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MODERNA SPIKEVAX (2022) COVID Vaccine Availability Autumn 2023 Uk
Hi all, As anyone had a Moderna COVID vaccine (2022 version Bivalent Spikevax) this autumn in the UK, I have a clinical need to avoid Pfizer and that is all that is being sent out at present. I have been in touch with UKHSA, NHS England, local Vaccine authority, Haematologist and GP without any joy.
Hi all, As anyone had a Moderna COVID vaccine (2022 version Bivalent Spikevax) this autumn in the UK, I have a clinical need to avoid Pfizer and that is all that is being sent out at present. I have been in touch with UKHSA, NHS England, local Vaccine authority, Haematologist and GP without any joy.
thyreoidea
in
Thyroid UK
7 months ago
covid vaccine
My Hematologist suggested I not take the flu or covid vaccine. She is concerned it will trigger another episode of low platelets. I had been in remission for 15 months last year and I thought I had beaten ITP. I got the vaccines last year then about 2 months later my platelets were back down to 1.
My Hematologist suggested I not take the flu or covid vaccine. She is concerned it will trigger another episode of low platelets. I had been in remission for 15 months last year and I thought I had beaten ITP. I got the vaccines last year then about 2 months later my platelets were back down to 1.
joecirillo
in
ITP Support Association
7 months ago
Finally some progress
Those who followed our Journey, know this is such a painful process of grief. Two weeks ago, the hospital wrote it would not change the factual information in my wife's chart. In her chart it had been written she had Biopys proven Nash Cirrhosis, which led doctors looking at ultrasounds that said
Those who followed our Journey, know this is such a painful process of grief. Two weeks ago, the hospital wrote it would not change the factual information in my wife's chart. In her chart it had been written she had Biopys proven Nash Cirrhosis, which led doctors looking at ultrasounds that said
Wolivere
in
British Liver Trust
8 months ago
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Not what I expected!
After feeling unwell, I’ve had a lousy night, tested in the early hours and have Covid! Had the booster 12 days ago and the flu jab on Saturday. it’s Sod’s Law , I was going to say a flare and low adrenal function feels like Covid with Mumps . Hopefully i can get antivirals , they wouldn’t give them
After feeling unwell, I’ve had a lousy night, tested in the early hours and have Covid! Had the booster 12 days ago and the flu jab on Saturday. it’s Sod’s Law , I was going to say a flare and low adrenal function feels like Covid with Mumps . Hopefully i can get antivirals , they wouldn’t give them
Greensleeves
in
PMRGCAuk
7 months ago
me again with the shingles questions! A specific one this time…
how long did you stop your arthritis meds when you had shingles? The a and e doc told me I could restart the Rinvoq once the blisters had crusted over…I’m keen not to be off it for too long … Thanks in advance all Bon X
how long did you stop your arthritis meds when you had shingles? The a and e doc told me I could restart the Rinvoq once the blisters had crusted over…I’m keen not to be off it for too long … Thanks in advance all Bon X
Bon1
in
NRAS
9 months ago
Flue or RLS
as I mentioned a day or so back I had my flue jab last Sunday 1st October and my RLS has got progressively worse Monday and Tuesday virtually all day and constant headaches. Went to bed at 9.45 Monday night woke at 11.30 pm had to get up and walk around tried to go back to sleep by gave up till 6am went
as I mentioned a day or so back I had my flue jab last Sunday 1st October and my RLS has got progressively worse Monday and Tuesday virtually all day and constant headaches. Went to bed at 9.45 Monday night woke at 11.30 pm had to get up and walk around tried to go back to sleep by gave up till 6am went
HipHop1972
in
Restless Legs Syndrome
7 months ago
A Shingrix thank you
Hi, I just wanted to thank so many of you who have spoken of your side effects with the second Shingrix, yet being worth it. It was when I recently read here that being only half vaccinated was still being open to Shingles that spurred me into getting the second one today, after 2 1/2 years. After
Hi, I just wanted to thank so many of you who have spoken of your side effects with the second Shingrix, yet being worth it. It was when I recently read here that being only half vaccinated was still being open to Shingles that spurred me into getting the second one today, after 2 1/2 years. After
