Search
Search
About
Log in
Join
Experiences with
Congenital infections
Posts
Communities
28,255 public posts
Filter results
If you get sick...cold, flu, Covid...what did you do?
I'm just over 9 months kidney transplant from a living donor. I've felt great but I do worry, since it is cold and flu season, about getting sick. Probably my biggest worry at this point. I try to wear masks when I am out and take all precautions. I just wondered though if I should get sick what are
I'm just over 9 months kidney transplant from a living donor. I've felt great but I do worry, since it is cold and flu season, about getting sick. Probably my biggest worry at this point. I try to wear masks when I am out and take all precautions. I just wondered though if I should get sick what are
Tankjsl
in
Kidney Transplant
3 months ago
covid
hello iam suffering with covid had it since Sunday , symptoms don’t seem to be going away , has anybody had covid , with hashimotos , am I wrong in thinking having this condition makes illness worse and longer to recover , sorry but been told I have hashimotos, but not sure on how it works thanks for
hello iam suffering with covid had it since Sunday , symptoms don’t seem to be going away , has anybody had covid , with hashimotos , am I wrong in thinking having this condition makes illness worse and longer to recover , sorry but been told I have hashimotos, but not sure on how it works thanks for
Prosecco1997
in
Thyroid UK
3 months ago
Pegasys Update 1.0
Finally getting around to sharing my experiences of starting Pegasys. First a little background. Diagnosed with ET JAK2+ in 2019 after a decade of scintillating scotomas with increasing frequency at almost weekly. Aspirin cut this to approx. 90 days! Over the next three years increasingly struggled with
Finally getting around to sharing my experiences of starting Pegasys. First a little background. Diagnosed with ET JAK2+ in 2019 after a decade of scintillating scotomas with increasing frequency at almost weekly. Aspirin cut this to approx. 90 days! Over the next three years increasingly struggled with
Crossefield
in
MPN Voice
3 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
D Mannose
Hello everyone Just wondered if anyone here has used D Mannose tablets to manage recurrent urinary tract infections and if so with what success? I’ve had this problem for a few years now and the Urologist suggested daily low dose antibiotics which I want to avoid. Despite trying all of the self
Hello everyone Just wondered if anyone here has used D Mannose tablets to manage recurrent urinary tract infections and if so with what success? I’ve had this problem for a few years now and the Urologist suggested daily low dose antibiotics which I want to avoid. Despite trying all of the self
RosaD
in
LUPUS UK
3 months ago
Covid and Myelofibrosis
hi I’ve just tested positive for Covid, I have post pv Myelofibrosis. I’m waiting on 111 to see whether I need to have some treatment. What are your thoughts and is this necessary now? I think it’s going to be a long wait, so it might be tomorrow. Thank you Mal
hi I’ve just tested positive for Covid, I have post pv Myelofibrosis. I’m waiting on 111 to see whether I need to have some treatment. What are your thoughts and is this necessary now? I think it’s going to be a long wait, so it might be tomorrow. Thank you Mal
Mal42
in
MPN Voice
3 months ago
dont give up the fight against Afib
I have been a member of this forum for some years and learned a few things from its members but up until now i have never posted anything but i thought my story may give some of you people a bit of hope. I first went into afib in 2018 sudenly without any warning my heart rate was 222 and the top line
I have been a member of this forum for some years and learned a few things from its members but up until now i have never posted anything but i thought my story may give some of you people a bit of hope. I first went into afib in 2018 sudenly without any warning my heart rate was 222 and the top line
Dikytiker
in
AF Association
3 months ago
Calcified tendonitis
Has anyone experienced calcified tendinitis? I have been diagnosed with this after 6 months of excruciating shoulder pain. GP kept just prescribing painkillers then I saw the physio who advised me to have an X-ray. I am now having a steroid injection in my shoulder followed by physio, and hopefully this
Has anyone experienced calcified tendinitis? I have been diagnosed with this after 6 months of excruciating shoulder pain. GP kept just prescribing painkillers then I saw the physio who advised me to have an X-ray. I am now having a steroid injection in my shoulder followed by physio, and hopefully this
