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help with results please
I’d be grateful if anyone could help with results please. I’m on combined therapy 50mg T4 and 35mg T3 TFT 0.02 (0.35-4.94) FT3 4.5 (2.4-6.00) FT4 8.1 (9.00-19.00) B12 433 (187-883) Vit D 126.1 >50 Thank you :)
I’d be grateful if anyone could help with results please. I’m on combined therapy 50mg T4 and 35mg T3 TFT 0.02 (0.35-4.94) FT3 4.5 (2.4-6.00) FT4 8.1 (9.00-19.00) B12 433 (187-883) Vit D 126.1 >50 Thank you :)
Bollieforme
in
Thyroid UK
4 months ago
Half moons on fingers
Hey guys, I have an underactive thyroid and know the importance of getting vitamin levela checked Is it true that lack of or small half moons can be a sign of deficiencies? Just took a photo or my fingers, what do people think? If zoomed in, can just about see half moon on some
Hey guys, I have an underactive thyroid and know the importance of getting vitamin levela checked Is it true that lack of or small half moons can be a sign of deficiencies? Just took a photo or my fingers, what do people think? If zoomed in, can just about see half moon on some
yewotc23
in
Thyroid UK
5 months ago
Tired weak hips when walking - is it still Pmr
Hi, I'm feeling despondent as it seems that I can walk less and less and I don't know what's wrong.I've been on 1mg, trying to get off for over a year. I have no pain except when I do sustained walking. It kicks in after about 3 minutes. Tired, aching hips and lower back and I have to stop. I've got
Hi, I'm feeling despondent as it seems that I can walk less and less and I don't know what's wrong.I've been on 1mg, trying to get off for over a year. I have no pain except when I do sustained walking. It kicks in after about 3 minutes. Tired, aching hips and lower back and I have to stop. I've got
Blossom20
in
PMRGCAuk
4 months ago
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Diabetic and Eye Damage
I have been insulin dependant diabetic for 40 years, which has been the cause of my eye conditions. I was one of the first patients my consultant gave eye injection, I've had three steroid implants, lots of Lazer and eye injections. Last year I had a sever bleed at the back of the eye resulting in
I have been insulin dependant diabetic for 40 years, which has been the cause of my eye conditions. I was one of the first patients my consultant gave eye injection, I've had three steroid implants, lots of Lazer and eye injections. Last year I had a sever bleed at the back of the eye resulting in
123charl
in
Macular Society
4 months ago
Headaches!
Hi everyone.....I'm started my PMR journey middle of January so have only been on Prednisolone for 6 weeks... I started on 20mg and now on 10mg I did up dosage for 2 weeks so was taking 12mg because I felt poorly... But my question is I've had a headache almost constantly for weeks....is it the press
Hi everyone.....I'm started my PMR journey middle of January so have only been on Prednisolone for 6 weeks... I started on 20mg and now on 10mg I did up dosage for 2 weeks so was taking 12mg because I felt poorly... But my question is I've had a headache almost constantly for weeks....is it the press
Tescohednesford
in
PMRGCAuk
4 months ago
Advice needed on thyroxine management
I am hoping someone can advise me about my thyroxine dose. Here's a little background: In September 2023, I was underweight and having trouble gaining weight and suffering from anxiety. I had been on 75mcg of levothyroxine daily for an underactive thyroid. I had recently developed pins and needles
I am hoping someone can advise me about my thyroxine dose. Here's a little background: In September 2023, I was underweight and having trouble gaining weight and suffering from anxiety. I had been on 75mcg of levothyroxine daily for an underactive thyroid. I had recently developed pins and needles
SarrahMay
in
Thyroid UK
5 months ago
Prednisone for treatment of AIG
I've just been started on Prednisone or Prednisolone, immunosuppressant steroids, for treatment of Autoimmune Gastritis/autoimmune PA. This has recently, within the last few years been shown to possibly heal AIG, although not entirely cure. It is also used to prevention immune system rejection of organ
I've just been started on Prednisone or Prednisolone, immunosuppressant steroids, for treatment of Autoimmune Gastritis/autoimmune PA. This has recently, within the last few years been shown to possibly heal AIG, although not entirely cure. It is also used to prevention immune system rejection of organ
Rexz
in
Pernicious Anaemia Society
5 months ago
Blood test
Had both Covid and flu jabs yesterday. Lipase blood test due today. I've been searching to see if it's wise. Leave it 48 hours is all I can see after a long search. Any advice if you've been in that position. I didn't do my weekly Benipali jab yesterday . My RA is in remission but sadly attacked my Pancreas
Had both Covid and flu jabs yesterday. Lipase blood test due today. I've been searching to see if it's wise. Leave it 48 hours is all I can see after a long search. Any advice if you've been in that position. I didn't do my weekly Benipali jab yesterday . My RA is in remission but sadly attacked my Pancreas
Jackie1947
in
NRAS
9 months ago
Berberine and iron?
