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lung nodule / proposed surgery / scared and confused
Hello, thank you for this site. My best to all on this site for health and happiness. I’m not even sure where I may be at on this journey but am certainly scared and confused . In March of 2022 I had a kidney stone and a lung nodule was detected on right lower lobe and suggested follow up in 3 -6 months
Hello, thank you for this site. My best to all on this site for health and happiness. I’m not even sure where I may be at on this journey but am certainly scared and confused . In March of 2022 I had a kidney stone and a lung nodule was detected on right lower lobe and suggested follow up in 3 -6 months
ghostyinmass
in
Lung Cancer Support
5 months ago
Biologic with covid
Testing positive for covid and am am taking a biologic.Like my head the info is a bit wooly, but I think it maybe that I should suspend the biologic until covid test is negative. Presume this is correct as i think it should make sense. Is anyone in similar circumstances able to confirm or otherwise?
Testing positive for covid and am am taking a biologic.Like my head the info is a bit wooly, but I think it maybe that I should suspend the biologic until covid test is negative. Presume this is correct as i think it should make sense. Is anyone in similar circumstances able to confirm or otherwise?
Wantplaytennis
in
NRAS
5 months ago
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
5 months ago
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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
5 months ago
Feeling poorly
Evening everyone, I have continued to feel increasingly unwell. Shoulder and neck pain continues and keeps me awake or wakes me up every night now. I sometimes wake up with sweat around my neck and chest. The steroid injection I had 13 days ago helped a bit to decrease the intensity of pain but it hasn
Evening everyone, I have continued to feel increasingly unwell. Shoulder and neck pain continues and keeps me awake or wakes me up every night now. I sometimes wake up with sweat around my neck and chest. The steroid injection I had 13 days ago helped a bit to decrease the intensity of pain but it hasn
MsWhistledown
in
Thyroid UK
5 months ago
GP appointment and blood tests - will recent steroid injection skew results?
Afternoon everyone, I had a GP appointment yesterday to discuss my symptoms. Went through everything that has happened since the summer. She sent me for blood tests today which included CRP, ESR, Rheumatoid factor and various other tests relating to autoimmune conditions. She insisted I call back for
Afternoon everyone, I had a GP appointment yesterday to discuss my symptoms. Went through everything that has happened since the summer. She sent me for blood tests today which included CRP, ESR, Rheumatoid factor and various other tests relating to autoimmune conditions. She insisted I call back for
MsWhistledown
in
PMRGCAuk
5 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
5 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
5 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
5 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
5 months ago
What do I tell my doctor?😢
Hi everyone! I am 3 months post op, and have been on the pill back to back since my first period after op. I still have periods and this is my third. This period I couldn't fight anymore, and I went to the ER where they did an intravaginal ultrasound and found a cyst. I bled for 5 days, stopped,
Hi everyone! I am 3 months post op, and have been on the pill back to back since my first period after op. I still have periods and this is my third. This period I couldn't fight anymore, and I went to the ER where they did an intravaginal ultrasound and found a cyst. I bled for 5 days, stopped,
Hooplove00
in
Endometriosis UK
10 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
5 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
5 months ago
PMR symptoms after steroid injection 12 days ago
Happy New Year everyone. I hope you all had a wonderful Christmas .🎄 I posted just before Christmas about awful shoulder and neck pain and that I saw a private doctor who thinks my symptoms are PMR. He gave me a steroid injection. It has helped dampen down the pain. It was excruciating but has since
Happy New Year everyone. I hope you all had a wonderful Christmas .🎄 I posted just before Christmas about awful shoulder and neck pain and that I saw a private doctor who thinks my symptoms are PMR. He gave me a steroid injection. It has helped dampen down the pain. It was excruciating but has since
MsWhistledown
in
PMRGCAuk
5 months ago
steroid injection
Hi everyone Happy New Year to you all. Can anyone answer my question if it's safe to have a steroid injection for frozen shoulder if you have open angle glaucoma? Don't know what to do. Many thanks in advance.
Hi everyone Happy New Year to you all. Can anyone answer my question if it's safe to have a steroid injection for frozen shoulder if you have open angle glaucoma? Don't know what to do. Many thanks in advance.
callie77
in
Glaucoma UK
5 months ago
steroid injection for back pain with pain team?
hello, I have had back pain for as long as I remember however 3 years ago was the first episode of severe spasm in my whole back making me collapse and couldn’t be moved for hours. I was put on gabapentin for 2.5 years which I have tapered off because I’m not sure the problem was nerve pain and the mri
hello, I have had back pain for as long as I remember however 3 years ago was the first episode of severe spasm in my whole back making me collapse and couldn’t be moved for hours. I was put on gabapentin for 2.5 years which I have tapered off because I’m not sure the problem was nerve pain and the mri
Louiseelaine
in
Stanmore Young Spine Group
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
5 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
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
5 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
5 months ago
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