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raised AST (SGOT) levels and your history with CLL
when i was DX 7 years ago, my AST levels were at around 30. my oncologist hasn't said much about the fluctuations, which have gone up to 50 on occasion. so when i went to see my GP who worked in oncology in another country, told me that i have mild fatty liver, i was shocked as i was obviously unaware
when i was DX 7 years ago, my AST levels were at around 30. my oncologist hasn't said much about the fluctuations, which have gone up to 50 on occasion. so when i went to see my GP who worked in oncology in another country, told me that i have mild fatty liver, i was shocked as i was obviously unaware
ninap
in
CLL Support
2 months ago
worrying results but not yet diagnosed
hi all I had some blood tests for something unrelated which showed high creatinine and a low egfr. Then I had a urine test which showed high albumin levels. Last week I had an ultrasound which showed normal size kidneys but inflammation. Does all this mean I have kidney disease? My appt to see a
hi all I had some blood tests for something unrelated which showed high creatinine and a low egfr. Then I had a urine test which showed high albumin levels. Last week I had an ultrasound which showed normal size kidneys but inflammation. Does all this mean I have kidney disease? My appt to see a
Meagain24
in
Early CKD Support
2 months ago
Caffeine
I’m on 87.5mcg levo for now (have been prescribed 100mcg, but am increasing slowly) and I plan to test again in another couple of weeks with MMH to see how my levels are doing. Over the past two weeks I’ve felt really well and have been out and about more - walking, shopping, out for coffee (only ever
I’m on 87.5mcg levo for now (have been prescribed 100mcg, but am increasing slowly) and I plan to test again in another couple of weeks with MMH to see how my levels are doing. Over the past two weeks I’ve felt really well and have been out and about more - walking, shopping, out for coffee (only ever
JoJoloveschocolate
in
Thyroid UK
2 months ago
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Looking for any Info for Recent PC Diagnosis
I’m a 62 year old, recently diagnosed with advanced prostate cancer. I’ve been on hormone therapy for 2 weeks and see my oncologist in a week. My PC seems to be aggressive and my PSA is off the charts 885! I would love any positive info I can get.
I’m a 62 year old, recently diagnosed with advanced prostate cancer. I’ve been on hormone therapy for 2 weeks and see my oncologist in a week. My PC seems to be aggressive and my PSA is off the charts 885! I would love any positive info I can get.
Iber
in
Advanced Prostate Cancer
2 months ago
Dosage question.
I was diagnosed with Graves and overactive thyroid forty four years ago. I had a thyroidectomy and started on synthetic thyroid hormone therapy. I’m 69 now and take 100 mcg of Levothyroxine daily, my TSH is 0.291, low. What dose should I be taking?
I was diagnosed with Graves and overactive thyroid forty four years ago. I had a thyroidectomy and started on synthetic thyroid hormone therapy. I’m 69 now and take 100 mcg of Levothyroxine daily, my TSH is 0.291, low. What dose should I be taking?
UndertheTuscanSun
in
Thyroid UK
2 months ago
New NICE guidelines
On the Pernicious Anaemia Society forum, there is a new thread re the newly released NICE guidelines for Pernicious Anaemia/B12 Deficiency Diagnosis and Treatment in Over 16s [i]
New NICE guidelines
[/i] https://healthunlocked.com/pasoc/posts/150619728/new-nice-guidelines Within that thread,
On the Pernicious Anaemia Society forum, there is a new thread re the newly released NICE guidelines for Pernicious Anaemia/B12 Deficiency Diagnosis and Treatment in Over 16s [i]
New NICE guidelines
[/i] https://healthunlocked.com/pasoc/posts/150619728/new-nice-guidelines Within that thread,
helvella
Thyroid UK
in
Thyroid UK
6 months ago
NICE guideline on B12 Deficiency diagnosis and monitoring in over 16s
The Vitamin B12 Deficiency Guideline in Over 16's has been published.
What does this mean for those with Pernicious Anaemia whether formally diagnosed or not?
What does it mean with those struggling to get sufficiently frequent treatment for their B12 deficiency?
What does
The Vitamin B12 Deficiency Guideline in Over 16's has been published.
