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covid and Thyroid tests
I have just tested positive for Covid. I am waiting for a Blue Horizon TFT kit. Can anyone advise how long I should wait before taking blood? Thanks
I have just tested positive for Covid. I am waiting for a Blue Horizon TFT kit. Can anyone advise how long I should wait before taking blood? Thanks
WeetabixSnacker
in
Thyroid UK
3 months ago
Some encouragement. If you’re looking for that.
disclaimer I will be going into detail so if you might be triggered know that it does end well. I started coming here around 2016. Anxiety had found me and I completely lost it. I let it take over and ended up spiraling for a few years. I would post how I was feeling, as many do and just hope that
disclaimer I will be going into detail so if you might be triggered know that it does end well. I started coming here around 2016. Anxiety had found me and I completely lost it. I let it take over and ended up spiraling for a few years. I would post how I was feeling, as many do and just hope that
Christory77
in
Anxiety Support
3 months ago
Latest COVID-19 guide for immunocompromised blood cancer patients from the International COVID-19 Blood Cancer Coalition (ICBCC)
The latest Patient Impact Statement has been released by the International COVID-19 Blood Cancer Coalition (ICBCC). Titled [i]"Navigating a post-pandemic world: A guide for immunocompromised blood cancer patients"[/i], it aims [i]"to help you navigate and manage the risks arising from the combination
The latest Patient Impact Statement has been released by the International COVID-19 Blood Cancer Coalition (ICBCC). Titled [i]"Navigating a post-pandemic world: A guide for immunocompromised blood cancer patients"[/i], it aims [i]"to help you navigate and manage the risks arising from the combination
CLLerinOz
Volunteer
in
CLL Support
3 months ago
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arrhythmia and the flu and Covid vaccine
Hi all! I had a physical on Wednesday and since I hadn’t received my flu and Covid vaccine yet this year went ahead and got them. I came home and did a workout and felt fine until evening when fever and chills hit along with some mild sporadic heart arrhythmia. I took it easy the next couple days and
Hi all! I had a physical on Wednesday and since I hadn’t received my flu and Covid vaccine yet this year went ahead and got them. I came home and did a workout and felt fine until evening when fever and chills hit along with some mild sporadic heart arrhythmia. I took it easy the next couple days and
CoCoLuna11
in
CLL Support
3 months ago
who cares for the carer?
Hello lovely people. In July 2023 i found myself needing to go the A and E as i was breathless and my GP sent me there for a chest xray but i ended up calling a ambulance and when they took my HR is was 200 beats a min i was taken straight in to the resuscitation area at the RSCH. I had no chest pains
Hello lovely people. In July 2023 i found myself needing to go the A and E as i was breathless and my GP sent me there for a chest xray but i ended up calling a ambulance and when they took my HR is was 200 beats a min i was taken straight in to the resuscitation area at the RSCH. I had no chest pains
Sindyblue
in
Atrial Fibrillation Support
3 months ago
Antibiotics and Increasing B12
Hi. I just got over a long bout with covid and am now on antibiotics (ceftin) for an ear infection (caused by covid). I've noticed since I began ceftin (8 days ago) that I'm experiencing fingers and toes tingling. Do you know if antibiotics can cause b12 depletion? I take daily 3000 mgs sublingually
Hi. I just got over a long bout with covid and am now on antibiotics (ceftin) for an ear infection (caused by covid). I've noticed since I began ceftin (8 days ago) that I'm experiencing fingers and toes tingling. Do you know if antibiotics can cause b12 depletion? I take daily 3000 mgs sublingually
LynetteinUSA
in
Pernicious Anaemia Society
4 months ago
Covid jabs to be sold in pharmacies
hi Has anyone else any information regarding selling of Covid jabs from next month . this was in the Times this morning. This will allow people who are not eligible for NHS booster jabs to get vaccinated . They are saying the cost will be £15-£20 .
hi Has anyone else any information regarding selling of Covid jabs from next month . this was in the Times this morning. This will allow people who are not eligible for NHS booster jabs to get vaccinated . They are saying the cost will be £15-£20 .
Main1234
in
Vasculitis UK
3 months ago
Rash any advice?
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
Geegee777
in
Thyroid UK
6 months ago
sjogens?
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
I have post PV Myelofibrosis. When I was dx with PV I took Pegasys from April 22 @ 45mg then 60mg then 90mg fortnightly. (On Jakavi since August 23) So took Pegasys for about 16 months After a couple of months on Pegasys I started to experience close vision problems which could not be corrected with
Yanico
in
MPN Voice
6 months ago
shingles vaccine
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Hi folks This is a brilliant site has keep me steady since my husband’s diagnosis of SLL now CLL. My Husband had been W&W for 6 years, now on acalabrutinib for two years with no side affect and doing well. He has been offered the shingles vaccine but he hasn’t had chickenpox’s, is it safe to get the
Charles4
in
CLL Support
6 months ago
anyone have achy legs
I’m learning so much from reading everyone’s posts. Unfortunately I am still trying to figure out what is going on with my legs. I know I have a component of RLS as my legs feel like a “current” is running through them when I am sitting for long periods, watching Tv in evenings and laying in bed.
I’m learning so much from reading everyone’s posts. Unfortunately I am still trying to figure out what is going on with my legs. I know I have a component of RLS as my legs feel like a “current” is running through them when I am sitting for long periods, watching Tv in evenings and laying in bed.
