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Statins - get informed and know the risks
This is my take on things - my personal experience and that of people I have met, known and loved (family members). If you are being pushed to take statins I would advise people to read up and consider risks before deciding to go on statins.. AND IT IS your decision. There’s loads of literature,
This is my take on things - my personal experience and that of people I have met, known and loved (family members). If you are being pushed to take statins I would advise people to read up and consider risks before deciding to go on statins.. AND IT IS your decision. There’s loads of literature,
Charlie-Farley
in
Thyroid UK
1 year ago
Dr Oliver Frey & Countryhealth
Hi, interested in this private GP practice on thyroid uk list specialising in underactive thyroid because they do telehealth, payment plans and can be seen quickly vs nearby private endocrinologist with a two month wait list and opaque charges. Please message me with any feedback. Thank you 🙌
Hi, interested in this private GP practice on thyroid uk list specialising in underactive thyroid because they do telehealth, payment plans and can be seen quickly vs nearby private endocrinologist with a two month wait list and opaque charges. Please message me with any feedback. Thank you 🙌
Insomania
in
Thyroid UK
1 year ago
Benefits
I am still not sure if you can get benefits if you have lupus?🤔 Any information would be helpful❤️🧡💛💚💙💜🌈
I am still not sure if you can get benefits if you have lupus?🤔 Any information would be helpful❤️🧡💛💚💙💜🌈
Butt3rf1y
in
LUPUS UK
1 year ago
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Is it lupus
Hi, on feb 12th this year a small circular spot appeared on my neck then 2 weeks later I had 2 ring shaped legions on my neck so assumed it was ringworm but after 2 months of treatment it has only gotten worse (over the counter creams then prescription medication) so I am now awaiting blood results to
Hi, on feb 12th this year a small circular spot appeared on my neck then 2 weeks later I had 2 ring shaped legions on my neck so assumed it was ringworm but after 2 months of treatment it has only gotten worse (over the counter creams then prescription medication) so I am now awaiting blood results to
Stephanie1980
in
LUPUS UK
1 year ago
lupus and shingles
Hey guys, I hope you’re all keeping safe and well. Just wondering if anyone has any tips or advice on how to manage having lupus and shingles! I got diagnosed on Wednesday and it’s safe to say I’m suffering a bit. Is there anything I should be looking out for? Avoiding? Thanks in advance!
Hey guys, I hope you’re all keeping safe and well. Just wondering if anyone has any tips or advice on how to manage having lupus and shingles! I got diagnosed on Wednesday and it’s safe to say I’m suffering a bit. Is there anything I should be looking out for? Avoiding? Thanks in advance!
Krishny18
in
LUPUS UK
1 year ago
post partum thyroditis
I’m in the process of thinking what the next step is and would really appreciate and thoughts. I had post partum thyroiditis after birth in October 2019, typical over active then underactive around 5 months pre birth. I have been on thyroxine since as I was very unwell and they were the results that
I’m in the process of thinking what the next step is and would really appreciate and thoughts. I had post partum thyroiditis after birth in October 2019, typical over active then underactive around 5 months pre birth. I have been on thyroxine since as I was very unwell and they were the results that
Courtney96
in
Thyroid UK
1 year ago
Discoid Lupus
hi I was wondering if fatigue and mind fog are associated with discoid lupus? Or is it just with systemic lupus?
hi I was wondering if fatigue and mind fog are associated with discoid lupus? Or is it just with systemic lupus?
