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Interstitial lung disease (ILD)
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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
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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
Just diagnosed scleroderma/myositis - any help or guidance appreciated
I have just been diagnosed with overlap autoimmune
disease
- systemic sclerosis/myositis - symptoms include raynauds,
interstitial
lung
disease
, (ILD), thickened fingers with pain and stiffness, achy thighs and upper arms.
I have just been diagnosed with overlap autoimmune
disease
- systemic sclerosis/myositis - symptoms include raynauds,
interstitial
lung
disease
, (ILD), thickened fingers with pain and stiffness, achy thighs and upper arms.
ruablue
in
Scleroderma & Raynaud's UK (SRUK)
2 years 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
SSc-related bronchiectasis
Does anyone know if you can have both bronchiectasis (which I've been diagnosed with) and
interstitial
lung
disease
(which I haven't)?
Does anyone know if you can have both bronchiectasis (which I've been diagnosed with) and
interstitial
lung
disease
(which I haven't)?
volvox45
in
Scleroderma & Raynaud's UK (SRUK)
2 years 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
Joint pain very common in lupus, affects patients’ life quality: Study
Joint pain very common in lupus, affects patients’ life quality: Study SLE marked by ache, discomfort, numbness in hands, wrists and knees Patricia Inacio, PhD The vast majority of people with systemic lupus erythematosus (SLE) experience musculoskeletal symptoms, marked by pain, ache, discomfort
Joint pain very common in lupus, affects patients’ life quality: Study SLE marked by ache, discomfort, numbness in hands, wrists and knees Patricia Inacio, PhD The vast majority of people with systemic lupus erythematosus (SLE) experience musculoskeletal symptoms, marked by pain, ache, discomfort
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
30 days ago
Lupus SLE feeling alone - needing some support or advice
Hi I am a 26 yr old female and I was diagnosed with SLE Lupus and FSGS a kidney disease at 18 in 2016.Recentley diagnosed with Sjogren's... I took high doses of Prednisone and Plaquenil and it put me into remission for about 7 years. I recently was hospitalized for swollen legs and ankles again and it
Hi I am a 26 yr old female and I was diagnosed with SLE Lupus and FSGS a kidney disease at 18 in 2016.Recentley diagnosed with Sjogren's... I took high doses of Prednisone and Plaquenil and it put me into remission for about 7 years. I recently was hospitalized for swollen legs and ankles again and it
amberb444
in
LUPUS UK
1 month ago
Bang for your buck
Supplements, medication, procedures Can someone tell me what supplements should be used with Parkinsons Among the various therapies that have shown at least some effect in the animal and/or human model are Carbadopa/Levadopa Actylcholine Actigal/Ursolic acid Adderil (amphetamine) Alcohol Alpha
Supplements, medication, procedures Can someone tell me what supplements should be used with Parkinsons Among the various therapies that have shown at least some effect in the animal and/or human model are Carbadopa/Levadopa Actylcholine Actigal/Ursolic acid Adderil (amphetamine) Alcohol Alpha
heartinmotion
in
Cure Parkinson's
6 months ago
Lupus
Yes I do and I don't really understand what to do for it brought on by lupus medicine
Yes I do and I don't really understand what to do for it brought on by lupus medicine
3139782852
in
LUPUS UK
1 month ago
Lupus
Thank you for accepting my request how do I download a app for this site
Thank you for accepting my request how do I download a app for this site
3139782852
in
LUpus Patients Understanding and Support
1 month ago
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