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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
6 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
6 months ago
Another Vaccine Dilemma! To have, or not to have a Tetanus Booster.
I've previously learnt on here that live vaccines are not recommended whilst on long term steroid medication, and that in many situations, alternative vaccines are available... as with the shingles vaccination program. Well, yesterday, whilst trimming my Wisteria, I accidentally pruned the tip of my
I've previously learnt on here that live vaccines are not recommended whilst on long term steroid medication, and that in many situations, alternative vaccines are available... as with the shingles vaccination program. Well, yesterday, whilst trimming my Wisteria, I accidentally pruned the tip of my
Kendrew
in
PMRGCAuk
1 month ago
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Good news/bad news
hi all. The nurse rang last week to say that my liver results had improved somewhat but were still outside normal range. Because I have such active disease she didn’t want to leave me with no meds at all, so we decided to restart the leflunomide and see how the blood results go in two week, then make
hi all. The nurse rang last week to say that my liver results had improved somewhat but were still outside normal range. Because I have such active disease she didn’t want to leave me with no meds at all, so we decided to restart the leflunomide and see how the blood results go in two week, then make
HeadInASpin
in
NRAS
3 months ago
Post covid oxygen levels.
Hi, I have recently had covid which left me with a dreadful COPD exacerbation. I was given anti virals and taken rescue pack followed by another course of Doxycycline. Although I feel a lot better my oxygen levels have dropped dreadfully. I am prescribed ambulatory oxygen but am finding I am using it
Hi, I have recently had covid which left me with a dreadful COPD exacerbation. I was given anti virals and taken rescue pack followed by another course of Doxycycline. Although I feel a lot better my oxygen levels have dropped dreadfully. I am prescribed ambulatory oxygen but am finding I am using it
Maggity
in
Lung Conditions Community Forum
3 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
6 months ago
Dreaded Covid
Having started with a bad cold last week after having a gastroscope, at my local hospital, I didn’t think too much about it at first, eventually went to doctors said it was a virus and chest was clear just drink plenty fluids, then my daughter thought best check covid and it was positive, can’t hear
Having started with a bad cold last week after having a gastroscope, at my local hospital, I didn’t think too much about it at first, eventually went to doctors said it was a virus and chest was clear just drink plenty fluids, then my daughter thought best check covid and it was positive, can’t hear
Alibongo60
in
Headway
3 months ago
clonazepam lethargy
has anyone experienced extreme fatigue since taking Clonazepam. My husband has been taking this now for around 10 days. He seems to be sleeping better at night but extremely tired during the day and i think this might be impacting his ability to walk as he can barely stand up without falling backwards
has anyone experienced extreme fatigue since taking Clonazepam. My husband has been taking this now for around 10 days. He seems to be sleeping better at night but extremely tired during the day and i think this might be impacting his ability to walk as he can barely stand up without falling backwards
Licquoricelover
in
PSP Association
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
6 months ago
Pneumococcal pneumonia vaccine - any link with PMR?
I have just realised that my recent flare, which led to the cancellation of my holiday, started the day after I had the pneumonia vaccine. I'm wondering if there could be a link?
I have just realised that my recent flare, which led to the cancellation of my holiday, started the day after I had the pneumonia vaccine. I'm wondering if there could be a link?
Broseley
in
PMRGCAuk
2 months ago
covid related?
does anyone feel ike the tinnitus started after covid? Just interested in any links, I’ve recently had a bad virus not tested for covid but it was quite nasty and I’m wondering if that’s why my tinnitus is worse
does anyone feel ike the tinnitus started after covid? Just interested in any links, I’ve recently had a bad virus not tested for covid but it was quite nasty and I’m wondering if that’s why my tinnitus is worse
Retailgirl
in
Tinnitus UK
3 months ago
Very worried about Mom
Hello everyone - wish you all a healthy path.My Mother was admitted to the hospital Monday morning and we found out she had urinary infection that went to her kidney and then blood. She had stopped taking venetoclax since Sunday. They are giving her antibiotics but her blood counts are out of whack.
Hello everyone - wish you all a healthy path.My Mother was admitted to the hospital Monday morning and we found out she had urinary infection that went to her kidney and then blood. She had stopped taking venetoclax since Sunday. They are giving her antibiotics but her blood counts are out of whack.
Hidden
in
CLL Support
5 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
6 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
6 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)
6 months ago
clavicle/collar bone swelling - YouTube Vid
hi there, A few of us have been talking about swelling in the pits of the collar bone. Instagram must’ve been listening 👂🏼 as this expert popped up in my feed. apparently this area is called the terminus, left and right so different jobs. I’ve watched this YouTube and immediately had gunk running
hi there, A few of us have been talking about swelling in the pits of the collar bone. Instagram must’ve been listening 👂🏼 as this expert popped up in my feed. apparently this area is called the terminus, left and right so different jobs. I’ve watched this YouTube and immediately had gunk running
Regenallotment
in
Thyroid UK
6 months ago
benign paroxysmal positional vertigo
I suffer with this occasionally. I take methotrexate and hydroxychloroquine. Is this a drug side effect and does anyone else suffer? Thanks.
I suffer with this occasionally. I take methotrexate and hydroxychloroquine. Is this a drug side effect and does anyone else suffer? Thanks.
Pognose123
in
NRAS
6 months ago
How do you get diagnosed on the NHS
Hello all. I've just joined this forum and have a bit of a perplexing question. For years I've suffered from food intolerances and mild allergies. I have had (and still have) various autoimmune issues. Post Covid in 2020, I developed hay fever along with an increasing number of food intolerances qand
Hello all. I've just joined this forum and have a bit of a perplexing question. For years I've suffered from food intolerances and mild allergies. I have had (and still have) various autoimmune issues. Post Covid in 2020, I developed hay fever along with an increasing number of food intolerances qand
Treetop33
in
The UK Mastocytosis Support Group
4 months ago
Covid, covid test and tapering
Very slow tapering (DL style and working well) currently at 5mg prednisolone. Just into my 3rd year PMR diagnosis, when I contracted covid. Staying put at 5 mg now. PMR bouts of fatigue and sleepiness much worse this time though just starting to improve a little. not the case on my previous covid infection
Very slow tapering (DL style and working well) currently at 5mg prednisolone. Just into my 3rd year PMR diagnosis, when I contracted covid. Staying put at 5 mg now. PMR bouts of fatigue and sleepiness much worse this time though just starting to improve a little. not the case on my previous covid infection
waltztherapy
in
PMRGCAuk
4 months ago
psoriasis flair and adalimumab
hi all, I am looking for some advice. I had severe psoriasis which was almost gone thanks to adalimumab. I saw my dermatology team back in April for my 6 monthly check where my psoriasis was flairing up. so I had an adalimumab blood test to see if it was meant to work. I got the results back a
hi all, I am looking for some advice. I had severe psoriasis which was almost gone thanks to adalimumab. I saw my dermatology team back in April for my 6 monthly check where my psoriasis was flairing up. so I had an adalimumab blood test to see if it was meant to work. I got the results back a
katienewland
in
Beyond Psoriasis
4 months ago
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