Search
Search
About
Log in
Join
Experiences with
Mitral valve disease
Posts
Communities
47,435 public posts
Filter results
Has anyone had these symptoms?
I’m on 200 Levothyroxine and just had a blood test. It’s out of range again. I’ve developed bad joint pains in pretty much all joints and it’s got progressively worse. In addition I’m getting cold hands and feet with pins and needles that also is causing pain. Felt very dizzy last week and ended up
I’m on 200 Levothyroxine and just had a blood test. It’s out of range again. I’ve developed bad joint pains in pretty much all joints and it’s got progressively worse. In addition I’m getting cold hands and feet with pins and needles that also is causing pain. Felt very dizzy last week and ended up
Pinkbutton
in
NRAS
22 days ago
organizing
I started organizing all my notes yesterday from the Summit. I will begin to share all of this with you today. One of the women I met was the Pediatrics and Rare Liver Diseases Director, Kristin Hatcher, from the Global Liver Institute. She is trying to lobby for a routine liver panel to be part
I started organizing all my notes yesterday from the Summit. I will begin to share all of this with you today. One of the women I met was the Pediatrics and Rare Liver Diseases Director, Kristin Hatcher, from the Global Liver Institute. She is trying to lobby for a routine liver panel to be part
DonnaBoll
Administrator
in
PBC Foundation
6 months ago
Underactive thyroid
I've had an underactive thyroid for 20 years, lm on 100mg thyroxine but last years and this years test show lm abnormal readings of TSH level 0.35 - 5.5, should my dose be increased as my health this year feels dreadful hair falling out, extreme fatigue and other bloods this test have affected my liver
I've had an underactive thyroid for 20 years, lm on 100mg thyroxine but last years and this years test show lm abnormal readings of TSH level 0.35 - 5.5, should my dose be increased as my health this year feels dreadful hair falling out, extreme fatigue and other bloods this test have affected my liver
Linann
in
Thyroid UK
23 days ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Watch Now - Successful Travel with MS
MSAA's newest webinar is now available to watch on our video page! Traveling with multiple sclerosis can present some unique challenges. Watch this discussion with Dr. Yolanda Wheeler for helpful tips to make your trip by boat, bus, plane, or even cruise ship enjoyable. Watch now by visiting MSAA's
MSAA's newest webinar is now available to watch on our video page! Traveling with multiple sclerosis can present some unique challenges. Watch this discussion with Dr. Yolanda Wheeler for helpful tips to make your trip by boat, bus, plane, or even cruise ship enjoyable. Watch now by visiting MSAA's
DanaMSAA
Partner
in
My MSAA Community
23 days ago
UCTD?
Hello ,Has anyone noticed that there now appears to be no reference to UCTD on the Lupus uk website. Spoke to someone there today who had heard of UCTD but didn't know what it was? And only talked about MCTD? Is UCTD still a recognised lupus connected diagnosis?
Hello ,Has anyone noticed that there now appears to be no reference to UCTD on the Lupus uk website. Spoke to someone there today who had heard of UCTD but didn't know what it was? And only talked about MCTD? Is UCTD still a recognised lupus connected diagnosis?
Narni21
in
LUPUS UK
23 days ago
Osteo or rheumatoid arthritis in fingers
At the same time as being diagnosed with rheumatoid arthritis, I started getting sharp pain and swelling in the joints closest to finger tips. I was told this is osteoarthritis (while it is also acknowledged that RA can affect any joint). The pain is getting worse and I expect that if I do contact my
At the same time as being diagnosed with rheumatoid arthritis, I started getting sharp pain and swelling in the joints closest to finger tips. I was told this is osteoarthritis (while it is also acknowledged that RA can affect any joint). The pain is getting worse and I expect that if I do contact my
Gottarelax
in
NRAS
23 days ago
confused about high b12 but now have PA
I started having small fiber neuropathy several years ago after being exposed to Lyme and Mold. Spent a lot of time treating with herbs to put both into remission, but I still deal with the small fiber neuropathy in my feet, my lips have a blue tinge to them as to the moons on my thumb nails. I just
I started having small fiber neuropathy several years ago after being exposed to Lyme and Mold. Spent a lot of time treating with herbs to put both into remission, but I still deal with the small fiber neuropathy in my feet, my lips have a blue tinge to them as to the moons on my thumb nails. I just
SunriseDaily
in
Pernicious Anaemia Society
23 days ago
What type of hypothyroidism do I have,?
