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Interstitial lung disease (ILD)
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coeliac safe Levo?
I have been taking levo for five years. 6 months into this I was diagnosed with coeliac disease (after my GP accused me of not taking my meds as my bloods kept coming back with no change and I was still very unwell). I asked my pharmacist at the drs to find me a gluten free levo tablet. They said TEVA
I have been taking levo for five years. 6 months into this I was diagnosed with coeliac disease (after my GP accused me of not taking my meds as my bloods kept coming back with no change and I was still very unwell). I asked my pharmacist at the drs to find me a gluten free levo tablet. They said TEVA
Coeliacmama
in
Thyroid UK
2 months ago
Stills disease or other arthritis pain
Adult onset Stills disease diagnosed aged 17 in 1979 now 62 and not on RA drugs just pain relief and self management by living within the boundaries of what the condition allows. 2023 brought stress and may be the cause of worsening joint pain and new symptoms possible down to autoimmune thyroiditis
Adult onset Stills disease diagnosed aged 17 in 1979 now 62 and not on RA drugs just pain relief and self management by living within the boundaries of what the condition allows. 2023 brought stress and may be the cause of worsening joint pain and new symptoms possible down to autoimmune thyroiditis
Stills
in
NRAS
2 months ago
low cortisol
I’ve been treated for hypothyroidism for 20 years, currently on 100/125 Levothyroxine. I’ve always remained symptomatic GP have fobbed me off..the usual CFS you’re depressed.. I’ve had to fight to see and endocrinologist NHS who was very uninterested.. However I had some blood test this am and the
I’ve been treated for hypothyroidism for 20 years, currently on 100/125 Levothyroxine. I’ve always remained symptomatic GP have fobbed me off..the usual CFS you’re depressed.. I’ve had to fight to see and endocrinologist NHS who was very uninterested.. However I had some blood test this am and the
JadeFox
in
Thyroid UK
6 months ago
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Can pernicious anaemia be caused by long term use of lansoprazole?
Hello everyone, I am a lady of 67. Ive been taking lansoprazole for years. Then I began to feel ill with various symptoms the doctor was not interested in or would virtually say I was a hypocondriac. I nagged and got sent to a consultant who said I had neurological problems caused by fibromylgia and
Hello everyone, I am a lady of 67. Ive been taking lansoprazole for years. Then I began to feel ill with various symptoms the doctor was not interested in or would virtually say I was a hypocondriac. I nagged and got sent to a consultant who said I had neurological problems caused by fibromylgia and
wiserlady
in
Pernicious Anaemia Society
2 months ago
LaRue44
My husband has metastatic prostate cancer. We went through all the treatments including 5 pluvicto treatments. Even though his scan shows improvement in some areas it continues to spread. Maybe this is due to no meds such as Xtandi to stop the spread. I'm trying to get more information by reading people's
My husband has metastatic prostate cancer. We went through all the treatments including 5 pluvicto treatments. Even though his scan shows improvement in some areas it continues to spread. Maybe this is due to no meds such as Xtandi to stop the spread. I'm trying to get more information by reading people's
LaRue44
in
Advanced Prostate Cancer
6 months ago
Advice on blood results please!
I had been waiting to see an endocrinologist for 7 months after a low cortisol result in August last year. I saw them last week and they said there was nothing wrong with me according to tests and it was probably medication related. Please could I use the knowledge of this forum to look at my blood results
I had been waiting to see an endocrinologist for 7 months after a low cortisol result in August last year. I saw them last week and they said there was nothing wrong with me according to tests and it was probably medication related. Please could I use the knowledge of this forum to look at my blood results
Tigghilly
in
Thyroid UK
6 months ago
Why am I being tested for Hep B?