FLS1
in
NRAS
4 months ago
Covid and Party
👋 Party is this coming Sat . I feel OK with going now after people's advice , so thank you all. Got my N95 mask. Will have sanitiser on me all the time . However I am now facing difficulties, flare up in both knees and one hip in agony and lower back , getting in and out of bed , turning in bed
👋 Party is this coming Sat . I feel OK with going now after people's advice , so thank you all. Got my N95 mask. Will have sanitiser on me all the time . However I am now facing difficulties, flare up in both knees and one hip in agony and lower back , getting in and out of bed , turning in bed
Stavrou1
in
CLL Support
3 months ago
Dizzy
Good morning to you all.I've been diagnosed with fibomyaigia in 2020 But I am getting real dizzy it's lasted for a couple of weeks now at first I got up at night and couldn't walk at all in a straight line everything was spinning so scary. The doctor said I have Benign paroxysmal positional vertigo
Good morning to you all.I've been diagnosed with fibomyaigia in 2020 But I am getting real dizzy it's lasted for a couple of weeks now at first I got up at night and couldn't walk at all in a straight line everything was spinning so scary. The doctor said I have Benign paroxysmal positional vertigo
Chellelo
in
Fibromyalgia Action UK
6 months ago
FET in 4 days and nasty cold
I am so worried now, our FET is this Thursday and some nasty cold got me this weekend. I am afraid to take any cold/flu meds so it won't mess up with my lining etc 🙈 Has anyone been not well before or during transfer and it affected the outcome?
I am so worried now, our FET is this Thursday and some nasty cold got me this weekend. I am afraid to take any cold/flu meds so it won't mess up with my lining etc 🙈 Has anyone been not well before or during transfer and it affected the outcome?
Glaedy
in
Fertility Network UK
2 months ago
latest results, confused, please advise!
My last results a month ago before treatment with 50 mcg were : Serum free t4 level. 10.2 pmo/L TSH level 7.28 IU/mL After a month of Levothyroxine my results are now:- serum free t4 level. 15.6 TSH 2.87 I asked for, and was told my T3 would be checked but I can’t see it on printout unless
My last results a month ago before treatment with 50 mcg were : Serum free t4 level. 10.2 pmo/L TSH level 7.28 IU/mL After a month of Levothyroxine my results are now:- serum free t4 level. 15.6 TSH 2.87 I asked for, and was told my T3 would be checked but I can’t see it on printout unless
Benjipuss
in
Thyroid UK
3 months ago
Will a COVID (or flu) vaccination affect my blood results?
If I have a blood test 3 or 7 days after a COVID (or flu) vaccination - will it affect my blood results? Should I perhaps make the vaccination after the blood test, so that there is no potential issue interpreting my blood results? If the vaccination affects blood results - how many days after the vaccination
If I have a blood test 3 or 7 days after a COVID (or flu) vaccination - will it affect my blood results? Should I perhaps make the vaccination after the blood test, so that there is no potential issue interpreting my blood results? If the vaccination affects blood results - how many days after the vaccination
mantana
in
CLL Support
3 months ago
B12 deficiency
I was diagnosed with a B12 deficiency. I'm recovering from covid it's been 3 weeks. Not sure if the covid knocked my B12 down. I had first injection today. I woke up out of my sleep my body burning and dry month. I had that feeling first week of covid it went away. Now I'm not sure if the B12 is fighting
I was diagnosed with a B12 deficiency. I'm recovering from covid it's been 3 weeks. Not sure if the covid knocked my B12 down. I had first injection today. I woke up out of my sleep my body burning and dry month. I had that feeling first week of covid it went away. Now I'm not sure if the B12 is fighting
Michbell45
in
Pernicious Anaemia Society
3 months ago
Current SUPERNOVA Clinical Trial for Reformulated EVUSHELD for preventing COVID-19 infection for immune-impaired individuals
A Phase II sub-study of SUPERNOVA clinical trial (2023) is currently operating to test the efficacy and safety of AZD3152 as a component of a reformulated version of EVUSHELD mAbs prophylaxis for immune-impaired individuals who cannot mount antibody responses to COVID-19 vaccines. Study Understanding