What does this mean for those with Pernicious Anaemia whether formally diagnosed or not?
What does it mean with those struggling to get sufficiently frequent treatment for their B12 deficiency?
What does
PAScomms
in
Pernicious Anaemia Society
6 months ago
Ascites
I’m going through the diagnosis process at the mo. Had CT scan last week. Follow up appointment isn’t until a week on Monday. I’m quite sure I’m suffering with ascites. Do I wait til that appointment to find out or should I call someone (consultant’s secretary or my own GP) to ask for it to be drained
I’m going through the diagnosis process at the mo. Had CT scan last week. Follow up appointment isn’t until a week on Monday. I’m quite sure I’m suffering with ascites. Do I wait til that appointment to find out or should I call someone (consultant’s secretary or my own GP) to ask for it to be drained
K-Bear88
in
My Ovacome
2 months ago
MRI HCC Scan and bloods.
Hi guys.I have just received my 6 months routine MRI Scan results . Like the other 5 scans I've had they've shown no features of concern and my next routine scan is booked for 6 months. The monitoring liver blood result was normal ( AFP <1). On the blood form for the next scan it shows Cirrhosis CPT
Hi guys.I have just received my 6 months routine MRI Scan results . Like the other 5 scans I've had they've shown no features of concern and my next routine scan is booked for 6 months. The monitoring liver blood result was normal ( AFP <1). On the blood form for the next scan it shows Cirrhosis CPT
Nip1
in
British Liver Trust
2 months ago
Fibroscan Frequency
I had a Fibroscan 3 months ago as an earlier US diagnosed I had cirrhosis. I have fatty liver and a LSM of 28.2 . I have given up alcohol completely since then. I asked the consultant when will I have another Fibroscan . He told me in about a year. I was hoping to have another one much sooner so
I had a Fibroscan 3 months ago as an earlier US diagnosed I had cirrhosis. I have fatty liver and a LSM of 28.2 . I have given up alcohol completely since then. I asked the consultant when will I have another Fibroscan . He told me in about a year. I was hoping to have another one much sooner so
Oldtag
in
British Liver Trust
2 months ago
Encouraging results
Went for 6 monthly US today and they also fitted me in for a fibroscan. Well...the US showed a regular shaped, smooth liver with no nodules and only mild fatty liver. Fibroscan was still high at 40, but much better than 10 months ago when it was 74. My liver is recovering from the years of alcohol I
Went for 6 monthly US today and they also fitted me in for a fibroscan. Well...the US showed a regular shaped, smooth liver with no nodules and only mild fatty liver. Fibroscan was still high at 40, but much better than 10 months ago when it was 74. My liver is recovering from the years of alcohol I
Ilovedavid
in
British Liver Trust
2 months ago
Seven years later.
hi all, Im 7 years post transplant.some bile duct problems, but a good recovery after the main operation. I unfortunately still have fatigue and others symptoms but am alive and kicking 🤣 In the 7years since my transplant I have been lucky enough to become nanna to 7 grandchildren… One for each
hi all, Im 7 years post transplant.some bile duct problems, but a good recovery after the main operation. I unfortunately still have fatigue and others symptoms but am alive and kicking 🤣 In the 7years since my transplant I have been lucky enough to become nanna to 7 grandchildren… One for each
Singlady
in
PBC Foundation
2 months ago
atypical trigeminal neuralgia
Recently diagnosed with atypical trigeminal neuralgia, pain on left side of face/eye/head. I also have rheumatoid arthritis which I take methotrexate 20mg once per week for. Does anyone else know anything about this, or what helps, in a lot of pain.
Recently diagnosed with atypical trigeminal neuralgia, pain on left side of face/eye/head. I also have rheumatoid arthritis which I take methotrexate 20mg once per week for. Does anyone else know anything about this, or what helps, in a lot of pain.
