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help with new test results
hi, could someone please help with these results.iv been on levothyroxine 75mg for about 4 years . Diagnosed in 2019 as underactive thyroid. Thyroid function test Serum TSH level 2.15 mu/L [0.35 - 4.94] Serum free T4 level 13.2 pmol/L [9.0 - 19.0] Thyroid Therapy Levothyroxine (T4) It has come
hi, could someone please help with these results.iv been on levothyroxine 75mg for about 4 years . Diagnosed in 2019 as underactive thyroid. Thyroid function test Serum TSH level 2.15 mu/L [0.35 - 4.94] Serum free T4 level 13.2 pmol/L [9.0 - 19.0] Thyroid Therapy Levothyroxine (T4) It has come
Norrahsjake
in
Thyroid UK
2 months ago
neuropathy source
hi all, Does anyone else on here have Sjögren’s as well as PA? I am experiencing constant tingling and occasional burning/numbness in my fingers and toes. (specific fingers and toes, not all)….It got worse when I did a reloading series of dosages of B12. I’m curious - does neuropathy usually flow from
hi all, Does anyone else on here have Sjögren’s as well as PA? I am experiencing constant tingling and occasional burning/numbness in my fingers and toes. (specific fingers and toes, not all)….It got worse when I did a reloading series of dosages of B12. I’m curious - does neuropathy usually flow from
Lhood08
in
Pernicious Anaemia Society
2 months ago
Teesside Lupus Support group meetings
We are a group in the North East of England. We had a very welcoming and successful Event on Lupus and other associated chronic illnesses awareness on the 20th of July 2024. We are inviting any Lupies within our area who are looking for a place to go and meet and chat and do activities as well as share
We are a group in the North East of England. We had a very welcoming and successful Event on Lupus and other associated chronic illnesses awareness on the 20th of July 2024. We are inviting any Lupies within our area who are looking for a place to go and meet and chat and do activities as well as share
Pipido36
in
LUPUS UK
2 months ago
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pernicious anemia diet
is there a certain diet that is recommended for pernicious anemia? I have been advised that even oats can be harmful? thanks
is there a certain diet that is recommended for pernicious anemia? I have been advised that even oats can be harmful? thanks
Damacian
in
Pernicious Anaemia Society
2 months ago
Do you stop Methotrexate whilst you have Covid?
Hi lovely people, I have Covid and am wondering if I should miss my Methotrexate out this week. I was given antivirals, but had to stop because of an allergic reaction after 24 hours. What have you done in the same position please? My Rheumatoid is well controlled at the moment.
Hi lovely people, I have Covid and am wondering if I should miss my Methotrexate out this week. I was given antivirals, but had to stop because of an allergic reaction after 24 hours. What have you done in the same position please? My Rheumatoid is well controlled at the moment.
Lotttie4
in
NRAS
2 months ago
Underactive thyroid
I Was diagnosed with under active thyroid 10 years ago age 50, I have struggled with tiredness my go will not change the 50mg dose of levothyroxine. I have just had it re tested and tsh level is 0.97 I am also anemic come back in the same blood tests so starting iron. Any thoughts please
I Was diagnosed with under active thyroid 10 years ago age 50, I have struggled with tiredness my go will not change the 50mg dose of levothyroxine. I have just had it re tested and tsh level is 0.97 I am also anemic come back in the same blood tests so starting iron. Any thoughts please
JUNEO
in
Thyroid UK
2 months ago
Addition of an ARSI to standard ADT significantly increases the risk of fractures and falls in men with prostate cancer
Jones C, Gray S, Brown M, et al. Risk of fractures and falls in men with advanced or metastatic prostate cancer receiving androgen deprivation therapy and treated with novel androgen receptor signalling inhibitors: a systematic review and meta-analysis of randomised controlled trials. Eur Urol Oncol.
Jones C, Gray S, Brown M, et al. Risk of fractures and falls in men with advanced or metastatic prostate cancer receiving androgen deprivation therapy and treated with novel androgen receptor signalling inhibitors: a systematic review and meta-analysis of randomised controlled trials. Eur Urol Oncol.
