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Forum Updates from 29 February 2024
Hello I would like to share the news with you all that our Charity Forums have recently been rebranded and renamed to reflect the condition to which each Forum provides information and support with. The Health Unlocked Team have assured us that all existing members will be unaffected by these changes
Hello I would like to share the news with you all that our Charity Forums have recently been rebranded and renamed to reflect the condition to which each Forum provides information and support with. The Health Unlocked Team have assured us that all existing members will be unaffected by these changes
TracyAdmin
ArrhythmiaAlliance
in
Heart Rhythm Disorders Support
3 months ago
Levothyroxine
does anyone know if Levothyroxine is definitely gluten free as I’m coeliac and unsure if it’s not helping with my immune system.
does anyone know if Levothyroxine is definitely gluten free as I’m coeliac and unsure if it’s not helping with my immune system.
1Cass
in
Thyroid UK
4 months ago
Moderate Calcification
Good morning all, I was recently invited for a lung check and have been recalled as the scan showed moderate Calcification. As I like to be proactive and believe this is due to fatty diet, are there any recommendations for menus that will halt (improve?) This condition. My brother dies with this condition
Good morning all, I was recently invited for a lung check and have been recalled as the scan showed moderate Calcification. As I like to be proactive and believe this is due to fatty diet, are there any recommendations for menus that will halt (improve?) This condition. My brother dies with this condition
1AnneMcC
in
Healthy Eating
3 months ago
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Post Amiodarone and waiting for ablation
I was on Amiodarone for 12 months after diagnosis of persistent AF post Covid and stopped taking it in October '23. I had a cardioversion in June and as far as I'm aware I'm still in sinus rhythm. I'm on the list for an ablation at the John Radcliffe in Oxford. I had a couple of blood tests, at my
I was on Amiodarone for 12 months after diagnosis of persistent AF post Covid and stopped taking it in October '23. I had a cardioversion in June and as far as I'm aware I'm still in sinus rhythm. I'm on the list for an ablation at the John Radcliffe in Oxford. I had a couple of blood tests, at my
JoDogBlue
in
Atrial Fibrillation Support
3 months ago
Pressure onback causing AF
I lay on my left side today and nasty afib came on within a couple minutes same on back. I then tried lying on right side and i felt ok with my EMAY ecg saying bradycardia. I qent to GP and she will book me in for xray back and front.Colin
I lay on my left side today and nasty afib came on within a couple minutes same on back. I then tried lying on right side and i felt ok with my EMAY ecg saying bradycardia. I qent to GP and she will book me in for xray back and front.Colin
Alphakiwi
in
Atrial Fibrillation Support
3 months ago
New meta-analysis shows docetaxel benefits those having high grade/low PSA prostate cancer
Reposting with more specific title - no one had replied to Maxone73's original post. Interesting results for those with a poor-prognosis cancer. https://www.miragenews.com/docetaxel-slashes-prostate-cancer-death-in-high-1115466/
Reposting with more specific title - no one had replied to Maxone73's original post. Interesting results for those with a poor-prognosis cancer. https://www.miragenews.com/docetaxel-slashes-prostate-cancer-death-in-high-1115466/
HikerWife
in
Advanced Prostate Cancer
7 months ago
Levothyroxine and coeliac disease
would someone please be kind enough to inform me if Levothyroxine is definitely gluten free with no traces of gluten and the brand name is Mand.
would someone please be kind enough to inform me if Levothyroxine is definitely gluten free with no traces of gluten and the brand name is Mand.
1Cass
in
Gluten Free Guerrillas
4 months ago
PS to Periodontal Abscess and Prednisone
Thanks to everyone who took the time to reply to my post about gum/tooth infections and prednisone. All the replies were helpful! I did manage to generate one last question. Did any of you who had tooth extractions go on to have dental implants? I am leaning against due to cost and issues related to
Thanks to everyone who took the time to reply to my post about gum/tooth infections and prednisone. All the replies were helpful! I did manage to generate one last question. Did any of you who had tooth extractions go on to have dental implants? I am leaning against due to cost and issues related to
Donna5658
in
PMRGCAuk
4 months ago
multaq and increased heart beat
Hi everyone haven’t posted for a while,but reading the site daily. Had my third ablation in October 2023 mostly for atypical flutter,procedure wasn’t long but quite extensive judging from post procedure troponin elevations over 20,000.Placed on Multaq afterwards as I already failed all other meds and
Hi everyone haven’t posted for a while,but reading the site daily. Had my third ablation in October 2023 mostly for atypical flutter,procedure wasn’t long but quite extensive judging from post procedure troponin elevations over 20,000.Placed on Multaq afterwards as I already failed all other meds and
55zuzanka61
in
AF Association
3 months ago
Cause of extremely low ALP on Liver Function Tests
27 years old male, heavy drinker for the past 11 years.I have been having this terrible pain on the right side, just below the ribs, gets worse when laughing or when I sleep on the same side. Also, my palms are red with visible dilated veins all over. Went to the doctor, last year and an abdominal
27 years old male, heavy drinker for the past 11 years.I have been having this terrible pain on the right side, just below the ribs, gets worse when laughing or when I sleep on the same side. Also, my palms are red with visible dilated veins all over. Went to the doctor, last year and an abdominal
African1
in
British Liver Trust
7 months ago
Lupus diagnosis yesterday
Hello everyone, been a tricky few months. You all know what it's like.just wanted to update and i feel a bit overwhelmed. In 2020 was diagnosed with UCTD. Positive ANA. Take hydroxychloquine. Last year ENT diagnosed sjogrens, it was an urgent 2 week referral as my throat had been sore for months
Hello everyone, been a tricky few months. You all know what it's like.just wanted to update and i feel a bit overwhelmed. In 2020 was diagnosed with UCTD. Positive ANA. Take hydroxychloquine. Last year ENT diagnosed sjogrens, it was an urgent 2 week referral as my throat had been sore for months
BonnyB
in
LUPUS UK
4 months ago
Reintroducing gluten for coeliac test?
