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Covid & dosing
Hi, I tested +ve for covid this morning. It's the first time I've had it. I've had 5 vacs. My temperature is high & I'm taking paracetamol for that.My question is, should I alter my T4/NDT dose? I haven't been ill at all since I started on thyroid meds in 2015. I wondered if I should increase, decrease
Hi, I tested +ve for covid this morning. It's the first time I've had it. I've had 5 vacs. My temperature is high & I'm taking paracetamol for that.My question is, should I alter my T4/NDT dose? I haven't been ill at all since I started on thyroid meds in 2015. I wondered if I should increase, decrease
amala57
in
Thyroid UK
9 months ago
Have COVID - should I get Paxlovid/
I have CLL and in W&W and also have ET. I am 67 yrs old, fully vaccinated and otherwise in good health Tested positive yesterday for COVID. Day three of my symptoms are uncomfortable but bearable. Should I get Paxlovid?
I have CLL and in W&W and also have ET. I am 67 yrs old, fully vaccinated and otherwise in good health Tested positive yesterday for COVID. Day three of my symptoms are uncomfortable but bearable. Should I get Paxlovid?
Lambo1
in
CLL Support
9 months ago
PBC and nails / gel polish / acrylic
hi everyone, just a quick question.. I wondered has anyone had any issues with having their nails done with gel polish. I had to switch from gel polish to acrylic as my nails kept having a reaction to the gel - and often developed a fungal infection. Once I switched to acrylic they were much better
hi everyone, just a quick question.. I wondered has anyone had any issues with having their nails done with gel polish. I had to switch from gel polish to acrylic as my nails kept having a reaction to the gel - and often developed a fungal infection. Once I switched to acrylic they were much better
Deemum
in
PBC Foundation
5 months ago
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Being taking off Pegasys. :( Looking for alternatives
Hi all, I have ET & PV with Jak2. I am 40. I have been on aspirin for over 10 years, but had to start Pegasys 3 months ago. I haven't tolerated it well. Severe shortness of breath etc. My hematologist reduced my dose to 30 per week, but I am suffering with hypertension (150 to 69/96 on average) and
Hi all, I have ET & PV with Jak2. I am 40. I have been on aspirin for over 10 years, but had to start Pegasys 3 months ago. I haven't tolerated it well. Severe shortness of breath etc. My hematologist reduced my dose to 30 per week, but I am suffering with hypertension (150 to 69/96 on average) and
JustKeepSw1mming
in
MPN Voice
10 months ago
Flu Symptoms
Hi I was recently diagnosed with Fibromylgia. I have had the flu and I am struggling to recover from it. I am 2 weeks in now and I am still feeling weak, dizzy, getting bad headache and have a rasping cough. Does anyone struggle to recover when having a virus..? Thanks
Hi I was recently diagnosed with Fibromylgia. I have had the flu and I am struggling to recover from it. I am 2 weeks in now and I am still feeling weak, dizzy, getting bad headache and have a rasping cough. Does anyone struggle to recover when having a virus..? Thanks
Mark1973
in
Fibromyalgia Action UK
5 months ago
Natural cycle FET likely to be cancelled due to ovulation on small follicle. What does this mean about my eggs/ ovaries? Having a wobble
Oh it's been a trial. Last month my cycle was cancelled due to COVID and this month, my bloods show I'm due to ovulate but follicle is only 12mm. I have been quite ill with Covid and pretty stressed getting ready to start a new job but was so hopeful to get this transfer done before Christmas but my
Oh it's been a trial. Last month my cycle was cancelled due to COVID and this month, my bloods show I'm due to ovulate but follicle is only 12mm. I have been quite ill with Covid and pretty stressed getting ready to start a new job but was so hopeful to get this transfer done before Christmas but my
Minniemouse88
in
Fertility Network UK
9 months ago
Prescribed Naproxine 250 twice a day for hip bursitis is that dangerous with Pred
I was prescribed Naproxine 250 twice a day yesterday for bursitis ? on right hip. Pain is so bad dr. gave a steroid injection. Suggested I take up to 4g of Paracetamol if necessary. Just read of NHS site that Naproxine and Pred are not compatible. Is this true for short time use? If so what
I was prescribed Naproxine 250 twice a day yesterday for bursitis ? on right hip. Pain is so bad dr. gave a steroid injection. Suggested I take up to 4g of Paracetamol if necessary. Just read of NHS site that Naproxine and Pred are not compatible. Is this true for short time use? If so what
Motida
in
PMRGCAuk
9 months ago
Companies that test liver biospy tissue to see what immunotherapy, parp inhibitors or ATK inhibitors would work?
