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Acalabrutinib and covid vaccines
I have been on acalabrutinib for 2 months and doing very well. It has been about 6 months since I have had my last covid vaccine , and I am due for another. My question is will the covid vaccines work while taking acalabrutinib?
I have been on acalabrutinib for 2 months and doing very well. It has been about 6 months since I have had my last covid vaccine , and I am due for another. My question is will the covid vaccines work while taking acalabrutinib?
Rrriver
in
CLL Support
1 year ago
Paxlovid
After keeping the dreaded Covid at bay for almost three years I finally tested positive last week. I had assumed this would happen at some point but being immunocompromised it goes without saying that it’s a worrying time. Fortunately I was able to access antivirals very easily and started taking them
After keeping the dreaded Covid at bay for almost three years I finally tested positive last week. I had assumed this would happen at some point but being immunocompromised it goes without saying that it’s a worrying time. Fortunately I was able to access antivirals very easily and started taking them
Hightower62
in
NRAS
1 year ago
Advice please
Sorry to bother all with non-lung incident but can anyone please throw any light on this? Awoke early today with flushing to face and need to get to bathroom urgently. Fainted twice to floor on the way. Had virtual colonoscopy (sorry!) Monday am this week, and wonder if this is related to that? Inclined
Sorry to bother all with non-lung incident but can anyone please throw any light on this? Awoke early today with flushing to face and need to get to bathroom urgently. Fainted twice to floor on the way. Had virtual colonoscopy (sorry!) Monday am this week, and wonder if this is related to that? Inclined
BronchyBronwen
in
Lung Conditions Community Forum
1 year ago
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Severe Cold, to Bronchitis; PMR has not returned
Had gotten a cold that became tenacious, as after 1 week of a head cold it progressed to my chest. A week later I had Bronchitis for the first time in my life and starting with week 3 my GP put me on a Prednisone routine of 40 mg, 30, 20, 10 over a course of 10 days. As if that wasn’t enough, she
Had gotten a cold that became tenacious, as after 1 week of a head cold it progressed to my chest. A week later I had Bronchitis for the first time in my life and starting with week 3 my GP put me on a Prednisone routine of 40 mg, 30, 20, 10 over a course of 10 days. As if that wasn’t enough, she
Boss302Fan
in
PMRGCAuk
2 years ago
Have just tested positive for Covid. Currently on 7.5mg prednisolone. Is it OK to take Snip twice a day or should I increase my dosage?
What I thought were standard cold symptoms - sore throat, runny nose and congestion - have turned out to be Covid. This is Day 2 and I don't feel too bad. I took a Snip last night and again this afternoon. It certainly helps but I seem to remember reading that you had to be careful taking this type
What I thought were standard cold symptoms - sore throat, runny nose and congestion - have turned out to be Covid. This is Day 2 and I don't feel too bad. I took a Snip last night and again this afternoon. It certainly helps but I seem to remember reading that you had to be careful taking this type
Pr0jection
in
PMRGCAuk
2 years ago
Research project update: COVID-19 vaccine responses in lupus patients
We have an update from one of the research projects LUPUS UK funded, which was looking at the response of people with lupus to COVID-19 vaccines. You can read about what they found on our website here: https://www.lupusuk.org.uk/understanding-covid-19-vaccine-responses-in-lupus-patients/ Feel free
We have an update from one of the research projects LUPUS UK funded, which was looking at the response of people with lupus to COVID-19 vaccines. You can read about what they found on our website here: https://www.lupusuk.org.uk/understanding-covid-19-vaccine-responses-in-lupus-patients/ Feel free
Debbie_kinsey
Administrator
in
LUPUS UK
2 years ago
CLL and Covid experiences
Hi, I am 65, have relapsed CLL after FCR treatment, made no antibodies to 6 Covid vaccinations. Otherwise I am healthy and physically very active. I'm so tire of the mask everywhere and so is my wife. Can anyone tell me if they have had Covid and how it went for them? Or anyone that can
Hi, I am 65, have relapsed CLL after FCR treatment, made no antibodies to 6 Covid vaccinations. Otherwise I am healthy and physically very active. I'm so tire of the mask everywhere and so is my wife. Can anyone tell me if they have had Covid and how it went for them? Or anyone that can
skipro
in
CLL Support
2 years ago
6 months post Covid and running shoes back on!
