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Hashimoto's & Multiple Sclerosis (apologies for two posts in very quick succession!)
Hello - first off, sorry for making two posts in quick succession asking for help! As I mentioned in my first question about an Endo Department, there has been a 'twist' in my Hashi's (I actually have Ord's: autoimmune thyroid disease with no goitre) story... Over the course of several blood tests,
Hello - first off, sorry for making two posts in quick succession asking for help! As I mentioned in my first question about an Endo Department, there has been a 'twist' in my Hashi's (I actually have Ord's: autoimmune thyroid disease with no goitre) story... Over the course of several blood tests,
ERIC107
in
Thyroid UK
5 months ago
Methotrexate
Been on methotrexate 15mg for 16 wks have psoriatic arthritis, rheumatoid arthritis helps my nails n skin but my joint feel worse now was out on another 5 mg from last Monday fell dreadfully n breathless n more pain n my feet and feel my blood vessels all tight n pulling any body else have this
Been on methotrexate 15mg for 16 wks have psoriatic arthritis, rheumatoid arthritis helps my nails n skin but my joint feel worse now was out on another 5 mg from last Monday fell dreadfully n breathless n more pain n my feet and feel my blood vessels all tight n pulling any body else have this
Teddie111
in
NRAS
5 months ago
Update B12 appointment . help needed
Thank you all for your advice . Had an appointment yesterday and despite feeling exhausted dizzy and having some pins and needles in my hand. (NHS website says 2_3months with malabsorption issues.) . I was told they cannot go against local NHS guidance and got to wait for 12 weeks for my B12 jab. I
Thank you all for your advice . Had an appointment yesterday and despite feeling exhausted dizzy and having some pins and needles in my hand. (NHS website says 2_3months with malabsorption issues.) . I was told they cannot go against local NHS guidance and got to wait for 12 weeks for my B12 jab. I
Welshtoffee
in
Pernicious Anaemia Society
5 months ago
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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
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
5 months ago
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
5 months ago
NZ made nutrient rescue.
Facebook keeps recommending this product to me. It’s made in NZ so might give it a shot as todays story was about a guy from NZ who has Parkinson’s and lives here in Christchurch! https://nutrientrescue.nz/ingredients “ When I was diagnosed 10 years ago, I was referred to a specialist in Oregon. Dr
Facebook keeps recommending this product to me. It’s made in NZ so might give it a shot as todays story was about a guy from NZ who has Parkinson’s and lives here in Christchurch! https://nutrientrescue.nz/ingredients “ When I was diagnosed 10 years ago, I was referred to a specialist in Oregon. Dr
LAJ12345
in
Cure Parkinson's
8 months ago
Good news
Evening ..some if you may know I've been on this site for a couple of years..I was on and off a drinker wine etc ..normal for spain.Anyway 2.5 years ago during the pandemic I knew that I wasn't right had a blood test ..not good . Fast tracked specialist apt . Different tests set up ..fatty liver diagnosed
Evening ..some if you may know I've been on this site for a couple of years..I was on and off a drinker wine etc ..normal for spain.Anyway 2.5 years ago during the pandemic I knew that I wasn't right had a blood test ..not good . Fast tracked specialist apt . Different tests set up ..fatty liver diagnosed
Spiff
in
British Liver Trust
8 months ago
Remission now flare.
