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š§¬UNC93B1 New genetic findings open up perspectives for future therapeutic approaches in Lupus
Hi lupis! šš¼ 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! šš¼ 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
5 months ago
Donepezil as an aid for PSP
Hi all you good people, A couple of weeks ago a fellow traveller here wrote about her husband with PSP that as his cognition and swallowing declined, his Doctor prescribed Donepezil. Originally, he was on 10 mg of Donepezil which improved his swallowing, alertness and cognition. Two years later when
Hi all you good people, A couple of weeks ago a fellow traveller here wrote about her husband with PSP that as his cognition and swallowing declined, his Doctor prescribed Donepezil. Originally, he was on 10 mg of Donepezil which improved his swallowing, alertness and cognition. Two years later when
Richard33
in
PSP Association
8 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
5 months ago
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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 āsymptomsā and wondered if my thyroid could be the cause and it showed I have Hashimotoās 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 āsymptomsā and wondered if my thyroid could be the cause and it showed I have Hashimotoās disease which I understand is an autoimmune
Philly2748
in
Thyroid UK
5 months ago
B6 - advice
Iām confused about B6. is the advice with Co-Careldopa not to take, at all. Or to take after Co-Careldopa has been absorbed. my recent blood tests showed me deficient in B6. thanks
Iām confused about B6. is the advice with Co-Careldopa not to take, at all. Or to take after Co-Careldopa has been absorbed. my recent blood tests showed me deficient in B6. thanks
Nb11
in
Cure Parkinson's
8 months ago
***NEW SUPPORT GROUPS!!***
[u][i]
ARE YOU INTERESTED IN GETTING SOME SUPPORT? - NEW GROUPS STARTING IN JULY
[/i][/u] [i]
GENETIC MUTATION LUNG CANCER - We are looking for people to join our Genetic Mutation Specific support group. This will be our third group and is a great way to get information and meet people in a similar
[u][i]
ARE YOU INTERESTED IN GETTING SOME SUPPORT? - NEW GROUPS STARTING IN JULY
[/i][/u] [i]
GENETIC MUTATION LUNG CANCER - We are looking for people to join our Genetic Mutation Specific support group. This will be our third group and is a great way to get information and meet people in a similar
ConnectRoyCastle
Administrator
in
The Roy Castle Lung Cancer Foundation
1 year ago
Adrenal cortisol expertise needed
Hi! I was diagnosed with adrenal fatigue / low cortisol 10-plus years ago and take 10 mg of hydrocortisone (tablet) in the morning and at noon. I just received results of diurnal saliva cortisol test and am surprised/confused at the results. Does this group help with adrenal issues, or is there a different
Hi! I was diagnosed with adrenal fatigue / low cortisol 10-plus years ago and take 10 mg of hydrocortisone (tablet) in the morning and at noon. I just received results of diurnal saliva cortisol test and am surprised/confused at the results. Does this group help with adrenal issues, or is there a different
Rileyfloof
in
Thyroid UK
8 months ago
Wheat Diet may Exacerbate Multiple Sclerosis Severity
Wheat diet may exacerbate multiple sclerosis severity, research finds - Jan 2024
by Natkritta HĆ¼ppe, UniversitƤtsmedizin der Johannes Gutenberg-UniversitƤt Mainz https://medicalxpress.com/news/2024-01-wheat-diet-exacerbate-multiple-sclerosis.html
Highlights:
A research team at the University
Wheat diet may exacerbate multiple sclerosis severity, research finds - Jan 2024
by Natkritta HĆ¼ppe, UniversitƤtsmedizin der Johannes Gutenberg-UniversitƤt Mainz https://medicalxpress.com/news/2024-01-wheat-diet-exacerbate-multiple-sclerosis.html
Highlights:
A research team at the University
Bolt_Upright
in
Cure Parkinson's
5 months ago
KardiaMobile and Apple Watch
I recently wore a heart monitor for two weeks. While on the monitor both my CardioMobile and my Apple Watch picked up several episodes of Afib, PACs, and Etopics. The results from the heart monitor test showed I had some episodes of PACs but otherwise the test was normal. It never picked one single
I recently wore a heart monitor for two weeks. While on the monitor both my CardioMobile and my Apple Watch picked up several episodes of Afib, PACs, and Etopics. The results from the heart monitor test showed I had some episodes of PACs but otherwise the test was normal. It never picked one single
Debjimmay
in
Atrial Fibrillation Support
4 months ago
Zytiga - Lupron
I was on Zytiga ( now Abi) with lup for several years and it kept my PSA to undetectable. I am now on 0rg0vyx instead of lup and my PSA remains undetectable after 6 years. Sode effects have been tolerable EXCEPT the I developed osteoporosis of the spin and now have multiple collapsed vertebrae and
I was on Zytiga ( now Abi) with lup for several years and it kept my PSA to undetectable. I am now on 0rg0vyx instead of lup and my PSA remains undetectable after 6 years. Sode effects have been tolerable EXCEPT the I developed osteoporosis of the spin and now have multiple collapsed vertebrae and
Schnab
in
Advanced Prostate Cancer
8 months ago
PAS blog - Dr Chandy
Hi All, Just posting this in case not posted already. https://pernicious-anaemia-society.org/pernicious-anaemia/dr-joseph-chandy-kayyalackom-a-reflection/
Hi All, Just posting this in case not posted already. https://pernicious-anaemia-society.org/pernicious-anaemia/dr-joseph-chandy-kayyalackom-a-reflection/
Sleepybunny
in
Pernicious Anaemia Society
5 months ago
I am so confused about bisoprolol...please help.
