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PMR & Cellulitis
Hi, some of you may remember that I posted a while back asking for tips to cope with long haul flights. Well, I arrived in Australia 6 weeks ago and didn’t have any problems after the flights, I just took an extra dose of Pred as suggested. However, two weeks ago I developed cellulitis in my left leg
Hi, some of you may remember that I posted a while back asking for tips to cope with long haul flights. Well, I arrived in Australia 6 weeks ago and didn’t have any problems after the flights, I just took an extra dose of Pred as suggested. However, two weeks ago I developed cellulitis in my left leg
GreatGranny4
in
PMRGCAuk
3 months ago
Shingles
Hi ladies, I tested positive on day 9 after FET but now have shingles. Has anyone been in a similar situation? GP says consult with fertility clinic, clinic says consult with GP....spent all day on the phone. Has anyone had shingles during pregnancy and did not use the medication? GP (prescribed aciclovir
Hi ladies, I tested positive on day 9 after FET but now have shingles. Has anyone been in a similar situation? GP says consult with fertility clinic, clinic says consult with GP....spent all day on the phone. Has anyone had shingles during pregnancy and did not use the medication? GP (prescribed aciclovir
Hope823
in
Fertility Network UK
3 months ago
reoccurring thrush on dienogest
Hello everyone, just thought I’d ask for some advice as I’m struggling with reoccurring thrush at the moment and although that doesn’t sound awful, on top of all the other pain it’s the last thing I want. Little bit of back story, I was diagnosed with endo last year. Had a laparoscopy and ablation
Hello everyone, just thought I’d ask for some advice as I’m struggling with reoccurring thrush at the moment and although that doesn’t sound awful, on top of all the other pain it’s the last thing I want. Little bit of back story, I was diagnosed with endo last year. Had a laparoscopy and ablation
Livylou1112
in
Endometriosis UK
3 months ago
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Shingles following AF
hi folks - seen a few posts recently about shingles and wondered about my own experience and if anyone had the same. I had an episode of AF in February which lasted 5.5hrs HR up to 182, next day a rash appeared on my collarbone and it turned out to be shingles. Cardiologist said it’s quite possible that
hi folks - seen a few posts recently about shingles and wondered about my own experience and if anyone had the same. I had an episode of AF in February which lasted 5.5hrs HR up to 182, next day a rash appeared on my collarbone and it turned out to be shingles. Cardiologist said it’s quite possible that
Jamontoast
in
Atrial Fibrillation Support
3 months ago
immunosuppressed, covid positive - anyone have an experience with antivirals?
hello lovely people of this wonderful forum - seeking any insight or guidance I was diagnosed (11 months ago) with scleroderma & myositis with lung involvement (ILD) on Mycophenolate for treatment. Despite being very cautious and careful, I have just tested positive for Covid, (having avoided it
hello lovely people of this wonderful forum - seeking any insight or guidance I was diagnosed (11 months ago) with scleroderma & myositis with lung involvement (ILD) on Mycophenolate for treatment. Despite being very cautious and careful, I have just tested positive for Covid, (having avoided it
ruablue
in
Myositis UK
6 months ago
Covid positive with ILD - antiviral experience ?
hello lovely people of this wonderful forum - seeking any insight or guidance I was diagnosed (11 months ago) with ILD. Despite being very cautious and careful, I have just tested positive for Covid, (having avoided it for last 4 years). I wonder if anyone could share their Covid experiences and
hello lovely people of this wonderful forum - seeking any insight or guidance I was diagnosed (11 months ago) with ILD. Despite being very cautious and careful, I have just tested positive for Covid, (having avoided it for last 4 years). I wonder if anyone could share their Covid experiences and
ruablue
in
Living with Interstitial Lung Disease (ILD)
6 months ago
Covid positive - anyone with antiviral experience
hello lovely people of this wonderful forum - seeking any insight or guidance I was diagnosed (11 months ago) with scleroderma & myositis with lung involvement (ILD) on Mycophenolate for treatment. Despite being very cautious and careful, I have just tested positive for Covid, (having avoided it
hello lovely people of this wonderful forum - seeking any insight or guidance I was diagnosed (11 months ago) with scleroderma & myositis with lung involvement (ILD) on Mycophenolate for treatment. Despite being very cautious and careful, I have just tested positive for Covid, (having avoided it
ruablue
in
Scleroderma & Raynaud's UK (SRUK)
6 months ago
More to deal with. Early birthday gift I guess.
