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Covid Treatments NHS Changes
Just had an email from the NHS saying that the Covid treatment contact is changing from the 27th June We are writing again because the way that you access treatment will change from Tuesday 27 June 2023. If you get COVID from Tuesday 27 June 2023: You will no longer be automatically contacted by
Just had an email from the NHS saying that the Covid treatment contact is changing from the 27th June We are writing again because the way that you access treatment will change from Tuesday 27 June 2023. If you get COVID from Tuesday 27 June 2023: You will no longer be automatically contacted by
Alan7690
in
PMRGCAuk
1 year ago
Email from NHS - suddenly COVID vulnerable
*****UPDATE******* Well I asked the Dr, about change in status. They have no idea. Then when I got home, I found that I have now been sent free COVID tests in the post. ****** anyone else had an email from the NHS, stating they are vulnerable to COVID and qualify for treatment if it's contracted? (It
*****UPDATE******* Well I asked the Dr, about change in status. They have no idea. Then when I got home, I found that I have now been sent free COVID tests in the post. ****** anyone else had an email from the NHS, stating they are vulnerable to COVID and qualify for treatment if it's contracted? (It
Wetsuiter
in
Thyroid UK
1 year ago
Small cell vasculitis and epidermis demostosis
Back in November last year,I got covered in a rash which was awful . Treatment initially was antibiotics and suspect strep infection. And then as it kept reappearing and visits to dermatology put down as vasculitis caused by covid vaccine of which I still don't really buy into. Here we are 8 months
Back in November last year,I got covered in a rash which was awful . Treatment initially was antibiotics and suspect strep infection. And then as it kept reappearing and visits to dermatology put down as vasculitis caused by covid vaccine of which I still don't really buy into. Here we are 8 months
cartwheels
in
CLL Support
1 year ago
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W&W, Sepsis, Pneumonia,Cellulitis, FEVERS ! - ???
Had my first visit to the Hematologist . He was patient, he was kind , he was very informative and most important to me , he asked me what my questions and concerns were. Unlike a lot of doctors I worked with as a nurse , ( who MANY have seemed to have lost their Sensitivity chip ) , he was full
Had my first visit to the Hematologist . He was patient, he was kind , he was very informative and most important to me , he asked me what my questions and concerns were. Unlike a lot of doctors I worked with as a nurse , ( who MANY have seemed to have lost their Sensitivity chip ) , he was full
Sillysand
in
CLL Support
1 year ago
Looks like even the covid vaccination has 2 sides to the story. (Rats. And just yesterday I had my 3rd booster.)
IgG4 Antibodies Induced by Repeated Vaccination May Generate Immune Tolerance to the SARS-CoV-2 Spike Protein May 17 https://pubmed.ncbi.nlm.nih.gov/37243095/ Abstract "Less than a year after the global emergence of the coronavirus SARS-CoV-2, a novel vaccine platform based on mRNA technology was
IgG4 Antibodies Induced by Repeated Vaccination May Generate Immune Tolerance to the SARS-CoV-2 Spike Protein May 17 https://pubmed.ncbi.nlm.nih.gov/37243095/ Abstract "Less than a year after the global emergence of the coronavirus SARS-CoV-2, a novel vaccine platform based on mRNA technology was
MBAnderson
in
Cure Parkinson's
1 year ago
significant drop in platelets after Covid Shot
I am wondering if anyone else experienced this, I received my first Covid shot in April. Within the next 3 weeks I had my labs drawn for my monthly phlebotomy. Since 2016 my platelets have consistently been in the mid 700’s. After receiving the covid shot( that was the only difference in the norm)
I am wondering if anyone else experienced this, I received my first Covid shot in April. Within the next 3 weeks I had my labs drawn for my monthly phlebotomy. Since 2016 my platelets have consistently been in the mid 700’s. After receiving the covid shot( that was the only difference in the norm)
Kids0901
in
MPN Voice
1 year ago
Microbiome in PD, RBD and 1st degree relatives
As much as I'd like to believe that one "bad" bacteria (desulfovibrio) is responsible for Parkinson's, I suspect the situation is more complicated than that, as this recently released study suggests; https://www.nature.com/articles/s41467-023-38248-4 Certainly the evidence is accumulating though, that
As much as I'd like to believe that one "bad" bacteria (desulfovibrio) is responsible for Parkinson's, I suspect the situation is more complicated than that, as this recently released study suggests; https://www.nature.com/articles/s41467-023-38248-4 Certainly the evidence is accumulating though, that
Rufous2
in
Cure Parkinson's
1 year ago
How can I reduce the swelling in my foot and ankle?