Well, it’s 6 months since I had Covid and then long Covid and at last I managed a 5 minute ‘jog’. It was slow but felt good. I mustn’t push it as until a month ago, I couldn’t even walk round the block without getting out of breath. So, I will soon be back doing C25K but may do each week twice!
Well, it’s 6 months since I had Covid and then long Covid and at last I managed a 5 minute ‘jog’. It was slow but felt good. I mustn’t push it as until a month ago, I couldn’t even walk round the block without getting out of breath. So, I will soon be back doing C25K but may do each week twice!
Phdgranny
Graduate
in
Couch to 5K
2 years ago
Reaction between thyroid meds and antibiotics and increased sensitivity to prescription drugs
I have really been suffering with a sinus infection following Covid in December last year. My gp prescribed Doxycycline 100 mg capsules. This was at my request. I had suffered with a sinus infection for almost eighteen months following a previous bout of Covid. The side affects were not pleasant but
I have really been suffering with a sinus infection following Covid in December last year. My gp prescribed Doxycycline 100 mg capsules. This was at my request. I had suffered with a sinus infection for almost eighteen months following a previous bout of Covid. The side affects were not pleasant but
dizzy864
in
Thyroid UK
2 years ago
🟨 Making Yellow Card Reports 🟨
🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨 In the UK, the
Medicines and Healthcare products Regulatory Agency (MHRA)
operates the Yellow Card scheme for reporting issues with medicines. They have slightly different approaches to: 🟡 Side Effects 🟡 Defective medicines 🟡 Counterfeit or
🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨 In the UK, the
Medicines and Healthcare products Regulatory Agency (MHRA)
operates the Yellow Card scheme for reporting issues with medicines. They have slightly different approaches to: 🟡 Side Effects 🟡 Defective medicines 🟡 Counterfeit or
helvella
Thyroid UK
in
Thyroid UK
2 years ago
ectopic beats
hi I’m 18 years old and I have always been in perfect health until around 2 years ago when I got covid for the first time, around 7-8 months after having covid i started experiencing rapid heart rate upon standing and suspect I have POTS but my beta blockers help massively in keeping my heart rate down
hi I’m 18 years old and I have always been in perfect health until around 2 years ago when I got covid for the first time, around 7-8 months after having covid i started experiencing rapid heart rate upon standing and suspect I have POTS but my beta blockers help massively in keeping my heart rate down
Maix
in
British Heart Foundation
2 years ago
Vaccinated People Have Fewer Cardiac Events after COVID-19
[i]In a study including data from almost two million individuals, COVID-19 vaccination seemed to have a protective effect against heart attacks, strokes, and cardiovascular problems linked to infection with SARS-CoV-2 [/i] ...begins this recent article https://www.insideprecisionmedicine.com/topics/
[i]In a study including data from almost two million individuals, COVID-19 vaccination seemed to have a protective effect against heart attacks, strokes, and cardiovascular problems linked to infection with SARS-CoV-2 [/i] ...begins this recent article https://www.insideprecisionmedicine.com/topics/
bennevisplace
in
CLL Support
2 years ago
post covid ibs/ digestive problems
Post covid (1mth). Weakness headaches tension light coloured poo acid reflux feel terrible. Anyone else s digestive probs worse after covid. Hoping will settle soon depressed and struggling daily.
Post covid (1mth). Weakness headaches tension light coloured poo acid reflux feel terrible. Anyone else s digestive probs worse after covid. Hoping will settle soon depressed and struggling daily.
