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Has anyone taken Paxlovid and PD Meds?
I may have been exposed to COVID and can’t find anything specific about interactions between Paxlovid and Carbidopa/levodopa (sinemet). I’m not sure I will take it even if I do come down with COVID, but I’m trying to be proactive.
I may have been exposed to COVID and can’t find anything specific about interactions between Paxlovid and Carbidopa/levodopa (sinemet). I’m not sure I will take it even if I do come down with COVID, but I’m trying to be proactive.
Juliegrace
in
Cure Parkinson's
2 years ago
Slow COVID recovery -- anti-inflammatory: berberine, anthocyanin, or?
It's been nearly four weeks since the whole family (and a few friends) all tested positive within a day or two of each other. Nothing severe for any of us. We all had "the usual" few days of fever, fatigue, body aches, cough, etc. But I'm the only one feeling lingering effects that include: weakness
It's been nearly four weeks since the whole family (and a few friends) all tested positive within a day or two of each other. Nothing severe for any of us. We all had "the usual" few days of fever, fatigue, body aches, cough, etc. But I'm the only one feeling lingering effects that include: weakness
noahware
in
Advanced Prostate Cancer
2 years ago
Update on Insurance Claim - Staysure
Remember this post about a fortnight ago? Hi Beaver. I am insured with Staysure and had to make a claim when we had to return from Scotland due to testing positive for Covid. I am CEV so had to return for Covid Antibody treatment and of course the moral issue. I made a claim the day after (June 23rd
Remember this post about a fortnight ago? Hi Beaver. I am insured with Staysure and had to make a claim when we had to return from Scotland due to testing positive for Covid. I am CEV so had to return for Covid Antibody treatment and of course the moral issue. I made a claim the day after (June 23rd
Investigator1
in
Vasculitis UK
2 years ago
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Lupus and COVID-19 Information & Guidance - UPDATED 06/04/2022
Hi everyone, We have updated our lupus and COVID-19 information and guidance to reflect the latest changes - https://www.lupusuk.org.uk/
coronavirus
/ For updates about vaccines and the "spring booster" go to https://www.lupusuk.org.uk/covid19-vaccination/ For updates about free lateral flow tests and
Hi everyone, We have updated our lupus and COVID-19 information and guidance to reflect the latest changes - https://www.lupusuk.org.uk/
coronavirus
/ For updates about vaccines and the "spring booster" go to https://www.lupusuk.org.uk/covid19-vaccination/ For updates about free lateral flow tests and
Paul_Howard
LUPUS UK
in
LUPUS UK
2 years ago
shingles and Covid at the same time
so I’ve been really stressed with work, a horrible accident my nephew was in, and just over all everything. So I’m not surprised I got shingles I am surprised I got Covid. I work in health care but I’m super careful and had 0 symptoms. I’m just wondering how hard this will hit my liver. I’m on Valtrex
so I’ve been really stressed with work, a horrible accident my nephew was in, and just over all everything. So I’m not surprised I got shingles I am surprised I got Covid. I work in health care but I’m super careful and had 0 symptoms. I’m just wondering how hard this will hit my liver. I’m on Valtrex
mtk0925
in
British Liver Trust
2 years ago
5k Runniversary update
Firstly, I would like to thank everyone who replied to my previous post regarding my 5k Runniversary. The response was very positive and only goes to show how good this community is. It gives people great encouragement spurs everyone on as a result. Just a bit of an update from my 10k run last Monday
Firstly, I would like to thank everyone who replied to my previous post regarding my 5k Runniversary. The response was very positive and only goes to show how good this community is. It gives people great encouragement spurs everyone on as a result. Just a bit of an update from my 10k run last Monday
Freecloud
Graduate
in
Couch to 5K
2 years ago
I have covid, can I have my laparoscopy next month?
hi guys, I have tested positive for covid for the second time as of today, and I’m worried about the implications on my planned laparoscopy. My pre op appointment is on the 13th of August (15 days away) and my surgery is scheduled for the 22nd (24 days away). I’m not sure what to do! Is it safe for me
hi guys, I have tested positive for covid for the second time as of today, and I’m worried about the implications on my planned laparoscopy. My pre op appointment is on the 13th of August (15 days away) and my surgery is scheduled for the 22nd (24 days away). I’m not sure what to do! Is it safe for me
Coco1860
in
Endometriosis UK
2 years ago
An antibody for myelofibrosis – “that’s a true discovery”
Recently, one of our MATES members showed me this (extract) article (MiaGrace), & I believe that many others might wish to see it too... A new monoclonal antibody, discovered by accident by Adelaide researchers, could become the world’s first effective treatment for primary myelofibrosis (MF).