I have had Budd Chiari for nearly 14 years, I have a shunt and luckily everything has been going fine since then. I have an app every 6 months for an ultrasound scan, then my outpatient app and bloods taken. I had an appointment yesterday and like normal I was in and out quite quickly as the scan showed
I have had Budd Chiari for nearly 14 years, I have a shunt and luckily everything has been going fine since then. I have an app every 6 months for an ultrasound scan, then my outpatient app and bloods taken. I had an appointment yesterday and like normal I was in and out quite quickly as the scan showed
Holsb
in
British Liver Trust
6 months ago
chronic pain interview
In case these might be of use, here’s a very good interview with Kirsty Young (who has fibromyalgia and rheumatoid arthritis) to coincide with the International Association for the Study of Pain World Congress in Amsterdam. And a link to a useful site on living with chronic pain. The interview is only
In case these might be of use, here’s a very good interview with Kirsty Young (who has fibromyalgia and rheumatoid arthritis) to coincide with the International Association for the Study of Pain World Congress in Amsterdam. And a link to a useful site on living with chronic pain. The interview is only
Sibelius5
in
PMRGCAuk
2 months ago
Is this real? Prevent & Reverse Autoimmune disease
Have you read, or do you know anyone who has, this book: 'Top 20 Foods to Help Prevent & Reverse Autoimmune Disease' ? It's available free as a download from Eric, Wisdom for Life if you enter your name and email address. It sounds too good to be true but perhaps you know better?
Have you read, or do you know anyone who has, this book: 'Top 20 Foods to Help Prevent & Reverse Autoimmune Disease' ? It's available free as a download from Eric, Wisdom for Life if you enter your name and email address. It sounds too good to be true but perhaps you know better?
thyr01d
in
Thyroid UK
2 months ago
Help in understanding drugs in Parkinsons
I've recently been diagnosed with Parkinsons and have been prescribed LevaDopa -1/2 tablet (125mg) 4 times per day. I understand that there are complimentary drugs such MAO-B Inhibitors (such as Selegiline, Rasagiline, and Safinamide) I've done some cursory reseach which indicates that MAO-B inhibitors
I've recently been diagnosed with Parkinsons and have been prescribed LevaDopa -1/2 tablet (125mg) 4 times per day. I understand that there are complimentary drugs such MAO-B Inhibitors (such as Selegiline, Rasagiline, and Safinamide) I've done some cursory reseach which indicates that MAO-B inhibitors
Mezmerric
in
Cure Parkinson's
6 months ago
New Drug May Repair Myelin
I received an article about clinical trials at the University of California San Francisco on a drug that can repair myelin. It uses venom from the green mamba snake. I'm wondering if the side effects include developing a lissssssp? 🤣 It's a long way from being available, but it sounds interesting
I received an article about clinical trials at the University of California San Francisco on a drug that can repair myelin. It uses venom from the green mamba snake. I'm wondering if the side effects include developing a lissssssp? 🤣 It's a long way from being available, but it sounds interesting
NanciG
in
My MSAA Community
2 months ago
belimumab Infusions
Hi all, I’m suppose to be starting belimumab infusions next week, however there is a shortage in the medication so I’m just waiting for a new date I’m on all the usual medication for lupus but nothing seems to be working, I have had rituximab last year and the first lot lasted 5 months which was great
Hi all, I’m suppose to be starting belimumab infusions next week, however there is a shortage in the medication so I’m just waiting for a new date I’m on all the usual medication for lupus but nothing seems to be working, I have had rituximab last year and the first lot lasted 5 months which was great
MaryannM
in
LUPUS UK
6 months ago
L-Theanine (not to be confused with Theanine B1)
Does anybody have any experience of supplementing with L-Theanine, (or drinking Green Tea, which contains L-Theanine) to help with sleep or any symptoms of Parkinsons? This video piqued by interest as it indicates that L-Theanine reduces the excitatory signals of Glutamate in the brain. https://www.youtube.com
Does anybody have any experience of supplementing with L-Theanine, (or drinking Green Tea, which contains L-Theanine) to help with sleep or any symptoms of Parkinsons? This video piqued by interest as it indicates that L-Theanine reduces the excitatory signals of Glutamate in the brain. https://www.youtube.com
Mezmerric
in
Cure Parkinson's
6 months ago
US FDA declines to approve Supernus' Parkinson's combination again