Music2
in
IBS Network
2 years ago
NICE share draft final recommendations for COVID-19 treatments
Hi everyone, NICE has published their draft final recommendations for COVID-19 treatments. We are pleased that they have included sotrovimab for people who are at high risk of severe COVID-19 but cannot have Paxlovid. This hopefully means most people with lupus will have a viable treatment option.
Hi everyone, NICE has published their draft final recommendations for COVID-19 treatments. We are pleased that they have included sotrovimab for people who are at high risk of severe COVID-19 but cannot have Paxlovid. This hopefully means most people with lupus will have a viable treatment option.
Paul_Howard
LUPUS UK
in
LUPUS UK
2 years ago
covid
hi, has anyone been given antiviral drugs for Covid? I am so ill, terrible throat and cough nurse said it will help prevent complications
hi, has anyone been given antiviral drugs for Covid? I am so ill, terrible throat and cough nurse said it will help prevent complications
jarujuda
in
NRAS
2 years ago
Good covid, bad downside.
I have refractory RLS and have been taking 20 mg of hydrocodone right before bed. The symptoms actually cycle during the year with the colder months coincide with reduced symptoms. A month ago I came down with covid. I was really sick for about a week and it took me another week to test negative. I took
I have refractory RLS and have been taking 20 mg of hydrocodone right before bed. The symptoms actually cycle during the year with the colder months coincide with reduced symptoms. A month ago I came down with covid. I was really sick for about a week and it took me another week to test negative. I took
JakeRLS
in
Restless Legs Syndrome
2 years ago
PMR pain and siatica post covid
I had a minor dose of covid in September last year. Following it I developed agonising siatica. I thought I’d broken my hip at least. This was all mixed in with a PMR flare. I’ve tapered back from a higher dose of 5 mg to 2mg of prednisolone only to have to give in again and try 6mg which is only just
I had a minor dose of covid in September last year. Following it I developed agonising siatica. I thought I’d broken my hip at least. This was all mixed in with a PMR flare. I’ve tapered back from a higher dose of 5 mg to 2mg of prednisolone only to have to give in again and try 6mg which is only just
Headwood
in
PMRGCAuk
2 years ago
Has anyone else had 10-13 hour seizures from covid?
Hello all, I am used to having 2-4 hours seizures regularly, but after I tested positive for Covid they now last 10-13 hours every single day for the last week. Has this happened to anyone else? Please tell me this won't last forever! No doctors are helping. Thank you!
Hello all, I am used to having 2-4 hours seizures regularly, but after I tested positive for Covid they now last 10-13 hours every single day for the last week. Has this happened to anyone else? Please tell me this won't last forever! No doctors are helping. Thank you!
Pattydancer2023
in
Functional Neurological Disorder - FND Hope
2 years ago
Help what should I do?
Good morning I had 2 unsuccessful attempts at ICSI with donor eggs a couple of years ago and we decided we would have one last try but then due to circumstances beyond my control our ivf journey had to be put on hold and we are unlikely to be able to move forward with another cycle until at least
Good morning I had 2 unsuccessful attempts at ICSI with donor eggs a couple of years ago and we decided we would have one last try but then due to circumstances beyond my control our ivf journey had to be put on hold and we are unlikely to be able to move forward with another cycle until at least
Miaow1975
in
Fertility Network UK
1 year ago
COVID-19 treatment options for those taking Warfarin
Hello. I have not contracted COVID-19, but most others I know have had it, and many treat successfully with Paxlovid. I learned recently that Paxlovid interacts with Warfarin in that it suppresses the body's ability to metabolize the Warfarin, thereby possibly causing increased INR while taking COVID
Hello. I have not contracted COVID-19, but most others I know have had it, and many treat successfully with Paxlovid. I learned recently that Paxlovid interacts with Warfarin in that it suppresses the body's ability to metabolize the Warfarin, thereby possibly causing increased INR while taking COVID
olleberj
in
Hughes Syndrome APS Forum
2 years ago
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