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Functional Endoscopic Sinus Surgery (FESS) for Mild-Sinusitis
(By the way, I am not Asthmetic, but this forum seemed the most relevant place to make this post...) I have
Chronic Sinusitis, without Nasal-Polyps
. This diagnosis came after having a CT-sinus scan earlier this year. I was told from the CT that it is ‘Mild’ Sinusitis (which sounds about right
(By the way, I am not Asthmetic, but this forum seemed the most relevant place to make this post...) I have
Chronic Sinusitis, without Nasal-Polyps
. This diagnosis came after having a CT-sinus scan earlier this year. I was told from the CT that it is ‘Mild’ Sinusitis (which sounds about right
reb_1951
in
Asthma Community Forum
1 year ago
Omicron variant
Hi all I have bronchiectasis (since 2012) and have been super careful during the pandemic. However, I missed my last vaccine (having had 4 over the years as well as both flu and shingles jabs) as the nearest place the NHS website could offer me for the 5th Covid jab was 22 miles away! With no public
Hi all I have bronchiectasis (since 2012) and have been super careful during the pandemic. However, I missed my last vaccine (having had 4 over the years as well as both flu and shingles jabs) as the nearest place the NHS website could offer me for the 5th Covid jab was 22 miles away! With no public
swimmer
in
Lung Conditions Community Forum
16 hours ago
Scared and lost
Hello, I am not too sure where to start, so much has happened. I am a 50 year-old female. A couple of years ago, I had a pain in my abdomen on the right side and my stools became orange. The GP sent me for an ultrasound where they saw I had polyps on my gallbladder. The GP phoned me on the 31st Dec to
Hello, I am not too sure where to start, so much has happened. I am a 50 year-old female. A couple of years ago, I had a pain in my abdomen on the right side and my stools became orange. The GP sent me for an ultrasound where they saw I had polyps on my gallbladder. The GP phoned me on the 31st Dec to
Foi24
in
British Liver Trust
1 day ago
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Hello
Hello Everyone, I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse. The support and suggestions you give each other in amazing. I was seen by a neurologist in August 2021
Hello Everyone, I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse. The support and suggestions you give each other in amazing. I was seen by a neurologist in August 2021
Trish_GlaucomaUK
in
FND Action
2 days ago
Hello
Hello Everyone, I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse. The support and suggestions you give each other in amazing. I was seen by a neurologist in August 2021
Hello Everyone, I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse. The support and suggestions you give each other in amazing. I was seen by a neurologist in August 2021
Trish_GlaucomaUK
in
Functional Neurological Disorder - FND Hope
2 days ago
Covid and extending NHS funded time
I am due to start long protocol in exactly a week, with a prostrap injection. My husband has tested positive for Covid today and although I am testing negative I think I’m bound to get it. Our clinic will delay by 7-10 weeks depending if we both test positive for Covid. I’m devastated as we are only
I am due to start long protocol in exactly a week, with a prostrap injection. My husband has tested positive for Covid today and although I am testing negative I think I’m bound to get it. Our clinic will delay by 7-10 weeks depending if we both test positive for Covid. I’m devastated as we are only
Rachiebabe
in
Fertility Network UK
2 days ago
Covid Booster Eligibility
I am 65 with compensated cirrhosis. I have portal hypertension and grade 1/2 oesophagal varices with bloods mostly in range. I do have anaemia and low platelets but thankfully no ascites or HE (fingers crossed). Following a post on here a few days ago about cirrhosis and eligibility for a spring Covid
I am 65 with compensated cirrhosis. I have portal hypertension and grade 1/2 oesophagal varices with bloods mostly in range. I do have anaemia and low platelets but thankfully no ascites or HE (fingers crossed). Following a post on here a few days ago about cirrhosis and eligibility for a spring Covid
AnxiousPete
in
British Liver Trust
3 days ago
shall CLL patient do Covid vaccination?
shall CLL patients do covid 19 vaccine?
shall CLL patients do covid 19 vaccine?
al444
in
CLL Support
3 days ago
Covid booster UK
Does anyone know if we can get spring boosters for Covid? I got the autumn one because of epilepsy, but it looks as though neurological conditions aren’t on the spring list.
Does anyone know if we can get spring boosters for Covid? I got the autumn one because of epilepsy, but it looks as though neurological conditions aren’t on the spring list.
GillyA
in
Epilepsy Action
4 days ago
No Cominarty Vaccine!!
I've had the call for my Spring covid booster, but unfortunately I can't have Spikevax (Moderna) as last time I was given it I spent the next 6mths sorting out a heart arrhythmia that seemed to have been triggered by it. My cardiologist said he'd seen a really significant number of new patients, all
I've had the call for my Spring covid booster, but unfortunately I can't have Spikevax (Moderna) as last time I was given it I spent the next 6mths sorting out a heart arrhythmia that seemed to have been triggered by it. My cardiologist said he'd seen a really significant number of new patients, all
Kendrew
in
PMRGCAuk
5 days ago
reaction to Spikevax XBB 1.5Moderna
Just want to share that I had the above covid booster on Thursday (2nd May) and it appears to have triggered a lupus flare (in my case, rash, aching joints, splitting headache, extreme fatigue). I normally take prednisolone when I have a flare but feel it would be counter productive to what the vaccination
Just want to share that I had the above covid booster on Thursday (2nd May) and it appears to have triggered a lupus flare (in my case, rash, aching joints, splitting headache, extreme fatigue). I normally take prednisolone when I have a flare but feel it would be counter productive to what the vaccination
Larks0ng
in
LUPUS UK
5 days ago
Do I need an ablation?
