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Antihistamine and probiotics
I have had long covid for 16 months now, and in the absence of any treatments on the horizon am thinking of trying antihistamine tablets and/or probiotic supplements. My RLS is currently much more controlled than it was, after iron infusion and am taking Gabapentin 400 mg- though insomnia still bad
I have had long covid for 16 months now, and in the absence of any treatments on the horizon am thinking of trying antihistamine tablets and/or probiotic supplements. My RLS is currently much more controlled than it was, after iron infusion and am taking Gabapentin 400 mg- though insomnia still bad
Edengirl58
in
Restless Legs Syndrome
1 year ago
Fecal Microbiota Transplantation (FMT) For PD And Much Much More
While many of us are aware of the potential that FMT has shown for PD, Clostridium difficile (C. diff) and IBS that has not responded to standard therapy, I wrote this to highlight the fact that FMT has shown the potential to also help a multitude of other diseases and health issues that are often seen
While many of us are aware of the potential that FMT has shown for PD, Clostridium difficile (C. diff) and IBS that has not responded to standard therapy, I wrote this to highlight the fact that FMT has shown the potential to also help a multitude of other diseases and health issues that are often seen
chartist
in
Cure Parkinson's
1 year ago
First 5 Tibetan Rites (7x) since Covid
First little exercise workout on my journey to return from latest Covid setback, and it feels great. I got surprisingly pretty sweaty quickly, just with these 5 minutes, but I felt strong. So aerobic fitness has suffered a bit the last week whilst in bed, but muscle strength and flexibility is all
First little exercise workout on my journey to return from latest Covid setback, and it feels great. I got surprisingly pretty sweaty quickly, just with these 5 minutes, but I felt strong. So aerobic fitness has suffered a bit the last week whilst in bed, but muscle strength and flexibility is all
CBDB
Administrator
in
Strength & Flex
1 year ago
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Endo appointment
Hey guys. I have finally got to see an endo. He was very nice and understood and listened to everything I said. So with my gp refusing to give me more levo for months was because my levels were 'within range' was 75mcg since September last year. Last week gp called to say I'm slightly hypo again tsh
Hey guys. I have finally got to see an endo. He was very nice and understood and listened to everything I said. So with my gp refusing to give me more levo for months was because my levels were 'within range' was 75mcg since September last year. Last week gp called to say I'm slightly hypo again tsh
Dollc86
in
Thyroid UK
1 year ago
Contribute your story to the Covid-19 Inquiry
Every Story Matters is your chance to share your experience of the pandemic with the UK Covid-19 Inquiry. Every story and experience is valuable in shaping the Inquiry’s recommendations for the future. Help them to hear the voices of people with lupus and their friends and loved ones. Your experience
Every Story Matters is your chance to share your experience of the pandemic with the UK Covid-19 Inquiry. Every story and experience is valuable in shaping the Inquiry’s recommendations for the future. Help them to hear the voices of people with lupus and their friends and loved ones. Your experience
Debbie_kinsey
Administrator
in
LUPUS UK
1 year ago
IVF and covid
Hello wonderful people, I’ve just started my second round of IVF after a failed transfer and no freezable embryos. Currently on day 3 of down regulation and have only gone and tested positive for covid. As this round has already been delayed due to a functional cyst and waiting for it to clear I’m
Hello wonderful people, I’ve just started my second round of IVF after a failed transfer and no freezable embryos. Currently on day 3 of down regulation and have only gone and tested positive for covid. As this round has already been delayed due to a functional cyst and waiting for it to clear I’m
Aansey
in
Fertility Network UK
1 year ago
Edema post transplant
So one year post transplant and what a complete shitshow.It has been nothing but one thing after another.First got covid from hospital when transplanted,then when being treated in hospital for that picked up COP and had 2 weeks in isolation on iv antibiotics 3 times daily.Finally got home suffer horrible
So one year post transplant and what a complete shitshow.It has been nothing but one thing after another.First got covid from hospital when transplanted,then when being treated in hospital for that picked up COP and had 2 weeks in isolation on iv antibiotics 3 times daily.Finally got home suffer horrible
Parkerbarker
in
Kidney Transplant
1 year ago
BHF Community Guidelines
Our latest interpretation of the evidence on COVID-19 and heart health is available here https://www.bhf.org.uk/informationsupport/
coronavirus
-and-you. We are committed to posting evidence-based information and maintaining a safe and inclusive environment for all members.
