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Mouthwash
I am on 320 of alvesco a day at present along with fostair mart taken with my trusty aero chamber. I was on 640 of alvesco, however for the first time I was starting to get some irritations from this, mild oral thrush, joint pain, weight gain and some odd eye issues. So my consultant said to drop
I am on 320 of alvesco a day at present along with fostair mart taken with my trusty aero chamber. I was on 640 of alvesco, however for the first time I was starting to get some irritations from this, mild oral thrush, joint pain, weight gain and some odd eye issues. So my consultant said to drop
Homely2
Administrator
in
Asthma Community Forum
5 months ago
From Prednisone to Morphine
I was wondering if anyone had been offered Morphine as an alternative to Prednisone? It’s been suggested to me by my new Rheumatologist recently. He’s questioning my diagnosis of PMR & suggests the pain is due to “wear & tear”. My pain is symmetrical, in all the usual places (knees, hips, shoulders,
I was wondering if anyone had been offered Morphine as an alternative to Prednisone? It’s been suggested to me by my new Rheumatologist recently. He’s questioning my diagnosis of PMR & suggests the pain is due to “wear & tear”. My pain is symmetrical, in all the usual places (knees, hips, shoulders,
Chelseadog
in
PMRGCAuk
3 months ago
COVID diagnosis
Just been on a 300 mile bike ride and returned with COVID. Don't feel too bad but should I contact consultant. I have had a vaccination about 3 weeks ago.
Just been on a 300 mile bike ride and returned with COVID. Don't feel too bad but should I contact consultant. I have had a vaccination about 3 weeks ago.
Guinness4822
in
CLL Support
2 months ago
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COVID, FND, and Cymbalta Ruined My Life
This is a long story, and I apologize in advance for any, bitter angry undertones. I'll skip all of the grief I've had in life and the hard times that I've experienced. I'll try to keep it to the medical issues. It will feel good to tell a part of my story, arguably the hardest I've been through.***Trigger
This is a long story, and I apologize in advance for any, bitter angry undertones. I'll skip all of the grief I've had in life and the hard times that I've experienced. I'll try to keep it to the medical issues. It will feel good to tell a part of my story, arguably the hardest I've been through.***Trigger
LoverOfAllThings
in
Functional Neurological Disorder - FND Hope
2 months ago
Increase in Synthroid Dose Worse Before Feeling Better?
Hello, I'm a long time hypothyroid patient but the last few years after covid have been a wild ride finding the right dose again. I'm curious if anyone can offer insight as to why the first one to two weeks of a medication dose increase I feel amazing and then I tank horribly after. All the hypo symptoms
Hello, I'm a long time hypothyroid patient but the last few years after covid have been a wild ride finding the right dose again. I'm curious if anyone can offer insight as to why the first one to two weeks of a medication dose increase I feel amazing and then I tank horribly after. All the hypo symptoms
Clarabethk
in
Thyroid UK
2 months ago
Hello
Hello again Hi. Ive had to shut down and rejoin the group. HU was playing up. Here is my original post. 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
Hello again Hi. Ive had to shut down and rejoin the group. HU was playing up. Here is my original post. 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
Trish_PBG
in
FND Action
2 months ago
Hello again
Hi. Ive had to shut down and rejoin the group. HU was,playing up. I have such great comments and ideas,already from Lady4 and others, so thank you. Below was, my original post Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are
Hi. Ive had to shut down and rejoin the group. HU was,playing up. I have such great comments and ideas,already from Lady4 and others, so thank you. Below was, my original post Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are
Trish_PBG
in
Functional Neurological Disorder - FND Hope
2 months ago
covid booster (Maderna)
morning all!! I have RA and I’m booked in for my annual covid booster!my concern is that from day one I’ve always had Pfizer vaccine but apparently there not using it this time around and it’s been replaced with Maderna it just makes me feel uneasy as I never had any problems with Pfizer!!have any you
morning all!! I have RA and I’m booked in for my annual covid booster!my concern is that from day one I’ve always had Pfizer vaccine but apparently there not using it this time around and it’s been replaced with Maderna it just makes me feel uneasy as I never had any problems with Pfizer!!have any you
Mybirthday1975
in
NRAS
2 months 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
3 months ago
Tinnitus and Meniere's
Has anyone ever received Intratympanic steroid injection in their ear(s) for Tinnitus or Meniere's? I was just curious if it was worth it and made matters better. Is the injection painful or create other issues? My ENT has recommended it for my left ear which has a variety of issues. Thanks.
Has anyone ever received Intratympanic steroid injection in their ear(s) for Tinnitus or Meniere's? I was just curious if it was worth it and made matters better. Is the injection painful or create other issues? My ENT has recommended it for my left ear which has a variety of issues. Thanks.
MrGC314
in
Tinnitus UK
3 months 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
3 months ago
Itching
Been diagnosed with fatty liver through ultrasound Went to the out of hours doctor's yesterday about servear back pain and dizziness also was diagnosed with psoriasis then shingles, she was too busy to deal with my other problems by running half hour late she gave me a prescription got home then read
Been diagnosed with fatty liver through ultrasound Went to the out of hours doctor's yesterday about servear back pain and dizziness also was diagnosed with psoriasis then shingles, she was too busy to deal with my other problems by running half hour late she gave me a prescription got home then read
Hidden
in
British Liver Trust
1 year ago
Finally a little light!
Many of you have been kind in giving me advice and support over the last year, especially when I was 'wading through treacle'. A few weeks ago I had another steroid injection and leflunomide added to my MTX. I hardly dare say this but I'm actually starting to feel better. My joints have gone down so
Many of you have been kind in giving me advice and support over the last year, especially when I was 'wading through treacle'. A few weeks ago I had another steroid injection and leflunomide added to my MTX. I hardly dare say this but I'm actually starting to feel better. My joints have gone down so
HeadInASpin
in
NRAS
3 months 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
3 months 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 months ago
Change in inhalers
I'm currently on sertide and being switched over to symbicort. I'm not sure of the dosage etc as need to discuss further with gp. I'm a little concerned as been on seretide for years. When I get switched it triggers flares and I've already had loads of time of work. I work part time. I also think I'm
I'm currently on sertide and being switched over to symbicort. I'm not sure of the dosage etc as need to discuss further with gp. I'm a little concerned as been on seretide for years. When I get switched it triggers flares and I've already had loads of time of work. I work part time. I also think I'm
spookylou
in
Asthma Community Forum
3 months 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 months ago
A return of the dreaded mongrel .......... ?????
'mornin' guys and gals ................... well it's almost 02.00 am for the second day in a row ..... funny feelings in the chest ............. my squadron of pet butterflies has returned - fluttering around in combat....... just like the olden days of mid 2010. Missed you ................ NOT !
'mornin' guys and gals ................... well it's almost 02.00 am for the second day in a row ..... funny feelings in the chest ............. my squadron of pet butterflies has returned - fluttering around in combat....... just like the olden days of mid 2010. Missed you ................ NOT !
BenHall1
in
Atrial Fibrillation Support
3 months 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
3 months 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
3 months ago
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