Schubert1870
in
CLL Support
2 months ago
COVID-19 immune cell vaccine eases SLE symptoms in girl: Report
Therapy helped 13-year-old by increasing immune tolerance, researchers say
A personalized vaccine kit designed to prevent COVID-19 infection eased systemic lupus erythematosus (SLE) manifestations in an adolescent girl in Indonesia whose symptoms had not been well-controlled with immunosuppressive
Therapy helped 13-year-old by increasing immune tolerance, researchers say
A personalized vaccine kit designed to prevent COVID-19 infection eased systemic lupus erythematosus (SLE) manifestations in an adolescent girl in Indonesia whose symptoms had not been well-controlled with immunosuppressive
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
7 months ago
A very special interview with Dr Patrick Harrington regarding Covid vaccines and MPN patients
In this interview Dr Patrick Harrington, Consultant Haematologist, Guy’s & St Thomas’ Hospital, talks to Nona about Covid vaccines for MPN patients, he starts off by describing the research he carried out at the start of the Covid pandemic, with Covid being a new condition it was an area that needed
In this interview Dr Patrick Harrington, Consultant Haematologist, Guy’s & St Thomas’ Hospital, talks to Nona about Covid vaccines for MPN patients, he starts off by describing the research he carried out at the start of the Covid pandemic, with Covid being a new condition it was an area that needed
Mazcd
MPNVoice
in
MPN Voice
7 months ago
First Post
Hi all, although this is my first post I have visited this site for the last 2 1/2 years. I was diagnosed with RA. Just as covid hit, I went from a healthy 52 year old to literally not being able to get out of bed overnight. I have never experienced pain like it, and I spiralled quickly in to a very
Hi all, although this is my first post I have visited this site for the last 2 1/2 years. I was diagnosed with RA. Just as covid hit, I went from a healthy 52 year old to literally not being able to get out of bed overnight. I have never experienced pain like it, and I spiralled quickly in to a very
Ryshta
in
NRAS
7 months ago
PV and lung problems/findings
Hello dear group, once again I am turning to you, in the hope somebody might share if they had a similar experience. A week ago, I went to the doctors office, totally unrelated to my PV journey, to check out a persisting cough. I wasn't extremely concerned, but wanted to make sure I was on the mend
Hello dear group, once again I am turning to you, in the hope somebody might share if they had a similar experience. A week ago, I went to the doctors office, totally unrelated to my PV journey, to check out a persisting cough. I wasn't extremely concerned, but wanted to make sure I was on the mend
love0826
in
MPN Voice
1 year ago
Drew Weissman, Katalin Karikó win Nobel in medicine for enabling mRNA COVID vaccines
[i]
A screen at the Karolinska Institute shows this year's laureates Katalin Kariko of Hungary (L) and Drew Weissman of the US during the announcement of the winners of the 2023 Nobel Prize in Physiology or Medicine at the Karolinska Institute in Stockholm on October 2, 2023.(Jonathan Nackstrand/AFP
[i]
A screen at the Karolinska Institute shows this year's laureates Katalin Kariko of Hungary (L) and Drew Weissman of the US during the announcement of the winners of the 2023 Nobel Prize in Physiology or Medicine at the Karolinska Institute in Stockholm on October 2, 2023.(Jonathan Nackstrand/AFP
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
7 months ago
Please someone reassure me that this is another IBS flare up
Last year I went through a bad phase with my bowels, had numerous doctor visits and blood/stool tests. The doctor said IBS again due to negative results and also based on my previous history of negative tests along with normal sigmoidoscopy. I've been having sporadic bad IBS flares which appear different
Last year I went through a bad phase with my bowels, had numerous doctor visits and blood/stool tests. The doctor said IBS again due to negative results and also based on my previous history of negative tests along with normal sigmoidoscopy. I've been having sporadic bad IBS flares which appear different
Tokai335
in
IBS Network
9 months ago
Seem to be stuck at 7.5mg