Corolla1
in
Restless Legs Syndrome
3 months ago
Steroid injection in shoulder joint
I had a steroid injection in my left shoulder on Thurs pm (after waiting about 6 months). The doctor administering it, advised me to postpone a forthcoming shingles jab, but I forgot to ask him if I should continue to take methotrexate (due Fri - i opted to skip it this week) and my 2 weekly Imraldi
I had a steroid injection in my left shoulder on Thurs pm (after waiting about 6 months). The doctor administering it, advised me to postpone a forthcoming shingles jab, but I forgot to ask him if I should continue to take methotrexate (due Fri - i opted to skip it this week) and my 2 weekly Imraldi
Cutes
in
NRAS
3 months ago
Groups eligible for covid-19 spring booster announced
The groups eligible for the spring 2024 Covid-19 booster vaccine have now been announced. But it is not yet clear what date invitations will be sent or when they will start. You can find more information about eligible groups on our website, where we will also provide updates when the NHS releases timings
The groups eligible for the spring 2024 Covid-19 booster vaccine have now been announced. But it is not yet clear what date invitations will be sent or when they will start. You can find more information about eligible groups on our website, where we will also provide updates when the NHS releases timings
Debbie_kinsey
Administrator
in
LUPUS UK
3 months ago
switching to a carnivore diet has put my PMR into total remission
I know the subject may be viewed as sensational or just plain wrong, but that is what I have concluded. At the time I was diagnosed with PMR, I already had diagnoses of psoriatic arthritis and fibromyalgia. My PMR started in 2019, about 8 months prior to covid. I was put on prednisone and experienced
I know the subject may be viewed as sensational or just plain wrong, but that is what I have concluded. At the time I was diagnosed with PMR, I already had diagnoses of psoriatic arthritis and fibromyalgia. My PMR started in 2019, about 8 months prior to covid. I was put on prednisone and experienced
benhemp
in
PMRGCAuk
3 months ago
Sciatica
Hi all. I have been suffering with back pain for several years. In regards to medication, you name it, I've tried it. I've have two lots of steroid injections which had no effect whatsoever and then finally in 2022 I had radio frequency ablation which was brilliant. I had instant relief from this. I
Hi all. I have been suffering with back pain for several years. In regards to medication, you name it, I've tried it. I've have two lots of steroid injections which had no effect whatsoever and then finally in 2022 I had radio frequency ablation which was brilliant. I had instant relief from this. I
Stormtrooper4
in
Pain Concern
3 months ago
Is there a test that you'd recommend for somebody suffering from long Covid and is the O.A.T useful?
Is there a test that you'd recommend for somebody suffering from long Covid and is the O.A.T useful? Answered by Dr. Jess Armine https://youtu.be/JTolpmzT4fk?si=lxwyGRkzE6HBAHzV
Is there a test that you'd recommend for somebody suffering from long Covid and is the O.A.T useful? Answered by Dr. Jess Armine https://youtu.be/JTolpmzT4fk?si=lxwyGRkzE6HBAHzV
Shewulf
Administrator
in
LDN Research Trust
3 months ago
Methotrexate and sinus/nasal issues
I've been on MTX for a year now and over the months I keep saying I feel like I'm coming down with a cold but it doesn't happen. I get a blockage in the back of my nasal passage and that causes post nasal drip and a sore throat. I was taking sulphasalazine but have stopped that as I felt so tired on
I've been on MTX for a year now and over the months I keep saying I feel like I'm coming down with a cold but it doesn't happen. I get a blockage in the back of my nasal passage and that causes post nasal drip and a sore throat. I was taking sulphasalazine but have stopped that as I felt so tired on
Gottarelax
in
NRAS
6 months ago
Silly me
I didn't get the latest Covid jab because I was afraid it would 'set off' pmr again. So of course I got Covid...thought it was a cold. Felt grotty for four days and definitely on the mend now. I take choi kwang do and that room is where I might have picked it up (one room, one door and @ 18 bodies
I didn't get the latest Covid jab because I was afraid it would 'set off' pmr again. So of course I got Covid...thought it was a cold. Felt grotty for four days and definitely on the mend now. I take choi kwang do and that room is where I might have picked it up (one room, one door and @ 18 bodies
whitefishbay
in
PMRGCAuk
3 months ago
Fostair Nexhaler - Side Effects after 2 months?
Hi everyone, Hope you can advise. I had asthma when I was in my teens but then it got better, now in my thirties my ashtma decided to come back. It appeared one year, but I was able to manage it by running so no inhaler was almost unnecessary, but sometimes would take the brown. Then had COVID (mild
Hi everyone, Hope you can advise. I had asthma when I was in my teens but then it got better, now in my thirties my ashtma decided to come back. It appeared one year, but I was able to manage it by running so no inhaler was almost unnecessary, but sometimes would take the brown. Then had COVID (mild
Othacon
in
Asthma Community Forum
3 months ago
Caring for mum with severe copd
Been following for a while but this is my first post. Mums a young 76 and had copd for around 15 years, it started deteriorating in 2022 starting with infection after infection and then ending up in hospital for 5 days late July with respiratory failure type 2, with infection they thought, she was put
Been following for a while but this is my first post. Mums a young 76 and had copd for around 15 years, it started deteriorating in 2022 starting with infection after infection and then ending up in hospital for 5 days late July with respiratory failure type 2, with infection they thought, she was put
Oioisaveloy
in
Lung Conditions Community Forum
3 months ago
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