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Polyunsaturated fats v saturated fats
I am so confused! I read on another site polyunsaturated fats are bad for people with hypothyroidism and saturated fats are recommended. I tend to follow the Mediterranean way of eating more for heart health and keep slim. This includes oily fish , avocados and nuts which are PUFAs. My GP wanted me
I am so confused! I read on another site polyunsaturated fats are bad for people with hypothyroidism and saturated fats are recommended. I tend to follow the Mediterranean way of eating more for heart health and keep slim. This includes oily fish , avocados and nuts which are PUFAs. My GP wanted me
GREENcard13
in
Thyroid UK
4 months ago
Thyroid scan
Clinical Indication: croaky voice, underactive thyroid Findings: Patient highlights known Hashimoto's. The thyroid is atrophic and hypoechoic in keeping with end stage diffuse thyroid disease. It has an overall volume of 2.1 cc; the right lobe has a volume of 1.3 cc, while the left a volume of
Clinical Indication: croaky voice, underactive thyroid Findings: Patient highlights known Hashimoto's. The thyroid is atrophic and hypoechoic in keeping with end stage diffuse thyroid disease. It has an overall volume of 2.1 cc; the right lobe has a volume of 1.3 cc, while the left a volume of
Flick9
in
Thyroid UK
5 months ago
Post Cardioversion
Well, after 3 years in Afib and a failed ablation I had a cardioversion just over a week ago, and I am pleased to say I am in Normal Sinus Rhythm ( well, fingers crossed )!..Just a point. I was a runner before getting Afib, so my pulse was always low ( High 40's, 50 )... Before cardioversion my resting
Well, after 3 years in Afib and a failed ablation I had a cardioversion just over a week ago, and I am pleased to say I am in Normal Sinus Rhythm ( well, fingers crossed )!..Just a point. I was a runner before getting Afib, so my pulse was always low ( High 40's, 50 )... Before cardioversion my resting
FSsimmer
in
Atrial Fibrillation Support
4 months ago
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Advice please - feeling worried
Hello all.
I need your thoughts and advice based on your experience.
Background
- I was diagnosed with AF four years ago, originally persistent and then intermittent doe to life style changes. I have lost 4 stone in weight (BMI now 29), cut out alcohol, gym 4 times a week and eat healthily
Hello all.
I need your thoughts and advice based on your experience.
Background
- I was diagnosed with AF four years ago, originally persistent and then intermittent doe to life style changes. I have lost 4 stone in weight (BMI now 29), cut out alcohol, gym 4 times a week and eat healthily
Steve101
in
Atrial Fibrillation Support
4 months ago
levothyroxine induced lupus erythematosus?
Hiya, I am fairly new to all this, I have been on Levothryroxine for Hypothyroid (Hashimoto’s disease.) since June. My initial symptoms started after my first covid infection. All was going well until November time when I started to develop a Malar rash in the classic butterfly shape on my face. I don
Hiya, I am fairly new to all this, I have been on Levothryroxine for Hypothyroid (Hashimoto’s disease.) since June. My initial symptoms started after my first covid infection. All was going well until November time when I started to develop a Malar rash in the classic butterfly shape on my face. I don
Baker16
in
Thyroid UK
5 months ago
blinding period success!
This week I will hit the 3 month blinding period date! I remain in Normal sinus rhythm and will be able to discontinue my Eliquis! However 3 nights ago I began to have PAC’s. Today I recorded them pretty consistently 3-6 per minute. So bummed as I haven’t really even been aware of my heart beat in last
This week I will hit the 3 month blinding period date! I remain in Normal sinus rhythm and will be able to discontinue my Eliquis! However 3 nights ago I began to have PAC’s. Today I recorded them pretty consistently 3-6 per minute. So bummed as I haven’t really even been aware of my heart beat in last
Acheybreakeyheart
in
Atrial Fibrillation Support
4 months ago
Answer's at last for my deficiency.