as above, so far pca Adenocarcinoma in liver biopsy tissue…. Anyone have a list?
as above, so far pca Adenocarcinoma in liver biopsy tissue…. Anyone have a list?
Shorehousejam
in
Advanced Prostate Cancer
2 months ago
Covid, strange beast.
I find Covid a bizarre virus. I have had 3 times , hospitalised once. I am in remission after stage 4 diagnosis in 2020. My wife last returned from a company business meeting in Malta attended by 500 employees. She and many of her work mates now in bed with Covid. This is the 4th time my wife has had
I find Covid a bizarre virus. I have had 3 times , hospitalised once. I am in remission after stage 4 diagnosis in 2020. My wife last returned from a company business meeting in Malta attended by 500 employees. She and many of her work mates now in bed with Covid. This is the 4th time my wife has had
stevesmith1964
in
CLL Support
9 months ago
Fod Map Diet
Good morning have been on Fodmap diet since March . Has been getting less strict as I eat some dairy but my diet is generally getting more and more restricted.Im also a Pescatarian and feel that I aren’t getting enough protein or variation . Main Symptoms are Anxiety,dizziness,tinnitus,Nausea,wind
Good morning have been on Fodmap diet since March . Has been getting less strict as I eat some dairy but my diet is generally getting more and more restricted.Im also a Pescatarian and feel that I aren’t getting enough protein or variation . Main Symptoms are Anxiety,dizziness,tinnitus,Nausea,wind
Imisspizza
in
IBS Network
9 months ago
Recovering after hospital stay
I’m wondering if anyone can tell me what to expect next. I had Covid at the end of January. I felt very flu like for a couple of days then okay for a few days. After that I got a cold and a chesty cough. The cough was only occasional. At the end of last week I started to feel flu like again. I decided
I’m wondering if anyone can tell me what to expect next. I had Covid at the end of January. I felt very flu like for a couple of days then okay for a few days. After that I got a cold and a chesty cough. The cough was only occasional. At the end of last week I started to feel flu like again. I decided
AppleOrchard
in
Asthma Community Forum
5 months ago
Afib worse since Ablation
I had Covid in Oct 2022. I was 57 at the time and in really great shape. I exercise everyday, average about 15,000 steps a day and fast 2 to 3 days a week. As my Covid was winding down and I was feeling better I started having Afib Episodes for the first time in my life. They started off
I had Covid in Oct 2022. I was 57 at the time and in really great shape. I exercise everyday, average about 15,000 steps a day and fast 2 to 3 days a week. As my Covid was winding down and I was feeling better I started having Afib Episodes for the first time in my life. They started off
filmguy5
in
AF Association
9 months ago
Coughing and AFib
I've been down for several days with what seems to be the flu (4 days of negative covid testing) and one of the most persistent symptoms has been a bad cough. I went into AFib a couple of days ago but blamed it on the fever. However, no fever today, but just went into AFib again. Anyone else have this
I've been down for several days with what seems to be the flu (4 days of negative covid testing) and one of the most persistent symptoms has been a bad cough. I went into AFib a couple of days ago but blamed it on the fever. However, no fever today, but just went into AFib again. Anyone else have this
hartbeast
in
Atrial Fibrillation Support
5 months ago
Mirena Coil Side Effects
hi everyone, I am desperate for some advice/help. I had the mirena coil fitted 6 months ago. 10 days after the coil was fitted I contacted my GP complaining of severe shoulder pain. I am still in agony most days, and nights are the worst. I am getting by on anywhere between 0-3 hours sleep due to being
hi everyone, I am desperate for some advice/help. I had the mirena coil fitted 6 months ago. 10 days after the coil was fitted I contacted my GP complaining of severe shoulder pain. I am still in agony most days, and nights are the worst. I am getting by on anywhere between 0-3 hours sleep due to being
Emily1107
in
Women's Health
9 months ago
Adrenal crisis or flare ?