The company plans to address the FDA's concerns and resubmit its application for the product, which aims to treat so-called "off episodes", which affects nearly all patients of Parkinson's, heightening symptoms such as tremors and difficulty in walking, as medication wears off. https://www.reuters.com
The company plans to address the FDA's concerns and resubmit its application for the product, which aims to treat so-called "off episodes", which affects nearly all patients of Parkinson's, heightening symptoms such as tremors and difficulty in walking, as medication wears off. https://www.reuters.com
Farooqji
in
Cure Parkinson's
6 months ago
Joint pain very common in lupus, affects patients’ life quality: Study
Joint pain very common in lupus, affects patients’ life quality: Study SLE marked by ache, discomfort, numbness in hands, wrists and knees by Patricia Inacio, PhD The vast majority of people with systemic lupus erythematosus (SLE) experience musculoskeletal symptoms, marked by pain, ache, discomfort
Joint pain very common in lupus, affects patients’ life quality: Study SLE marked by ache, discomfort, numbness in hands, wrists and knees by Patricia Inacio, PhD The vast majority of people with systemic lupus erythematosus (SLE) experience musculoskeletal symptoms, marked by pain, ache, discomfort
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
2 months ago
Protein discovery could help solve prostate cancer drug resistance Date:January 22, 2024 Source:Washington State University
I found this information while researching my husband's PSA rising issues. Found it interesting and want to share. Click on link to read the entire article https://www.sciencedaily.com/ Protein discovery could help solve prostate cancer drug resistance Date: January 22, 2024 Source: Washington
I found this information while researching my husband's PSA rising issues. Found it interesting and want to share. Click on link to read the entire article https://www.sciencedaily.com/ Protein discovery could help solve prostate cancer drug resistance Date: January 22, 2024 Source: Washington
MsHope
in
Advanced Prostate Cancer
6 months ago
child low cortisol
Hi, I would be very grateful for any advice etc on the following. My 9 year old daughter has had a blood test come back with borderline low cortisone ( that’s what the doctor has described it as). She is waiting for a test but apparently it can take months. The doctor has mentioned Addisons and under
Hi, I would be very grateful for any advice etc on the following. My 9 year old daughter has had a blood test come back with borderline low cortisone ( that’s what the doctor has described it as). She is waiting for a test but apparently it can take months. The doctor has mentioned Addisons and under
Karatesarah
in
Thyroid UK
6 months ago
Fibroscan result waiting time?
Please can somebody tell me how long it takes to receive results for a fibroscan? I started this journey in November 2023 after asking for a general check-up at my GP surgery because of some non-liver related issues. I had no awareness at all that my liver could be damaged. After a few rounds of blood
Please can somebody tell me how long it takes to receive results for a fibroscan? I started this journey in November 2023 after asking for a general check-up at my GP surgery because of some non-liver related issues. I had no awareness at all that my liver could be damaged. After a few rounds of blood
Trotter2024
in
British Liver Trust
6 months ago
Hashimoto's and gut
Hi there, I have really sluggish digestion that's been getting worse and now I realise I have Hashi's it's starting to make sense. I've also discovered from this forum that we often have low stomach acidity and I'd like to understand more about this...how do we find out if that's definitely something
Hi there, I have really sluggish digestion that's been getting worse and now I realise I have Hashi's it's starting to make sense. I've also discovered from this forum that we often have low stomach acidity and I'd like to understand more about this...how do we find out if that's definitely something
LifeintheMed
in
Thyroid UK
2 months ago
feeling unwell
hello I have underactive thyroid , but now it is overactive I’ve been told , since reducing my meds , I have had such an awful feeling oh painful sensitive throat , wierd flutter with tounge and very sensitive gums , I have hashimotos and have nodules, keep getting hot and cold , any advise on what I
hello I have underactive thyroid , but now it is overactive I’ve been told , since reducing my meds , I have had such an awful feeling oh painful sensitive throat , wierd flutter with tounge and very sensitive gums , I have hashimotos and have nodules, keep getting hot and cold , any advise on what I
Prosecco1997
in
Thyroid UK
2 months ago
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