Some will already know from my previous posts I went for an ultrasound scan today on my intestines. When I arrived home I had recieved rather a lot of post. I waded through the various bills and then opened one from the hospital, it was from the endocrine dept. Some of you will know I have both hypothroidism
Some will already know from my previous posts I went for an ultrasound scan today on my intestines. When I arrived home I had recieved rather a lot of post. I waded through the various bills and then opened one from the hospital, it was from the endocrine dept. Some of you will know I have both hypothroidism
Jillymo
in
Pernicious Anaemia Society
7 months ago
A Happy Anniversary
Dear AFA forum family. Isn't life wonderful? I joined the AFA forum some four years ago and had it not been for chance encounters, who knows where I would be today. It started with an AFA post titled "Tim' Story". At the time of his post (several years ago) Tim was 55 and his story mirrored my own
Dear AFA forum family. Isn't life wonderful? I joined the AFA forum some four years ago and had it not been for chance encounters, who knows where I would be today. It started with an AFA post titled "Tim' Story". At the time of his post (several years ago) Tim was 55 and his story mirrored my own
saulger
in
AF Association
7 months ago
PSA rise from initial Pluvicto treatment
I am curious if most of you that have been through Pluvicto experienced a PSA rise initially? I just finished my first injection, and did see a bit of a jump in PSA level. I had a similar experience in the SPLASH trial last year. After the first Lu177 injection, my PSA shot up quite a lot. This got
I am curious if most of you that have been through Pluvicto experienced a PSA rise initially? I just finished my first injection, and did see a bit of a jump in PSA level. I had a similar experience in the SPLASH trial last year. After the first Lu177 injection, my PSA shot up quite a lot. This got
joeguy
in
Advanced Prostate Cancer
7 months ago
Slight ache near heart
I had abdominal surgery in November. They used inappropriate dressings despite being warned and I had very inflamed skin on the stomach area. This all triggered paraxsysmal af. I then had terrible burning/itcing all over the torso for which I was prescribed strong pills. I have had a bad yeast problem
I had abdominal surgery in November. They used inappropriate dressings despite being warned and I had very inflamed skin on the stomach area. This all triggered paraxsysmal af. I then had terrible burning/itcing all over the torso for which I was prescribed strong pills. I have had a bad yeast problem
GrannyE
in
Atrial Fibrillation Support
4 months ago
feeling a bit overwhelmed and lost
In September 2023 I found out by chance that I had apparently been diagnosed with lupus 15-20 years ago. I haven’t been told at any point in this time by a doctor - I found out almost by accident from my GP physio. Since then my current GP has been initially verbally supportive although said they knew
In September 2023 I found out by chance that I had apparently been diagnosed with lupus 15-20 years ago. I haven’t been told at any point in this time by a doctor - I found out almost by accident from my GP physio. Since then my current GP has been initially verbally supportive although said they knew
opalescenthope
in
LUPUS UK
5 months ago
a newby to Lupus
Hello folks, I was only diagnosed with lupus a few days ago, after six months of being told I have stage4 CKD, currently at 21% .Eight years ago I was diagnosed with severe anaemia by my GP, which with retrospect I think was a symptom of Lupus and the cause wasn’t looked into. I don’t have the energy
Hello folks, I was only diagnosed with lupus a few days ago, after six months of being told I have stage4 CKD, currently at 21% .Eight years ago I was diagnosed with severe anaemia by my GP, which with retrospect I think was a symptom of Lupus and the cause wasn’t looked into. I don’t have the energy
C0rnflakes
in
LUPUS UK
5 months ago
Dr. Jones' Knowledge
Several times a week I want to share some of Dr. Jones' statements regarding PBC These are all taken from his book [u][i]The Definitive Guide for Patients Who Have Primary Biliary Cholangitis. I [/i][/u]think it's important to share some of the basics of this complicated disease. If you have any questions
Several times a week I want to share some of Dr. Jones' statements regarding PBC These are all taken from his book [u][i]The Definitive Guide for Patients Who Have Primary Biliary Cholangitis. I [/i][/u]think it's important to share some of the basics of this complicated disease. If you have any questions
DonnaBoll
Administrator
in
PBC Foundation
27 days ago
Fibro medication and alcahol
Diagnosed a few years ago but decided not to take medication. The only meds I take are for my underactive Thyroid,i also have Ostioarthritis and Scoliosis but finding my pain is gradually feeling worse. What medication would you recommend? I am sociable and enjoy a sociable beer so is there anything
Diagnosed a few years ago but decided not to take medication. The only meds I take are for my underactive Thyroid,i also have Ostioarthritis and Scoliosis but finding my pain is gradually feeling worse. What medication would you recommend? I am sociable and enjoy a sociable beer so is there anything
henrythewasp
in
Fibromyalgia Action UK
5 months ago
New treatment for neurodegenerative diseases may be found in used coffee grounds
New treatment for neurodegenerative diseases may be found in used coffee grounds
: Caffeic-acid based Carbon Quantum Dots have the potential to be transformative in the treatment of neurodegenerative disorders 2023 https://www.caledonianrecord.com/features/health/used-coffee-grounds-may-help-prevent-alzheimer-s-and-parkinson-s-study
New treatment for neurodegenerative diseases may be found in used coffee grounds
: Caffeic-acid based Carbon Quantum Dots have the potential to be transformative in the treatment of neurodegenerative disorders 2023 https://www.caledonianrecord.com/features/health/used-coffee-grounds-may-help-prevent-alzheimer-s-and-parkinson-s-study
Bolt_Upright
in
Cure Parkinson's
7 months ago
Do you know your pulse?