Bhudhi
in
LUPUS UK
1 year ago
NRAS Live: Mental Health & Wellbeing with Rheumatoid Arthritis
Join our NRAS Live on Wednesday 19 April at 7pm for a chat discussing ways to keep on top of your mental health and wellbeing while living with inflammatory arthritis. Submit your questions 👉 https://bit.ly/3KZa7Tl We are delighted to be joined by Dr. Emma Dures, Chartered Psychologist and Associate
Join our NRAS Live on Wednesday 19 April at 7pm for a chat discussing ways to keep on top of your mental health and wellbeing while living with inflammatory arthritis. Submit your questions 👉 https://bit.ly/3KZa7Tl We are delighted to be joined by Dr. Emma Dures, Chartered Psychologist and Associate
Aribah-NRAS
NRAS
in
NRAS
1 year ago
Not PCa related but sounds like a very promising approach
When I read "advanced pancreatic cancer" and "overall disease control of 94%" in the same document...I feel like smiling.... https://ascopost.com/news/april-2024/advanced-pancreatic-cancer-oncolytic-virus-based-immunostimulatory-gene-therapy-plus-chemotherapy/
When I read "advanced pancreatic cancer" and "overall disease control of 94%" in the same document...I feel like smiling.... https://ascopost.com/news/april-2024/advanced-pancreatic-cancer-oncolytic-virus-based-immunostimulatory-gene-therapy-plus-chemotherapy/
Maxone73
in
Advanced Prostate Cancer
1 month ago
Thyroid Panel Re-Test
Hi, I recently posted asking some questions about my Thyroid panel. I had these tested 2 months ago. Originally, my T4 came back as 11, with the preferred range being 12-22. The doctor wanted me to come back in 8-12 weeks for a retest. I went last week, in the mid afternoon without fasting (not sure
Hi, I recently posted asking some questions about my Thyroid panel. I had these tested 2 months ago. Originally, my T4 came back as 11, with the preferred range being 12-22. The doctor wanted me to come back in 8-12 weeks for a retest. I went last week, in the mid afternoon without fasting (not sure
rubyroo23
in
Thyroid UK
1 year ago
Scottish Medicines appraisal of voclosporin
Do you live in Scotland? Do you have lupus nephritis or care for someone with lupus nephritis? The Scottish Medicines Consortium (SMC) are currently conducting an appraisal to decide whether voclosporin, a new treatment for lupus nephritis, will be commissioned for use by the NHS in Scotland. LUPUS
Do you live in Scotland? Do you have lupus nephritis or care for someone with lupus nephritis? The Scottish Medicines Consortium (SMC) are currently conducting an appraisal to decide whether voclosporin, a new treatment for lupus nephritis, will be commissioned for use by the NHS in Scotland. LUPUS
Debbie_kinsey
Administrator
in
LUPUS UK
10 months ago
Are you interested in helping with the design of a piece of research looking at infections in people with lupus?
We have been contacted by a Clinical Research Fellow at the University of Manchester who is looking for 5 or 6 volunteers, who would be willing and able to travel to Manchester Royal Infirmary for a face to face discussion about this project. We are looking for people of all ethnicities and from all
We have been contacted by a Clinical Research Fellow at the University of Manchester who is looking for 5 or 6 volunteers, who would be willing and able to travel to Manchester Royal Infirmary for a face to face discussion about this project. We are looking for people of all ethnicities and from all
Alida_Bennett
LUPUS UK
in
LUPUS UK
1 year ago
I’m new to this forum
hi folks, new to this forum. basically was referred to consultant some 6 years ago and started on NSAID naproxen which I had been taking for a while prior and which seemed to be holding pain control quite well. Declined to start DMARDs at that point as a bit scared of side effects and have managed with
hi folks, new to this forum. basically was referred to consultant some 6 years ago and started on NSAID naproxen which I had been taking for a while prior and which seemed to be holding pain control quite well. Declined to start DMARDs at that point as a bit scared of side effects and have managed with
Isla-baby
in
NRAS
1 year ago
Hello from a (UK based) Pernicious Anaemia sufferer...