I get all my shots as soon as they are available. Besides, Lupron had current flu, covid and RVS. Thought I must have caught flu and but feeling different about it. Worst sore throat every and continually spit phlegm and spittle. Went to our local ER and came up with the winner, COVID! Caught it
I get all my shots as soon as they are available. Besides, Lupron had current flu, covid and RVS. Thought I must have caught flu and but feeling different about it. Worst sore throat every and continually spit phlegm and spittle. Went to our local ER and came up with the winner, COVID! Caught it
SpencerBoy11
in
Advanced Prostate Cancer
6 months ago
Stomach pain common with IBS?
Is stomach pain common with IBS?If so, where do you feel the pain? I feel pain right in the center pit of my stomach... sometimes gnawing sensation, sometimes a cramping sensation Do you feel it there in the center pit of your stomach too?
Is stomach pain common with IBS?If so, where do you feel the pain? I feel pain right in the center pit of my stomach... sometimes gnawing sensation, sometimes a cramping sensation Do you feel it there in the center pit of your stomach too?
Catsandsunsets
in
IBS Network
3 months ago
Famotidine
I have been on 20mg of Famotidine for about a year, over the past 6 months while taking Famotidine I seem to have developed heartburn has any one else suffered with heartburn while on Famotidine? I was on Omeprazole previously for nearly 3 years without any problems but a blood test revealed low sodium
I have been on 20mg of Famotidine for about a year, over the past 6 months while taking Famotidine I seem to have developed heartburn has any one else suffered with heartburn while on Famotidine? I was on Omeprazole previously for nearly 3 years without any problems but a blood test revealed low sodium
Phed
in
PMRGCAuk
3 months ago
Shingles vaccine and atrial fibrillation
Hi, My GP is recommending shingles vaccine. I am just concerned if it will cause atrial fibrillation. Any one had shingles vaccines with no adverse effects like atrial fibrillationThanks Padma
Hi, My GP is recommending shingles vaccine. I am just concerned if it will cause atrial fibrillation. Any one had shingles vaccines with no adverse effects like atrial fibrillationThanks Padma
Poluneeru
in
Atrial Fibrillation Support
3 months ago
Shingles
I posted over 9 weeks ago about my shingles outbreak. I still have horrible pain and can't stand clothing even to touch me. I have had 2 epidurals for the pain and they didn't even help at all. Someone wrote back and said that they had shingles since last December and I couldn't find the post. If you
I posted over 9 weeks ago about my shingles outbreak. I still have horrible pain and can't stand clothing even to touch me. I have had 2 epidurals for the pain and they didn't even help at all. Someone wrote back and said that they had shingles since last December and I couldn't find the post. If you
mlp3434
in
Atrial Fibrillation Support
3 months ago
Father has had PBC for 16 years - Odd complications since COVID?
Hello all, I wonder if anyone here who has PBC (or has a family member with PBC) has had similar experiences post covid? My father was diagnosed 16 years ago. Recently he contracted COVID and was hospitalised (he's also been a type 1 diabetic since birth, so 60 years). Within a day of getting COVID
Hello all, I wonder if anyone here who has PBC (or has a family member with PBC) has had similar experiences post covid? My father was diagnosed 16 years ago. Recently he contracted COVID and was hospitalised (he's also been a type 1 diabetic since birth, so 60 years). Within a day of getting COVID
Kylewillmott
in
PBC Foundation
6 months ago
Should I go ahead with Covid Jab?