Hello everyone, After going gluten free in mid-November 2023 I have today had a blood test request come in which involves a coeliac test. I was tested for coeliac in 2017 too (negative) but didn't know I was being tested for it and had been eating strictly low carb for about 2 years at that point
Hello everyone, After going gluten free in mid-November 2023 I have today had a blood test request come in which involves a coeliac test. I was tested for coeliac in 2017 too (negative) but didn't know I was being tested for it and had been eating strictly low carb for about 2 years at that point
Myalikki
in
Thyroid UK
4 months ago
Teeth sensitivity at the dentist
I have been diagnosed with SLE Lupus for a year now. Does anyone find their teeth really sensitive during ordinary dental treatment such as cleaning? I’m also having a problem with the injections to numb the mouth not working . Is this Lupus related or is it just me? Any advice on the problem would
I have been diagnosed with SLE Lupus for a year now. Does anyone find their teeth really sensitive during ordinary dental treatment such as cleaning? I’m also having a problem with the injections to numb the mouth not working . Is this Lupus related or is it just me? Any advice on the problem would
Chocolate1956
in
LUPUS UK
4 months ago
eye sight affected with af
hello again to all, been off the site for a long while but like to check in now and again. My af usually only lasts a few seconds several times a day but I do get what I call bad episodes where it really affects my daily life I.e very tired more than a fair bit. The other night while moving from settee
hello again to all, been off the site for a long while but like to check in now and again. My af usually only lasts a few seconds several times a day but I do get what I call bad episodes where it really affects my daily life I.e very tired more than a fair bit. The other night while moving from settee
rubble4356
in
AF Association
3 months ago
🧬UNC93B1 New genetic findings open up perspectives for future therapeutic approaches in Lupus
Hi lupis! 👋🏼 New study demonstrates a direct causal link between an overactive UNC93B1/TLR7 axis and lupus pathogenesis and indicates that blocking overactive TLR7 might be therapeutically effective. Their findings are expected to accelerate further development of TLR7 inhibitors for patients with
Hi lupis! 👋🏼 New study demonstrates a direct causal link between an overactive UNC93B1/TLR7 axis and lupus pathogenesis and indicates that blocking overactive TLR7 might be therapeutically effective. Their findings are expected to accelerate further development of TLR7 inhibitors for patients with
Naladog
in
LUPUS UK
4 months ago
Results
Hello I messaged on here recently about my symptoms and was recommended to take a private blood test, which I've done. So I'm surprised that they've all come back normal! I screenshot them but not all together. Think I need to now think it is actually not my thyroid, but rheumatoid after all!
Hello I messaged on here recently about my symptoms and was recommended to take a private blood test, which I've done. So I'm surprised that they've all come back normal! I screenshot them but not all together. Think I need to now think it is actually not my thyroid, but rheumatoid after all!
Flo2021
in
Thyroid UK
4 months ago
Hashimoto advice please
hello, I have had an underactive thyroid and been on Levothyroxine 75mg since 2015. Last November I had a private blood test done as I had been struggling with lots of ‘symptoms’ and wondered if my thyroid could be the cause and it showed I have Hashimoto’s disease which I understand is an autoimmune
hello, I have had an underactive thyroid and been on Levothyroxine 75mg since 2015. Last November I had a private blood test done as I had been struggling with lots of ‘symptoms’ and wondered if my thyroid could be the cause and it showed I have Hashimoto’s disease which I understand is an autoimmune
Philly2748
in
Thyroid UK
4 months ago
lowering prednisolone
I have had pmg since last September and have very gradually lowered my dose from 15mg to 1mg. which I have been on for the last six weeks. I decided to try to go without steroids for the last two days and apart from the usual shoulder ach when getting up, so far so good, I am now worried about getting
I have had pmg since last September and have very gradually lowered my dose from 15mg to 1mg. which I have been on for the last six weeks. I decided to try to go without steroids for the last two days and apart from the usual shoulder ach when getting up, so far so good, I am now worried about getting
Guilluame
in
PMRGCAuk
7 months ago
Lynne
Hi,My name is Lynne and I am new to the Forum and to Asthma! Looking back I have been breathless going up two flights of stairs at home for a while,but another respiratory virus in November left me with fatigue,cough and breathlessness. My G.P started me on inhalers while waiting for a Spiro test.
Hi,My name is Lynne and I am new to the Forum and to Asthma! Looking back I have been breathless going up two flights of stairs at home for a while,but another respiratory virus in November left me with fatigue,cough and breathlessness. My G.P started me on inhalers while waiting for a Spiro test.
Budd1ngart1st
in
Asthma Community Forum
3 months ago
Feeling fed up
I’ve had deranged LFTS on and off for at least 6 years now with Alt going up over 1000. Second time seeing specialist and apart from signs in liver biopsy pointing to AIH the scans don’t seem to show much. Don’t seem to get told much by Specialist and don’t seem to keep me updated. Had a MRCP on October
I’ve had deranged LFTS on and off for at least 6 years now with Alt going up over 1000. Second time seeing specialist and apart from signs in liver biopsy pointing to AIH the scans don’t seem to show much. Don’t seem to get told much by Specialist and don’t seem to keep me updated. Had a MRCP on October
MrMidnight2021
in
British Liver Trust
7 months ago
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