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NICE: Teprotumumab for treating thyroid eye disease ID 6432 - being scoped
setid=3e6c54a1-cefd-4a5b-a855-ab9f268b6cce [i]Home > NICE Guidance >
Conditions
and
diseases
> Diabetes
and
other endocrinal, nutritional and metabolic
conditions
> Thyroid disorders[/i] [i]
Teprotumumab for treating thyroid eye disease ID 6432
[/i] [i][/i] [i]Awaiting development [GID-TA11531
setid=3e6c54a1-cefd-4a5b-a855-ab9f268b6cce [i]Home > NICE Guidance >
Conditions
and
diseases
> Diabetes
and
other endocrinal, nutritional and metabolic
conditions
> Thyroid disorders[/i] [i]
Teprotumumab for treating thyroid eye disease ID 6432
[/i] [i][/i] [i]Awaiting development [GID-TA11531
helvella
Thyroid UK
in
Thyroid UK
2 months ago
Anyone tried celery juice
Hello, my friend bought me a book at Christmas from medical medium where he believes our kind of condition comes from the EBV (virus), along with many other
conditions
and
diseases
. I am finding it interesting. He has an article on rls and recommends celery juice and cilantro.
Hello, my friend bought me a book at Christmas from medical medium where he believes our kind of condition comes from the EBV (virus), along with many other
conditions
and
diseases
. I am finding it interesting. He has an article on rls and recommends celery juice and cilantro.
Lespenney
in
Restless Legs Syndrome
5 months ago
Peace of Mind
Over the past several months I've not been quite as active on the forum. This has been because I've been busy attending a host of appointments with different medical professionals, ranging from the practise nurse to various consultants, all in order to discover the cause of some uncomfortable and worrying
Over the past several months I've not been quite as active on the forum. This has been because I've been busy attending a host of appointments with different medical professionals, ranging from the practise nurse to various consultants, all in order to discover the cause of some uncomfortable and worrying
Kendrew
in
PMRGCAuk
15 hours ago
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Started bleeding with BMs again.
Good afternoon, I was diagnosed with Ulcerative colitis at the start of May 2024 via colonoscopy. Start of June , I had a bad flare up where I had lots of blood and diarrhea ( up to 12 times day) worse cramps ever. Finding mesalasine tablets in poo. Got admitted 3 days in hospital for dehydration and
Good afternoon, I was diagnosed with Ulcerative colitis at the start of May 2024 via colonoscopy. Start of June , I had a bad flare up where I had lots of blood and diarrhea ( up to 12 times day) worse cramps ever. Finding mesalasine tablets in poo. Got admitted 3 days in hospital for dehydration and
Raerae2781
in
Crohn's and Colitis Support
18 hours ago
Parkinson’s Active Immunotherapy Medicine Phase 1 Study Positive Results Published
The Phase 1 successfully met its primary outcome measures, demonstrating that UB-312 was generally well-tolerated and induced anti-aggregated α-synuclein (αSyn) antibody responses in healthy volunteers and PD patients. Specifically, 12 of 13 PD patients who completed dosing developed anti-αSyn antibodies
The Phase 1 successfully met its primary outcome measures, demonstrating that UB-312 was generally well-tolerated and induced anti-aggregated α-synuclein (αSyn) antibody responses in healthy volunteers and PD patients. Specifically, 12 of 13 PD patients who completed dosing developed anti-αSyn antibodies
Farooqji
in
Cure Parkinson's
2 days ago
Frozen transfer tips
Hi everyone. I am preparing for a frozen transfer after my fresh transfer failed in February. I had wanted to wait until my cycle was back too normal . I had become disillusioned with all the acupuncture and reflexology and just all the things I’d stopped doing because of TTC for 3 years . Now I
Hi everyone. I am preparing for a frozen transfer after my fresh transfer failed in February. I had wanted to wait until my cycle was back too normal . I had become disillusioned with all the acupuncture and reflexology and just all the things I’d stopped doing because of TTC for 3 years . Now I
Lemons1986
in
Fertility Network UK
3 days ago
autoimmune gastritis
