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He lived a wonderful life
My father passed away on Sunday, 10/15/2023, at the age of 91. We initially learned of his very high PSA level on 10/14/2021 (two years prior), with the diagnosis of Stage 4 metastatic prostate cancer soon thereafter. In addition to advanced prostate cancer, he had dementia that progressed significantly
My father passed away on Sunday, 10/15/2023, at the age of 91. We initially learned of his very high PSA level on 10/14/2021 (two years prior), with the diagnosis of Stage 4 metastatic prostate cancer soon thereafter. In addition to advanced prostate cancer, he had dementia that progressed significantly
Merlot1
in
Advanced Prostate Cancer
8 months ago
Hello
Introducing myself, as I'll be looking through posts in the coming weeks... I'm 61, recently diagnosed with AF, but reckon I've been suffering for about 2 years. Biosprolol, Apixaban and Digoxin. Due to do the 'zaps' in 8-12 weeks.
Introducing myself, as I'll be looking through posts in the coming weeks... I'm 61, recently diagnosed with AF, but reckon I've been suffering for about 2 years. Biosprolol, Apixaban and Digoxin. Due to do the 'zaps' in 8-12 weeks.
MausenMumma
in
AF Association
5 months ago
Update
Well this is a long story,Mick started loosing weight In February. We then went too the GP in March,who did a blood, when I rang up they said it was normal.Mick continued to loose weight so went back to the GP on April 9th,who then said his blood test showed dangerously high blood sugars,this is the
Well this is a long story,Mick started loosing weight In February. We then went too the GP in March,who did a blood, when I rang up they said it was normal.Mick continued to loose weight so went back to the GP on April 9th,who then said his blood test showed dangerously high blood sugars,this is the
very
in
CLL Support
6 months ago
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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
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
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
Coming home
So after 4.5 years in Nigeria and an APS diagnosis in summer 2020 I’m coming back to the U.K. In many ways I’m looking forward to it and I know my consultants - all 3 of them - will be much more comfortable with me being near better medical care (APS, warfarin and epilepsy are not a good combination
So after 4.5 years in Nigeria and an APS diagnosis in summer 2020 I’m coming back to the U.K. In many ways I’m looking forward to it and I know my consultants - all 3 of them - will be much more comfortable with me being near better medical care (APS, warfarin and epilepsy are not a good combination
GillyA
in
Hughes Syndrome APS Forum
7 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
B12 made symptoms go away
Hi. I had ME/CFS and it seemed to clear up 16 years later. About 3 years ago, I had fatigue, myclonic jerks especially while sleeping which woke me up and tremor feeling inside me. I took B12 sublingual for 2 or 3 weeks and the symptoms subsided. But then I stopped taking the B12 supplements and I have
Hi. I had ME/CFS and it seemed to clear up 16 years later. About 3 years ago, I had fatigue, myclonic jerks especially while sleeping which woke me up and tremor feeling inside me. I took B12 sublingual for 2 or 3 weeks and the symptoms subsided. But then I stopped taking the B12 supplements and I have
MEguy
in
Pernicious Anaemia Society
8 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
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
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
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
Introduction
Hello everyone, I am new to this site so let me introduce myself I live with my husband on the outskirts of Llandudno on the North Wales coast. I am very fortunate that both my children & grandchildren live locally. We have a 2 year old cavapoo who together with our 2 year old grand-twins provide
Hello everyone, I am new to this site so let me introduce myself I live with my husband on the outskirts of Llandudno on the North Wales coast. I am very fortunate that both my children & grandchildren live locally. We have a 2 year old cavapoo who together with our 2 year old grand-twins provide
Ildivolover
in
Scleroderma & Raynaud's UK (SRUK)
26 days 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
AF and MAD
anyone else have AF and MAD (mitral annular disjunction) . It was picked up during cardiac MRI. The displacement is 5mm, mild mitral valve prolapse and regurgitation. Neither my cardiologist or EP have said anything about it apart from put me on another very long waiting list to see a more specialist
anyone else have AF and MAD (mitral annular disjunction) . It was picked up during cardiac MRI. The displacement is 5mm, mild mitral valve prolapse and regurgitation. Neither my cardiologist or EP have said anything about it apart from put me on another very long waiting list to see a more specialist
LoveRowing
in
Atrial Fibrillation Support
29 days 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
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
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