Hi all, Not been on here for a while. I have sero neg rheumatoid arthritis, diagnosed 2010. Have been luckily in remission for a long time probably 10 years anyway seem to be having a flare, pain in shoulder, both knees and one hip plus pain in jaw. But bloods show no inflammation, not sure what is going
Hi all, Not been on here for a while. I have sero neg rheumatoid arthritis, diagnosed 2010. Have been luckily in remission for a long time probably 10 years anyway seem to be having a flare, pain in shoulder, both knees and one hip plus pain in jaw. But bloods show no inflammation, not sure what is going
pool0009
in
NRAS
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
5 months ago
Hello
Hi I'm under going tests for lupus I have symptoms, I'm just looking for more information at the moment
Hi I'm under going tests for lupus I have symptoms, I'm just looking for more information at the moment
Tray68
in
LUPUS UK
5 months ago
switching to a carnivore diet has put my PMR into total remission
I know the subject may be viewed as sensational or just plain wrong, but that is what I have concluded. At the time I was diagnosed with PMR, I already had diagnoses of psoriatic arthritis and fibromyalgia. My PMR started in 2019, about 8 months prior to covid. I was put on prednisone and experienced
I know the subject may be viewed as sensational or just plain wrong, but that is what I have concluded. At the time I was diagnosed with PMR, I already had diagnoses of psoriatic arthritis and fibromyalgia. My PMR started in 2019, about 8 months prior to covid. I was put on prednisone and experienced
benhemp
in
PMRGCAuk
5 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
5 months ago
Beta blockers
I'm 68, female with NASH/ Cirrhosis which is compensated. I have recently been prescribed 1.25 mg of Bisoprolol Fumarate (beta blocker) but I'm so anxious about taking it as my GP seemed unsure about any effect on my liver. I was wondering if any members take beta blockers with no ill effects? I'm also
I'm 68, female with NASH/ Cirrhosis which is compensated. I have recently been prescribed 1.25 mg of Bisoprolol Fumarate (beta blocker) but I'm so anxious about taking it as my GP seemed unsure about any effect on my liver. I was wondering if any members take beta blockers with no ill effects? I'm also
Robert1220
in
British Liver Trust
2 months ago
lupus
hi everyone I’m new on here. Im currently waiting for a lupus diagnosis. I’m due to go in to hospital tomorrow for a skin biopsy on my face. Has any one ever had one ? Also do you think my rash looks like a lupus rash ? Thanks everyone.
hi everyone I’m new on here. Im currently waiting for a lupus diagnosis. I’m due to go in to hospital tomorrow for a skin biopsy on my face. Has any one ever had one ? Also do you think my rash looks like a lupus rash ? Thanks everyone.
Pea_m
in
LUPUS UK
5 months ago
Lupie Diary - International 4+Syamsi Dhuha Foundation
This FREE Application is developed to help people with lupus (and also people with other diseases) to record and monitor her/his medication, treatment received from her/his doctor, or other consultation with medical professionals (such as pharmacist). Personal medical record will help both patient and
This FREE Application is developed to help people with lupus (and also people with other diseases) to record and monitor her/his medication, treatment received from her/his doctor, or other consultation with medical professionals (such as pharmacist). Personal medical record will help both patient and
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
5 months ago
Low Volume Low PSA Metastatic PC.
When my Oncologist refers to Low volume, Low PSA Oglimetastic PC, what is he saying about my disease? I’ve been oo Abiraterone followed by Xtandi with Lupron every 3 months and Zometa every 6.
When my Oncologist refers to Low volume, Low PSA Oglimetastic PC, what is he saying about my disease? I’ve been oo Abiraterone followed by Xtandi with Lupron every 3 months and Zometa every 6.
NDJIM
in
Advanced Prostate Cancer
8 months ago
1st patient doesd in Phase 2 trial testing vaccine for Parkinson's
------------ The first patient has been dosed in a Phase 2 clinical trial testing AC Immune’s ACI-7104.056, an investigational vaccine targeting toxic alpha-synuclein forms to [u][i]
prevent nerve cell degeneration in Parkinson’s disease.
[/i][/u] AC Immune expects to complete the enrollment
------------ The first patient has been dosed in a Phase 2 clinical trial testing AC Immune’s ACI-7104.056, an investigational vaccine targeting toxic alpha-synuclein forms to [u][i]
prevent nerve cell degeneration in Parkinson’s disease.
[/i][/u] AC Immune expects to complete the enrollment
PDWarrior1900
in
Cure Parkinson's
8 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
5 months ago
20 years of drinking and want to stop but don’t dare’nt get a liver test.!!
iv been drinking beer for 20 year's, 4 to 5 pints most evenings at home after work. I know I must have damaged my liver in some way, I’m not stupid.! But my problem is that I dare’nt go for a liver function test as I also suffer with heath anxiety which doesn’t help ? Not that anyone one has asked me
iv been drinking beer for 20 year's, 4 to 5 pints most evenings at home after work. I know I must have damaged my liver in some way, I’m not stupid.! But my problem is that I dare’nt go for a liver function test as I also suffer with heath anxiety which doesn’t help ? Not that anyone one has asked me
Jetcat
in
British Liver Trust
8 months ago
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