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t3 blood test at gp
hi my gp practice has been kindly filling my medichecks container for t3 test when I get my tsh/t4 nhs test done. However now they’ve decided it’s not possible to do private tests. Has anyone taken their gp on over this. It seems crazy that for the 10 seconds it takes to fill one more container I now
hi my gp practice has been kindly filling my medichecks container for t3 test when I get my tsh/t4 nhs test done. However now they’ve decided it’s not possible to do private tests. Has anyone taken their gp on over this. It seems crazy that for the 10 seconds it takes to fill one more container I now
Mag999
in
Thyroid UK
5 months ago
The RLS nightmare
My name is Tim and RLS sucks!!!!! In 2013 i was put on disability because I have flat back syndrome and it has caused chronic pain for over 20 years non stop 24/7 and I am addicted to opioids. On June 20th of this yr I received a dbl laminectomy on my l4 and l5 vertebra and the knife was removed. Now
My name is Tim and RLS sucks!!!!! In 2013 i was put on disability because I have flat back syndrome and it has caused chronic pain for over 20 years non stop 24/7 and I am addicted to opioids. On June 20th of this yr I received a dbl laminectomy on my l4 and l5 vertebra and the knife was removed. Now
Miloboy23
in
Restless Legs Syndrome
5 months ago
Advice on where to get blood tests done privately
Hi all, I hope you can help with my query. I've always had issues with T4 but after a good few years of a boost on dessicated thyroid (Erfa) the weight is piling on again. My private doctor has recommended I get the following tested but I'm struggling to find a company that can test my fasting glucose
Hi all, I hope you can help with my query. I've always had issues with T4 but after a good few years of a boost on dessicated thyroid (Erfa) the weight is piling on again. My private doctor has recommended I get the following tested but I'm struggling to find a company that can test my fasting glucose
Tiredofthis77
in
Thyroid UK
5 months ago
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Leflunomide, Mycophenolate, Azathioprine instead of TCZ, that was the question
Thanks for your help in answering this question. It seems Leflunomide is the only real contender. So much so that my cynical self wonders if the other two are only there to give the illusion of choice! Any more info about your experience of Leflunomide is very welcome. Not rushing into anything, and
Thanks for your help in answering this question. It seems Leflunomide is the only real contender. So much so that my cynical self wonders if the other two are only there to give the illusion of choice! Any more info about your experience of Leflunomide is very welcome. Not rushing into anything, and
Japsquar
in
PMRGCAuk
5 months ago
Living with Long Covid but now Tinnitus too!
Hello everybody, I am new to this site today and have spoken to a very helpful gentleman on the helpline. I have had Long Covid subsequent to catching Covid in April and November 2020 and January 2022. One of the major problems for me is fatigue which is very debilitating. I usually have nausea with
Hello everybody, I am new to this site today and have spoken to a very helpful gentleman on the helpline. I have had Long Covid subsequent to catching Covid in April and November 2020 and January 2022. One of the major problems for me is fatigue which is very debilitating. I usually have nausea with
santosha72
in
Tinnitus UK
5 months ago
BC Which Hospital Update _ and eyesl
I got a call saying I could go into local hospital for my flexy cystoscopy There is a 25 mile difference. My last rigid cystoscopy showed that 5 out of 6 biopsies was low grade, hence the flexy cystoscopy.. I have not long ago finished my 3 x BCG infusions - Have they worked, my flexy cystoscopy
I got a call saying I could go into local hospital for my flexy cystoscopy There is a 25 mile difference. My last rigid cystoscopy showed that 5 out of 6 biopsies was low grade, hence the flexy cystoscopy.. I have not long ago finished my 3 x BCG infusions - Have they worked, my flexy cystoscopy
Ern007
in
Lung Conditions Community Forum
5 months ago
GI BLEED
Had small gi bleed 16mths ago increased omoprazole for 8wks & had repeat endoscopy everything ok.Had stomach bug 2 wks ago & stool was partly black which got less over 2days & now ok, so think i may have had another bleed even with omeprazole 20mg morning & night. Also seem to be having loose stools
Had small gi bleed 16mths ago increased omoprazole for 8wks & had repeat endoscopy everything ok.Had stomach bug 2 wks ago & stool was partly black which got less over 2days & now ok, so think i may have had another bleed even with omeprazole 20mg morning & night. Also seem to be having loose stools
Fybo
in
IBS Network
5 months ago
What does having a NEW KIDNEY feel like?