Hello my friends , I have been stuck at this dose for approaching 3 years . Sometimes going a little higher on sick days and throughout extremely stressful times. I’ve lost my Mum this year after years of caring , grief is a dreadful experience, the price we pay for love eh ! I only have to drop
Hello my friends , I have been stuck at this dose for approaching 3 years . Sometimes going a little higher on sick days and throughout extremely stressful times. I’ve lost my Mum this year after years of caring , grief is a dreadful experience, the price we pay for love eh ! I only have to drop
Greensleeves
in
PMRGCAuk
7 months ago
unbearably cold hands
Hi all, Please can you help/advise what I can do in regards to my hands being cold , the coldness gets worse each evening, I have to get in a really hot bath and use a hot water bottle to try and raise temperature, other symptoms are usual under active , brittle nails, hair loss, unbearable weight gain
Hi all, Please can you help/advise what I can do in regards to my hands being cold , the coldness gets worse each evening, I have to get in a really hot bath and use a hot water bottle to try and raise temperature, other symptoms are usual under active , brittle nails, hair loss, unbearable weight gain
J2506
in
Thyroid UK
1 year ago
Post Covid
Morning all ,hoping for advice plz. I had covid 6 weeks ago,it was very unpleasant. Worse still is now ive been left with vertigo. Im actually struggling more with this than the covid. My RA nurse also stopped my meds due to how poorly i was. So far no flare. Please has anyone else had vertigo and how
Morning all ,hoping for advice plz. I had covid 6 weeks ago,it was very unpleasant. Worse still is now ive been left with vertigo. Im actually struggling more with this than the covid. My RA nurse also stopped my meds due to how poorly i was. So far no flare. Please has anyone else had vertigo and how
Ninnin67
in
NRAS
7 months ago
weird mouth symptoms on Sulfasalazine
Has anyone experienced anything like the following? I’ve been on Sulf for 7 weeks, max dose from 4 weeks. In the last 3 days I’ve had a sore tongue which has now settled but I’ve completely lost my sense of taste. I’ve tested and am negative for covid. I can’t think what else it could be!
Has anyone experienced anything like the following? I’ve been on Sulf for 7 weeks, max dose from 4 weeks. In the last 3 days I’ve had a sore tongue which has now settled but I’ve completely lost my sense of taste. I’ve tested and am negative for covid. I can’t think what else it could be!
Charlongo79
in
NRAS
5 months ago
thrush……again
For the past three months I’ve been trying to get rid of a bad taste in my mouth. The roof of my mouth feels like I’ve burned my mouth on a too hot pizza. The middle of my tongue is coated the tip is somewhat red. My dentist said X-rays show no infection. GP looked in my mouth and said
For the past three months I’ve been trying to get rid of a bad taste in my mouth. The roof of my mouth feels like I’ve burned my mouth on a too hot pizza. The middle of my tongue is coated the tip is somewhat red. My dentist said X-rays show no infection. GP looked in my mouth and said
Mstiles
in
PMRGCAuk
10 months ago
itch and bilirubin, long covid
1) since startin* urso I continue to have an itchy abdomen and scalp. My family dr does not think itch is related to PBC because my bilirubin is fine… I think I’m early stage. Enzymes starting to come down but the gi doc says nothing gets added or changed until we see how I do after being on it for a
1) since startin* urso I continue to have an itchy abdomen and scalp. My family dr does not think itch is related to PBC because my bilirubin is fine… I think I’m early stage. Enzymes starting to come down but the gi doc says nothing gets added or changed until we see how I do after being on it for a
Artsy123
in
PBCers Organization
7 months ago
Covid prior to FET with a positive outcome
Hope everyone is doing ok! I just wondered if anyone tested positive for covid the month before their FET and then had a positive result? I know it’s different for everyone but just making sure it has actually happened and if I go ahead with my FET next month I’m not starting on the back foot! (Well
Hope everyone is doing ok! I just wondered if anyone tested positive for covid the month before their FET and then had a positive result? I know it’s different for everyone but just making sure it has actually happened and if I go ahead with my FET next month I’m not starting on the back foot! (Well
Booda21
in
Fertility Network UK
7 months ago
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