Evening all, I've been a casual observer for many months now - my PMR was 'gone' (ie in remission/on holiday/not troubling me) and I had adjusted to Adrenal Insufficiency and a likely permanent dose of Hydrocortisone and Vitamin D. I recovered from a dose of covid about 3 weeks ago. On Saturday
Evening all, I've been a casual observer for many months now - my PMR was 'gone' (ie in remission/on holiday/not troubling me) and I had adjusted to Adrenal Insufficiency and a likely permanent dose of Hydrocortisone and Vitamin D. I recovered from a dose of covid about 3 weeks ago. On Saturday
Cyclo5
in
Thyroid UK
9 months ago
Adrenal Crisis or a Flare?
Evening all, I've been a casual observer for many months now - my PMR was 'gone' (ie in remission/on holiday/not troubling me) and I had adjusted to Adrenal Insufficiency and a likely permanent dose of Hydrocortisone and Vitamin D. I recovered from a dose of covid about 3 weeks ago. On Saturday afternoon
Evening all, I've been a casual observer for many months now - my PMR was 'gone' (ie in remission/on holiday/not troubling me) and I had adjusted to Adrenal Insufficiency and a likely permanent dose of Hydrocortisone and Vitamin D. I recovered from a dose of covid about 3 weeks ago. On Saturday afternoon
Cyclo5
in
PMRGCAuk
9 months ago
advice please
My thyroid results from 2.5 weeks ago were: TSH 0.78 (0.4 to 4.9) previously 0.21 in Feb 23 T4 16.8 (9 to 19) previously Feb 23 - 15.7 (9.0 to 19.0) T3 3.9 (2.4 to 6) previously Feb 23 - 4.4 (2.4 to 6.0) Could anyone advise on the percentages and if they are okay? Feeling underactive at present
My thyroid results from 2.5 weeks ago were: TSH 0.78 (0.4 to 4.9) previously 0.21 in Feb 23 T4 16.8 (9 to 19) previously Feb 23 - 15.7 (9.0 to 19.0) T3 3.9 (2.4 to 6) previously Feb 23 - 4.4 (2.4 to 6.0) Could anyone advise on the percentages and if they are okay? Feeling underactive at present
Sailing14
in
Thyroid UK
9 months ago
Ginkgo - possible adverse side effect: Nervous anxiety
It's me again. On about Ginkgo as usual... Having taken Ginkgo for over 6 months, and having planned relief from Tinnitus by doing so, I may have experienced a side effect. Recent bouts of nervous anxiety. This is not the kind of anxiety you might experience in a dentist waiting room. No, this is
It's me again. On about Ginkgo as usual... Having taken Ginkgo for over 6 months, and having planned relief from Tinnitus by doing so, I may have experienced a side effect. Recent bouts of nervous anxiety. This is not the kind of anxiety you might experience in a dentist waiting room. No, this is
Ray200
in
Tinnitus UK
2 months ago
Hearing aids and work
Hi, I started using hearing aids earlier in the year (moderate to severe loss, with profound at the highest frequencies). I’m only in my mid 50s and have close to 10 years working left. As with a lot of office workers I’m now spending an awful lot of time on MS teams. I’m really struggling with headphones
Hi, I started using hearing aids earlier in the year (moderate to severe loss, with profound at the highest frequencies). I’m only in my mid 50s and have close to 10 years working left. As with a lot of office workers I’m now spending an awful lot of time on MS teams. I’m really struggling with headphones
GillyA
in
Tinnitus UK
2 months ago
A COLD AND VENETOCLAX
Hi all….has anyone had a cold and paused Venetoclax? Still waiting to hear back from my Oncologist. Thanks…Diana
Hi all….has anyone had a cold and paused Venetoclax? Still waiting to hear back from my Oncologist. Thanks…Diana
difor29
in
CLL Support
5 months ago
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