PurpleDuckie
in
PMRGCAuk
6 months ago
Pluvicto and PSA
Hi Gents, Prior to starting Pluvicto my PSA was 29.29, after round 1, 23.67, after round 2, 14.47, after round 3, 17.70. I then had a PSMA-PET scan. It showed all bone metastases except one were either receding or gone. After round 4, my PSA is now 21.51. I don’t get it. If almost all my metastases
Hi Gents, Prior to starting Pluvicto my PSA was 29.29, after round 1, 23.67, after round 2, 14.47, after round 3, 17.70. I then had a PSMA-PET scan. It showed all bone metastases except one were either receding or gone. After round 4, my PSA is now 21.51. I don’t get it. If almost all my metastases
MJCA
in
Advanced Prostate Cancer
2 months ago
Updates to de novo metastatic prostate cancer treatment
Q. Is the current standard of care has changed in just one year? Docetaxel may now be considered in low volume and de novo disease together with an AR pathway inhibitor and radiation therapy indications should be extended not only to low volume but also to high-volume de novo disease? A. Yes, there
Q. Is the current standard of care has changed in just one year? Docetaxel may now be considered in low volume and de novo disease together with an AR pathway inhibitor and radiation therapy indications should be extended not only to low volume but also to high-volume de novo disease? A. Yes, there
Seasid
in
Advanced Prostate Cancer
2 months ago
Help Interpreting PET Scan Results
This is for my son's father (and my best friend). His biopsy showed prostate cancer, Gleason Score 7 (3+4), Grade 2, cancer found in all 12 cores. Yesterday he went in for a PSMA PET Scan and the results were delivered to his online account this morning. His Dr is closed for the holiday weekend so
This is for my son's father (and my best friend). His biopsy showed prostate cancer, Gleason Score 7 (3+4), Grade 2, cancer found in all 12 cores. Yesterday he went in for a PSMA PET Scan and the results were delivered to his online account this morning. His Dr is closed for the holiday weekend so
Autumn911
in
Advanced Prostate Cancer
2 months ago
to anyone new to the group.....
Hi - and welcome! My name is Donna - I facilitate this support group for The PBC Foundation - Health Unlocked. If you are new to your diagnosis, first of all, take a breath. It’s ok. We all, myself included, have been exactly where you are right now…. scared, unsure, mad, sad, and so much more. Stop
Hi - and welcome! My name is Donna - I facilitate this support group for The PBC Foundation - Health Unlocked. If you are new to your diagnosis, first of all, take a breath. It’s ok. We all, myself included, have been exactly where you are right now…. scared, unsure, mad, sad, and so much more. Stop
DonnaBoll
Administrator
in
PBC Foundation
2 months ago
Wednesday's Word
[i]
encephalopathy
[/i] This is a term used for a condition of toxic brain dysfunction. In those with PBC, it is known as hepatic encephalopathy. This occurs in advanced cirrhosis as the liver fails to filter the toxins. It occurs rarely, a liver transplant being the only help. HE (Hepatic Encephalopathy
[i]
encephalopathy
[/i] This is a term used for a condition of toxic brain dysfunction. In those with PBC, it is known as hepatic encephalopathy. This occurs in advanced cirrhosis as the liver fails to filter the toxins. It occurs rarely, a liver transplant being the only help. HE (Hepatic Encephalopathy
DonnaBoll
Administrator
in
PBC Foundation
2 months ago
Organ Donation for Transplant and Research
This post is talking about Organ Donation upon Death, so please take care to choose to read on further.
I recently went down to the Blood and Transplant Service Head Office in Bristol and attended a workshop on the importance of organ research. There were four of us fellow liver transplantees
This post is talking about Organ Donation upon Death, so please take care to choose to read on further.
I recently went down to the Blood and Transplant Service Head Office in Bristol and attended a workshop on the importance of organ research. There were four of us fellow liver transplantees
Richard-Allen
in
British Liver Trust
2 months ago
Newly Diagnosed
Hello, I’m new to this forum and was only diagnosed with SLE in late December. I’ve also got secondary triple positive antiphospholipid antibodies. I’m 26 and I’ve always lived a very active/outgoing lifestyle and have always tried to be healthy so it I’m finding it all a bit difficult to process.
Hello, I’m new to this forum and was only diagnosed with SLE in late December. I’ve also got secondary triple positive antiphospholipid antibodies. I’m 26 and I’ve always lived a very active/outgoing lifestyle and have always tried to be healthy so it I’m finding it all a bit difficult to process.
ChloeScotland
in
LUPUS UK
6 months ago
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