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Sub-clinical hypothyroidism
4 years ago in 2019 my thyroid levels were showing underactive borderline I managed to get into normal range and all I did was take Seamoss gel. However it's returned and now my TSH is 10.38 and T4 around 9. I do feel lethargic and fatigued and the GP wants to stick me on to a low dose of levo.. I don't
4 years ago in 2019 my thyroid levels were showing underactive borderline I managed to get into normal range and all I did was take Seamoss gel. However it's returned and now my TSH is 10.38 and T4 around 9. I do feel lethargic and fatigued and the GP wants to stick me on to a low dose of levo.. I don't
Jbl65
in
Thyroid UK
16 days ago
Working with inflammatory arthritis
Hi, I missed the Working with Inflammatory Arthritis online meeting on 17th June 2024, Does anyone know if this was recorded & if so where I could listen. Thank you very much
Hi, I missed the Working with Inflammatory Arthritis online meeting on 17th June 2024, Does anyone know if this was recorded & if so where I could listen. Thank you very much
cosmos55
in
NRAS
17 days ago
Can't lose weight !
I have underactive thyroid, and am really overweight ( 138 kg ). For the past 4 weeks I have been on 1500 calorie diet and walking one hour a day. The result = 1 lb loss ! What am I doing wrong ? I take 125mg Levothyroxine daily and wait an hour before having breakfast. I am thinking of taking a Blue
I have underactive thyroid, and am really overweight ( 138 kg ). For the past 4 weeks I have been on 1500 calorie diet and walking one hour a day. The result = 1 lb loss ! What am I doing wrong ? I take 125mg Levothyroxine daily and wait an hour before having breakfast. I am thinking of taking a Blue
Bigsi
in
Thyroid UK
17 days ago
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Father with Stage 4 prostate cancer in 8 bones.
On 10/25/22 I took my dad (79 at the time) to the ER at the VA for escalating back pain and we walked out with a stage 4 prostate cancer diagnosis. When I brought him to the ER I expected them to tell me he had lung cancer as he is a lifelong smoker. Additionally, I had been worried about him all year
On 10/25/22 I took my dad (79 at the time) to the ER at the VA for escalating back pain and we walked out with a stage 4 prostate cancer diagnosis. When I brought him to the ER I expected them to tell me he had lung cancer as he is a lifelong smoker. Additionally, I had been worried about him all year
lgutman
in
Advanced Prostate Cancer
6 months ago
A clinical picture of a B12 deficiency and PA explained.........
Hopefully the following will be of interest to newbies on the sight and give a little insight of the condition and how to treat............ https://www.bmj.com/content/383/bmj-2022-071725
What is a patient with a lack of B12 would have pa?
Pernicious anemia (PA) is a decrease in red blood
Hopefully the following will be of interest to newbies on the sight and give a little insight of the condition and how to treat............ https://www.bmj.com/content/383/bmj-2022-071725
What is a patient with a lack of B12 would have pa?
Pernicious anemia (PA) is a decrease in red blood
Jillymo
in
Pernicious Anaemia Society
18 days ago
Gastric Parietal Cell Antibody
Just wondering whether any members have had this test? I'm not really thinking about those who have had a B12 deficiency (or suspected Pernicious Anaemia) followed up by this test. Rather has anyone had done spontaneously as the link below [i]appears[/i] to imply. As I read it, the words say GPC should
Just wondering whether any members have had this test? I'm not really thinking about those who have had a B12 deficiency (or suspected Pernicious Anaemia) followed up by this test. Rather has anyone had done spontaneously as the link below [i]appears[/i] to imply. As I read it, the words say GPC should
helvella
Thyroid UK
in
Thyroid UK
19 days ago
Is it worth doing pernicious anemia test with active B12 of 68?
