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Hypo on Aristo
I have been taking 62.5 mcg mercury pharma plus 15T3 for a couple of years Every time I try and increase the Thyroxine I get itchy eyes and a runny nose ( with stomach pain) so eventually I got a prescription for Aristo.. but since being on it I am so hypothyroid, I’m struggling to walk and spend most
I have been taking 62.5 mcg mercury pharma plus 15T3 for a couple of years Every time I try and increase the Thyroxine I get itchy eyes and a runny nose ( with stomach pain) so eventually I got a prescription for Aristo.. but since being on it I am so hypothyroid, I’m struggling to walk and spend most
Bean101
in
Thyroid UK
4 months ago
What deficiencies could B12 injection cause?
Some of you might remember me writing about how, since moving to Pascoe vials from Dr Myhill's multi use vial, I've been experiencing whole of body mini vibrations / electricity / agitation. It's particularly bad in the night and I wake with it. I had worked out that it's tolerable by reducing injection
Some of you might remember me writing about how, since moving to Pascoe vials from Dr Myhill's multi use vial, I've been experiencing whole of body mini vibrations / electricity / agitation. It's particularly bad in the night and I wake with it. I had worked out that it's tolerable by reducing injection
Sunnysidoop
in
Pernicious Anaemia Society
4 months ago
Should I be asking for an increase in Levo?
I have an appt with my endo on Thursday to discuss my latest results and those from last August and April when I was taking different amounts of levo. I always follow the suggested procedure of stopping Vit B complex a week before, early blood test and not taking levo for 24 hours. My most recent
I have an appt with my endo on Thursday to discuss my latest results and those from last August and April when I was taking different amounts of levo. I always follow the suggested procedure of stopping Vit B complex a week before, early blood test and not taking levo for 24 hours. My most recent
Feelingrubbish
in
Thyroid UK
4 months ago
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FYI: New data on progression of visceral mets without PSA progression (discordance) and ARAT/docetaxel therapy
Interesting study, folks. We know physical progression of PCa (i.e., new metastases) can occur without PSA progression. This is known as a discordance. But we don't know how often it occurs or why it occurs. In these instances, our greatest fear is "therapy-induced neuroendocrine prostate cancer
Interesting study, folks. We know physical progression of PCa (i.e., new metastases) can occur without PSA progression. This is known as a discordance. But we don't know how often it occurs or why it occurs. In these instances, our greatest fear is "therapy-induced neuroendocrine prostate cancer
SeosamhM
in
Advanced Prostate Cancer
10 months ago
Liothyronine T3
Is anyone having difficulty getting Mercury Pharma Liothyronine? The pharmacy I’ve been getting mine from for 8 years are now saying they can’t get them as there is a supplier issue. If they can’t get them what’s the best alternative?
Is anyone having difficulty getting Mercury Pharma Liothyronine? The pharmacy I’ve been getting mine from for 8 years are now saying they can’t get them as there is a supplier issue. If they can’t get them what’s the best alternative?
130396
in
Thyroid UK
4 months ago
raising levothyroxne give you headaches and brain fog
last two weeks i raised lt4 levo to 75mg from 50mg i get stomach upset brain fog headahes at back of my neck high near the scull and painfull ear and i am hungry all the time i am bloated and dont feel well i have appointment in a month with endocrinologist my dr says is no side effects
last two weeks i raised lt4 levo to 75mg from 50mg i get stomach upset brain fog headahes at back of my neck high near the scull and painfull ear and i am hungry all the time i am bloated and dont feel well i have appointment in a month with endocrinologist my dr says is no side effects
morcan54
in
Thyroid UK
4 months ago
carbimazole and iron supplements
hi all, I have very low ferritin and need to supplement iron. Do I need to take my carbimazole away from iron or it doesn’t matter?
hi all, I have very low ferritin and need to supplement iron. Do I need to take my carbimazole away from iron or it doesn’t matter?
Kari55
in
Thyroid UK
4 months ago
Newly detectable PSA after prostatectomy: RT + ADT planned; add Erleada?
