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A question on 'high' dosage
So I'm currently on 150mcg of levo and 30mcg T3 and my latest results were still only 65% and 62% respectively. I've just started HRT so I may well continue to see improvements but I'm curious about my dosing. I'm 6'1" and roughly 65kg so I'm on the cusp of underweight. I know we need what we need
So I'm currently on 150mcg of levo and 30mcg T3 and my latest results were still only 65% and 62% respectively. I've just started HRT so I may well continue to see improvements but I'm curious about my dosing. I'm 6'1" and roughly 65kg so I'm on the cusp of underweight. I know we need what we need
WitchingHour2point0
in
Thyroid UK
6 months ago
Picking
My husband with PD has been picking at his skin. Especially his hands. Dermatologist recommended lotions for dry skin. Neurologist says it’s not due to PD. He thinks he is peeling skin, but I don’t see anything. Seems to me to be more like a habit, like biting nails. Has anyone else had this feeling?
My husband with PD has been picking at his skin. Especially his hands. Dermatologist recommended lotions for dry skin. Neurologist says it’s not due to PD. He thinks he is peeling skin, but I don’t see anything. Seems to me to be more like a habit, like biting nails. Has anyone else had this feeling?
Shirleyam
in
Cure Parkinson's
6 months ago
Modified Citrus Pectin
New study below [1]. Earlier (2021) results [2] - full text. The study was on men with non-metastatic biochemically relapsed PCa. There was no placebo arm. Dr. Isaac Eliaz created PectaSol - Modified Citrus Pectin [P-MCP] thirty years ago. There are 110 PubMed references to it - Eliaz claims
New study below [1]. Earlier (2021) results [2] - full text. The study was on men with non-metastatic biochemically relapsed PCa. There was no placebo arm. Dr. Isaac Eliaz created PectaSol - Modified Citrus Pectin [P-MCP] thirty years ago. There are 110 PubMed references to it - Eliaz claims
pca2004
in
Fight Prostate Cancer
10 months ago
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SIBO!!! But fearing taking antibiotics, especially Neomicyn… I’ve heard of terrible side effects ( tinnitus and hearing loss).
Hello, here is my doctor's report: ''The report of your hydrogen and methane breath test is positive, both for small intestinal bacterial overgrowth as well as excessive methane-producing bacteria in the large bowel. It may be sensible to consider treatment with non-absorbable antibiotics. If you would
Hello, here is my doctor's report: ''The report of your hydrogen and methane breath test is positive, both for small intestinal bacterial overgrowth as well as excessive methane-producing bacteria in the large bowel. It may be sensible to consider treatment with non-absorbable antibiotics. If you would
Clara62
in
IBS Network
6 months ago
Too much or too little fibre?
Hi everyone, sorry I know I post a lot on here.. it just seems to be the only place I can get help! I rang my GP the other day.. quite clearly seeking help and he sent me a link to the nhs IBS website.. and told me not to eat sweeteners. EYE ROLL... My current situation is daily loose stools with gas
Hi everyone, sorry I know I post a lot on here.. it just seems to be the only place I can get help! I rang my GP the other day.. quite clearly seeking help and he sent me a link to the nhs IBS website.. and told me not to eat sweeteners. EYE ROLL... My current situation is daily loose stools with gas
JT1992
in
IBS Network
1 year ago
Why does everyone seem to have permanent tinnitus here?
What is the cause of permanent tinnitus? This is so worrying, as my tinnitus started this month due to ear canal infection. Would this be permanent? I have been prescribed otomize. Would that be helpful?
What is the cause of permanent tinnitus? This is so worrying, as my tinnitus started this month due to ear canal infection. Would this be permanent? I have been prescribed otomize. Would that be helpful?