Hi, So glad to have found this wonderful forum! I am a 74 year female who recently started taking pregabalin for RLS. I just got back my ferritin level and it is 12. I will order some iron and would like to know how many mg is a good dose. Also, I started taking niacin 500mg daily for my cholesterol
Hi, So glad to have found this wonderful forum! I am a 74 year female who recently started taking pregabalin for RLS. I just got back my ferritin level and it is 12. I will order some iron and would like to know how many mg is a good dose. Also, I started taking niacin 500mg daily for my cholesterol
glorious-granny
in
Restless Legs Syndrome
4 months ago
Lupus flare
Hi has anyone experience a lupus flare which was tiggered by a suspected infection? Ended up in hospital but they couldnt detect where the infection / virus was dispite full blood tests, urine tests as well as blood and urine culuture tests. Pretty scary.Thanks
Hi has anyone experience a lupus flare which was tiggered by a suspected infection? Ended up in hospital but they couldnt detect where the infection / virus was dispite full blood tests, urine tests as well as blood and urine culuture tests. Pretty scary.Thanks
Flows
in
LUPUS UK
5 months ago
sulfasalazine side effects
Hi. I am on sulfasalazine for mixed connective tissue disease (similar to rheumatoid arthritis and lupus), which I started taking again after many years of my disease being in remission. I was initially on sulfasalazine 10 years ago and it is a horrid medication. Was, and am again, terribly dizzy
Hi. I am on sulfasalazine for mixed connective tissue disease (similar to rheumatoid arthritis and lupus), which I started taking again after many years of my disease being in remission. I was initially on sulfasalazine 10 years ago and it is a horrid medication. Was, and am again, terribly dizzy
girldoc
in
NRAS
5 months ago
New here 🤗
Hi everyone, I’m looking for any information about bloods and Thyroid please. I was diagnosed in 2017 with chronic pain, chronic fatigue and osteoarthritis. I have tried all pain medications the NHS has, and nothing touches the pain. I have had horrendous pain in my feet, left one for over a year,
Hi everyone, I’m looking for any information about bloods and Thyroid please. I was diagnosed in 2017 with chronic pain, chronic fatigue and osteoarthritis. I have tried all pain medications the NHS has, and nothing touches the pain. I have had horrendous pain in my feet, left one for over a year,
Pammygtf
in
Thyroid UK
5 months ago
updated journey
I’m getting so frustrated with this underactive thyroid. My only symptom before I was diagnosed again was unexplained weight gain. I had put on half a stone but hadn’t changed any habits. After starting on levothyroxine I put on another 2 stone. This may have been made worse due to all my joints seizing
I’m getting so frustrated with this underactive thyroid. My only symptom before I was diagnosed again was unexplained weight gain. I had put on half a stone but hadn’t changed any habits. After starting on levothyroxine I put on another 2 stone. This may have been made worse due to all my joints seizing
ScriptMaz
in
Thyroid UK
5 months ago
Tapering with a high ESR Reading?