Diagnosed 12/21, PSA 7, negative PSMA PET. Radical prostatectomy with extended lymph node dissection in Mar 2022. Gleason 4+5, +cribriform, +intraductal, + bilat SVI, +ECE. Margins negative (barely) and 1/34 lymph nodes positive with very small focus of cancer. PSA was undetectable until Jun 2023, then
Diagnosed 12/21, PSA 7, negative PSMA PET. Radical prostatectomy with extended lymph node dissection in Mar 2022. Gleason 4+5, +cribriform, +intraductal, + bilat SVI, +ECE. Margins negative (barely) and 1/34 lymph nodes positive with very small focus of cancer. PSA was undetectable until Jun 2023, then
Brokedown_Palace
in
Advanced Prostate Cancer
10 months ago
Flare
Thursday, my husband had his follow-up appointment with Oncologist. I was very alarmed at some of his blood test results. His PSA went up to 1600. Doctor said other blood work was to be expected. I researched surged in PSA and found this, The PSA flare is a well-known phenomenon. The post chemotherapy
Thursday, my husband had his follow-up appointment with Oncologist. I was very alarmed at some of his blood test results. His PSA went up to 1600. Doctor said other blood work was to be expected. I researched surged in PSA and found this, The PSA flare is a well-known phenomenon. The post chemotherapy
MsHope
in
Advanced Prostate Cancer
5 months ago
Brain metastasis
New (Portuguese) anecdotal case study below. [1] When I began reading PCa studies on PubMed, I saw a lot of cell studies that used LNCaP (from a lymph PCa cell), PC3 (from a bone PCa cell) &/or DU145 (supposedly a brain met cell, but now described as "derived from a central nervous system metastasis
New (Portuguese) anecdotal case study below. [1] When I began reading PCa studies on PubMed, I saw a lot of cell studies that used LNCaP (from a lymph PCa cell), PC3 (from a bone PCa cell) &/or DU145 (supposedly a brain met cell, but now described as "derived from a central nervous system metastasis
pca2004
in
Fight Prostate Cancer
10 months ago
AUA 2023: PSA Response and Time-to-Castration Resistance Among Patients with mCSPCa Initiated on Apalutamide, Enzalutamide, or Abiraterone
The objective of this study was to describe a “real-world” experience of mCSPC patients treated with apalutamide, enzalutamide, and abiraterone acetate, with a focus on PSA response and development of castration resistance outcomes. This study identified patients with mCSPC newly initiated on apalutamide
The objective of this study was to describe a “real-world” experience of mCSPC patients treated with apalutamide, enzalutamide, and abiraterone acetate, with a focus on PSA response and development of castration resistance outcomes. This study identified patients with mCSPC newly initiated on apalutamide
skiingfiend
in
Advanced Prostate Cancer
10 months ago
Restless Legs - changing treatment.
Can anyone advise me? I have had RLS for more than 30 years, familial predisposition. Been on Pramipexole for about 10 years - started with 0.088 mg. Over the years with the need to increase the dose - now 0.7 mg. Sleeps only about 2 + 2 hours a night. Has severe restlessness in the legs, like a wasps
Can anyone advise me? I have had RLS for more than 30 years, familial predisposition. Been on Pramipexole for about 10 years - started with 0.088 mg. Over the years with the need to increase the dose - now 0.7 mg. Sleeps only about 2 + 2 hours a night. Has severe restlessness in the legs, like a wasps
Gibbel
in
Restless Legs Syndrome
4 months ago
preds down but flare ups again
hi all, I have not been on for a while so my apologies, once again I am down to 2 mg and hence flare up again 😭 every joint and muscle are back. When I was on 2.5mg I wasn’t to bad for a month on that dose, every time I try 2mg flare up starts and agony. 13 years this year now from 60mg to 2, am I ever
hi all, I have not been on for a while so my apologies, once again I am down to 2 mg and hence flare up again 😭 every joint and muscle are back. When I was on 2.5mg I wasn’t to bad for a month on that dose, every time I try 2mg flare up starts and agony. 13 years this year now from 60mg to 2, am I ever
Margaret1951
in
PMRGCAuk
4 months ago
Suboptimal Cortisol levels following Synacthen test
I’ve just turned 60 and used to be a sportsperson. I’ve been on predisolene for 5 1/2 years and unable to get below 5mg despite several slow attempts. My rheumy suggested a short synacthen test via Endo which was 8 months later. I barely function on 5mg with doing bare minimum, giving up my small flower
I’ve just turned 60 and used to be a sportsperson. I’ve been on predisolene for 5 1/2 years and unable to get below 5mg despite several slow attempts. My rheumy suggested a short synacthen test via Endo which was 8 months later. I barely function on 5mg with doing bare minimum, giving up my small flower
Heucera1
in
PMRGCAuk
4 months ago
Liver Screening Results
Good morning to you all, Well after asking for my blood results to be emailed to me I am pleased to see that most antibody tests were negative however the EBNA igg one was positive which after reading online says it is a virus probably caught years ago that lies dormant like the cold sore virus, my
Good morning to you all, Well after asking for my blood results to be emailed to me I am pleased to see that most antibody tests were negative however the EBNA igg one was positive which after reading online says it is a virus probably caught years ago that lies dormant like the cold sore virus, my
Sophia1968
in
British Liver Trust
4 months ago
Tiromol T3 - Any good etc?
