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Could chronic urticaria be related to underactive thyroid?
I've had under active thyroid for 5/6 years and have been on a dose of 50mcg of Levothyroxine for all of this time. This year I developed chronic urticaria and then a different kind of dermatitis/eczema and I want to rip my skin off it's so itchy. This week I did an Advanced Thyroid Function Blood Test
I've had under active thyroid for 5/6 years and have been on a dose of 50mcg of Levothyroxine for all of this time. This year I developed chronic urticaria and then a different kind of dermatitis/eczema and I want to rip my skin off it's so itchy. This week I did an Advanced Thyroid Function Blood Test
Chestercheese
in
Thyroid UK
6 months ago
blood test results
Hi all. I am age 24 male. History with excessive alcohol for the past 5 years. I recently got a full blood work carried out at my GP and my liver enzymes came back as ok, but I don’t really understand what any of it means. I tried calling my GP and it’s like trying to milk blood out of a stone
Hi all. I am age 24 male. History with excessive alcohol for the past 5 years. I recently got a full blood work carried out at my GP and my liver enzymes came back as ok, but I don’t really understand what any of it means. I tried calling my GP and it’s like trying to milk blood out of a stone
Uplight99
in
British Liver Trust
8 months ago
LUPUS 100 Answers to the most important questions about lupus, verified by world renowned lupus doctors
LUPUS 100
Answers to the most important questions about lupus, verified by world renowned lupus doctors in Europe.
LUPUS CHALLENGES
LUPUS MANIFESTATION
LUPUS MANAGEMENT
LIVING WITH LUPUS
LUPUS EUROPE is the European umbrella organisation that brings together
LUPUS 100
Answers to the most important questions about lupus, verified by world renowned lupus doctors in Europe.
LUPUS CHALLENGES
LUPUS MANIFESTATION
LUPUS MANAGEMENT
LIVING WITH LUPUS
LUPUS EUROPE is the European umbrella organisation that brings together
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
6 months ago
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Nausea - Levo/Thyroid symptom?
I am at a complete and utter loss. Why as I optimise dose do I feel nauseated for days now? As of a few weeks ago I’ve been alternating doses of 75mcg own day, followed by 100mcg of Levothyroxine only for hypothyroidism (Hashimoto). Same brand throughout treatment thus far. Perhaps it’s nothing to
I am at a complete and utter loss. Why as I optimise dose do I feel nauseated for days now? As of a few weeks ago I’ve been alternating doses of 75mcg own day, followed by 100mcg of Levothyroxine only for hypothyroidism (Hashimoto). Same brand throughout treatment thus far. Perhaps it’s nothing to
HealthStarDust
in
Thyroid UK
8 months ago
Car-T cell therapy might cure Systemic Autoimmune Diseases
Hi my dear lupies, I hope you are well. Another promising article about car-T cell therapy 😍🙏💚💜: https://www.medscape.com/viewarticle/car-t-cell-therapy-cure-systemic-autoimmune-diseases-2023a1000usm?src=WNL_conf_ash_231220_MSCPEDIT&uac=342465EY&impID=6175634
Hi my dear lupies, I hope you are well. Another promising article about car-T cell therapy 😍🙏💚💜: https://www.medscape.com/viewarticle/car-t-cell-therapy-cure-systemic-autoimmune-diseases-2023a1000usm?src=WNL_conf_ash_231220_MSCPEDIT&uac=342465EY&impID=6175634
Naladog
in
LUPUS UK
6 months ago
What the Heck? I thought boosting Short Chain Fatty Acids (SCFAs) was a Good Thing?
So... I'm digging into PDTom's post: Propionic acid (sodium propionate) - Does anyone have any experience? https://healthunlocked.com/cure-parkinsons/posts/150101092/propionic-acid-sodium-propionate-does-anyone-have-any-experience
And the feedback seems to be "Go Propionic Acid!" so I start
So... I'm digging into PDTom's post: Propionic acid (sodium propionate) - Does anyone have any experience? https://healthunlocked.com/cure-parkinsons/posts/150101092/propionic-acid-sodium-propionate-does-anyone-have-any-experience
And the feedback seems to be "Go Propionic Acid!" so I start
Bolt_Upright
in
Cure Parkinson's
8 months ago
My son’s PSA rose a bit today.
