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HRT and Lupus
I’m 44 and have just been diagnosed with lupus and sjogrens in the last couple of months- there’s an awful lot to Learn. My GP thought my joint pain and anxiety was perimenopause related, and I was prescribed Evorel patches but after a month the pain was increasing rather than decreasing and autoimmune
I’m 44 and have just been diagnosed with lupus and sjogrens in the last couple of months- there’s an awful lot to Learn. My GP thought my joint pain and anxiety was perimenopause related, and I was prescribed Evorel patches but after a month the pain was increasing rather than decreasing and autoimmune
RachelMaryS
in
LUPUS UK
6 months ago
Blood test help required
Hi all! Please could anyone advise me on my blood tests which were done as my hair is shedding like crazy. I have an underactive thyroid and about 8 weeks ago my GP increased my thyroxine to 200mcg as my TSH was 6 (she didn’t test anything else). Since the shedding has continued and I feel really tired
Hi all! Please could anyone advise me on my blood tests which were done as my hair is shedding like crazy. I have an underactive thyroid and about 8 weeks ago my GP increased my thyroxine to 200mcg as my TSH was 6 (she didn’t test anything else). Since the shedding has continued and I feel really tired
happykath
in
Thyroid UK
6 months ago
Omega 3
Does anyone take Omega 3 supplements for Rheumatoid Arthritis if so do they help so many brands out there.
Does anyone take Omega 3 supplements for Rheumatoid Arthritis if so do they help so many brands out there.
welsh12
in
NRAS
6 months ago
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Top tips on celebrating Diwali with Rheumatoid Arthritis
Join us in this heartfelt celebration of Diwali, the festival of lights🪔✨ Living with Rheumatoid Arthritis shouldn't mean you miss out on celebrating Diwali. Joti Reehal shares her personal experiences, tips, and inspiration to help you make the most of the festival while managing your Rheumatoid
Join us in this heartfelt celebration of Diwali, the festival of lights🪔✨ Living with Rheumatoid Arthritis shouldn't mean you miss out on celebrating Diwali. Joti Reehal shares her personal experiences, tips, and inspiration to help you make the most of the festival while managing your Rheumatoid
Aribah-NRAS
NRAS
in
NRAS
6 months ago
Thyroid antibodies test
My daughter had a thyroid antibodies test in May which was quite high. The hospital referred her back to our GP to be monitored for underactive thyroid. I have seen some posts that say antibodies test is a sign of Hashimoto's or Graves disease so I am just looking for some advice and guidance as I
My daughter had a thyroid antibodies test in May which was quite high. The hospital referred her back to our GP to be monitored for underactive thyroid. I have seen some posts that say antibodies test is a sign of Hashimoto's or Graves disease so I am just looking for some advice and guidance as I
Briggsi
in
Thyroid UK
6 months ago
Seeking advice - underactive thyroid
so my doctors have queried that I may have an under active thyroid and have recently been tested for the antibodies, can someone explain if my result is in range or if not, can you explain it to me - normal ranges etc. Serum thyroid peroxidase antibody concentration (XabCy) 21 kU/L [0 - 75] what is
so my doctors have queried that I may have an under active thyroid and have recently been tested for the antibodies, can someone explain if my result is in range or if not, can you explain it to me - normal ranges etc. Serum thyroid peroxidase antibody concentration (XabCy) 21 kU/L [0 - 75] what is
Klpanda080907
in
Thyroid UK
6 months ago
Books on Pernicious Anemia
Hi everyone, could you tell me which is Martin's most informative book, thanks
Hi everyone, could you tell me which is Martin's most informative book, thanks
Helliborous
in
Pernicious Anaemia Society
6 months ago
Webinar on financial planning with lupus
Monday 20th November at 5:30pm we are hosting a webinar with specialist financial planners from the Stonewood Group. They will talk through some information, and you will have the opportunity to ask them questions. The topics discussed will come directly from what people highlighted was important in
Monday 20th November at 5:30pm we are hosting a webinar with specialist financial planners from the Stonewood Group. They will talk through some information, and you will have the opportunity to ask them questions. The topics discussed will come directly from what people highlighted was important in
Debbie_kinsey
Administrator
in
LUPUS UK
6 months ago
Rash on Feet
hello everyone, I recently just joined after discovering this. For the last few days I’ve been suffering burning on the top of my feet as well as swelling in my feet and ankles. I’ve been diagnosed with Lupus earlier this year as well as raynauds and sjogrens. I’m starting to get concerned with my current
hello everyone, I recently just joined after discovering this. For the last few days I’ve been suffering burning on the top of my feet as well as swelling in my feet and ankles. I’ve been diagnosed with Lupus earlier this year as well as raynauds and sjogrens. I’m starting to get concerned with my current
Hidden
in
LUPUS UK
6 months ago
Advice
I'm seeing a neurologist for balance problems and occasional slurring of words. I was diagnosed with Pernicious Anaemia (currently on B12 injections) in July this year and have had vitiligo for over 20 years. One of the blood test done was for TPO antibodies with were 78 which apparently had been
I'm seeing a neurologist for balance problems and occasional slurring of words. I was diagnosed with Pernicious Anaemia (currently on B12 injections) in July this year and have had vitiligo for over 20 years. One of the blood test done was for TPO antibodies with were 78 which apparently had been
Mark2027
in
Thyroid UK
6 months ago
ANY MALES WITH LUPUS/SLE, SJOGREN'S OR UNDIFFERENTIATED CONNECTIVE TISSUE DISEASE?