Kiitty
in
Tinnitus UK
6 months ago
Hi, Everyone
My name is Ali. I am nearly 52 and live on our dairy farm in Pembrokeshire. Had IBS for all of my life, I think, but diagnosed back in early 2000s. It did settle when I moved to West Wales in 2003 and completely changed my lifestyle, only really flaring on stressful journeys. I do get bloating
My name is Ali. I am nearly 52 and live on our dairy farm in Pembrokeshire. Had IBS for all of my life, I think, but diagnosed back in early 2000s. It did settle when I moved to West Wales in 2003 and completely changed my lifestyle, only really flaring on stressful journeys. I do get bloating
MiRiderGirl
in
IBS Network
1 year ago
Interesting Article (please read)
came across this article today and would like to know your thoughts: i was swayed by flashy advertising in the late 1990s featuring medical stars like Professor Lord Winston, who convinced me that omega-3 fish oil supplements were essential for my brain and my heart. Fast forward to today, and
came across this article today and would like to know your thoughts: i was swayed by flashy advertising in the late 1990s featuring medical stars like Professor Lord Winston, who convinced me that omega-3 fish oil supplements were essential for my brain and my heart. Fast forward to today, and
Padayn01
in
AF Association
6 months ago
Newbie 0
Hi, I've recently been diagnosed with Gilbert's syndrome/disease. It was picked up via blood tests. I'm waiting to have a liver scan but the GP hasn't come up with any other plan. My main question at the minute is does anyone suffer with itching. Its not put down as one of the main symptoms but it's
Hi, I've recently been diagnosed with Gilbert's syndrome/disease. It was picked up via blood tests. I'm waiting to have a liver scan but the GP hasn't come up with any other plan. My main question at the minute is does anyone suffer with itching. Its not put down as one of the main symptoms but it's
HomerJSimpson
in
British Liver Trust
6 months ago
EYE HEALTH: RELATIONSHIP OF PMR, PRED & MTX TO GLAUCOMA, CATARACTS, & DRY EYE
Hello everyone. Vacillated on a title for this post. I'll bet I covered it all. I've been on my hard PMR journey for 4+ years. Currently on 4mg Pred daily & 20mg MTX weekly. PMR pain is under control. My eyes have wept for the past 2 yrs; at times, non stop. Eyedrops are the common advice from my Optometrist
Hello everyone. Vacillated on a title for this post. I'll bet I covered it all. I've been on my hard PMR journey for 4+ years. Currently on 4mg Pred daily & 20mg MTX weekly. PMR pain is under control. My eyes have wept for the past 2 yrs; at times, non stop. Eyedrops are the common advice from my Optometrist
DrRon
in
PMRGCAuk
6 months ago
Corneal transplant
Hi all. A very happy Christmas to you all. I apologise if this is not an acceptable question on here as it is not related to RA but it is a great platform to air the question. I am desparately worried about my brother who needs a corneal transplant. Has anyone on here had one or knows of anyone who has
Hi all. A very happy Christmas to you all. I apologise if this is not an acceptable question on here as it is not related to RA but it is a great platform to air the question. I am desparately worried about my brother who needs a corneal transplant. Has anyone on here had one or knows of anyone who has
Sheila_G
in
NRAS
6 months ago
How food additives can perhaps affect us: a chocolate story.
