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Alk phos on Xeloda
Moms just started her 3 cycle today of xeloda. So she’s been on it 6 weeks. Her T bili is normal her ast and alt are normal . But her Alk phos is up. Her doctor said they would continue to monitor it. Anyone else have this elevate on Xeloda ? Thanks so much!
Moms just started her 3 cycle today of xeloda. So she’s been on it 6 weeks. Her T bili is normal her ast and alt are normal . But her Alk phos is up. Her doctor said they would continue to monitor it. Anyone else have this elevate on Xeloda ? Thanks so much!
Flower1513
in
SHARE Metastatic Breast Cancer
5 months ago
Thoughts and Help
Hello all! I am new here. I know this is a lupus / autoimmune group, but before joining I noticed some helpful posts for other conditions, so I am hoping I can find some advice here. I have been dealing with declining health for a few years now, but have not received any diagnoses. I do have a positive
Hello all! I am new here. I know this is a lupus / autoimmune group, but before joining I noticed some helpful posts for other conditions, so I am hoping I can find some advice here. I have been dealing with declining health for a few years now, but have not received any diagnoses. I do have a positive
Hidden
in
LUPUS UK
6 months ago
sueky
Does this sound like a DILI? History of erythromycin use sine Christmas 2022 to control rosacea but altho a GP herself my daughter didnt follow the rules and stopped and started, also increasing and decreasing dose acc to how bad her rosacea was. On June 30th 2023 half an hour after going to bed absolutely
Does this sound like a DILI? History of erythromycin use sine Christmas 2022 to control rosacea but altho a GP herself my daughter didnt follow the rules and stopped and started, also increasing and decreasing dose acc to how bad her rosacea was. On June 30th 2023 half an hour after going to bed absolutely
suekaty
in
British Liver Trust
6 months ago
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Effective Management of Polycythemia Vera With Ropeginterferon Alfa-2b Treatment
Discussion; The results in our study demonstrate that the new dosing regimen of 250-350-500 µg of ropeginterferon alfa-2b is well-tolerated and highly efficacious in patients suffering from PV. This dosing regimen was associated with a rapid achievement of CHR without the need for phlebotomy or erythrocyte
Discussion; The results in our study demonstrate that the new dosing regimen of 250-350-500 µg of ropeginterferon alfa-2b is well-tolerated and highly efficacious in patients suffering from PV. This dosing regimen was associated with a rapid achievement of CHR without the need for phlebotomy or erythrocyte
Manouche
in
MPN Voice
1 month ago
update
hello everyone hope you’re all keeping as well as possible, I’ve had a blood test on the 22/ feb with nhs no thyroid’s done They were done as medichecks test for cpr was very high I would like to add a little more t3 as it’s not very high at the moment and feel as I need a good. Boost , to get
hello everyone hope you’re all keeping as well as possible, I’ve had a blood test on the 22/ feb with nhs no thyroid’s done They were done as medichecks test for cpr was very high I would like to add a little more t3 as it’s not very high at the moment and feel as I need a good. Boost , to get
Kowbie
in
Thyroid UK
3 months ago
Need your advice please
For the last 60 years I have been a vigilant weight watcher, daily exerciser and have watched my calorie intake. When I commenced treatment for my Essential Thrombocytosis in January 2021, my weight was 53.5kg. Three years later this has ballooned to 60.3kg, despite my efforts to control any
For the last 60 years I have been a vigilant weight watcher, daily exerciser and have watched my calorie intake. When I commenced treatment for my Essential Thrombocytosis in January 2021, my weight was 53.5kg. Three years later this has ballooned to 60.3kg, despite my efforts to control any
Goosebumps52
in
MPN Voice
3 months ago
Do I have lupus?