I'm working on getting my levels of B12, folate, ferritin and D up to ideal levels, if I can, for my thyroid. I recently got a B12 result from monitor my health of 68 pmol/L (range 38-210). I have read that you can still have B12 deficiency even if your B12 is around my level (I heard over 70 is needed
I'm working on getting my levels of B12, folate, ferritin and D up to ideal levels, if I can, for my thyroid. I recently got a B12 result from monitor my health of 68 pmol/L (range 38-210). I have read that you can still have B12 deficiency even if your B12 is around my level (I heard over 70 is needed
Carrie234
in
Thyroid UK
19 days ago
New PA diagnosis
Hi all Recently found to have autoimmune gastritis with stomach polyps. I also have Hashimotos (autoimmune thyroid addressed & on meds) and ckd stage 3 I was given the B12 loading dose of 6 injections. I read since a high intake of B12 is not good for the kidneys? Does anyone know if this is the case
Hi all Recently found to have autoimmune gastritis with stomach polyps. I also have Hashimotos (autoimmune thyroid addressed & on meds) and ckd stage 3 I was given the B12 loading dose of 6 injections. I read since a high intake of B12 is not good for the kidneys? Does anyone know if this is the case
Bacca
in
Pernicious Anaemia Society
19 days ago
Graves disease and Pregnancy
Hi guys, so I was diagnosed with graves disease causing hyperthyroidism and celiac disease in June last year. I have been on 40mg carbimazole per day and 80mg propanalol per day since. I had a consultation with my endocrinologist yesterday, she has now reduced my dose to 30mg carbimazole per day. I expressed
Hi guys, so I was diagnosed with graves disease causing hyperthyroidism and celiac disease in June last year. I have been on 40mg carbimazole per day and 80mg propanalol per day since. I had a consultation with my endocrinologist yesterday, she has now reduced my dose to 30mg carbimazole per day. I expressed
Candice197
in
Thyroid UK
6 months ago
Successful Pluvicto Treatment
I completed six Pluvicto treatments in December 2023 and returned to Mayo in Rochester on January 31, 2024 for a Choline Pet scan to see if it would reveal any non-PSMA PCa. My doctor reviewed the report and scans and informed me that my cancer appears to be in complete remission. The findings of the
I completed six Pluvicto treatments in December 2023 and returned to Mayo in Rochester on January 31, 2024 for a Choline Pet scan to see if it would reveal any non-PSMA PCa. My doctor reviewed the report and scans and informed me that my cancer appears to be in complete remission. The findings of the
Skifanatic
in
Advanced Prostate Cancer
6 months ago
Different Types of MS
I was reading a post on another online group earlier today and realized I really needed this for clarity. Maybe you do too. Robbie Multiple sclerosis (MS) is a chronic disease that affects the brain and spinal cord. It is thought to be an autoimmune disease. This means that the body's immune system
I was reading a post on another online group earlier today and realized I really needed this for clarity. Maybe you do too. Robbie Multiple sclerosis (MS) is a chronic disease that affects the brain and spinal cord. It is thought to be an autoimmune disease. This means that the body's immune system
robster1
in
My MSAA Community
20 days ago
Terrified Before Appointment
Hey all! I’m a female, in my 30s and looking for a little support as I freak out about an upcoming doctor appointment. Long story short, I have diagnosed hypothyroidism and have been treated for years for it. Low thyroid is my issue (important fact). My MD referred me to an endocrinologist, who is
Hey all! I’m a female, in my 30s and looking for a little support as I freak out about an upcoming doctor appointment. Long story short, I have diagnosed hypothyroidism and have been treated for years for it. Low thyroid is my issue (important fact). My MD referred me to an endocrinologist, who is
Totmama
in
My MSAA Community
20 days ago
and more promising (in vitro) CRISPR, this time used directly against cancer and not to help studying it
we are moving… https://crisprmedicinenews.com/news/crispr-targets-pancreatic-cancer-mutations/
we are moving… https://crisprmedicinenews.com/news/crispr-targets-pancreatic-cancer-mutations/
Maxone73
in
Advanced Prostate Cancer
21 days ago
Hello 👋🏿
Hi everyone! My name is Taress (rhymes with caress). I was diagnosed with Multiple Sclerosis 6 months ago. It's been a long time coming. I have had symptoms of it, on and off, since 2005. I am one of three of my family members whose been diagnosed with it. My main symptoms are fatigue, dizziness, neuropathy
