has abscess in pelvic area such as fallopian tubes or near ovaries?
Hannah818
in
Pelvic Pain Support Network
4 months ago
Hep B immunity blood test positive
Hi all I was asked by my clinic to do a Hep B core blood test which I believe is same as immunity one and I asked my GP for the tests. It’s come back as not immune to hep b. Does that mean I won’t be entitled to a donor egg treatment? I’m freaking out 😟 Please share your thoughts and experience
Hi all I was asked by my clinic to do a Hep B core blood test which I believe is same as immunity one and I asked my GP for the tests. It’s come back as not immune to hep b. Does that mean I won’t be entitled to a donor egg treatment? I’m freaking out 😟 Please share your thoughts and experience
Milo2011
in
Fertility Network UK
4 months ago
FISH TESTING - ‘Admin Edit’ - please read sad update on this post before replying.
I apologize if I am incorrect with the name of the testing results below. My husbands first CLL Dr 5 years ago had him on watch and wait. When he received the following results Tumor/ Prognostic Markers: CD38+ ZAP70+ Trisomy 12. IgVH unmutated, I researched the results which were very concerning to
I apologize if I am incorrect with the name of the testing results below. My husbands first CLL Dr 5 years ago had him on watch and wait. When he received the following results Tumor/ Prognostic Markers: CD38+ ZAP70+ Trisomy 12. IgVH unmutated, I researched the results which were very concerning to
Debcap61
in
CLL Support
6 months ago
PAF well controlled till I got covid
hi, I’m new to this forum and hope you can give me some hope. I’ve had PAF for 13 years, well controlled on propranolol 80mg slow release - other beta blockers seem to affect my chest/throat and give me dreadful indigestion and can’t tolerate the newer ones. However in November whilst on holiday in
hi, I’m new to this forum and hope you can give me some hope. I’ve had PAF for 13 years, well controlled on propranolol 80mg slow release - other beta blockers seem to affect my chest/throat and give me dreadful indigestion and can’t tolerate the newer ones. However in November whilst on holiday in
Clifflove
in
Atrial Fibrillation Support
6 months ago
On Venetoclax, lymph node appeared
Trying not to worry but a lymph node in my armpit swelled up. I feel fine, no colds, fevers or recent vaccinations. Even did a Covid test because I have had Covid totally asymptomatic but negative. Has anyone have this happen and it turned out to be nothing. Hoping this is just a fluke but it seems
Trying not to worry but a lymph node in my armpit swelled up. I feel fine, no colds, fevers or recent vaccinations. Even did a Covid test because I have had Covid totally asymptomatic but negative. Has anyone have this happen and it turned out to be nothing. Hoping this is just a fluke but it seems
Alex830
in
CLL Support
6 months ago
Shingles
Has anyone had shingles? I've been hit with it, I havent had any treatment for my CLL, it's been 11 years. I need to know what to do about the shingles pain. In the almost 3 week.
Has anyone had shingles? I've been hit with it, I havent had any treatment for my CLL, it's been 11 years. I need to know what to do about the shingles pain. In the almost 3 week.
sallylou
in
CLL Support
4 months ago
First Injection of Pegasys
I FINALLY got approved for Pegasys, and am to pick it up at the pharmacy by Wednesday. My question is does the first injection happen in the Drs. office, or at home?? Were you given physical instructions for how to give the injection? I have written instructions that were sent to me with the approval
I FINALLY got approved for Pegasys, and am to pick it up at the pharmacy by Wednesday. My question is does the first injection happen in the Drs. office, or at home?? Were you given physical instructions for how to give the injection? I have written instructions that were sent to me with the approval
dogsandhorses
in
MPN Voice
4 months ago
Covid 19 vaccine UK
Hi there, I’d welcome any information you have on eligibility for Covid 19 vaccination in the U.K. I’ve looked at the .gov.uk website and in one place it includes epilepsy under neurological conditions, in another place it doesn’t. I did have an in invitation from my GP for flu, but not for Covid.
Hi there, I’d welcome any information you have on eligibility for Covid 19 vaccination in the U.K. I’ve looked at the .gov.uk website and in one place it includes epilepsy under neurological conditions, in another place it doesn’t. I did have an in invitation from my GP for flu, but not for Covid.
GillyA
in
Epilepsy Action
6 months ago
INVOLVEMENT OPPORTUNITY: Have you been diagnosed with hepatitis C and interested in sharing your story? (England)
Have you been diagnosed with hepatitis C and would you be interested in sharing your story with the national press to promote an NHS campaign? The NHS has launched a new service for people to test at home for hepatitis C. To help make more people aware, we are looking for individuals in England who
Have you been diagnosed with hepatitis C and would you be interested in sharing your story with the national press to promote an NHS campaign? The NHS has launched a new service for people to test at home for hepatitis C. To help make more people aware, we are looking for individuals in England who
BritishLiverTrust1
Partner
in
British Liver Trust
4 months ago
Update after3years
I was in a covid coma 3years ago and posted in here to soon after I got home my brain was so hyper for a bout a month I felt so.guilty that I survived when ppl were loosing husband's wives children mum's dad's etc when I still do but I did survive I went to therapist who helped a lot and helped me
I was in a covid coma 3years ago and posted in here to soon after I got home my brain was so hyper for a bout a month I felt so.guilty that I survived when ppl were loosing husband's wives children mum's dad's etc when I still do but I did survive I went to therapist who helped a lot and helped me
Drewc
in
ICUsteps
6 months ago
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