Several years ago I was having a lot of joint pains in my legs and fevers. I was referred to haematology who then referred me on to infectious diseases. The consultant did blood tests and told me I had a positive ANA test and anti-Double stranded dna antibody test which was positive, he diagnosed me
Several years ago I was having a lot of joint pains in my legs and fevers. I was referred to haematology who then referred me on to infectious diseases. The consultant did blood tests and told me I had a positive ANA test and anti-Double stranded dna antibody test which was positive, he diagnosed me
Poppy-12345
in
LUPUS UK
8 months ago
all phos
hi, my alk phos started last year at 152. Went on urso and 6 months later it dropped to 118. Today whic is 6 month later alk went back up to 146. Have not discussed with doctor yet. Has anyone else experienced the fluctuation? Thank you
hi, my alk phos started last year at 152. Went on urso and 6 months later it dropped to 118. Today whic is 6 month later alk went back up to 146. Have not discussed with doctor yet. Has anyone else experienced the fluctuation? Thank you
Samanthaann
in
PBC Foundation
8 months ago
GP insisting on using CRP & ESR as inflammatory markers...and managing to get a creatine kinase blood test ordered...legs are still an issue
Hello I was called in to my GP surgery yesterday, by one of the GPs, the letter indicating it was for a medication review. She's not one of the GPs I prefer to see, she can be a little vague etc. But we ended up going through my meds and she asked about steroids being on my repeat....I said that although
Hello I was called in to my GP surgery yesterday, by one of the GPs, the letter indicating it was for a medication review. She's not one of the GPs I prefer to see, she can be a little vague etc. But we ended up going through my meds and she asked about steroids being on my repeat....I said that although
Wendy39
in
LUPUS UK
8 months ago
Should I push for a test?
Update - I have realised that a few more results have come through. He ordered dsDNA but apparently the sample was lost or there wasn't enough? He ordered ENA Antibody test but the result says unknown? ANA Test - Anti-nuclear factor level POSITIVE - Titre > 1:640 ANA PATTERN SPECKLED In the presence
Update - I have realised that a few more results have come through. He ordered dsDNA but apparently the sample was lost or there wasn't enough? He ordered ENA Antibody test but the result says unknown? ANA Test - Anti-nuclear factor level POSITIVE - Titre > 1:640 ANA PATTERN SPECKLED In the presence
EllsBells591
in
Pernicious Anaemia Society
8 months ago
COVID-19 immune cell vaccine eases SLE symptoms in girl: Report
Therapy helped 13-year-old by increasing immune tolerance, researchers say
A personalized vaccine kit designed to prevent COVID-19 infection eased systemic lupus erythematosus (SLE) manifestations in an adolescent girl in Indonesia whose symptoms had not been well-controlled with immunosuppressive
Therapy helped 13-year-old by increasing immune tolerance, researchers say
A personalized vaccine kit designed to prevent COVID-19 infection eased systemic lupus erythematosus (SLE) manifestations in an adolescent girl in Indonesia whose symptoms had not been well-controlled with immunosuppressive
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
8 months ago
immune system
Hi Everyone Can anyone tell me what affect Pegasys has on the immune system. A few tears ago I had a positive ANA and Anti-Ro blood test, was seen by a Rheumatologist who said I had Sicca symptoms but not Sjogrens. Another recent blood test has shown the same, positive ANA and Anti Ro. Now I am having
Hi Everyone Can anyone tell me what affect Pegasys has on the immune system. A few tears ago I had a positive ANA and Anti-Ro blood test, was seen by a Rheumatologist who said I had Sicca symptoms but not Sjogrens. Another recent blood test has shown the same, positive ANA and Anti Ro. Now I am having
lindyloulou
in
MPN Voice
8 months ago
Individualized Dosing of Ropeginterferon Alfa-2b Ensures Optimal Response in Patients with Low-Risk Polycythemia Vera (PV)
Conclusions: High long-term response rates (80.4% at 24 months; 73.2% at 72 months) were achieved with ropeginterferon alfa-2b treatment in the low-risk PV population when the dose was optimized on an individual basis. No specific baseline characteristics among low-risk PV patients appear to be associated
Conclusions: High long-term response rates (80.4% at 24 months; 73.2% at 72 months) were achieved with ropeginterferon alfa-2b treatment in the low-risk PV population when the dose was optimized on an individual basis. No specific baseline characteristics among low-risk PV patients appear to be associated
Manouche
in
MPN Voice
6 months ago
Help with blood test results please
Hi All I've recently had 2 blood tests - one was a private finger prick test through monitormyhealth.com. The reason I took the tests was because I've not felt 'right' for quite some months. Insomnia (but then falling asleep at my desk during the day), constant aches and pains, headaches, unable
Hi All I've recently had 2 blood tests - one was a private finger prick test through monitormyhealth.com. The reason I took the tests was because I've not felt 'right' for quite some months. Insomnia (but then falling asleep at my desk during the day), constant aches and pains, headaches, unable
haysmarie
in
Thyroid UK
2 days ago
Fibrosis?
