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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
Live vaccine for dengue fever
My son lives in Bali. He is in the middle of a very severe bout of dengue fever. I am going to visit him for 3 weeks in July. He has suggested I should have a vaccine before I go. I can find that it is called a " live attenuated dengue tetravalent vaccine". Even the vaccine side effects can be pretty
My son lives in Bali. He is in the middle of a very severe bout of dengue fever. I am going to visit him for 3 weeks in July. He has suggested I should have a vaccine before I go. I can find that it is called a " live attenuated dengue tetravalent vaccine". Even the vaccine side effects can be pretty
Graham64
in
CLL Support
4 months ago
My husband still on sedation after 30 days going in for a peritonitis
Hello my husband went in the ER for stomach pains and could not really breath .He was admitted immediately with the diagnosis peritonitis which leaked in his stomach so he got surgery soon after surgery he started septic shock and next thing we knew he wasn't able to get off the ventilator and in the
Hello my husband went in the ER for stomach pains and could not really breath .He was admitted immediately with the diagnosis peritonitis which leaked in his stomach so he got surgery soon after surgery he started septic shock and next thing we knew he wasn't able to get off the ventilator and in the
CarlMc116
in
ICUsteps
4 months ago
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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
7 months ago
Advice request - going in circles with doctors
Hi all, I've been suffering with endometriosis for years but I'm really struggling to get proper help with it, and the doctors seem to be thinking now it might be something else. I've had surgery to remove endometriosis twice (and the second time I also had an ovarian cyst removed which was larger than
Hi all, I've been suffering with endometriosis for years but I'm really struggling to get proper help with it, and the doctors seem to be thinking now it might be something else. I've had surgery to remove endometriosis twice (and the second time I also had an ovarian cyst removed which was larger than
Bookworm321123
in
Endometriosis UK
4 months 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
7 months ago
Does asthma severity tend to reflect that of sinuses?
I wasn’t sure where to post this but please tell me if it’s out of place as I’l move it. Basically I’ve had chronic sinusitis with polyps for over a decade. It is more chronic inflammation that’s the issue, with meds the polyps are only small/secondary to the inflammation. I don’t have asthma but
I wasn’t sure where to post this but please tell me if it’s out of place as I’l move it. Basically I’ve had chronic sinusitis with polyps for over a decade. It is more chronic inflammation that’s the issue, with meds the polyps are only small/secondary to the inflammation. I don’t have asthma but
Unfocusedarrow
in
Asthma Community Forum
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
7 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
7 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
7 months ago
trauma after icu stay
hi in2020 I was rushed to kings hospital London with septic shock due to ulcers on my liver. I was in an induced coma for a week and in hospital for 5 weeks. During the last 3 months I have been having really bad nightmares about being in a coma, specifically that my doctor is trying to kill me (i really
hi in2020 I was rushed to kings hospital London with septic shock due to ulcers on my liver. I was in an induced coma for a week and in hospital for 5 weeks. During the last 3 months I have been having really bad nightmares about being in a coma, specifically that my doctor is trying to kill me (i really
ZoeH1974
in
ICUsteps
5 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
7 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
7 months ago
Has anyone had good success with Low Dose Naltrexone (LDN) for chronically reactivated EBV?
Has anyone had good success with Low Dose Naltrexone (LDN) for chronically reactivated EBV? Answered by Sebastian Denison, RPh https://youtu.be/ifWvF7Yz52Y
Has anyone had good success with Low Dose Naltrexone (LDN) for chronically reactivated EBV? Answered by Sebastian Denison, RPh https://youtu.be/ifWvF7Yz52Y
Shewulf
Administrator
in
LDN Research Trust
5 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
7 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
7 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
7 months ago
Keep getting chest infections
hello I had open heart surgery in June to repair my mitral valve. The surgery was a great success, I’ve recovered well and I am back to working full time. However, whereas before surgery I very rarely got Ill , I now seem to pick up every big going 🤦🏻♀️ And end up quite poorly. I am on statins and
hello I had open heart surgery in June to repair my mitral valve. The surgery was a great success, I’ve recovered well and I am back to working full time. However, whereas before surgery I very rarely got Ill , I now seem to pick up every big going 🤦🏻♀️ And end up quite poorly. I am on statins and
Plum44
in
British Heart Foundation
7 months ago
pneumonia vaccination
I have been told to get my pneumonia jab , i’m not worried about sore arm, but i’m just a bit concerned i might feel poorly after. I didn’t feel poorly after my flu jab or covid booster. Any reassurance would be appreciated. Thank you.
I have been told to get my pneumonia jab , i’m not worried about sore arm, but i’m just a bit concerned i might feel poorly after. I didn’t feel poorly after my flu jab or covid booster. Any reassurance would be appreciated. Thank you.
Collie4
in
Lung Conditions Community Forum
5 months ago
Covid day four....U.K
Hi all. This sounds so stupid but I thought it was a regular cold. Just did a COVID test and it's positive. I think it maybe too late to access antivirals now? What should I do? Sorry, just a bit panicked. Thank you in advance.
Hi all. This sounds so stupid but I thought it was a regular cold. Just did a COVID test and it's positive. I think it maybe too late to access antivirals now? What should I do? Sorry, just a bit panicked. Thank you in advance.
Basil01
in
CLL Support
7 months ago
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