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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
9 months ago
immunosuppressants and Covid vaccine
I was told by my nephrologist that I should wait 3 months to get the current Covid vaccine until my immunosuppressive medication (rituximab) wears off because I won’t mount a good response if I get it now. Has anyone been told similar advice?
I was told by my nephrologist that I should wait 3 months to get the current Covid vaccine until my immunosuppressive medication (rituximab) wears off because I won’t mount a good response if I get it now. Has anyone been told similar advice?
MsAmyM
in
Kidney Disease
9 months ago
covid vaccination
Thankyou to everyone who replied to my previous post . Most people seem to be having the covid booster . It isn’t the initial jab that bothers me but what it’s doing long term . I had my last one in November and since then I’ve developed polymyalgia rheumatica, another auto immune disease . Who knows
Thankyou to everyone who replied to my previous post . Most people seem to be having the covid booster . It isn’t the initial jab that bothers me but what it’s doing long term . I had my last one in November and since then I’ve developed polymyalgia rheumatica, another auto immune disease . Who knows
Juliet46
in
MPN Voice
9 months ago
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Covid jab, to be or not to be
I really don't know what to think about the covid jab, i have had them all until now, but having contracted covid 4 weeks ago, and ended up feeling terrible, and even now i feel pretty dire, and it certainly heightened my depression, and so i do question if it's really worth bothering. Several people
I really don't know what to think about the covid jab, i have had them all until now, but having contracted covid 4 weeks ago, and ended up feeling terrible, and even now i feel pretty dire, and it certainly heightened my depression, and so i do question if it's really worth bothering. Several people
secrets22
in
Anxiety and Depression Support
9 months ago
Has anyone succeeded using bluetooth microphone to amplify patients voice so it can be heard on bluetooth hearing aids?
Hi, My wife (78) was diagnosed with PSP about 30 months ago and is in slow decline. Her voice is getting weaker and I am finding it difficult to hear what she says, much of it is mumbled. My hearing aids are bluetooth enabled, so I wondered if anyone had managed to amplify a patient's voice using
Hi, My wife (78) was diagnosed with PSP about 30 months ago and is in slow decline. Her voice is getting weaker and I am finding it difficult to hear what she says, much of it is mumbled. My hearing aids are bluetooth enabled, so I wondered if anyone had managed to amplify a patient's voice using
Legobuilder
in
PSP Association
3 months ago
Covid autumn booster
Usually get invite for Covid booster. Has the criteria changed recently only severe asthma sufferers are eligible now. Did not get any invited%? Thanks
Usually get invite for Covid booster. Has the criteria changed recently only severe asthma sufferers are eligible now. Did not get any invited%? Thanks
ahfat41
in
Asthma Community Forum
9 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
8 months ago
A question on breathing, possible long-covid ?
Strange thing, and need your help, just to see if anyone else has the same symptom, so Dec 2021, came down with covid, and then had a upper respiratory infection, which lasted around 4 months. During these months, I had wheezing, and at times very bad, but there was one other symptom, which I need
Strange thing, and need your help, just to see if anyone else has the same symptom, so Dec 2021, came down with covid, and then had a upper respiratory infection, which lasted around 4 months. During these months, I had wheezing, and at times very bad, but there was one other symptom, which I need
Fitbit-Joe
in
British Heart Foundation
9 months ago
anxious about CAD - MRI result
Hi all, Does anyone know if a cardiac MRI would pick up coronary heart disease , or at least see some part of the arteries? I’m awaiting a CT scan with dye to look into CAD, but my consultant thinks it’s unlikely as I’m 32 , I am overweight and an ex-smoker so I do have some risk factors. My cardiac
Hi all, Does anyone know if a cardiac MRI would pick up coronary heart disease , or at least see some part of the arteries? I’m awaiting a CT scan with dye to look into CAD, but my consultant thinks it’s unlikely as I’m 32 , I am overweight and an ex-smoker so I do have some risk factors. My cardiac
Amy190
in
British Heart Foundation
9 months ago
nervous about covid
this morning I woke up congested and with a lot of post nasal drip, which caused my throat to be slightly sore. I tested last night for covid and was negative. These past few weeks I’ve been fighting a cold/allergies but I feel like yesterday and today have been slightly worse. I’m supposed to go to
this morning I woke up congested and with a lot of post nasal drip, which caused my throat to be slightly sore. I tested last night for covid and was negative. These past few weeks I’ve been fighting a cold/allergies but I feel like yesterday and today have been slightly worse. I’m supposed to go to
Daisy425
in
Anxiety and Depression Support
9 months ago
Check your Thyroid
For about a year I’ve been struggling. Fatigue getting worse, frozen shoulder, dry mouth and eyes, aching, brain fog, palpitations. It really got worse after last years autumn Covid booster when I thought I was having a heart attack. Heart all checked out fine. So I talked to my consultant at my clinic
For about a year I’ve been struggling. Fatigue getting worse, frozen shoulder, dry mouth and eyes, aching, brain fog, palpitations. It really got worse after last years autumn Covid booster when I thought I was having a heart attack. Heart all checked out fine. So I talked to my consultant at my clinic
Readlots
in
British Liver Trust
9 months ago
covid vaccination
I was wondering if most people are having the covid vaccine ?