My mother had a goitre and my sister born with no functioning thyroid. I realise I had thyroid problems from childhood but not treated until nearly 50 50 is this hashimotos or autoimmune considering familial connection?
My mother had a goitre and my sister born with no functioning thyroid. I realise I had thyroid problems from childhood but not treated until nearly 50 50 is this hashimotos or autoimmune considering familial connection?
Dodds
in
Thyroid UK
24 days ago
Blood Test Results advice please!
I have now had Blue Horizon Thyroid and Vitamin test results. Blood was taken 24 hrs after last Thyroxine and early in morning on Sept 3rd). I am on 75gms Thyroxine daily for Underactive Thyroid and am currently not taking any Vitamins or supplements. Vit D(25 OH)
I have now had Blue Horizon Thyroid and Vitamin test results. Blood was taken 24 hrs after last Thyroxine and early in morning on Sept 3rd). I am on 75gms Thyroxine daily for Underactive Thyroid and am currently not taking any Vitamins or supplements. Vit D(25 OH)
Rolbo
in
Thyroid UK
24 days ago
Advice for blood-test redo after loading doses
Hi you lovely lot! I posted in July regarding my symptoms and your kind words helped give me the motivation to continue pushing my doctor surgery before they finally agreed to give me B12 injections. They started on 6 loading doses which I've just finished and now I need to wait the dreaded 12 weeks
Hi you lovely lot! I posted in July regarding my symptoms and your kind words helped give me the motivation to continue pushing my doctor surgery before they finally agreed to give me B12 injections. They started on 6 loading doses which I've just finished and now I need to wait the dreaded 12 weeks
Battypatty2
in
Pernicious Anaemia Society
24 days ago
Lab results. Please help!!!
Hi all. I have a question to ask, because my gp wasn't very helpfull as we all experienced that. I just done my thyroid bloods with medichecks. Results are back and I would like to share tho with you ask for advice what to do. I am not feeling well myself. I have heat intolerance, sweeting a lot. I am
Hi all. I have a question to ask, because my gp wasn't very helpfull as we all experienced that. I just done my thyroid bloods with medichecks. Results are back and I would like to share tho with you ask for advice what to do. I am not feeling well myself. I have heat intolerance, sweeting a lot. I am
ErikaGJ
in
Thyroid UK
25 days ago
test result gluten
coeliac test came back fine , so can I still have gluten with hashimotos?
coeliac test came back fine , so can I still have gluten with hashimotos?
Prosecco1997
in
Thyroid UK
25 days ago
Will Anti TPO - Thyroid peroxidase antibodies show the same thing as Thyroglobulin antibodies ?
Years ago I had a full thyroid panel which included tsh , free t4 , free t3 and Thyroid Peroxidase Ab IU/mL . My result was : 0.84 IU/mL The Range: 0 - 5 IU/mL But my GP didn’t check thyroglobulin antibody levels surely if I had any autoimmune thyroid problems wouldn’t the Thyroid peroxidase pick
Years ago I had a full thyroid panel which included tsh , free t4 , free t3 and Thyroid Peroxidase Ab IU/mL . My result was : 0.84 IU/mL The Range: 0 - 5 IU/mL But my GP didn’t check thyroglobulin antibody levels surely if I had any autoimmune thyroid problems wouldn’t the Thyroid peroxidase pick
Watermelonsugarr
in
Thyroid UK
26 days ago
hi im new and would like a 2nd opinion on thyroid/other test results please
i am on 125mg of levo for my underactive thyroid have been this way over 2 yrs. ive recently had slight headaches /extreme tiredness/generally no get up an go in me i go the gym well force myself recently and have an active job in construction i very rarely drink or smoke and my diet is id say
i am on 125mg of levo for my underactive thyroid have been this way over 2 yrs. ive recently had slight headaches /extreme tiredness/generally no get up an go in me i go the gym well force myself recently and have an active job in construction i very rarely drink or smoke and my diet is id say
fullban
in
Thyroid UK
27 days ago
Ruxience is a new Bio similar , Rituximab
I have Rheumatoid arthritis and myasenthia gravis and have been Rituximab for about 5 years. That had work good me. Now they are doing a new Bio similar drug Ruxience by Pfizer. Has anyone taken the Ruxience ? If so did you have side effects? Did it help?