Would be people be so kind as to tell me how they got on with the T3 brand tiromol? I am just trying the odd 25mcg tablet here and there along with my Thybon Henning. Tiromol is a little easier on the wallet which is one of the reasons I have decided to try it. Many thanks.
Would be people be so kind as to tell me how they got on with the T3 brand tiromol? I am just trying the odd 25mcg tablet here and there along with my Thybon Henning. Tiromol is a little easier on the wallet which is one of the reasons I have decided to try it. Many thanks.
joey82
in
Thyroid UK
4 months ago
Iron Infusion
Sue perhaps you can help me, I have been successfully relying on diet for years but RLS seems to be catching up. I am in Australia. Perhaps its simply a matter of getting older (currently 79) but a couple of other things might be a problem. I tore a hamstring muscle or tendon that apparently caused
Sue perhaps you can help me, I have been successfully relying on diet for years but RLS seems to be catching up. I am in Australia. Perhaps its simply a matter of getting older (currently 79) but a couple of other things might be a problem. I tore a hamstring muscle or tendon that apparently caused
Graham3196
in
Restless Legs Syndrome
4 months ago
Ferritin and B12D/PA
Some time ago (on this forum?) I read that 80% of PA people had peripheral neuropathy and 20% did not. I have dizziness, brain fog and tinnitus but not PN. I believe the above are related to the central nervous system rather than the peripheral nervous system.What I'm discovering in my case is that the
Some time ago (on this forum?) I read that 80% of PA people had peripheral neuropathy and 20% did not. I have dizziness, brain fog and tinnitus but not PN. I believe the above are related to the central nervous system rather than the peripheral nervous system.What I'm discovering in my case is that the
Orchard33
in
Pernicious Anaemia Society
4 months ago
Should I be worried about suppressed TSH
I am extremely well and all my bloods seem within normal range to me (but not the GP)! I am 61 years old and was diagnosed with Hashimotos Thyroditis and Chronic Fatigue in 2004. My only health issue is very erratic sleep (one night 8 and a half hours, the next 4) which I handle by resting in the afternoon
I am extremely well and all my bloods seem within normal range to me (but not the GP)! I am 61 years old and was diagnosed with Hashimotos Thyroditis and Chronic Fatigue in 2004. My only health issue is very erratic sleep (one night 8 and a half hours, the next 4) which I handle by resting in the afternoon
YoginiDancer
in
Thyroid UK
9 days ago
Could someone PM me T3 sites?
Hi. I come back here every two years when my supply runs low and my former go-to site has vanished (or at least is giving me a security warning) to ask again. I need a site that takes paypal/debit card. Cynomel is my holy grail but I don't know if anyone can access that now without a scrip. Tiromel
Hi. I come back here every two years when my supply runs low and my former go-to site has vanished (or at least is giving me a security warning) to ask again. I need a site that takes paypal/debit card. Cynomel is my holy grail but I don't know if anyone can access that now without a scrip. Tiromel
GentleOrange
in
Thyroid UK
4 months ago
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