hi everyone, anyone have any knowledge on links between hashimotos and gastric mucosal disease/autoimmune atrophic gastritis/ biermans disease / thyroid gastric autoimmune syndrome. I spoke to an immunologist who told me links to the above and the association between hashimotos . I have also been tested
hi everyone, anyone have any knowledge on links between hashimotos and gastric mucosal disease/autoimmune atrophic gastritis/ biermans disease / thyroid gastric autoimmune syndrome. I spoke to an immunologist who told me links to the above and the association between hashimotos . I have also been tested
Rowing2
in
Thyroid UK
4 days ago
hello
After searching through the web I came across this website. I finally went to go see a GI doctor. He asked what were my symptoms? But before I say, he told me he needed blood work done, colonoscopy, an ultrasound. My symptoms are bloating, excess amounts of gas, constipation, diarrhea. I do have a hard
After searching through the web I came across this website. I finally went to go see a GI doctor. He asked what were my symptoms? But before I say, he told me he needed blood work done, colonoscopy, an ultrasound. My symptoms are bloating, excess amounts of gas, constipation, diarrhea. I do have a hard
32321
in
Colon Cancer Connected
4 days ago
Calprotectin still 1800
Calprotectin test back again after last check in February which was 1800 after having alot of blood loss and diarrhea flare-up yet it is still 1800.Gastro appointment on 1st of July booked to discuss but feel very down by this number as I have been eating nothing but oats, almond milk, fish and rice
Calprotectin test back again after last check in February which was 1800 after having alot of blood loss and diarrhea flare-up yet it is still 1800.Gastro appointment on 1st of July booked to discuss but feel very down by this number as I have been eating nothing but oats, almond milk, fish and rice
Sooty712
in
Crohn's and Colitis Support
5 days ago
10dp5dt and less that 1 on Beta hcg blood test so think this must have failed this time.
my clinic still wants me to continue with PIO injections pessaries and test again at 14 days which I think is a bit excessive and a waste of money, pain and even more anguish. I thought the latest clinics say is 12 days post transfer. Does anyone else clinic say 14 days?
my clinic still wants me to continue with PIO injections pessaries and test again at 14 days which I think is a bit excessive and a waste of money, pain and even more anguish. I thought the latest clinics say is 12 days post transfer. Does anyone else clinic say 14 days?
ladybd
in
Fertility Network UK
5 days ago
Fecal Calprotectin & CRC
Hey all, I am waiting on a colonoscopy I have scheduled for June 27th due to some symptoms and have a question for you all. Did any of you that got a CRC diagnosis have a really low fecal calprotectin score? I have been worried (as we all are) about what will be found on this colonoscopy, but I had a
Hey all, I am waiting on a colonoscopy I have scheduled for June 27th due to some symptoms and have a question for you all. Did any of you that got a CRC diagnosis have a really low fecal calprotectin score? I have been worried (as we all are) about what will be found on this colonoscopy, but I had a
nowayoutofthis1
in
Colon Cancer Connected
7 days ago
My IBS
I wonder if anyone can tell me have they suffered extreme stomach pressure due to ibs which realy restricts their mobility to move around and also to relax,my gp has recently told me she thinks I have ibs as I have all the symptoms a distended stomach which makes me look heavily pregnant,constipation
I wonder if anyone can tell me have they suffered extreme stomach pressure due to ibs which realy restricts their mobility to move around and also to relax,my gp has recently told me she thinks I have ibs as I have all the symptoms a distended stomach which makes me look heavily pregnant,constipation
Green1967
in
IBS Network
11 days ago
New but familiar
Hello, I was diagnosed with IBS in 2018. My symptoms were abdominal pain with diarrhea which turned into constipation. Started the low fodmap diet in 2021, and stopped eating gluten, and cut out sugar. My symptoms improved until recently. Now I'm having daily abdominal pain and I'm not passing as much