I can eat Galaxy chocolate. No problem, and it doesn't trigger my IBS. The other day I ate a Galaxy Ripple bar instead of the ordinary block chocolate. I thought nothing of it, just thought it would be the same as the block chocolate. But it affected my bowel movements the next day, and there
I can eat Galaxy chocolate. No problem, and it doesn't trigger my IBS. The other day I ate a Galaxy Ripple bar instead of the ordinary block chocolate. I thought nothing of it, just thought it would be the same as the block chocolate. But it affected my bowel movements the next day, and there
Luisa22
in
IBS Network
1 year ago
help :(
I have had symptoms of a UTI since 31st October. I had Nitrofuration twice at the start of all this and things started to settle until I had a bath. I was then given 7 days of trimethoprim- I felt no real difference with this. Dipstick tests never really show infection so 3 urines have been sent to lab
I have had symptoms of a UTI since 31st October. I had Nitrofuration twice at the start of all this and things started to settle until I had a bath. I was then given 7 days of trimethoprim- I felt no real difference with this. Dipstick tests never really show infection so 3 urines have been sent to lab
Kimbad1990
in
Bladder Health UK
6 months ago
GCA or Dry eye pain
Yesterday was the first day both my eyes hurt. I have been having dry eyes and drops are not doing too much. The pain in both eyes feel like pressure or strain pain. I am worried not knowing if it’s just dry eyes or my GCA acting up. Currently taking 10 mg if prednisone since the last GCA temple pain
Yesterday was the first day both my eyes hurt. I have been having dry eyes and drops are not doing too much. The pain in both eyes feel like pressure or strain pain. I am worried not knowing if it’s just dry eyes or my GCA acting up. Currently taking 10 mg if prednisone since the last GCA temple pain
Plains
in
PMRGCAuk
6 months ago
German tara
HI EVERYONE went docter or could be inhalers s bout dry mouth told her it's like sandpaper my tongue abit sore doesn't stop me eating but my taste not good docter says there's nothing I can give you only thing we have is for peaple wh on end life care so was waste off time just have to
HI EVERYONE went docter or could be inhalers s bout dry mouth told her it's like sandpaper my tongue abit sore doesn't stop me eating but my taste not good docter says there's nothing I can give you only thing we have is for peaple wh on end life care so was waste off time just have to
Germantara
in
Lung Conditions Community Forum
6 months ago
Possible relapse, trouble seeing Rheumatologist.
Hi, I have not posted in quite some time. Read other's mostly, and since I have been in remission for 7-8 years I have not had much I could add to conversation. I was diagnosed with GPA in 2015. Put on pred and mycophenolate initially, then two rounds of rituximab. I have been med free since 2016
Hi, I have not posted in quite some time. Read other's mostly, and since I have been in remission for 7-8 years I have not had much I could add to conversation. I was diagnosed with GPA in 2015. Put on pred and mycophenolate initially, then two rounds of rituximab. I have been med free since 2016
lollypocket
in
Vasculitis UK
6 months ago
Pip help
Hi lovely people I have a question i am waiting on a decision for pip and have just found out my Dr has diagnosed me with fibromyalgia amongst other ting do I need to tell pip now This is me not my husband 🫣 Thanks in advance ☺️
Hi lovely people I have a question i am waiting on a decision for pip and have just found out my Dr has diagnosed me with fibromyalgia amongst other ting do I need to tell pip now This is me not my husband 🫣 Thanks in advance ☺️
Suzeinwoody
in
Fibromyalgia Action UK
20 days ago
My Bladder Cancer Update.
My latest flexy cystoscopy showed I had no tumour in my bladder, backing up what was said in Autumn 2023 and that was a complete turn-around. Seems my BCG has worked in as far as there si no tumour growth. I still have cancer cells because I have cancer in situ (CIS) but at moment is low grade. So
My latest flexy cystoscopy showed I had no tumour in my bladder, backing up what was said in Autumn 2023 and that was a complete turn-around. Seems my BCG has worked in as far as there si no tumour growth. I still have cancer cells because I have cancer in situ (CIS) but at moment is low grade. So
Ern007
in
Lung Conditions Community Forum
4 months ago
Bleeding 3 weeks on desogesterel
I have been taking Desogesterel since March and at first it was fine, I still had a monthly bleed on it which was not painful. In July I discussed future conception with a GP who told me that i would be fine coming off the pill and ignored my endo diagnosis because i had it done privately.. I came off
I have been taking Desogesterel since March and at first it was fine, I still had a monthly bleed on it which was not painful. In July I discussed future conception with a GP who told me that i would be fine coming off the pill and ignored my endo diagnosis because i had it done privately.. I came off
Mushroom40
in
Endometriosis UK
6 months ago
Wednesday The 14th.
I promised a painting for the 14 and being a heart shape canvas I could not use the easel. I ruined the picture with my sleeve going in paint on palate and it got onto painting - Ruined. I have done one not as good by painting the canvas black, and painted a picture ok for black canvas, Could not
I promised a painting for the 14 and being a heart shape canvas I could not use the easel. I ruined the picture with my sleeve going in paint on palate and it got onto painting - Ruined. I have done one not as good by painting the canvas black, and painted a picture ok for black canvas, Could not
Ern007
in
Lung Conditions Community Forum
4 months ago
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