Recently, one of our MATES members showed me this (extract) article (MiaGrace), & I believe that many others might wish to see it too... A new monoclonal antibody, discovered by accident by Adelaide researchers, could become the world’s first effective treatment for primary myelofibrosis (MF).
socrates_8
in
MPN Voice
2 years ago
RLS improved after covid?
I've had RLS for years and have been on Ropinirole for several years. 3 Weeks ago, I tested positive for Covid. I had mild symptoms - a sore throat, cough, slight wheeziness and fatigue. Other than ongoing tiredness and a cough - pretty common - I'm over it and have had 2 negative tests. The thing
I've had RLS for years and have been on Ropinirole for several years. 3 Weeks ago, I tested positive for Covid. I had mild symptoms - a sore throat, cough, slight wheeziness and fatigue. Other than ongoing tiredness and a cough - pretty common - I'm over it and have had 2 negative tests. The thing
Mattly
in
Restless Legs Syndrome
2 years ago
Husband beginning V+O treatment for unmutated CLL
My husband will be beginning the combo Ventaclax and Obinutuzumab for unmutated CLL which will continue for 1 year. We would love any helpful advice about how this treatment affects most people, and how folks are coping in an unmasked COVID world. Are patients staying in a bubble for the entire year
My husband will be beginning the combo Ventaclax and Obinutuzumab for unmutated CLL which will continue for 1 year. We would love any helpful advice about how this treatment affects most people, and how folks are coping in an unmasked COVID world. Are patients staying in a bubble for the entire year
lisakc1
in
CLL Support
2 years ago
does having covid recently stop treatment from starting?
so I had a reactivation of EPstein Barr Virus in May that caused a Monk infection so we put off treatment until I see my doc again next week. To give me time to resolve it. Then , on July 3rd I got Covid and am still with many symptoms. I did have the monoclonal antibodies, but everything is lingering
so I had a reactivation of EPstein Barr Virus in May that caused a Monk infection so we put off treatment until I see my doc again next week. To give me time to resolve it. Then , on July 3rd I got Covid and am still with many symptoms. I did have the monoclonal antibodies, but everything is lingering
WittyApricot
in
CLL Support
2 years ago
sudden onset of fibromyalgia. Is it possible ?
I would like to know if anyone experienced a sudden onset of fibromyalgia. In June 2021 I caught covid (delta variant) and the virus caused me afib (atrial fibrillation) but i was misdiagnosed for many months due to cardiologists' mistakes. At the end of December 2021 unfortunately i got covid again
I would like to know if anyone experienced a sudden onset of fibromyalgia. In June 2021 I caught covid (delta variant) and the virus caused me afib (atrial fibrillation) but i was misdiagnosed for many months due to cardiologists' mistakes. At the end of December 2021 unfortunately i got covid again
JoseT
in
Fibromyalgia Action UK
2 years ago
Covid and Prednisolone
Hi I am recovering from Covid It got.me for my birthday!! One day up one day down but improving so that's good.I increased my pred by 5mg to 10mg.Dr said to increase for a week.He wanted me to increase to 25mg but I thought I would see how I went.Will it be OK to drop straight back to 5mg when I am
Hi I am recovering from Covid It got.me for my birthday!! One day up one day down but improving so that's good.I increased my pred by 5mg to 10mg.Dr said to increase for a week.He wanted me to increase to 25mg but I thought I would see how I went.Will it be OK to drop straight back to 5mg when I am
Raewynne
in
PMRGCAuk
2 years ago
COVID Hazy not Stupid Lazy
I started in my new position when COVID hit. I'm in Healthcare and manage a team of nearly 200 nurses and CNAs in a very busy emergency dept. This is my first job managing a team this size. At first I was excited about advancing into such an important cause, but then things became overwhelmingly difficult
I started in my new position when COVID hit. I'm in Healthcare and manage a team of nearly 200 nurses and CNAs in a very busy emergency dept. This is my first job managing a team this size. At first I was excited about advancing into such an important cause, but then things became overwhelmingly difficult
TADHD69
in
CHADD's Adult ADHD Support
2 years ago
Covid and Ibrance
hello,I tested positive for Covid 2 days ago just now heard back from my oncologist. She said stop Ibrance for 2-3 weeks but to continue with letrozol. Has anyone been told to do that when they have gotten Covid?