i’ve been on the waiting list for an ablation and the appointment has finally come up however I am really having second thoughts about having this procedure as I’ve finally been feeling very well lately after three years of highly symptomatic long Covid. Also I’ve only had one episode of AF in the last
i’ve been on the waiting list for an ablation and the appointment has finally come up however I am really having second thoughts about having this procedure as I’ve finally been feeling very well lately after three years of highly symptomatic long Covid. Also I’ve only had one episode of AF in the last
Midnight2022
in
Atrial Fibrillation Support
5 days ago
Headaches / update, also Spring Covid Vaccine update.
I was grateful for everyone’s’ replies to my recent post and I telephoned my Haematologist who advised a blood test and to see a doctor as soon as possible If I couldn’t see my GP the Haematologist said they’d fit me in at the hospital clinic. However, I had a full blood test that day at my G.P’s and
I was grateful for everyone’s’ replies to my recent post and I telephoned my Haematologist who advised a blood test and to see a doctor as soon as possible If I couldn’t see my GP the Haematologist said they’d fit me in at the hospital clinic. However, I had a full blood test that day at my G.P’s and
azaelea
in
MPN Voice
6 days ago
Covid booster
I had my Covid booster jab yesterday,my ibs was settling down ,but has got worse since I had it.Has anybody else experienced this ?
I had my Covid booster jab yesterday,my ibs was settling down ,but has got worse since I had it.Has anybody else experienced this ?
mousey1
in
IBS Network
6 days ago
First time COVID
I got really poorly on the 7th September last year, I phoned the doctors and they wouldn't see me at all, don't really blame them, they are under so much strain.I phoned 111 and when I told them me my illnesses, they wanted to send an ambulance, three different people I talked to all wanted to send an
I got really poorly on the 7th September last year, I phoned the doctors and they wouldn't see me at all, don't really blame them, they are under so much strain.I phoned 111 and when I told them me my illnesses, they wanted to send an ambulance, three different people I talked to all wanted to send an
Itsmeok
in
Lung Conditions Community Forum
7 days ago
Reactions to COVID boosters
Hi, I've been getting the COVID boosters in the UK on a regular basis, but my reaction each time has gotten worse. With the one six months ago and the one last week, I was wiped out for 24 hours afterward, which hadn't happened with the previous boosters. The pharmacist last week was surprised at my
Hi, I've been getting the COVID boosters in the UK on a regular basis, but my reaction each time has gotten worse. With the one six months ago and the one last week, I was wiped out for 24 hours afterward, which hadn't happened with the previous boosters. The pharmacist last week was surprised at my
SAT_poet
in
CLL Support
7 days ago
Upcoming hospital appointment
I was diagnosed with a 25mm AN last October. It totally came out of the blue. I'd been suffering from Long Covid for over a year and I started to have dizziness and body veer to the left when walking. I was also struggling with being in a room where multiple conversations were happening, as I couldn't
I was diagnosed with a 25mm AN last October. It totally came out of the blue. I'd been suffering from Long Covid for over a year and I started to have dizziness and body veer to the left when walking. I was also struggling with being in a room where multiple conversations were happening, as I couldn't
EssEmBee
in
Acoustic Neuroma Support
8 days ago
Covid vaccine
this morning I paid for a Covid vaccine £65. I was given the Novavax. Excellent service, not far to travel but annoying that I was not given it on the NHS as live with someone who is clinically extremely vulnerable.
this morning I paid for a Covid vaccine £65. I was given the Novavax. Excellent service, not far to travel but annoying that I was not given it on the NHS as live with someone who is clinically extremely vulnerable.
Main1234
in
Vasculitis UK
8 days ago
PMR and covid vaccination
I’ve been asked to have a seasonal covid vaccination because of my weakened autoimmune system, due to PMR. There’s a lot online about covid vaccines and PMR, mainly about PMR onset after a vaccination. Does anyone know if there’s any evidence between a seasonal vaccination and worsening of PMR symptoms
I’ve been asked to have a seasonal covid vaccination because of my weakened autoimmune system, due to PMR. There’s a lot online about covid vaccines and PMR, mainly about PMR onset after a vaccination. Does anyone know if there’s any evidence between a seasonal vaccination and worsening of PMR symptoms
Freshairfiend
in
PMRGCAuk
9 days ago
do I need the spring Covid shot?
I have had 7 covid shots since the start of Covid. On October 10 of 2023 I received the Moderna bivalent booster, as well as the flu shot and RSV shot. I came down with Covid, for the second time, on March 20 of 2024. First time was April of 2022, I am doing fine now. My wife tells me she received
I have had 7 covid shots since the start of Covid. On October 10 of 2023 I received the Moderna bivalent booster, as well as the flu shot and RSV shot. I came down with Covid, for the second time, on March 20 of 2024. First time was April of 2022, I am doing fine now. My wife tells me she received
Claybuster
in
CLL Support
9 days ago
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