Your heartbeat is the most fundamental rhythm in your life, signalling the regular pumping of your heart as it propels blood carrying oxygen and nutrients to the rest of your body. We take the regular beating completely for granted, never giving it a second thought until the elegant control process
Your heartbeat is the most fundamental rhythm in your life, signalling the regular pumping of your heart as it propels blood carrying oxygen and nutrients to the rest of your body. We take the regular beating completely for granted, never giving it a second thought until the elegant control process
TracyAdmin
Partner
in
Sudden Cardiac Arrest & Heart Attack
4 months ago
Autoimmune Diseases
Saw this news article today and found it interesting. https://www.ctvnews.ca/health/lupus-and-other-autoimmune-diseases-strike-far-more-women-than-men-now-there-s-a-clue-why-1.6751469 Really found this part interesting. “Scientists have long thought it takes a combination of genetic susceptibility
Saw this news article today and found it interesting. https://www.ctvnews.ca/health/lupus-and-other-autoimmune-diseases-strike-far-more-women-than-men-now-there-s-a-clue-why-1.6751469 Really found this part interesting. “Scientists have long thought it takes a combination of genetic susceptibility
Swift20
in
Pernicious Anaemia Society
5 months ago
Hashis and Graves? Watch and Wait has now caught up.
About 15 months or so, I had an appointment for a thyroid specialist as my thyroid tests pointed towards Graves. I had been hypothyroid for about 17years when my different results meant my gp prescribing less and less levo. When the amount became 12.5mcg, (after an original 150 mcg) I asked to be
About 15 months or so, I had an appointment for a thyroid specialist as my thyroid tests pointed towards Graves. I had been hypothyroid for about 17years when my different results meant my gp prescribing less and less levo. When the amount became 12.5mcg, (after an original 150 mcg) I asked to be
Bluebell999
in
Thyroid UK
7 months ago
Article: Why autoimmune disease is more common in women
I thought people might be interested in this article from Nature about why autoimmune diseases are more common in women: https://www.nature.com/articles/d41586-024-00267-6 "A new explanation for the discrepancy has emerged: a molecular coating typically found on half of a woman’s X chromosomes — but
I thought people might be interested in this article from Nature about why autoimmune diseases are more common in women: https://www.nature.com/articles/d41586-024-00267-6 "A new explanation for the discrepancy has emerged: a molecular coating typically found on half of a woman’s X chromosomes — but
cyberbarn
in
NRAS
5 months ago
Some new science on why women are more prone to autoimmune disease
This is an interesting read that suggests the preponderance of systemic autoimmune conditions in women is linked to incomplete X chromosome inactivation. Sadly, it doesnt have any immediate practical implications for us lot, but may be a pointer for the future. https://www.nature.com/articles/d41586
This is an interesting read that suggests the preponderance of systemic autoimmune conditions in women is linked to incomplete X chromosome inactivation. Sadly, it doesnt have any immediate practical implications for us lot, but may be a pointer for the future. https://www.nature.com/articles/d41586
whisperit
in
LUPUS UK
5 months ago
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