hello,I tested positive for Covid 2 days ago just now heard back from my oncologist. She said stop Ibrance for 2-3 weeks but to continue with letrozol. Has anyone been told to do that when they have gotten Covid?
Gmaoftriplets
in
SHARE Metastatic Breast Cancer
2 years ago
Enc, covid and pneumonia - life on an NHS 'covid ward'
Waited 18 hours for a bed with junkies sleeping on the floor and accident/assault victims. Went in with covid and pneumonia, staff never looked at my medical case notes which require about a dozen medications for life threatening issues and conditions including, epilepsy, seizures, ptsd, auto immune
Waited 18 hours for a bed with junkies sleeping on the floor and accident/assault victims. Went in with covid and pneumonia, staff never looked at my medical case notes which require about a dozen medications for life threatening issues and conditions including, epilepsy, seizures, ptsd, auto immune
Gandalf2
in
Encephalitis International
2 years ago
NCT classes when Covid cases are high?
Hi all, Hope you are all having a lovely week! Just wondering how everyone else approached NCT or similar when Covid cases are high ( as they're expected to be this autumn)? From the research I've done it sounds like third trimester, when you would do an antenatal course, is the riskiest time to catch
Hi all, Hope you are all having a lovely week! Just wondering how everyone else approached NCT or similar when Covid cases are high ( as they're expected to be this autumn)? From the research I've done it sounds like third trimester, when you would do an antenatal course, is the riskiest time to catch
Redsequin
in
Fertility Network UK - Pregnancy Support
2 years ago
What should I do now please?
Hi all I am wondering if you would be able to help me please? I have been stabilised on 7mg of prednisolone since last month June 2022. Unfortunately three weeks ago both my husband and myself picked up a nasty respiratory virus that was reported to be circulating around this area of Spain. I immediately
Hi all I am wondering if you would be able to help me please? I have been stabilised on 7mg of prednisolone since last month June 2022. Unfortunately three weeks ago both my husband and myself picked up a nasty respiratory virus that was reported to be circulating around this area of Spain. I immediately
Elispeth
in
PMRGCAuk
2 years ago
Follow up to Rituximab COVID paxlovid...
Follow up: I finished paxlovid 7/16. Felt ok until 7/22 with Different symptoms from 7/11 ED visit but similar to pneumonia and sinus congestion. First available GP appt was today. COVID positive again! (Yes, fully vaxxed, wear mask, live alone, isolate, etc.) Also, flu neg. Doctor also suspects bacterial
Follow up: I finished paxlovid 7/16. Felt ok until 7/22 with Different symptoms from 7/11 ED visit but similar to pneumonia and sinus congestion. First available GP appt was today. COVID positive again! (Yes, fully vaxxed, wear mask, live alone, isolate, etc.) Also, flu neg. Doctor also suspects bacterial
irishponies
in
Vasculitis UK
2 years ago
Post Covid infection - nearly 4 weeks since positive test and treated with antivirals - have ET and still feel awful
Hi I tested positive with covid 4 weeks ago and was prescribed antivirals as I have ET. I tested positive for 6 days only and after 10 days felt loads better - however on day 19 i ended up in a and e with a suspected heart arithymia and body going into shock, I couldn’t walk or stand, couldn’t eat,
Hi I tested positive with covid 4 weeks ago and was prescribed antivirals as I have ET. I tested positive for 6 days only and after 10 days felt loads better - however on day 19 i ended up in a and e with a suspected heart arithymia and body going into shock, I couldn’t walk or stand, couldn’t eat,
BeckyDing
in
MPN Voice
2 years ago
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