Hi All, I have been in the transplant list for a year now and still waiting to get called. I can’t just help to wonder what having a kidney transplant will feel like. Apart from the fact that it will be a gift of life and freedom from being tied down to dialysis. What does it feel like? Will you
Hi All, I have been in the transplant list for a year now and still waiting to get called. I can’t just help to wonder what having a kidney transplant will feel like. Apart from the fact that it will be a gift of life and freedom from being tied down to dialysis. What does it feel like? Will you
Imaanforever
in
Kidney Dialysis
6 months ago
omeprazole at night
I take 20 mg of Omeprazole before breakfast under instruction from my GP although I have not suffered from acid reflux/ heartburn. I do however suffer from a hoarse voice which I was told by others who have the same that it may be “silent reflux” which is where the stomach acid is pushed up into the
I take 20 mg of Omeprazole before breakfast under instruction from my GP although I have not suffered from acid reflux/ heartburn. I do however suffer from a hoarse voice which I was told by others who have the same that it may be “silent reflux” which is where the stomach acid is pushed up into the
Nanatoo
in
PMRGCAuk
5 months ago
Advice on statins and vascular atheroma please
Story so far.... Had a recent hospitalisation in Cyprus for a problem unconnected to the thyroid (acute diverticular episode after 30 years of no major issues) which resulted in me having to have a CT scan when I returned from holiday. The scan was OK on the original issue, nothing sinister revealed
Story so far.... Had a recent hospitalisation in Cyprus for a problem unconnected to the thyroid (acute diverticular episode after 30 years of no major issues) which resulted in me having to have a CT scan when I returned from holiday. The scan was OK on the original issue, nothing sinister revealed
ATVMWF
in
Thyroid UK
5 months ago
Post nasal drip
Greetings from VERY COLD Ohio. Does anyone have issues with chronic post nasal drip due to CLL? I do t know if I'm just hyper aware now or what..I know I've had this issue prior to be diagnosed and my pcp just said it was due to vasomotor rhinitis...but it seems like it never gets better..no infections
Greetings from VERY COLD Ohio. Does anyone have issues with chronic post nasal drip due to CLL? I do t know if I'm just hyper aware now or what..I know I've had this issue prior to be diagnosed and my pcp just said it was due to vasomotor rhinitis...but it seems like it never gets better..no infections
ANewMe2024
in
CLL Support
5 months ago
ra associated eye ulcers
hi everyone, I posted in this community quite a while ago about an ulcer in my eye which the rheumatologist said was caused by the ra. At the time, I was given some very helpful advice and information by Kags1068. Since then, I have had 4 more ulcers (my eyes take it in turns), and am currently in week
hi everyone, I posted in this community quite a while ago about an ulcer in my eye which the rheumatologist said was caused by the ra. At the time, I was given some very helpful advice and information by Kags1068. Since then, I have had 4 more ulcers (my eyes take it in turns), and am currently in week
Emye343
in
NRAS
5 months ago
Mr Alan M
I have been missed diagnosed with liver disease for years I believe that I am still around because I do not drink and I am quite strict with my diet etc. I have also taken a lot of over the counter medication for liver disease. I believe that the disease has been caused by DILI / prescribed medication
I have been missed diagnosed with liver disease for years I believe that I am still around because I do not drink and I am quite strict with my diet etc. I have also taken a lot of over the counter medication for liver disease. I believe that the disease has been caused by DILI / prescribed medication
TillySyd
in
British Liver Trust
5 months ago
Devices to wear in case I fall.