Hello, I was diagnosed with IBS in 2018. My symptoms were abdominal pain with diarrhea which turned into constipation. Started the low fodmap diet in 2021, and stopped eating gluten, and cut out sugar. My symptoms improved until recently. Now I'm having daily abdominal pain and I'm not passing as much
Hidden
in
IBS Network
12 days ago
Foot surgery
Hi. Has anyone used a lady wee after having non weight baring surgery. If so, do you have any recommendations. Thank you
Hi. Has anyone used a lady wee after having non weight baring surgery. If so, do you have any recommendations. Thank you
Lematt
in
NRAS
12 days ago
When to take meds
I have been on levothyroxine 75mg for few years now I have to take alendronic acid and adcal d3 for my bones. I now read you should not take aa and levo at same time been prescribed to take in morn. The adcal d3 at night wondered if anyone on same how they take them. Has anyone got side effects from
I have been on levothyroxine 75mg for few years now I have to take alendronic acid and adcal d3 for my bones. I now read you should not take aa and levo at same time been prescribed to take in morn. The adcal d3 at night wondered if anyone on same how they take them. Has anyone got side effects from
bellsjet
in
Thyroid UK
12 days ago
IBS ok with daily loperamide
Male, for the Last 4 years have suffered from IBS -D ( mainly diarrhoea )diagnosis after colonoscopy & associated blood tests I was advised by a specialist to take Imodium (loperamide) daily after first poo, I follow the FODMAP diet & LOW insoluble fibre. And try to eat Prebiotic foods e.g Oats, also
Male, for the Last 4 years have suffered from IBS -D ( mainly diarrhoea )diagnosis after colonoscopy & associated blood tests I was advised by a specialist to take Imodium (loperamide) daily after first poo, I follow the FODMAP diet & LOW insoluble fibre. And try to eat Prebiotic foods e.g Oats, also
Kestrel66
in
IBS Network
13 days ago
Bisacodyl
Taken Senna, Fybogel and Laxido and haven’t had any bowel movements. I’ve seen people say to take Bisacodyl as this is quite strong. What are people’s experiences with this? Does it work? When is the best time to take it?
Taken Senna, Fybogel and Laxido and haven’t had any bowel movements. I’ve seen people say to take Bisacodyl as this is quite strong. What are people’s experiences with this? Does it work? When is the best time to take it?
HI1237
in
IBS Network
14 days ago
Stomach cramps
Hi lovely ladies! My mum is 6 weeks post primary debulking surgery, and bowel resection and is still having some bowel issues. She's had pretty bad stomach cramping all day today. Is this normal? Does anyone have any tips? She's still on laxatives and drinking peppermint tea for gas. Would love to hear
Hi lovely ladies! My mum is 6 weeks post primary debulking surgery, and bowel resection and is still having some bowel issues. She's had pretty bad stomach cramping all day today. Is this normal? Does anyone have any tips? She's still on laxatives and drinking peppermint tea for gas. Would love to hear
georgiageorgia182
in
My Ovacome
15 days ago
Diverticulitis
Just been diagnosed with diverticulitis after colonoscopy, luckily no cancer found. Unfortunately I’m having to wear pads as I am experiencing “leaking” after a bowel movement. Any help with diet or tips, I would appreciate, as I am reluctant to take Loperamide on a regular basis.
Just been diagnosed with diverticulitis after colonoscopy, luckily no cancer found. Unfortunately I’m having to wear pads as I am experiencing “leaking” after a bowel movement. Any help with diet or tips, I would appreciate, as I am reluctant to take Loperamide on a regular basis.
Sinnelg
in
British Liver Trust
15 days ago
Managing Pudendal Neuralgia pain
Hi all, I joined this forum to remain on top of developments around the complex pelvic floor issues affecting women and to seek support from others. In my experience these are generally poorly understood by doctors in the UK especially at consultant level and there is an absence of multi agency support
Hi all, I joined this forum to remain on top of developments around the complex pelvic floor issues affecting women and to seek support from others. In my experience these are generally poorly understood by doctors in the UK especially at consultant level and there is an absence of multi agency support
Elfcreature
in
Pelvic Pain Support Network
15 days ago
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