Hello I was diagnosed with RA about six weeks ago and am on 20 mg methotrexate and 5 mg folic acid and have had a steroid injection. I can see improvement in other places but my right foot and ankle are swollen so I can only walk really short distances with a limp. I am worried that I will not be able
Hello I was diagnosed with RA about six weeks ago and am on 20 mg methotrexate and 5 mg folic acid and have had a steroid injection. I can see improvement in other places but my right foot and ankle are swollen so I can only walk really short distances with a limp. I am worried that I will not be able
spartacus101
in
NRAS
1 year ago
Pnuemonia post ablation
Hi. Not sure if anyone can advise me I am three weeks post AV node ablation (Pace and Ablate) I was in hospital extra four days because of breathlessness and dehydration. I had a chest crackle but thought no more about it on leaving hospital. Had a rough week felt really ill finally went to GP who
Hi. Not sure if anyone can advise me I am three weeks post AV node ablation (Pace and Ablate) I was in hospital extra four days because of breathlessness and dehydration. I had a chest crackle but thought no more about it on leaving hospital. Had a rough week felt really ill finally went to GP who
Lamplight37
in
AF Association
1 year ago
Covid tips
hi , I’m ten days in on Covid that to be fair was not too bad ,,,,just like a bad flu , so not complaining really I just wondered if anyone had any good tip for getting stamina back , I’m no athlete but I feel so exhausted it’s horrible……since Christmas I’ve had pneumonia, pleurisy, three chest infections
hi , I’m ten days in on Covid that to be fair was not too bad ,,,,just like a bad flu , so not complaining really I just wondered if anyone had any good tip for getting stamina back , I’m no athlete but I feel so exhausted it’s horrible……since Christmas I’ve had pneumonia, pleurisy, three chest infections
Hazel1010
in
British Heart Foundation
1 year ago
Is there any hope?
My OTD is tomorrow, but I took a test this morning to prepare myself for the worst. It was negative. This is our 4th ICSI round (all been fresh rounds) and we had 3 embryos transferred day 3. Including this one I would have had 9 embryos transferred and not once have we had a positive. I'm nearly 41.
My OTD is tomorrow, but I took a test this morning to prepare myself for the worst. It was negative. This is our 4th ICSI round (all been fresh rounds) and we had 3 embryos transferred day 3. Including this one I would have had 9 embryos transferred and not once have we had a positive. I'm nearly 41.
40plusTTC
in
Fertility Network UK
10 months ago
Waltz therapy
Due for my 6th covid vaccination, (spring booster) one month after having covid. Currently on 9 mg prednisolone (slow tapering). Not expecting a problem, am I right please. Will check with the moderator at the vaccination site.Thankyou for any advice.
Due for my 6th covid vaccination, (spring booster) one month after having covid. Currently on 9 mg prednisolone (slow tapering). Not expecting a problem, am I right please. Will check with the moderator at the vaccination site.Thankyou for any advice.
