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Covid and under active thyroid
I have just had covid for first time, and it hit me pretty badly, like a bad flu. My glands felt really swollen during it, particularly before, and still do. I'm also so tired. Sleeping a lot. Feel sluggish. Fat for no reason and constipated. This is all the feeling for me that my thyroid is under
I have just had covid for first time, and it hit me pretty badly, like a bad flu. My glands felt really swollen during it, particularly before, and still do. I'm also so tired. Sleeping a lot. Feel sluggish. Fat for no reason and constipated. This is all the feeling for me that my thyroid is under
Billy2023
in
Thyroid UK
8 months ago
clinical trial vyd222 monoclonal AB against covid update science 37
thought i'd give an update on my experience with this study. i got my first infusion on oct 17th and had no ill effects other than my blood pressure getting super high. but i think that was from the last minute fumbles in planning thru science 37. my infusion medicine was supposed to arrive the afternoon
thought i'd give an update on my experience with this study. i got my first infusion on oct 17th and had no ill effects other than my blood pressure getting super high. but i think that was from the last minute fumbles in planning thru science 37. my infusion medicine was supposed to arrive the afternoon
bachplayer13
in
CLL Support
8 months ago
Tuberculosis
I have been talking medication for lymph node tb for 4 months now, however i have been developing fever and night sweats for the past few day. Is it common to have fever and nights sweats 4 months into the treatment? My lymph node is secreting pus and is very itchy.
I have been talking medication for lymph node tb for 4 months now, however i have been developing fever and night sweats for the past few day. Is it common to have fever and nights sweats 4 months into the treatment? My lymph node is secreting pus and is very itchy.
Premika
in
TB Alert
6 months ago
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COVID-19 Infection effect on Urinary Incontinence and Mirabegron.
Dear Simon Foundation, I'm an old member of HU as a CLL type Leukaemia patient in the UK, but only just discovered your Simon foundation. Now I've always had poor bladder control and that could be due to bladder sensitivity, BPH, or damaged nerves in my lower back or all three, or more. I've gone through
Dear Simon Foundation, I'm an old member of HU as a CLL type Leukaemia patient in the UK, but only just discovered your Simon foundation. Now I've always had poor bladder control and that could be due to bladder sensitivity, BPH, or damaged nerves in my lower back or all three, or more. I've gone through
Ernest2
in
The Simon Foundation for Continence
8 months ago
Covid vax and AFIB
just as an FYI, I had a Covid vaccination (Pfizer) a couple of days ago and I developed AFIB within a few hours. It did resolve itself overnight after I took extra metoprolol.
just as an FYI, I had a Covid vaccination (Pfizer) a couple of days ago and I developed AFIB within a few hours. It did resolve itself overnight after I took extra metoprolol.
Awksom
in
CLL Support
8 months ago
thrush……again
For the past three months I’ve been trying to get rid of a bad taste in my mouth. The roof of my mouth feels like I’ve burned my mouth on a too hot pizza. The middle of my tongue is coated the tip is somewhat red. My dentist said X-rays show no infection. GP looked in my mouth and said
For the past three months I’ve been trying to get rid of a bad taste in my mouth. The roof of my mouth feels like I’ve burned my mouth on a too hot pizza. The middle of my tongue is coated the tip is somewhat red. My dentist said X-rays show no infection. GP looked in my mouth and said
Mstiles
in
PMRGCAuk
1 year ago
Anti viral?
Does anyone know if they're still giving anti viral medication for a positive covid patient? I'm on rituximab and azathioprine aswell as prednisolone. I've not yet done a test but have been feeling breathless and coughing more than normal. I'm not allowed to have my covid or flu vaccinations due to
Does anyone know if they're still giving anti viral medication for a positive covid patient? I'm on rituximab and azathioprine aswell as prednisolone. I've not yet done a test but have been feeling breathless and coughing more than normal. I'm not allowed to have my covid or flu vaccinations due to
Vqueen
in
Vasculitis UK
8 months ago
B12 Ampoules
Hello everyone. I hope you are all keeping well 🙏 I am slowly recovering from Covid which I caught 6 weeks ago. I had the booster vaccine- the 4th vaccine-It takes 2 weeks to become effective and I managed to catch Covid before the vaccine kicked in. Just my luck ! 🙄Wish I could be so lucky with
Hello everyone. I hope you are all keeping well 🙏 I am slowly recovering from Covid which I caught 6 weeks ago. I had the booster vaccine- the 4th vaccine-It takes 2 weeks to become effective and I managed to catch Covid before the vaccine kicked in. Just my luck ! 🙄Wish I could be so lucky with
dollcat
in
Pernicious Anaemia Society
8 months ago
Starting Pegasys soon
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
IsabelleHo
in
MPN Voice
6 months ago
COPD and Pneumonia
Hello. My mom has severe COPD and got out of the hospital last week after a 3 week stay for pneumonia. She’s had COPD for 16 years and just went on O2 about a year ago. She’s always done well with the COPD and never had an exacerbation until the pneumonia. I know it can take a very long time for the
Hello. My mom has severe COPD and got out of the hospital last week after a 3 week stay for pneumonia. She’s had COPD for 16 years and just went on O2 about a year ago. She’s always done well with the COPD and never had an exacerbation until the pneumonia. I know it can take a very long time for the
nyla668
in
Lung Conditions Community Forum
2 months ago
enlarged lymp node
I had a ct scan yesterday and got the results today. I have enlarged left axillary lymph nodes, largest measuring 19x14 mm, previously subcentimeter and measured 10x8.5. Enlarged left subpectoral lymph nodes are identified. Nothing on the right side. I had a covid vacine about 2-3 weeks ago. The
I had a ct scan yesterday and got the results today. I have enlarged left axillary lymph nodes, largest measuring 19x14 mm, previously subcentimeter and measured 10x8.5. Enlarged left subpectoral lymph nodes are identified. Nothing on the right side. I had a covid vacine about 2-3 weeks ago. The
DianeSH
in
CLL Support
8 months ago
Covid
Hello, everyone I have severe emphysema and I did a test yesterday and I got covid 😱 I am scared it gonna attack my lungs, my chest feeling tighter.Anyone else had covid with emphysema, how did you take care of yourself to stop it going to the lungs.