Hi i was prescibed 1.25 dose of bisoprolol after being admitted to a+e on 7 Feb. I have known Afib, not permanent afib. Over past year i have been told by EP, top thorasic surgeon, and several cardiologists that anti arrthymia meds and rate control meds are not an option open for me to be presribed this
Hi i was prescibed 1.25 dose of bisoprolol after being admitted to a+e on 7 Feb. I have known Afib, not permanent afib. Over past year i have been told by EP, top thorasic surgeon, and several cardiologists that anti arrthymia meds and rate control meds are not an option open for me to be presribed this
DizzyD
in
Atrial Fibrillation Support
4 months ago
Post Ablation advice please??
I underwent an RFA for Afib and Aflutter in late last year (coming up on end of blanking period) for paroxysmal afib/flutter first diagnosed 5 years ago. I have been on Flecainide and Diltiazem for several years. Prior to the ablation, I would experience episodes about 2x a week for about 12-24 hours
I underwent an RFA for Afib and Aflutter in late last year (coming up on end of blanking period) for paroxysmal afib/flutter first diagnosed 5 years ago. I have been on Flecainide and Diltiazem for several years. Prior to the ablation, I would experience episodes about 2x a week for about 12-24 hours
Jonboggs
in
AF Association
4 months ago
OK bloods...Still plateauing??
Hi again šAbout 7 weeks ago I increased my levo from 50mcg to 75mcg after discussing here. Initially, revved up again. Happy days- more energy, lost a small bit of weight, mood improved etc. I have started slipping back again and thought I'd get my bloods done again before I do anymore 'tinkering'.
Hi again šAbout 7 weeks ago I increased my levo from 50mcg to 75mcg after discussing here. Initially, revved up again. Happy days- more energy, lost a small bit of weight, mood improved etc. I have started slipping back again and thought I'd get my bloods done again before I do anymore 'tinkering'.
Caffeinefreezone
in
Thyroid UK
8 months ago
blue horizon premium gold
hi would this test also provide results to determine autoimmune conditions such as Gravesā disease? Thanks matty
hi would this test also provide results to determine autoimmune conditions such as Gravesā disease? Thanks matty
Mattydonald1984
in
Thyroid UK
5 months ago
Low hemoglobin
I started hemodialysis in Aug with an emergency chest catheter. I had 2 units of blood as my hemoglobin was low while in hospital. Then in hospital again in September and another 2 units of blood. Got my labs today and hemoglobin was 6.8 so they gave me Mircera and iron. When I did PD I got Mircera
I started hemodialysis in Aug with an emergency chest catheter. I had 2 units of blood as my hemoglobin was low while in hospital. Then in hospital again in September and another 2 units of blood. Got my labs today and hemoglobin was 6.8 so they gave me Mircera and iron. When I did PD I got Mircera
horsie63
in
Kidney Dialysis
8 months ago
Post 2nd Ablation Recovery
Hi All, I am 11-days in to my recovery from my second ablation procedure and wanted to check if anyone else has/had the symptoms I am suffering from; as I didn't have them after the first ablation procedure. I have two key ones as follows; 1. After walking for a few minutes and then standing still
Hi All, I am 11-days in to my recovery from my second ablation procedure and wanted to check if anyone else has/had the symptoms I am suffering from; as I didn't have them after the first ablation procedure. I have two key ones as follows; 1. After walking for a few minutes and then standing still
trevs7
in
AF Association
4 months ago
No Afib after all
Hi everyone, well i finally had my cardio phone appointment after a 7 month wait since the GP 24 holter showed suspected PAF. (Only symptom really was a prolonged drop in blood pressure) Apparently i do not have AF after all. I should add i also had a 72 hour holter monitor from cardiology. He did say
Hi everyone, well i finally had my cardio phone appointment after a 7 month wait since the GP 24 holter showed suspected PAF. (Only symptom really was a prolonged drop in blood pressure) Apparently i do not have AF after all. I should add i also had a 72 hour holter monitor from cardiology. He did say
Tropicaltaurus
in
AF Association
4 months ago
WHY WHY WHY
Suddenly my afib is visiting me a lot more frequently ā¦ it used to be every six months ā¦ now itās every three weeks but it only lasts an hour or so and it converts to nsr. Today it happened when l returned from the gym and l was carrying very heavy bolders to put into a plant that keeps falling over
Suddenly my afib is visiting me a lot more frequently ā¦ it used to be every six months ā¦ now itās every three weeks but it only lasts an hour or so and it converts to nsr. Today it happened when l returned from the gym and l was carrying very heavy bolders to put into a plant that keeps falling over
Janith
in
Atrial Fibrillation Support
4 months ago
Just diagnosed with autoimmune atrophic gastritis with intestinal metaplasia
I assume this is the root cause of my pernicious anemia? I have an appointment this week to discuss with GI, but want to go into the appointment educated. Does anyone else have this? Any treatment for this? Iām already on EOD (for last two weeks) B12 shots and multivitamins. Thanks in advance for your
I assume this is the root cause of my pernicious anemia? I have an appointment this week to discuss with GI, but want to go into the appointment educated. Does anyone else have this? Any treatment for this? Iām already on EOD (for last two weeks) B12 shots and multivitamins. Thanks in advance for your
ReallyWondering
in
Pernicious Anaemia Society
5 months ago
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