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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
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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
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
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
2 months 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
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
2 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 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 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
2 months ago
vaginal estrogen and vag valium question
I was wondering if any of you lovely ladies are using both vaginal estrogen cream and vaginal valium suppositories. I'm supposed to insert a valium suppository every night (10mg) and I also insert 1 gram of estradiol cream three nights a week. I'm worried that the valium will keep the estrogen cream
I was wondering if any of you lovely ladies are using both vaginal estrogen cream and vaginal valium suppositories. I'm supposed to insert a valium suppository every night (10mg) and I also insert 1 gram of estradiol cream three nights a week. I'm worried that the valium will keep the estrogen cream
sungirl55
in
Pelvic Pain Support Network
1 year 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
2 months ago
rubella immunity blood tests
Hi I’m about to start another round of IVF after 7 cancelled transfers and 3 failed but using a new clinic. My blood tests have come back that I don’t have a rubella immunity but I have checked my results from my IVF cycle in 2020 which blessed me with my son and my pregnancy results and I did have an
Hi I’m about to start another round of IVF after 7 cancelled transfers and 3 failed but using a new clinic. My blood tests have come back that I don’t have a rubella immunity but I have checked my results from my IVF cycle in 2020 which blessed me with my son and my pregnancy results and I did have an
Chowlady14
in
Fertility Network UK
5 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
2 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
2 months 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
3 months 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
3 months ago
Tirosint
Hi, I posted earlier about Tirosint in Gel capsules possibly giving me a rash. I stopped taking them 4 weeks ago and the rash continues. Not as bad but still all down my legs and arms. My question. Can it take so long to leave the body? Or am I blaming the wrong thing for my rash? Blood tests were
Hi, I posted earlier about Tirosint in Gel capsules possibly giving me a rash. I stopped taking them 4 weeks ago and the rash continues. Not as bad but still all down my legs and arms. My question. Can it take so long to leave the body? Or am I blaming the wrong thing for my rash? Blood tests were
jand123
in
Thyroid UK
5 months ago
Pes Anserine Bursitis - steroid injection offered.
On Thursday I had an appointment with a rheumatologist who had previously been quite impatient and dismissive of me. I made up my mind to give him the briefest details of my woes over the last 9 months. (This is a 6 monthly appointment 😂). He was happy for me to continue with my slow tapering and then
On Thursday I had an appointment with a rheumatologist who had previously been quite impatient and dismissive of me. I made up my mind to give him the briefest details of my woes over the last 9 months. (This is a 6 monthly appointment 😂). He was happy for me to continue with my slow tapering and then
Sukydee
in
PMRGCAuk
3 months ago
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