My son’s last PSA three months ago was <.01 but today it was <.10.It was previously as high as 22. He’s also tertiary five. His Mayo doctor told him to continue to test every three months, stay on current meds Lupron, Abiraterone/prednisone for another year and two months then stop meds and wait
My son’s last PSA three months ago was <.01 but today it was <.10.It was previously as high as 22. He’s also tertiary five. His Mayo doctor told him to continue to test every three months, stay on current meds Lupron, Abiraterone/prednisone for another year and two months then stop meds and wait
Cactus297
in
Advanced Prostate Cancer
8 months ago
My first endocrinologist visit
Hi everyone, On the 27th I have my first appointment with an endo. He ordered blood tests for me before he even spoke to me or knew what dose of pred I was taking. (I'm taking 7 mg a day now. Was doing 6.5 for a week but decided better to go back to 7 and stay for a while as I was feeling so bad with
Hi everyone, On the 27th I have my first appointment with an endo. He ordered blood tests for me before he even spoke to me or knew what dose of pred I was taking. (I'm taking 7 mg a day now. Was doing 6.5 for a week but decided better to go back to 7 and stay for a while as I was feeling so bad with
sferios
in
PMRGCAuk
8 months ago
Some key differences found in lupus symptoms in men vs. women: Study
Men at higher risk of heart attack; women more likely to have arthritis Men with systemic lupus erythematosus (SLE) are more likely to experience kidney failure and heart attacks, while women with SLE are at higher risk of other symptoms, such as skin problems and arthritis, according to a new study
Men at higher risk of heart attack; women more likely to have arthritis Men with systemic lupus erythematosus (SLE) are more likely to experience kidney failure and heart attacks, while women with SLE are at higher risk of other symptoms, such as skin problems and arthritis, according to a new study
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
6 months ago
Hope for the future
New research into autoimmune liver condition suggests unique cell movements may be driving disease A Birmingham study reveals a novel cellular phenomenon could be responsible for the onset of primary biliary cholangitis (PBC). Research suggests that a recent understanding of cell movements may
New research into autoimmune liver condition suggests unique cell movements may be driving disease A Birmingham study reveals a novel cellular phenomenon could be responsible for the onset of primary biliary cholangitis (PBC). Research suggests that a recent understanding of cell movements may
DonnaBoll
Administrator
in
PBC Foundation
4 months ago
When's the "best" time to do the scan?
Well, it appears the salvage radiation done in January '23 (RP in 2019) may have been unsuccessful, as my latest PSA came back at 0.06, 3 months prior was 0.02. Obviously not yet actionable and not yet definitive for failure, but the indication that the barbarian hordes might be regrouping is apparent
Well, it appears the salvage radiation done in January '23 (RP in 2019) may have been unsuccessful, as my latest PSA came back at 0.06, 3 months prior was 0.02. Obviously not yet actionable and not yet definitive for failure, but the indication that the barbarian hordes might be regrouping is apparent
Cackalacky_cyclist
in
Advanced Prostate Cancer
8 months ago
Medication and Memory
I was diagnosed with AFib in July and my daily medication is 12-5 Bisoprolol, as well as Digoxin, Rivaroxaban and Perindopril. I’ve always had a brilliant memory but have recently become concerned that I cannot retain information for very long at all. I also seem to get spurts of random, fleeting and
I was diagnosed with AFib in July and my daily medication is 12-5 Bisoprolol, as well as Digoxin, Rivaroxaban and Perindopril. I’ve always had a brilliant memory but have recently become concerned that I cannot retain information for very long at all. I also seem to get spurts of random, fleeting and
Jonhel
in
Atrial Fibrillation Support
5 months ago
Is it possible for me to get back to skateboard with autoimmune disease ever?Or do I need to give it up forever?