I am aged 80 and have my 5th Covid jab booked for Thursday I am steady on 5mg pred with no PRM symptoms. Should I go ahead with the jab and if so, what might I look out for?
I am aged 80 and have my 5th Covid jab booked for Thursday I am steady on 5mg pred with no PRM symptoms. Should I go ahead with the jab and if so, what might I look out for?
kangaroojohn
in
PMRGCAuk
6 months ago
Next instalment. I thought I`d better do this now before I start working.
In fact, I don't remember ever seeing my dad drunk, except for one occasion when he had had, perhaps, an excess of drink. We were on a family holiday in Ireland, in a horse drawn caravan, which in itself was an experience, especially for the horse as we had no prior experience whatsoever of the care
In fact, I don't remember ever seeing my dad drunk, except for one occasion when he had had, perhaps, an excess of drink. We were on a family holiday in Ireland, in a horse drawn caravan, which in itself was an experience, especially for the horse as we had no prior experience whatsoever of the care
LissacFrance
in
Lung Conditions Community Forum
3 months ago
Travelling with interferon/pegasys
Hi , I have just recently started on the pegasys weekly injections . I am travelling to Greece and wonder if anyone can recomend the best way to keep the medication at the correct temperature whilst flying and travelling. Is there a chargeable medication box which I could charge using a battery pack
Hi , I have just recently started on the pegasys weekly injections . I am travelling to Greece and wonder if anyone can recomend the best way to keep the medication at the correct temperature whilst flying and travelling. Is there a chargeable medication box which I could charge using a battery pack
Sunnyhunny
in
MPN Voice
3 months ago
Covid and testing
Good morning all, My daughter, diagnosed last summer, has thyroid blood tests scheduled for Monday morning (GP). However, she actively has Covid at the moment. Should we reschedule? Thanks
Good morning all, My daughter, diagnosed last summer, has thyroid blood tests scheduled for Monday morning (GP). However, she actively has Covid at the moment. Should we reschedule? Thanks
J972
in
Thyroid UK
6 months ago
Streptococcal Bacterial Meningitis
Hi, everyone! I was admitted to the hospital on March 11 and diagnosed with Streptococcal Bacterial Meningitis and hospitalized for 17 days. Just released last Thursday. This was all brought on by an ear infection that I guess turned into meningitis. I had all the tests and scans and was told I was lucky
Hi, everyone! I was admitted to the hospital on March 11 and diagnosed with Streptococcal Bacterial Meningitis and hospitalized for 17 days. Just released last Thursday. This was all brought on by an ear infection that I guess turned into meningitis. I had all the tests and scans and was told I was lucky
Fjreed23
in
Meningitis Now
3 months ago
Interferon and the liver
question to all my MPN people on here who are taking pegasys or besremi, how do you manage elevated liver enzymes? Do they cycle up and down? Is there anything we can do to bring them down? What is acceptable to y’all? My hematologist says not to worry until they hit 2-300.. My blood numbers actually
question to all my MPN people on here who are taking pegasys or besremi, how do you manage elevated liver enzymes? Do they cycle up and down? Is there anything we can do to bring them down? What is acceptable to y’all? My hematologist says not to worry until they hit 2-300.. My blood numbers actually
dbus1417
in
MPN Voice
3 months ago
Finger nails and raynauds
Hi ..I have raynauds and limited schleroderma and was wondering if anyone has the problem of there finger nails being discoloured and lifting off the nail bed ..I have tried lots of treatments but nothing seems to work and am now worried that I may lose some nails altogether!
Hi ..I have raynauds and limited schleroderma and was wondering if anyone has the problem of there finger nails being discoloured and lifting off the nail bed ..I have tried lots of treatments but nothing seems to work and am now worried that I may lose some nails altogether!
Tmontana
in
Scleroderma & Raynaud's UK (SRUK)
3 months ago
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