waltztherapy
in
PMRGCAuk
1 year ago
Atrial fibrillation after steroids
Has anyone experienced atrial fibrillation after starting steroids? 4 years ago I had steroid injections in both knees, and less than 48 hours later suddenly went into persistent rapid AF, having no previous history of it. I found some Dutch research that found new atrial fibrillation was more common
Has anyone experienced atrial fibrillation after starting steroids? 4 years ago I had steroid injections in both knees, and less than 48 hours later suddenly went into persistent rapid AF, having no previous history of it. I found some Dutch research that found new atrial fibrillation was more common
Belle11
in
AF Association
1 year ago
Cystatin C
Hi, .. recently done my bloods, and once again everything seems normal other then creatinine 129 umol- egfr 58 and little blood in urine(not visiable)Doctor suggests it's iga n. The real reason I'm on here is that I'm quite muscular and train a lot. I keep hearing about. A cystatin C test as it's
Hi, .. recently done my bloods, and once again everything seems normal other then creatinine 129 umol- egfr 58 and little blood in urine(not visiable)Doctor suggests it's iga n. The real reason I'm on here is that I'm quite muscular and train a lot. I keep hearing about. A cystatin C test as it's
Train1674
in
Early CKD Support
1 year ago
ivf/ICSI Sept/oct 2023 tww
Anyone in the TWW? 5dp5dt and all symptoms gone again. :( Any reassuring stories ?
Anyone in the TWW? 5dp5dt and all symptoms gone again. :( Any reassuring stories ?
Pkm4321
in
Fertility Network UK
10 months ago
covid - any benefit from Azithromycin 250
yesterday I spend several hours in car with someone who may now have covid, although she’s only presently showing a sore throat. Someone she spent last weekend with has now tested positive. Do I get any protection from the daily dose of Azithromycin 250. I have problem wearing mask as result of broken
yesterday I spend several hours in car with someone who may now have covid, although she’s only presently showing a sore throat. Someone she spent last weekend with has now tested positive. Do I get any protection from the daily dose of Azithromycin 250. I have problem wearing mask as result of broken
Morrison10
in
Lung Conditions Community Forum
1 year ago
Otelza Drug for Plaque Psoriasis
Hi all, just a quick question. Not PMR but for another AI disease. Has anyone come across or have experience of using Otelza (Apremilast, Aplex)? An earlier post got me thinking as my daughter has just been diagnosed (maybe) with Palmoplantar Pustulosis Psoriasis. I thought she might be put on Methotrexate
Hi all, just a quick question. Not PMR but for another AI disease. Has anyone come across or have experience of using Otelza (Apremilast, Aplex)? An earlier post got me thinking as my daughter has just been diagnosed (maybe) with Palmoplantar Pustulosis Psoriasis. I thought she might be put on Methotrexate
Bcol
in
PMRGCAuk
1 year ago
HU and prefibrotic myelofibrosis
Recently diagnosed first with ET. put on 500mg hydroxyurea daily with platelets at 617. After bone marrow aspiration and biopsy, diagnosis changed to prefibrotic myelofibrosis. HU had brought platelets down to 270 but I suffered from bad side effects. Dr didn’t want to change med or dosage. I resisted
Recently diagnosed first with ET. put on 500mg hydroxyurea daily with platelets at 617. After bone marrow aspiration and biopsy, diagnosis changed to prefibrotic myelofibrosis. HU had brought platelets down to 270 but I suffered from bad side effects. Dr didn’t want to change med or dosage. I resisted
Apple238
in
CLL Support
1 year ago
UTI and microscopic haematuria
After years of recurring uti and a diagnosis of cystitis cystica after camera jobby I was prescribed vagifem. This worked for 7 years until mother of infection which took 2 lots of antibiotics to subside, and has left me with microscopic haematuria. Don't want further tests, has anyone else experienced
After years of recurring uti and a diagnosis of cystitis cystica after camera jobby I was prescribed vagifem. This worked for 7 years until mother of infection which took 2 lots of antibiotics to subside, and has left me with microscopic haematuria. Don't want further tests, has anyone else experienced
Poshdog
in
PMRGCAuk
1 year ago
Running and Long Covid
When we went into the first lockdown, I was already ill in bed with Covid. It totally knocked me for six. I was ill for a month. Okay for a few days. Ill for a couple of weeks. Okay for a week. And then it really began. It developed into pneumonia that took some shifting. When I finally got out of bed
When we went into the first lockdown, I was already ill in bed with Covid. It totally knocked me for six. I was ill for a month. Okay for a few days. Ill for a couple of weeks. Okay for a week. And then it really began. It developed into pneumonia that took some shifting. When I finally got out of bed
Gthants
in
Couch to 5K
1 year ago
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