Graham49
in
Advanced Prostate Cancer
6 months ago
Cortisol test result
Hi, I have just had some blood test results come back today. Currently on 5.5mg, but have been taking 6mg (Sat 30th..Sun, Mon, Tues) as have had lots going on, bit stressful but good stress not bad! the 0.5mg did help. All results are ok including PV, ESR, CRP. Also had a basal cortisol test (partially
Hi, I have just had some blood test results come back today. Currently on 5.5mg, but have been taking 6mg (Sat 30th..Sun, Mon, Tues) as have had lots going on, bit stressful but good stress not bad! the 0.5mg did help. All results are ok including PV, ESR, CRP. Also had a basal cortisol test (partially
Saffron23
in
PMRGCAuk
6 months ago
'Wednesday Word"
Since my question yesterday was concerning 'brain fog', I thought my word for today should be [u][i]
encephalopathy
[/i][/u] - here are specifics about the word This is a blanket term referring to any brain dysfunction. It can commonly be called 'brain fog'. However, [u][i]
encephalopathy
Since my question yesterday was concerning 'brain fog', I thought my word for today should be [u][i]
encephalopathy
[/i][/u] - here are specifics about the word This is a blanket term referring to any brain dysfunction. It can commonly be called 'brain fog'. However, [u][i]
encephalopathy
DonnaBoll
Administrator
in
PBC Foundation
6 months ago
Macrophages, type of immune cell, tied to lupus nephritis in children
M1 macrophages may cause more severe kidney disease in young patients Inflammatory macrophages, a type of immune cell tasked with clearing the body of harmful invaders and dead cells, may be linked to more severe lupus nephritis in children with systemic lupus erythematosus, a small study suggests.
M1 macrophages may cause more severe kidney disease in young patients Inflammatory macrophages, a type of immune cell tasked with clearing the body of harmful invaders and dead cells, may be linked to more severe lupus nephritis in children with systemic lupus erythematosus, a small study suggests.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
5 months ago
PSA after chemo # 4
Hi My husbands last chemo was # 3 and PSA was 0.14, he just got the results from Chemo # 4 and it was at 0.12. This is the slowest decline if you look in the profile Iisted all his PSA results. Should we be worried that this last one barely moved ? Or is this slower decline good news? Thanks for any
Hi My husbands last chemo was # 3 and PSA was 0.14, he just got the results from Chemo # 4 and it was at 0.12. This is the slowest decline if you look in the profile Iisted all his PSA results. Should we be worried that this last one barely moved ? Or is this slower decline good news? Thanks for any
positive-thinking
in
Advanced Prostate Cancer
6 months ago
How Much Carbidopa Levodopa After 5-10 Years? Any other meds?
I am about to "celebrate" the six year anniversary of my Parkinson's disease diagnosis. I currently take five 25/100 Carbidopa Levodopa tablets per day, usually around 9:00 a.m., noon, 3:00 p.m., 6:00 p.m., and 9:00 p.m. although timing varies slightly from day to day. Lately, I have noticed that I
I am about to "celebrate" the six year anniversary of my Parkinson's disease diagnosis. I currently take five 25/100 Carbidopa Levodopa tablets per day, usually around 9:00 a.m., noon, 3:00 p.m., 6:00 p.m., and 9:00 p.m. although timing varies slightly from day to day. Lately, I have noticed that I
jimcaster
in
Cure Parkinson's
6 months ago
Addison's disease
Spoke with my GP yesterday regarding the extreme fatigue & rollercoaster of crashing following activity. He is now going to test & look at the possibility of Addison's. How does this mesh with PMR and Pred? I'd welcome any advice or better knowledge. Thanks.
Spoke with my GP yesterday regarding the extreme fatigue & rollercoaster of crashing following activity. He is now going to test & look at the possibility of Addison's. How does this mesh with PMR and Pred? I'd welcome any advice or better knowledge. Thanks.