A Phase II sub-study of SUPERNOVA clinical trial (2023) is currently operating to test the efficacy and safety of AZD3152 as a component of a reformulated version of EVUSHELD mAbs prophylaxis for immune-impaired individuals who cannot mount antibody responses to COVID-19 vaccines. Study Understanding
Classicaljazz
in
CLL Support
4 months ago
Trimbow update
I have been on the Trimbow three weeks now and it does seem to be working , I noticed I was walking faster and the use of my ventolin is much reduced . I still have a chesty cough lingering on after a cold but no infection , I need to ask the question does Trimbow make you cough? Just wondered as I
I have been on the Trimbow three weeks now and it does seem to be working , I noticed I was walking faster and the use of my ventolin is much reduced . I still have a chesty cough lingering on after a cold but no infection , I need to ask the question does Trimbow make you cough? Just wondered as I
MrsP70
in
Lung Conditions Community Forum
2 months ago
Declined lupus Centre help
Hi all, hope you're all doing as well as you can be. Just thought I'd give you an update on something that went from being so hopeful to now being left to struggle once again. If you know my previous posts just before Christmas I'd had a steroid injection and was waiting to see professor D'cruz in London
Hi all, hope you're all doing as well as you can be. Just thought I'd give you an update on something that went from being so hopeful to now being left to struggle once again. If you know my previous posts just before Christmas I'd had a steroid injection and was waiting to see professor D'cruz in London
Haylz2109
in
LUPUS UK
4 months ago
⭐️⭐️my COVID journey ⭐️⭐️
⭐️covid survivors let’s keep on fighting, let’s help each other & spread awareness of the real impact & life changing difficulties we face❤️❤️ Ladysurvivor1 profile image Ladysurvivor1 2 days ago•0 Replies 🧏🏽♀️My COVID Journey: A Tale of Resilience and Hope (Part 1) In the depths of January
⭐️covid survivors let’s keep on fighting, let’s help each other & spread awareness of the real impact & life changing difficulties we face❤️❤️ Ladysurvivor1 profile image Ladysurvivor1 2 days ago•0 Replies 🧏🏽♀️My COVID Journey: A Tale of Resilience and Hope (Part 1) In the depths of January
Ladysurvivor1
in
ICUsteps
4 months ago
Finally failed at side-stepping the “rona”
Well I guess sooner or later it had to happen. Four years of avoiding covid and now I caught it whilst traveling for work in the Far East. Started with a cold and a general malaise, then a few days later, last night, I had a slight temperature so I thought I’d check (had packed some tests just in
Well I guess sooner or later it had to happen. Four years of avoiding covid and now I caught it whilst traveling for work in the Far East. Started with a cold and a general malaise, then a few days later, last night, I had a slight temperature so I thought I’d check (had packed some tests just in
Aldebaran25
in
MPN Voice
4 months ago
Worried About (Possible) Recent Diagnosis of PMR.
Around 3 months ago I became aware of increasing aches and pains in my arms and legs and an overwhelming exhaustion. I’m normally a fit and active 73 year old. My neck felt stiff but I put that down to wear and tear as I also have worn discs in my lower spine which I manage with Pilates. GP sent me
Around 3 months ago I became aware of increasing aches and pains in my arms and legs and an overwhelming exhaustion. I’m normally a fit and active 73 year old. My neck felt stiff but I put that down to wear and tear as I also have worn discs in my lower spine which I manage with Pilates. GP sent me
GlesgaGal
in
PMRGCAuk
4 months ago
Interesting article about the effects of Covid19 on your blood
Having caught Covid19 a short time after my allo SCT and with my anaemia ongoing, I was interested to see this article. This is not CLL specific but worth a read. "[i]Several studies have reported, in COVID-19 patients, hematological abnormalities. Most of these alterations are associated with a higher
Having caught Covid19 a short time after my allo SCT and with my anaemia ongoing, I was interested to see this article. This is not CLL specific but worth a read. "[i]Several studies have reported, in COVID-19 patients, hematological abnormalities. Most of these alterations are associated with a higher
Jm954
Administrator
in
CLL Support
4 months ago
1
...
19
20
21
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Lung Conditions Community Forum
2927 results
Fertility Network UK
2784 results
NRAS
2333 results
View top 10 communities
Sort by
Most Relevant
Newest