Hi everyone I have an autoimmune disease they say it might be lupus and myosis and Systemic Sclerosis. I don't even now which one it is or if it's all of them combined. I got diagnosed in 2022 and at this point all exercise and sports declined to none. I used to skate board, do boxing and play basketball
Hi everyone I have an autoimmune disease they say it might be lupus and myosis and Systemic Sclerosis. I don't even now which one it is or if it's all of them combined. I got diagnosed in 2022 and at this point all exercise and sports declined to none. I used to skate board, do boxing and play basketball
Crow9
in
LUPUS UK
6 months ago
Proctitis ? 🙏
Good morning, I am French and I come here on English-speaking forums to be able to find answers to my questions 😁 Has anyone here ever been diagnosed with proctitis? or inflammation of the intestines without pain? Thank you in advance have a good evening
Good morning, I am French and I come here on English-speaking forums to be able to find answers to my questions 😁 Has anyone here ever been diagnosed with proctitis? or inflammation of the intestines without pain? Thank you in advance have a good evening
Carl33150
in
Colon Cancer Connected
8 months ago
First dialysis.... not for a wuss
As I promised, I am going to document my journey as I have done before. Now it is hemodialysis. Holy mackerel. Anyone who thinks this is easy, let them sit in the chair for a turn and see what they think. My husband came with me and will be attending the training with me for the next five weeks. I am
As I promised, I am going to document my journey as I have done before. Now it is hemodialysis. Holy mackerel. Anyone who thinks this is easy, let them sit in the chair for a turn and see what they think. My husband came with me and will be attending the training with me for the next five weeks. I am
Bassetmommer
in
Kidney Dialysis
8 months ago
Intrinsic factor antibody
I'm posting on here as I been advised to. I've just been back to my GP because I had a blood test done the other week for intrinsic factor antibody. I had a result of 3.66 which I thought was positive but my GP just said it's negative ? I had the test done because my vitamins b12 is 211.
I'm posting on here as I been advised to. I've just been back to my GP because I had a blood test done the other week for intrinsic factor antibody. I had a result of 3.66 which I thought was positive but my GP just said it's negative ? I had the test done because my vitamins b12 is 211.
suzybear
in
Pernicious Anaemia Society
8 months ago
Ablation question
Hi I’ had my 3rd CV last Thursday . It was reverted after 1st go, and everything was great first time in over 3 years in sinus ryrhmn, I was elated and loved checking my Kardia seeing HR in sinus rythmn! However today I’ve gone back to AF mode , whilst I’m pleased it lasted almost 6 days last two previous
Hi I’ had my 3rd CV last Thursday . It was reverted after 1st go, and everything was great first time in over 3 years in sinus ryrhmn, I was elated and loved checking my Kardia seeing HR in sinus rythmn! However today I’ve gone back to AF mode , whilst I’m pleased it lasted almost 6 days last two previous
Janelr
in
Atrial Fibrillation Support
5 months ago
Cardio and thyroidism
5and a half years ago I suffered a heart attack. I had a stent implanted and went to cardio rehab. I have noticed over the last year I get tired quickly and have shortage of breath. I was shocked to be told by my new doctor that I have an underactive thyroid. My question is this! Is my heart contributing
5and a half years ago I suffered a heart attack. I had a stent implanted and went to cardio rehab. I have noticed over the last year I get tired quickly and have shortage of breath. I was shocked to be told by my new doctor that I have an underactive thyroid. My question is this! Is my heart contributing
gunnerred67
in
Thyroid UK
6 months ago
Latest results from the INSPIRE project - how doctors diagnose neuropsychiatric symptoms in lupus
A new study has found that doctors have a variety of opinions on whether different neuropsychiatric symptoms are directly caused by lupus. Doctors rated their assessment as most helpful in diagnosis & patient reports as least helpful. The researchers are calling for more inclusion of the patient voice
A new study has found that doctors have a variety of opinions on whether different neuropsychiatric symptoms are directly caused by lupus. Doctors rated their assessment as most helpful in diagnosis & patient reports as least helpful. The researchers are calling for more inclusion of the patient voice
Debbie_kinsey
Administrator
in
LUPUS UK
6 months ago
Only One Chance - B12 deficiency
Recommended article on the Pernicious Anaemia Society website. Quite an easy read and very much worth reading - whether you have a B12 issue, or think you don't have a B12 issue! [i]
Only One Chance
[/i] [i]Bruce Wolffenbuttel[/i] https://pernicious-anaemia-society.org/blog/only-one-chance/
Recommended article on the Pernicious Anaemia Society website. Quite an easy read and very much worth reading - whether you have a B12 issue, or think you don't have a B12 issue! [i]
Only One Chance
[/i] [i]Bruce Wolffenbuttel[/i] https://pernicious-anaemia-society.org/blog/only-one-chance/
helvella
Thyroid UK
in
Thyroid UK
6 months ago
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