Our latest interpretation of the evidence on COVID-19 and heart health is available here https://www.bhf.org.uk/informationsupport/
coronavirus
-and-you. We are committed to posting evidence-based information and maintaining a safe and inclusive environment for all members.
Luke_BHF
Partner
in
British Heart Foundation
3 months ago
You're not a fraud!
https://www.theguardian.com/science/2023/jul/09/microbiome-chronic-fatigue-me-long-covid-research Hello all, I'm also on the Thyroid forum, but was originally diagnosed with CFS in the early '90's. A couple of years later I developed Thyroid Cancer and hence, life has been confusing for doctors.
https://www.theguardian.com/science/2023/jul/09/microbiome-chronic-fatigue-me-long-covid-research Hello all, I'm also on the Thyroid forum, but was originally diagnosed with CFS in the early '90's. A couple of years later I developed Thyroid Cancer and hence, life has been confusing for doctors.
Sluggishandtired
in
Myalgic Encephalomyelitis Community
1 year ago
Evaluating Success
See profile for current understanding of my life long B12 deficiency and self designed supplementation regiment. [u]July 2023[/u] Over time I changed by supplementation starting 90 days ago. Before that I was improving to some degree. I used the pain from Peripheral Neuropathy to monitor improvement
See profile for current understanding of my life long B12 deficiency and self designed supplementation regiment. [u]July 2023[/u] Over time I changed by supplementation starting 90 days ago. Before that I was improving to some degree. I used the pain from Peripheral Neuropathy to monitor improvement
WIZARD6787
in
Pernicious Anaemia Society
1 year ago
Sore throat 1dp5dt (FET)
Hi guys, So I feel like I’m going nuts… I’ve had a verrry slight sore throat in the few days leading up to my 2nd FET. Nothing bad, I swear I had it leading up to my first FET in December (I was so worried about getting covid and it being cancelled). But of course both times it was not covid so have
Hi guys, So I feel like I’m going nuts… I’ve had a verrry slight sore throat in the few days leading up to my 2nd FET. Nothing bad, I swear I had it leading up to my first FET in December (I was so worried about getting covid and it being cancelled). But of course both times it was not covid so have
Esb27
in
Fertility Network UK
1 year ago
Covid, meds do they help?
I have CKD stage 3a, I just got covid. I was thinking about calling my doctor tomorrow to see if I need meds to help. I have body aches, headache, and sore throat. I was vaccinated in Nov. Not sure if it’s worth it to take meds and if it hurts the kidneys..could you share your experiences?
I have CKD stage 3a, I just got covid. I was thinking about calling my doctor tomorrow to see if I need meds to help. I have body aches, headache, and sore throat. I was vaccinated in Nov. Not sure if it’s worth it to take meds and if it hurts the kidneys..could you share your experiences?
Sarah_402
in
Kidney Disease
1 year ago
🟨 Making Yellow Card Reports 🟨
[i]
Coronavirus
Yellow Card reporting site[/i] https://
coronavirus
-yellowcard.mhra.gov.uk/ 🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨
Outside the UK
There are other routes outside the UK. For example the USA's FDA has a reporting mechanism.
[i]
Coronavirus
Yellow Card reporting site[/i] https://
coronavirus
-yellowcard.mhra.gov.uk/ 🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨🟨
Outside the UK
There are other routes outside the UK. For example the USA's FDA has a reporting mechanism.
helvella
Thyroid UK
in
Thyroid UK
1 year ago
⭐️Update - 5/4/2013 🙂 Spring 2023 Covid-19 booster for most vulnerable.