Hi there. Continuing my journey to recovery, I was today told by my doctor that I need to have a blood test to see if I have any scarring of the liver. My LFT’s are better than they were in June last year. An ultrasound in August 23 noticed a fatty liver. So, can you still get scarring of the liver
Hi there. Continuing my journey to recovery, I was today told by my doctor that I need to have a blood test to see if I have any scarring of the liver. My LFT’s are better than they were in June last year. An ultrasound in August 23 noticed a fatty liver. So, can you still get scarring of the liver
Chris7746
in
British Liver Trust
10 days ago
Newly diagnosed with PBC
Hi there! I just got my official diagnosis today and was started on Ursodiol. I have been feeling fatigued for about 13 years and no one could find a reason. In the last 3 years, my liver enzymes went up and I started getting even weirder symptoms. Neurological impairments, heart pain, muscle pain.
Hi there! I just got my official diagnosis today and was started on Ursodiol. I have been feeling fatigued for about 13 years and no one could find a reason. In the last 3 years, my liver enzymes went up and I started getting even weirder symptoms. Neurological impairments, heart pain, muscle pain.
Pawsandchoc
in
PBCers Organization
8 months ago
help with blood test results
Hi, I have just had the results of my blood test and they are all within the normal range which is obviously great news but not so great as to knowing why I’m feeling so tired, aching, gut issues and cramping, brain fog. Could any of you lovely people just take a look and see why I maybe feeling like
Hi, I have just had the results of my blood test and they are all within the normal range which is obviously great news but not so great as to knowing why I’m feeling so tired, aching, gut issues and cramping, brain fog. Could any of you lovely people just take a look and see why I maybe feeling like
Luckygirl1
in
Thyroid UK
21 days ago
update
morning everyone hope your as well as can be , I’ve now had my gallbladder removed, I’m putting on my latest results and would like to know if I can raise t3 a little bit more , I had bloods done 8/20 nothing to eat and drank only water,the only thing I did wrong was take all meds at the same time as
morning everyone hope your as well as can be , I’ve now had my gallbladder removed, I’m putting on my latest results and would like to know if I can raise t3 a little bit more , I had bloods done 8/20 nothing to eat and drank only water,the only thing I did wrong was take all meds at the same time as
Kowbie
in
Thyroid UK
29 days ago
Peginterferon alfa-2a
Hola! I'm new to this group and newly diagnosed with essential thrombocythemia. The treatment prescribed is peginterferon alfa-2a. So far I have done one treatment and wow does it suck! I haven't seen anyone else talking about this course of treatment. Is anyone else doing this? I sure could use some
Hola! I'm new to this group and newly diagnosed with essential thrombocythemia. The treatment prescribed is peginterferon alfa-2a. So far I have done one treatment and wow does it suck! I haven't seen anyone else talking about this course of treatment. Is anyone else doing this? I sure could use some
LisaLoveTacos
in
MPN Voice
6 months ago
Nosebleeds and thyroid / blood test query / going private
Hi there :) You were all so helpful when I was first diagnosed with hypothyroidism last year, and I was hoping I could trouble you all with another question. - My levothyroxine was raised to 75mg a day in February based on my NHS blood test (TSH 5.91 mU/L, free T4 15.8pmol/L). - Not really sure if
Hi there :) You were all so helpful when I was first diagnosed with hypothyroidism last year, and I was hoping I could trouble you all with another question. - My levothyroxine was raised to 75mg a day in February based on my NHS blood test (TSH 5.91 mU/L, free T4 15.8pmol/L). - Not really sure if
Fweb
in
Thyroid UK
1 month ago
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