I was wondering if most people are having the covid vaccine ?
Juliet46
in
MPN Voice
9 months ago
Temporary AF during Covid?
Hi. Following an ablation nearly 2 years ago I have been AF free. I have PIP Flecainide and Bisoprolol that I have never needed to take since the ablation. I take Edoxaban daily. I currently have Covid and yesterday had a jumping feeling so checked my Apple Watch and it said AF. I immediately did several
Hi. Following an ablation nearly 2 years ago I have been AF free. I have PIP Flecainide and Bisoprolol that I have never needed to take since the ablation. I take Edoxaban daily. I currently have Covid and yesterday had a jumping feeling so checked my Apple Watch and it said AF. I immediately did several
Buttercups22
in
AF Association
9 months ago
Rapid Onset of Symptoms
Hello, I was wondering if anyone can help me…. My dad has been diagnosed with PSP only a few months ago but has had symptoms for about 18months. His recent symptoms were textbook stage 2 but quite independent ….. this past Sunday morning he woke up feeling a bit off and then suddenly lost feeling in
Hello, I was wondering if anyone can help me…. My dad has been diagnosed with PSP only a few months ago but has had symptoms for about 18months. His recent symptoms were textbook stage 2 but quite independent ….. this past Sunday morning he woke up feeling a bit off and then suddenly lost feeling in
IPinkie
in
PSP Association
4 months ago
covid
Have just had the Pfizer Covid jab will keep you informed as to what if any side effects I have. Fingers crossed for none🤞
Have just had the Pfizer Covid jab will keep you informed as to what if any side effects I have. Fingers crossed for none🤞
Givemestrength23
in
CLL Support
9 months ago
Tinnitus fades after noise exposure
Hello all, hope you’re doing ok! I’ve had low frequency tinnitus for 18 months or so, some days better than others. One thing I’ve noticed is that my tinnitus almost entirely disappears after I’ve been in loud environments. I was at a gig on Monday and I forgot my loop earplugs and for 3 days and nights
Hello all, hope you’re doing ok! I’ve had low frequency tinnitus for 18 months or so, some days better than others. One thing I’ve noticed is that my tinnitus almost entirely disappears after I’ve been in loud environments. I was at a gig on Monday and I forgot my loop earplugs and for 3 days and nights
Ponay
in
Tinnitus UK
9 months ago
Covid is lasting a long time this time round
Today I’m day 16 of testing strong positive. I caught covid visiting my hubby in hospital. I wore a mask when I visited and sanitised my hands but still caught it. My GP thinks I’ve had 2 strains as I’ve had 2 lots of symptoms. I visited the hospital on the Saturday afternoon, hubby was told that evening
Today I’m day 16 of testing strong positive. I caught covid visiting my hubby in hospital. I wore a mask when I visited and sanitised my hands but still caught it. My GP thinks I’ve had 2 strains as I’ve had 2 lots of symptoms. I visited the hospital on the Saturday afternoon, hubby was told that evening
bernese1225
in
NRAS
9 months ago
Leflunomide and tapering. Update on flare this Summer
I posted in late July about getting into a yo-yo situation trying to control a flare of PMR and got excellent advice from DL which sorted it out. I've been on 3.5mg ever since (I was at 2mg when the flare started). I've tried using DSNS taper. But the PMR isn't ready to cooperate yet!On Monday I had
I posted in late July about getting into a yo-yo situation trying to control a flare of PMR and got excellent advice from DL which sorted it out. I've been on 3.5mg ever since (I was at 2mg when the flare started). I've tried using DSNS taper. But the PMR isn't ready to cooperate yet!On Monday I had
PastelsinArt
in
PMRGCAuk
9 months ago
AF back 6 days after Covid vacc
I'd been in NSR for over 3 1/2 years following a cardioversion after 9 months of persistent AF, but I woke for the loo at 3.30am on Monday and found I was back in AF - which is so far persisting. Sigh! My first thought about the trigger was that I was dehydrated. We were staying with friends, and
I'd been in NSR for over 3 1/2 years following a cardioversion after 9 months of persistent AF, but I woke for the loo at 3.30am on Monday and found I was back in AF - which is so far persisting. Sigh! My first thought about the trigger was that I was dehydrated. We were staying with friends, and
Belle11
in
AF Association
9 months ago
It Had To Happen!! Covid-19 Strikes!
It has been 18 months since I completed my CLL Obinutuzumab plus Venclexta treatment protocol. I was in remission. I have had four Covid-19 vaccinations and two Evusheld vaccinations over that time. So, last week is the first time I ventured into the public transportation system in 2-1/2 years. I
It has been 18 months since I completed my CLL Obinutuzumab plus Venclexta treatment protocol. I was in remission. I have had four Covid-19 vaccinations and two Evusheld vaccinations over that time. So, last week is the first time I ventured into the public transportation system in 2-1/2 years. I
DanBro1
in
CLL Support
9 months ago
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