The Joint Committee on Vaccination and Immunisation (JCVI) has confirmed its advice for a 2023 spring
coronavirus
(COVID-19) booster programme.
The Joint Committee on Vaccination and Immunisation (JCVI) has confirmed its advice for a 2023 spring
coronavirus
(COVID-19) booster programme.
Moomin8
in
NRAS
1 year ago
ZERO TASTE AFTER PAXLOVID COVID
I had Covid back in September 2022. I am pretty healthy at 71 and had my shots. First time to get it and it was pretty intense. I was given Paxlovid and afte 2 weeks I felt better however my taste was zero with little smell. I went through the holdups with no taste and come March I got it again out in
I had Covid back in September 2022. I am pretty healthy at 71 and had my shots. First time to get it and it was pretty intense. I was given Paxlovid and afte 2 weeks I felt better however my taste was zero with little smell. I went through the holdups with no taste and come March I got it again out in
oznaf
in
Acid Reflux Support
1 year ago
Duration of a first NHS Endocrinologist Appointment
Is a first, initial NHS Endocrinology appointment for hypothyroidism, which appears to be possible central hypo, genetic and suggestive of a pituitary tumour of 30 minutes duration, then thrown out regardless of time required to discuss the problem? G.P. appointments are 10 mins. maximum. Are hospital
Is a first, initial NHS Endocrinology appointment for hypothyroidism, which appears to be possible central hypo, genetic and suggestive of a pituitary tumour of 30 minutes duration, then thrown out regardless of time required to discuss the problem? G.P. appointments are 10 mins. maximum. Are hospital
Wua13262348
in
Thyroid UK
1 year ago
Internal tremble - frequency and cause
Since having covid in 2020 there are times when I suddenly feel trembly inside. I feel less steady, movement and sensation can be affected slightly. Nobody would notice but I don't feel right. This happens after being very busy, more stressful times (eg, being in a meeting) or having to be out in the
Since having covid in 2020 there are times when I suddenly feel trembly inside. I feel less steady, movement and sensation can be affected slightly. Nobody would notice but I don't feel right. This happens after being very busy, more stressful times (eg, being in a meeting) or having to be out in the
StriatedCaracara
in
LUPUS UK
1 year ago
Covid jab and return of PMR symptoms
I had successfully reduced to 3mg after a year of taking pred. A week after having the covid jab as I was supposedly vulnerable my PMR symptoms are bad again. Neck ,shoulders and buttock pains as before. Have gone upto 5mg for the past four days on GPs recommendation but no relief . Had blood test
I had successfully reduced to 3mg after a year of taking pred. A week after having the covid jab as I was supposedly vulnerable my PMR symptoms are bad again. Neck ,shoulders and buttock pains as before. Have gone upto 5mg for the past four days on GPs recommendation but no relief . Had blood test
simps999
in
PMRGCAuk
1 year ago
bronchiectasis, asthma and long covid
Hi, I’m about 3 months into my bronchiectasis journey since my diagnosis earlier this year. My 3 month azithromycin trial went well and is now on my repeat prescription list (with it feels like a million other things ) I went for assessment for pulmonary rehab and the physio decided I’m too affected
Hi, I’m about 3 months into my bronchiectasis journey since my diagnosis earlier this year. My 3 month azithromycin trial went well and is now on my repeat prescription list (with it feels like a million other things ) I went for assessment for pulmonary rehab and the physio decided I’m too affected
Emily-G
in
Lung Conditions Community Forum
1 year ago
Bronchiectasis and long covid
Hi, I’m about 3 months into my bronchiectasis journey since my diagnosis earlier this year. My 3 month azithromycin trial went well and is now on my repeat prescription list (with it feels like a million other things ) I went for assessment for pulmonary rehab and the physio decided I’m too affected
Hi, I’m about 3 months into my bronchiectasis journey since my diagnosis earlier this year. My 3 month azithromycin trial went well and is now on my repeat prescription list (with it feels like a million other things ) I went for assessment for pulmonary rehab and the physio decided I’m too affected
Emily-G
in
Bronchiectasis Support
1 year ago
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