I am like so many others trying to jump the health hurdles I keep facing and recently feel like I've been running straight into them instead of avoiding. I am currently waiting for a Endocrinology appointment to have a test for Addison's having had some recent blood tests that showed concerning low
I am like so many others trying to jump the health hurdles I keep facing and recently feel like I've been running straight into them instead of avoiding. I am currently waiting for a Endocrinology appointment to have a test for Addison's having had some recent blood tests that showed concerning low
f1ddle_st1cks
in
Pernicious Anaemia Society
1 year ago
Lupus Information Day - Sat, 13th May in Cardiff, Wales
LUPUS UK will be having their Lupus Information Day in Cardiff, Wales on Saturday 13th May. The information day event is open to anyone, providing they book a ticket which is free of charge. Refreshments will be provided in the afternoon. We hope that many members will be able to join us for the event
LUPUS UK will be having their Lupus Information Day in Cardiff, Wales on Saturday 13th May. The information day event is open to anyone, providing they book a ticket which is free of charge. Refreshments will be provided in the afternoon. We hope that many members will be able to join us for the event
Chanpreet_Walia
LUPUS UK
in
LUPUS UK
1 year ago
Stage 4 fibrosis of the Liver
I contracted Hepatitis A in 2020, undiagnosed for 2 months. Six months later I was told I had NALD and last year I was sent for ultrasound scans and blood tests to check for cancer. In March this year, I was told I had Stage 4 Fibrosis of the liver. Does anyone know if this can be reversed, any treatments
I contracted Hepatitis A in 2020, undiagnosed for 2 months. Six months later I was told I had NALD and last year I was sent for ultrasound scans and blood tests to check for cancer. In March this year, I was told I had Stage 4 Fibrosis of the liver. Does anyone know if this can be reversed, any treatments
Wi-llow
in
British Liver Trust
1 month ago
Osteoarthritis, B12, Underactive Thyroid,Hypertension
Morning all Just wondering if anyone who has similar problems has or is trying Weygovy ? My arthritis is so bad and at the moment I also have piriformis syndrome I struggle to get upstairs let alone do anything else ? Thanks for reading😄
Morning all Just wondering if anyone who has similar problems has or is trying Weygovy ? My arthritis is so bad and at the moment I also have piriformis syndrome I struggle to get upstairs let alone do anything else ? Thanks for reading😄
Hidden
in
Cure Arthritis Community
1 year ago
Wednesday Word
[u][i]
ALT - Alanine Transaminase
[/i][/u] This is a blood test performed as part of your routine liver panel test. It is released more so by the [u][i]
hepatocytes -(liver cells)
[/i][/u] so it's associated more with hepatitis rather than PBC. ALT can be elevated in both non responders
[u][i]
ALT - Alanine Transaminase
[/i][/u] This is a blood test performed as part of your routine liver panel test. It is released more so by the [u][i]
hepatocytes -(liver cells)
[/i][/u] so it's associated more with hepatitis rather than PBC. ALT can be elevated in both non responders
DonnaBoll
Administrator
in
PBC Foundation
2 months ago
Phase 1 trial testing CAR T-cell therapy GC012F in SLE
“This study of GC012F in SLE marks an important next step in GC012F’s development as we look to confirm its potential in
autoimmune
diseases
and prepare the IND submission in both U.S. and China,” William Cao, PhD, Gracell’s founder, chairman, and CEO, said in a company press release.
“This study of GC012F in SLE marks an important next step in GC012F’s development as we look to confirm its potential in
autoimmune
diseases
and prepare the IND submission in both U.S. and China,” William Cao, PhD, Gracell’s founder, chairman, and CEO, said in a company press release.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
1 year ago
cannot lose weight - hashimoto’s
hi everyone! hashimoto’s thyroiditus was diagnosed privately in August 2022 and now nhs is treating me with 75mg levothyroxine (teva brand) and things are improving. Goitre reducing and t3,t4,TSH all in normal range now. On b12 supplement for deficiency, was tested for all major vitamins, coeliac,
hi everyone! hashimoto’s thyroiditus was diagnosed privately in August 2022 and now nhs is treating me with 75mg levothyroxine (teva brand) and things are improving. Goitre reducing and t3,t4,TSH all in normal range now. On b12 supplement for deficiency, was tested for all major vitamins, coeliac,
08ambo1
in
Thyroid UK
1 year ago
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