There was a great response to the invite for interviewees for zoom or email interviews for the Swansea University Medical School diagnostic journeys study; and the interviews have been incredibly helpful. We are not too far off the total number of interviewees we need at this stage. But have had very
There was a great response to the invite for interviewees for zoom or email interviews for the Swansea University Medical School diagnostic journeys study; and the interviews have been incredibly helpful. We are not too far off the total number of interviewees we need at this stage. But have had very
RupertW-SUMS
in
LUPUS UK
6 months ago
Lupus information and stories
https://lupusnewstoday.com/category/news/ This link works I hope. If you are not aware of it, it could be helpful and real time stories of people with lupus.
https://lupusnewstoday.com/category/news/ This link works I hope. If you are not aware of it, it could be helpful and real time stories of people with lupus.
MrsMarigold
in
LUPUS UK
6 months ago
What is the best app for lupus diet.
I’m struggling with my weight and what to avoid .
I’m struggling with my weight and what to avoid .
Gabriel8
in
LUPUS UK
6 months ago
Do anyone have a movement disorder?
I haven't got lupus but have aps and from what I've been told you can have a movement disorder with lupus. I have involuntary movements from what looks like I'm being electrocuted (like whole body spasms that bring my whole body in) tics, left side facial spasms (also tongue) and hand movements. It's
I haven't got lupus but have aps and from what I've been told you can have a movement disorder with lupus. I have involuntary movements from what looks like I'm being electrocuted (like whole body spasms that bring my whole body in) tics, left side facial spasms (also tongue) and hand movements. It's
Charts
in
LUPUS UK
6 months ago
Advice please 😌
Hi everybody, It’s nice to meet you all! So I’m sure you have loads of people posting on here about their frustrations with the NHS/GPs etc. therefore I won’t bore you with all of the details. My journey began in Dec 22 with what I thought was a bout of viral infection-induced joint pain in my hands
Hi everybody, It’s nice to meet you all! So I’m sure you have loads of people posting on here about their frustrations with the NHS/GPs etc. therefore I won’t bore you with all of the details. My journey began in Dec 22 with what I thought was a bout of viral infection-induced joint pain in my hands
Rocinante_89
in
LUPUS UK
6 months ago
updated Sjögren’s leaflet
https://sjogrensresearch-ireland.eu/wp-content/uploads/2022/09/Sjogrens-information-leaflet_2023-1.pdf Might be of interest!
https://sjogrensresearch-ireland.eu/wp-content/uploads/2022/09/Sjogrens-information-leaflet_2023-1.pdf Might be of interest!
weathervane
in
LUPUS UK
6 months ago
when to test child for CD?
Those of you with CD diagnosed in adulthood but with children - is there any evidence to suggest it’s beneficial to limit gluten in the diet? A fellow coeliac recently told me age 4 is when to get tested but he couldn’t recall where he got that info from. My daughter has no obvious signs and we haven
Those of you with CD diagnosed in adulthood but with children - is there any evidence to suggest it’s beneficial to limit gluten in the diet? A fellow coeliac recently told me age 4 is when to get tested but he couldn’t recall where he got that info from. My daughter has no obvious signs and we haven
Anj1a
in
Gluten Free Guerrillas
6 months ago
Hello - I'm a new member
Hello, I've just joined today and wanted to say hello. I was diagnosed with Rheumatoid Arthritis around 26 years ago, and it's been quite a journey. I've been on numerous treatments over the years, and had several surgeries. Fortunately, I've managed to keep working - although it's becoming more
Hello, I've just joined today and wanted to say hello. I was diagnosed with Rheumatoid Arthritis around 26 years ago, and it's been quite a journey. I've been on numerous treatments over the years, and had several surgeries. Fortunately, I've managed to keep working - although it's becoming more
WendyB123
in
NRAS
6 months ago
Just joined
Hi everyone, just want to say hello and am pleased that I am now part of this online community. I've had Rheumatoid Arthritis for over 30 years now and it's good to be able to hear from others in the same situation .
Hi everyone, just want to say hello and am pleased that I am now part of this online community. I've had Rheumatoid Arthritis for over 30 years now and it's good to be able to hear from others in the same situation .
AcerGirl
in
NRAS
6 months ago
Stating and underactive thyroid
Hi I suffer with underactive thyroid and fibromalarga reciently I got put on stating for high colesteral after 3 day I stopped them my muscles felt like I'd been hit buy a bus i
Hi I suffer with underactive thyroid and fibromalarga reciently I got put on stating for high colesteral after 3 day I stopped them my muscles felt like I'd been hit buy a bus i
shazzafloyd
in
Thyroid UK
6 months ago
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