I have Rheumatoid arthritis and myasenthia gravis and have been Rituximab for about 5 years. That had work good me. Now they are doing a new Bio similar drug Ruxience by Pfizer. Has anyone taken the Ruxience ? If so did you have side effects? Did it help?
65_women
in
PMRGCAuk
28 days ago
Bone metastasis good news: OsteoDex got to phase 3 at last
in phase 2 it behaved well, now starting phase 3 https://healthunlocked.com/advanced-prostate-cancer/posts/150487940/osteodex-for-mcrpc-bone-metastasis
in phase 2 it behaved well, now starting phase 3 https://healthunlocked.com/advanced-prostate-cancer/posts/150487940/osteodex-for-mcrpc-bone-metastasis
Maxone73
in
Advanced Prostate Cancer
6 months ago
blood test results for liver. Advice welcome please
maybe I don’t need to be on this page, but thought I’d put the question out there. Up until recently my husband’s blood test results have always been pretty good. But around the time he was diagnosed with chronic degenerative spinal disease, his liver results have gone a bit awry. However, at the
maybe I don’t need to be on this page, but thought I’d put the question out there. Up until recently my husband’s blood test results have always been pretty good. But around the time he was diagnosed with chronic degenerative spinal disease, his liver results have gone a bit awry. However, at the
Doraflora
in
British Liver Trust
6 months ago
Just a touch away: CT-optimal touch perception and its influence on pain and itch
Psychologist Larissa Meijer has discovered that gentle caresses from a partner can provide relief from chronic pain. This treatment has no side effects and can be done at home. It should normally be free too 🙂 Meijer has demonstrated the effect of light stroking on pain and itchiness in Parkinson's
Psychologist Larissa Meijer has discovered that gentle caresses from a partner can provide relief from chronic pain. This treatment has no side effects and can be done at home. It should normally be free too 🙂 Meijer has demonstrated the effect of light stroking on pain and itchiness in Parkinson's
Esperanto
in
Cure Parkinson's
6 months ago
Sourcing levothyroxine without prescription in the UK
Hello, As per my reply to another post earlier, the endo that I saw regarding adrenal insufficiency recently included a throw-away line in the subsequent letter to my GP recommending that the levothyroxine that I have been taking for 12 years be stopped. Unfortunately, the GP instantly removed levothyroxine
Hello, As per my reply to another post earlier, the endo that I saw regarding adrenal insufficiency recently included a throw-away line in the subsequent letter to my GP recommending that the levothyroxine that I have been taking for 12 years be stopped. Unfortunately, the GP instantly removed levothyroxine
JumpJiving
in
Thyroid UK
6 months ago
The importance of advocacy in the chronic illness world
The importance of advocacy in the chronic illness world How to get started if you feel called to become an advocate Marisa Zeppieri Earlier today, the speaker of a faith-based class I participated in was discussing the ancient Greek term “parakletos,” which meant “advocate.” My ears perked up,
The importance of advocacy in the chronic illness world How to get started if you feel called to become an advocate Marisa Zeppieri Earlier today, the speaker of a faith-based class I participated in was discussing the ancient Greek term “parakletos,” which meant “advocate.” My ears perked up,
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
30 days ago
1
...
44
45
46
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Thyroid UK
7177 results
British Liver Trust
4583 results
Advanced Prostate Cancer
4546 results
View top 10 communities
Sort by
Most Relevant
Newest