Hi everyone! My name is Taress (rhymes with caress). I was diagnosed with Multiple Sclerosis 6 months ago. It's been a long time coming. I have had symptoms of it, on and off, since 2005. I am one of three of my family members whose been diagnosed with it. My main symptoms are fatigue, dizziness, neuropathy
RessieBare02
in
My MSAA Community
21 days ago
No thyroid
Hi, all the posts are about thyroid problems and taking levo for underactive thyroid, I'm taking levo 50mg and 75mg on alternate days. Can anyone tell me if taking tiromel or the unipharma tablets would be any use fo r someone who has had a total thyroidectomy. At the moment I feel as though I'm sleeping
Hi, all the posts are about thyroid problems and taking levo for underactive thyroid, I'm taking levo 50mg and 75mg on alternate days. Can anyone tell me if taking tiromel or the unipharma tablets would be any use fo r someone who has had a total thyroidectomy. At the moment I feel as though I'm sleeping
Sleepyasf--k
in
Thyroid UK
21 days ago
Medication not working
I’ve had rheumatoid arthritis for nearly 20years. I’ve tried, methotrexate, Arava, adalimimab, entanercept, ruituxan, filgotinib, baracitinib and a few others that aren’t biologics. The problem is, they don’t work for me. Has anyone else had this issue and if so what are you taking now. I’m at my wits
I’ve had rheumatoid arthritis for nearly 20years. I’ve tried, methotrexate, Arava, adalimimab, entanercept, ruituxan, filgotinib, baracitinib and a few others that aren’t biologics. The problem is, they don’t work for me. Has anyone else had this issue and if so what are you taking now. I’m at my wits
Lornap1
in
NRAS
21 days ago
biologics
hi all! I have rheumatoid arthritis I’m currently injecting 15 mg of Metratrexate but just had all my screening including TB all come back clear so now I have the green light to start Himera but I’m really nervous of this medication!🤦🏽♀️I’m staying on the metratrexate but adding in the biologic as
hi all! I have rheumatoid arthritis I’m currently injecting 15 mg of Metratrexate but just had all my screening including TB all come back clear so now I have the green light to start Himera but I’m really nervous of this medication!🤦🏽♀️I’m staying on the metratrexate but adding in the biologic as
Mybirthday1975
in
NRAS
22 days ago
Heat does it cause problems
Hi allBoth ankles and knees swollen does this often happen with underactive thyroid I am on 75 to 100mg daily which I alternate as recommended by you lovely lot which has helped me become stable and feel better for last year I do have inflammatory arthritis also and am on DMARS for Any advise tips will
Hi allBoth ankles and knees swollen does this often happen with underactive thyroid I am on 75 to 100mg daily which I alternate as recommended by you lovely lot which has helped me become stable and feel better for last year I do have inflammatory arthritis also and am on DMARS for Any advise tips will
Castroll
in
Thyroid UK
22 days ago
so. Is Undifferentiated Connective Tissue Disease latent lupus or lupus?
diagnosed with UCTD in October 2023. Fatigue, weird blood results which sent down rabbit hole for heart, liver. Scans showed all okay… fatigue, dry eyes, dry mouth, ulcers on parotid glands, thyroid, testes, mouth ulcers, Yesterday taken into hospital for suspected brain bleed, aneurism. One protein
diagnosed with UCTD in October 2023. Fatigue, weird blood results which sent down rabbit hole for heart, liver. Scans showed all okay… fatigue, dry eyes, dry mouth, ulcers on parotid glands, thyroid, testes, mouth ulcers, Yesterday taken into hospital for suspected brain bleed, aneurism. One protein
Bigdave79
in
LUPUS UK
22 days ago
Post Transplant Fatigue
Hello, I had my liver transplant just over 6 years ago now and apart from an issue right at the beginning, I have been well. I’ve not even had covid! Recently though I’ve begun to feel very tired again, almost as if I’d never had the transplant at all. My question is, has anyone else experienced chronic
Hello, I had my liver transplant just over 6 years ago now and apart from an issue right at the beginning, I have been well. I’ve not even had covid! Recently though I’ve begun to feel very tired again, almost as if I’d never had the transplant at all. My question is, has anyone else experienced chronic
Dawnejoy
in
British Liver Trust
6 months ago
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