My GP rang me yesterday because my ESR reading was 48 in a range of 1-30. He suggested I should increase the Pred. Because my cataract operation was cancelled for a fourth time yesterday, I dropped to 7 mg yesterday after being told, from 31 days on 7.5mg. I have read that ESR could denote
My GP rang me yesterday because my ESR reading was 48 in a range of 1-30. He suggested I should increase the Pred. Because my cataract operation was cancelled for a fourth time yesterday, I dropped to 7 mg yesterday after being told, from 31 days on 7.5mg. I have read that ESR could denote
Motida
in
PMRGCAuk
4 months ago
frustrated and anxious re appt
just feel this Is a safe space to have a rant was diagnosed beginning of October with NTG ( quite a lot of damage already , nerve damage, some peripheral vision loss ) Started on medication and was due to have a follow up appt after. 2 months ( so should have been December) However the hospital
just feel this Is a safe space to have a rant was diagnosed beginning of October with NTG ( quite a lot of damage already , nerve damage, some peripheral vision loss ) Started on medication and was due to have a follow up appt after. 2 months ( so should have been December) However the hospital
Crafty-gran
in
Glaucoma UK
4 months ago
Sore dry eyes
Good morning folks. I’ve been switched from Latanoprost to Monopost drops for both eyes. Bilateral NTG. I was getting a lot of headaches, eye pain and swelling around my right eye and a duty A&E ophthalmologist suggested I could be reacting to the preservatives in the Latanoprost drops. I’ve been on
Good morning folks. I’ve been switched from Latanoprost to Monopost drops for both eyes. Bilateral NTG. I was getting a lot of headaches, eye pain and swelling around my right eye and a duty A&E ophthalmologist suggested I could be reacting to the preservatives in the Latanoprost drops. I’ve been on
Maisie79
in
Glaucoma UK
4 months ago
crohns and immunosuppressants???
hello all first time poster after being recently diagnosed with crohns post colonoscopy which showed long term inflammation, ulcers and some restriction in the intestine. First presented with mild stomach pain and some blood in poo but NO other symptoms. I feel lucky to have so few symptoms compared
hello all first time poster after being recently diagnosed with crohns post colonoscopy which showed long term inflammation, ulcers and some restriction in the intestine. First presented with mild stomach pain and some blood in poo but NO other symptoms. I feel lucky to have so few symptoms compared
Awbee23
in
Crohn's and Colitis Support
9 months ago
worried
hi I was diagnosed with nafld in November and told to lose weight I was about 2 stone overweight I have now hit healthy weight but my liver is showing still problems in the bloods so I have now been referred for autoimmune screening and mri scan also my urine is very dark have anyone gone through this
hi I was diagnosed with nafld in November and told to lose weight I was about 2 stone overweight I have now hit healthy weight but my liver is showing still problems in the bloods so I have now been referred for autoimmune screening and mri scan also my urine is very dark have anyone gone through this
Candycru
in
British Liver Trust
5 months ago
Extremely high eye pressure while sleeping.
Hi, I have been diagnosed with glaucoma for about 12 years now and I also have uveitis since I was 2 years old. The last 4/5 years the main focus has been managing glaucoma as my uveitis is in remission. Recently I managed to get self monitoring eye pressure machine from Icare so I can keep track of
Hi, I have been diagnosed with glaucoma for about 12 years now and I also have uveitis since I was 2 years old. The last 4/5 years the main focus has been managing glaucoma as my uveitis is in remission. Recently I managed to get self monitoring eye pressure machine from Icare so I can keep track of
Biggs87
in
Glaucoma UK
4 months ago
cochlear implants and tinnitus
Hi , does anyone have a cochlear implant and still have bad tinnitus?
Hi , does anyone have a cochlear implant and still have bad tinnitus?
1Dar
in
Tinnitus UK
4 months ago
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