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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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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
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
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
The Shelagh Cheesman Lupus Information Day - 16th March
The Cambridgeshire Lupus Group will be hosting an Information Day on Saturday 16th March, in memory of Shelagh Cheesman, who died as a result of cancer in March 2018. To register for your free ticket, please visit - https://lupusuk.org.uk/shelagh-cheesman-lupus-day/ If you have any questions, please
The Cambridgeshire Lupus Group will be hosting an Information Day on Saturday 16th March, in memory of Shelagh Cheesman, who died as a result of cancer in March 2018. To register for your free ticket, please visit - https://lupusuk.org.uk/shelagh-cheesman-lupus-day/ If you have any questions, please
michaellasmith
Administrator
in
LUPUS UK
5 months ago
lupus and surgery
hi my name is Diana I have lupus and I am looking to do a hip dip and bum filler. I and on medication my lupus is topical it only affects my skin making it really dry and also my scalp really dry. I am on medication once a day It only affects my skins in the sun here in the uk but not when I’m home
hi my name is Diana I have lupus and I am looking to do a hip dip and bum filler. I and on medication my lupus is topical it only affects my skin making it really dry and also my scalp really dry. I am on medication once a day It only affects my skins in the sun here in the uk but not when I’m home
Shawna3g
in
LUPUS UK
5 months ago
High ALT and Bilirubin and worried
my ‘urgent blood’ tests have come back and I am stressed to pieces as following my ultrasound I was told I had a fatty liver. My LFTs were all normal apart from my ALT which was 45 and needed to be less than 33, and Serum Bilirubin which was 27 and should be less than 21. Both readings end of March
my ‘urgent blood’ tests have come back and I am stressed to pieces as following my ultrasound I was told I had a fatty liver. My LFTs were all normal apart from my ALT which was 45 and needed to be less than 33, and Serum Bilirubin which was 27 and should be less than 21. Both readings end of March
Owlie
in
British Liver Trust
1 hour ago
Need some positivity
I have been diagnosed with liver cirrhosis I'm April/ may I have been alcohol free for 3 months but I am having a very anxious day today about my life expectancy and was hoping to hear of some positive news or advice please
I have been diagnosed with liver cirrhosis I'm April/ may I have been alcohol free for 3 months but I am having a very anxious day today about my life expectancy and was hoping to hear of some positive news or advice please
Lifefan
in
British Liver Trust
57 minutes ago
Looking for support in supporting my husband
This community has been so informative and I truly appreciate the information I have received from so many incredible people. Thank you! This is the first time I am posting to this group. In October 2023 my husband noticed more frequent use of the bathroom. He had his PSA tested in January which was
This community has been so informative and I truly appreciate the information I have received from so many incredible people. Thank you! This is the first time I am posting to this group. In October 2023 my husband noticed more frequent use of the bathroom. He had his PSA tested in January which was
Smmac15
in
Advanced Prostate Cancer
2 hours ago
ELF test
hi all, If you see my previous liver posts I’ve had varying fibroscan scores, mostly overestimated because of my BMI. Lost a ton of weight and got it down to 7.2-7.5. Had another recently after regaining most of the weight and the score is up to 10KPA. Had an ultrasound in March this year and liver
hi all, If you see my previous liver posts I’ve had varying fibroscan scores, mostly overestimated because of my BMI. Lost a ton of weight and got it down to 7.2-7.5. Had another recently after regaining most of the weight and the score is up to 10KPA. Had an ultrasound in March this year and liver
Amy190
in
British Liver Trust
2 hours ago
CRISPR Identifies New Genes as Drivers of Prostate Cancer Metastasis
Three research groups recently independently elucidated the genetic and epigenetic mechanisms driving prostate cancer metastasis. The innovative use of CRISPR technology not only facilitated the discovery of the genes but also opened potential new avenues for targeted cancer therapies to prevent metastasis
Three research groups recently independently elucidated the genetic and epigenetic mechanisms driving prostate cancer metastasis. The innovative use of CRISPR technology not only facilitated the discovery of the genes but also opened potential new avenues for targeted cancer therapies to prevent metastasis
No_stone_unturned
in
Advanced Prostate Cancer
4 hours ago
Can Exercise Help People with Parkinson’s Disease? 5 Things to Know
According to a study that tracked 237 patients over a five-year period, those with early-stage Parkinson’s disease who were more active had better physical outcomes than less active people with the disease. “Higher physical activity levels were strongly associated with better functioning in activities
According to a study that tracked 237 patients over a five-year period, those with early-stage Parkinson’s disease who were more active had better physical outcomes than less active people with the disease. “Higher physical activity levels were strongly associated with better functioning in activities
Farooqji
in
Cure Parkinson's
14 hours ago
There's Hope
Being a dialysis patient can have its difficulty, but when you have dual diagnosis like being a diabetic sometimes it feels like all he'll breaks through. But I decided to reach out to my medical team and I got the support I needed as well as understanding my situation. I have a plan that I and my
Being a dialysis patient can have its difficulty, but when you have dual diagnosis like being a diabetic sometimes it feels like all he'll breaks through. But I decided to reach out to my medical team and I got the support I needed as well as understanding my situation. I have a plan that I and my
Quita55
in
Kidney Dialysis
17 hours ago
RUQ of abdomen
Can someone have an ache in the right upper quadrant of their abdomen without it being something seriously wring with the liver like cirrhosis? Thanks, Terry
Can someone have an ache in the right upper quadrant of their abdomen without it being something seriously wring with the liver like cirrhosis? Thanks, Terry
ToughToes
in
British Liver Trust
19 hours ago
please help
hello I’ve been on here a few times now, at first it started being my TSH and T3 suggesting hyperthyroidism, I was then referred to an endocrinologist and retested and that was then fine however my cortisol was low at 220 so I had a SST yesterday and the results have come back as below which they have
hello I’ve been on here a few times now, at first it started being my TSH and T3 suggesting hyperthyroidism, I was then referred to an endocrinologist and retested and that was then fine however my cortisol was low at 220 so I had a SST yesterday and the results have come back as below which they have
Lollipop93
in
Thyroid UK
1 day ago
Considering a change of dialysis centers
So, my nephrologist just up and left. I'm sure there was more going on behind the scenes than I'm aware of, but it was so sudden for me. He was also the consulting MD at the dialysis clinic. I'm not worried about finding another nephro, though. The nephrology department I deal with is a crack team
So, my nephrologist just up and left. I'm sure there was more going on behind the scenes than I'm aware of, but it was so sudden for me. He was also the consulting MD at the dialysis clinic. I'm not worried about finding another nephro, though. The nephrology department I deal with is a crack team
PeaB4YouGo
in
Kidney Dialysis
1 day ago
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