Naim1
in
PMRGCAuk
2 months ago
Excess Folic Acid and Vitamin B12 Deficiency: Clinical Implications?
This is a very recent paper. Some of the areas covered are well-known. Such as not treating B12 deficiency with folic acid. But, in the more speculative parts, I think it does raise questions over the prescribing of high dose (e.g. 5 milligrams a day) of folic acid in those who are currently low in
This is a very recent paper. Some of the areas covered are well-known. Such as not treating B12 deficiency with folic acid. But, in the more speculative parts, I think it does raise questions over the prescribing of high dose (e.g. 5 milligrams a day) of folic acid in those who are currently low in
helvella
in
Pernicious Anaemia Society
2 months ago
Crohns/IBD
I have undiagnosed Crohns/IBD and continuous flares. I had surgery in 2011 resection of 20cm colon. What treatments are effective?
I have undiagnosed Crohns/IBD and continuous flares. I had surgery in 2011 resection of 20cm colon. What treatments are effective?
Lalande
in
Thyroid UK
6 months ago
Rising PCA - on ADT Holiday
Diagnosed Stage 4 oligometastatic (low volume) PCA in 2021. Gleason 7, 4+3 . Completed RT and 18 months on ADT (Nubeqa) paused the ADT in September after PSA non detectable and a fresh set of scans showed no “evidence of disease”. Continued to do bloodwork quarterly and PSA remained at 0. Until
Diagnosed Stage 4 oligometastatic (low volume) PCA in 2021. Gleason 7, 4+3 . Completed RT and 18 months on ADT (Nubeqa) paused the ADT in September after PSA non detectable and a fresh set of scans showed no “evidence of disease”. Continued to do bloodwork quarterly and PSA remained at 0. Until
Kkash
in
Advanced Prostate Cancer
6 months ago
Telephone Consultation Results of:
So, I have just finished my phone consultation. I had my list of questions which I wasn't able to put over to the Consultant without being accused of being rude. This is how it went before I forget: My symptoms as they appear at the moment do not entitle me to any thing other than a 3 day ECG monitor
So, I have just finished my phone consultation. I had my list of questions which I wasn't able to put over to the Consultant without being accused of being rude. This is how it went before I forget: My symptoms as they appear at the moment do not entitle me to any thing other than a 3 day ECG monitor
CavendishCool
in
LUPUS UK
1 month ago
Confused
UPDATE: April 5, 2024 Yesterday was very disappointing as my husbands PSA increased again by 183 points, last month his PSA was 1546 and now it is 1730. All his other CBC results were good. His Alkaline Phosphatase increased 6 points, last month 127 and now 133 but still in range of 40-150. Questioned
UPDATE: April 5, 2024 Yesterday was very disappointing as my husbands PSA increased again by 183 points, last month his PSA was 1546 and now it is 1730. All his other CBC results were good. His Alkaline Phosphatase increased 6 points, last month 127 and now 133 but still in range of 40-150. Questioned
MsHope
in
Advanced Prostate Cancer
6 months ago
Psa level
Just came off degarlix as psa level was rising, now on xtadi apalutamide how long does it take for psa level to fall and by how much?
Just came off degarlix as psa level was rising, now on xtadi apalutamide how long does it take for psa level to fall and by how much?
littlemount
in
Advanced Prostate Cancer
6 months ago
New diagnosis - what to expect/demand from GP
I had my second child in August 2022 and to be honest I've not felt right since. Since going back to work in June last year I've been permanently exhausted but it's just got worse and worse. Totally mental fog, can't focus, constantly yawning my head off. My body aches constantly but all the while I
I had my second child in August 2022 and to be honest I've not felt right since. Since going back to work in June last year I've been permanently exhausted but it's just got worse and worse. Totally mental fog, can't focus, constantly yawning my head off. My body aches constantly but all the while I
Whatdidyousay
in
Thyroid UK
2 months ago
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