Hello, everyone I have severe emphysema and I did a test yesterday and I got covid 😱 I am scared it gonna attack my lungs, my chest feeling tighter.Anyone else had covid with emphysema, how did you take care of yourself to stop it going to the lungs.
Madonna1
in
COPD Friends
8 months ago
Pituitary gland not producing TSH
Oct 14, 2022 I had a 3rd Covid Booster shot. The next day I had the "normal" flu symptoms. Oct 20, six days later, I felt I had been hit by a bus, hurting literally from head to toe with different kinds of pain along with heartburn and leg swelling. I figured this was just a reaction that would subside
Oct 14, 2022 I had a 3rd Covid Booster shot. The next day I had the "normal" flu symptoms. Oct 20, six days later, I felt I had been hit by a bus, hurting literally from head to toe with different kinds of pain along with heartburn and leg swelling. I figured this was just a reaction that would subside
Cricket-mas
in
Thyroid UK
8 months ago
Exercise and PMR
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
Indigo2417
in
PMRGCAuk
8 months ago
treatment for thin lining?
Hello, I’ve got PCOS but ovulate and have an average cycle of 32 days. I’ve been told I have a thin lining 4-5mm. I saw a private dr who gave me cyclogest post ovulation and I’ve used it for two cycles, which have both resulted in a negative test. Does anyone know what the treatment is for a thin lining
Hello, I’ve got PCOS but ovulate and have an average cycle of 32 days. I’ve been told I have a thin lining 4-5mm. I saw a private dr who gave me cyclogest post ovulation and I’ve used it for two cycles, which have both resulted in a negative test. Does anyone know what the treatment is for a thin lining
tarka123
in
Fertility Network UK
4 months ago
ADT and crying
Does anyone else that has been on ADT drugs for years have trouble with tears or crying for no real reason? I tear up anymore at just the thought of something sad. It’s a major pain in the ass, not to mention embarrassing because I am still employed. Wondering if there is a solution other than stopping
Does anyone else that has been on ADT drugs for years have trouble with tears or crying for no real reason? I tear up anymore at just the thought of something sad. It’s a major pain in the ass, not to mention embarrassing because I am still employed. Wondering if there is a solution other than stopping
joeguy
in
Advanced Prostate Cancer
6 months ago
TINGLY FEET
Has anyone on here experienced tingly feet during the night after having steroid injections in the knees. I had the injections in both of my knees for arthritis only four days ago. The tingly feeling seems just like having a flare when I need to increase my steroids. It goes as soon as I get up in the
Has anyone on here experienced tingly feet during the night after having steroid injections in the knees. I had the injections in both of my knees for arthritis only four days ago. The tingly feeling seems just like having a flare when I need to increase my steroids. It goes as soon as I get up in the
Wallydb
in
PMRGCAuk
4 months ago
GPA flare, is it likely even if I only have 1 symptom
I was diagnosed with GPA in 2017, I have had 3 flares since initial diagnosis and although the symptoms have got milder each time, I always have the same symptoms - pain and loss of hearing in my ear, discomfort and blood in my nose, pain and stiffness in my finger joints and extreme fatigue. I regularly
I was diagnosed with GPA in 2017, I have had 3 flares since initial diagnosis and although the symptoms have got milder each time, I always have the same symptoms - pain and loss of hearing in my ear, discomfort and blood in my nose, pain and stiffness in my finger joints and extreme fatigue. I regularly
stuc
in
Vasculitis UK
6 months ago
enlarged sore breasts
hi - rather embarrassing but here goes! Approximately 2 weeks ago I had to increase levothyroxine to 100 mcgs- breasts are now enlarged and sore. I can’t be pregnant- I happen to of had routine breast scan just prior to meds increase and no abnormalities detected. Has anyone else experienced this
hi - rather embarrassing but here goes! Approximately 2 weeks ago I had to increase levothyroxine to 100 mcgs- breasts are now enlarged and sore. I can’t be pregnant- I happen to of had routine breast scan just prior to meds increase and no abnormalities detected. Has anyone else experienced this
Purplepuffin
in
Thyroid UK
6 months ago
Arnica cream for jab reactions
Just posting in case it's useful to anyone else...🤞 I've posted previously about a hive style reaction I get after SC injections on my tummy. I've tried allsorts, including strong antihistamines and mild steroid cream, to ease the itch and calm the redness. I've now found that Arnica cream is the
Just posting in case it's useful to anyone else...🤞 I've posted previously about a hive style reaction I get after SC injections on my tummy. I've tried allsorts, including strong antihistamines and mild steroid cream, to ease the itch and calm the redness. I've now found that Arnica cream is the
ClaireWF1346
in
Pernicious Anaemia Society
6 days ago
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