I am looking at wearing a device for if I fall whilst alone. Over the last few years I have had three falls where I haven’t tripped. Tiny blackout. Also a few weeks ago I had severe dizziness/vertigo with sickness high blood pressure and tinnitus. Rang 999 and was taken to hospital. Within a few
I am looking at wearing a device for if I fall whilst alone. Over the last few years I have had three falls where I haven’t tripped. Tiny blackout. Also a few weeks ago I had severe dizziness/vertigo with sickness high blood pressure and tinnitus. Rang 999 and was taken to hospital. Within a few
5lupins
in
PMRGCAuk
5 months ago
Enlarged Prostate
I have an enlarged prostate and I am trying to determine if I should be taking medicines or have a procedure such as TURP. I would like to get some experiences of people that have taken Flomax or other medicines to reduce the prostate size. I have an allergy to sulfa, what makes me a little nervous about
I have an enlarged prostate and I am trying to determine if I should be taking medicines or have a procedure such as TURP. I would like to get some experiences of people that have taken Flomax or other medicines to reduce the prostate size. I have an allergy to sulfa, what makes me a little nervous about
Cachito
in
Atrial Fibrillation Support
5 months ago
Waiting and Wondering
Hello everyone. I'm a 61 year old male and I started experiencing tinnitus in my left ear around July of 2023. In December of 2023 I began experiencing irregular/occasional bouts of dizziness which would last an hour or so then go recede. In January 2024 the occasional bouts of dizziness continue
Hello everyone. I'm a 61 year old male and I started experiencing tinnitus in my left ear around July of 2023. In December of 2023 I began experiencing irregular/occasional bouts of dizziness which would last an hour or so then go recede. In January 2024 the occasional bouts of dizziness continue
murphyzlaw
in
Acoustic Neuroma Support
5 months ago
10k or bust
this week my daughter and I decided we will run the Rotherham 10k on May 19th. Every year we as a family raise money for the hospital special baby care unit. This is because my 2nd granddaughter died there aged 7 weeks of sepsis. Ironically the same thing that killed my wife. So today I walked 10k!
this week my daughter and I decided we will run the Rotherham 10k on May 19th. Every year we as a family raise money for the hospital special baby care unit. This is because my 2nd granddaughter died there aged 7 weeks of sepsis. Ironically the same thing that killed my wife. So today I walked 10k!
Kevin1604
in
Couch to 5K
5 months ago
psoas Muscle Tumors
my OVCA metastasized to my Psoas muscle 6 years after preliminary OVCA diagnosis. Various chemo and immunotherapy are helping keep it contained. Has anyone had surgery for removal of a psoas tumor? I’d love to hear from you. Thank you.
my OVCA metastasized to my Psoas muscle 6 years after preliminary OVCA diagnosis. Various chemo and immunotherapy are helping keep it contained. Has anyone had surgery for removal of a psoas tumor? I’d love to hear from you. Thank you.
Leniko
in
My Ovacome
5 months ago
Does anyone have any feedback on Wegener's Gramgranulomatosis?
I have Wegener's and it has primarily affected my eyes and lungs. I've been on rituximab and 25mg methotrexate for two years but I have a host of issues from taking the rituximab.
I have Wegener's and it has primarily affected my eyes and lungs. I've been on rituximab and 25mg methotrexate for two years but I have a host of issues from taking the rituximab.
Youelbeverly
in
NRAS
5 months ago
Diagnosis
Hello, my first post 😁 I have had Tinnitus for many years. I live with it and I cope well most of the time. No one has ever looked at my ears apart from my GP. He looked in my ears and said 'yes you just have a bit of wax' you probably have Tinnitus' I complain of pain I frequently get in my right
Hello, my first post 😁 I have had Tinnitus for many years. I live with it and I cope well most of the time. No one has ever looked at my ears apart from my GP. He looked in my ears and said 'yes you just have a bit of wax' you probably have Tinnitus' I complain of pain I frequently get in my right
Idontknow71
in
Tinnitus UK
5 months ago
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