Experiences with

Alkaline phosphatase test

Hello friends, I am having a hard time sleeping due to a nagging suspicion. My husband has very high risk, hormone sensitive M1a pc which has been kept undetectable since January, ‘24 with doublet (Elgard/Abi/Pred and IMRT. His ALP baseline was 62 at initial dx in 4/22 and rose to 88 when he had a clinical

Hello everyone! My name is Ashley and I set up an account here for my dad (60 years old) who has been recently diagnosed with advanced prostate cancer that has metastasized to the bones. I have been reading many of the posts on this website and have learned so much already. It has helped me reassure

[u][i]AMA - Anti - mitochrondial Antibody[/i][/u] This classic antibody type is seen in PBC. Combined with elevated alkaline phosphatase, part of your liver panel blood work, a positive AMA is about 95% certain for the diagnosis of PBC.

Once again I am asking for any information that can be provided from this great group. Would appreciate any information for Jevtana treatment. At doctor's appt yesterday, my husband's hemoglobin had decreased to 7.6 and he had to have a blood transfusion. His Alkaline Phosphatase went up again.

Once again I am asking for any information that can be provided from this great group. Would appreciate any information for Jevtana treatment. At doctor's appt yesterday, my husband's hemoglobin had decreased to 7.6 and he had to have a blood transfusion. His Alkaline Phosphatase went up again. He

I'm 3 weeks into a clinical trial for ARV-766, an AR degrader. At 2 weeks, my PSA had dropped from 133 to 66! Bone pain is much less. All my liver numbers are fine, but alkaline phosphatase has gone from 199 when I started to 429 at two weeks and 519 at three weeks. Doc thinks may just be a surge, but

Hoping all is well with others on this site. UPDATE May 15 2024 I am concerned about results of the Right frontal skull SUV 5.3 previously 0.75. I have researched and really can't find any information that I can understand. Any replies would be greatly appreciated My husband had his PSMA PET/

The first part is in my profile. It makes me feel vulnerable to share, but we have benefited enormously from reading others' stories, so I'm sharing. UPDATE: 8/18/21 PSA =0.45 9/6/21 last dose Orgovyx 9/7/21 First Eligard 3 month shot 9/17/21 PSA =0.78 10/18/21 PSA =1.28 Nov not tested 12

The words this week I want to define are alkaline phosphatase. Alkaline phosphatase (ALP) is an enzyme that is released by the bile ducts cells ( among other organs). The release of ALP is a marker of stress or injury. So the more injury or stress to the bile duct cells, the higher

I am in ARX517 trials Last PSA : 2.18 (Check BIO for more) I am trying understand what going on with Aspartate Aminotransferase , Alanine Aminotransferase and Alkaline Phosphatase Alanine Aminotransferase Aspartate Aminotransferase Alkaline Phosphatase

Hi everyone, just joined the forum and would be interested in people's opinion of my latest liver test results.My cholesterol is showing as 6.1 also. Received: 26 Jul 2024 Provider Sample ID: BP274508V Pathology Investigations Liver function tests Serum total bilirubin level 17 umol/L [0.0 - 21.0]

[u][i]Alkaline phosphatase [/i][/u] It is an enzyme released as a response to injury to the bile ducts - not the liver itself. As more cells are injured, the more alk phos is released. Alk phos is not in itself harmful. Higher levels in the blood does not mean more tissue damage. Even lowering

Hi everyone, my Dad’s PSA at the end of 2023 was 0.008. This year (2024), PSA had some fluctuations: 0.024, 0.029, 0.026, 0.025. PSMA Pet showed one small spot on the rib which was radiated by Dr. Kishan at UCLA. After SBRT, PSA was 0.015, and then in August was 0.022. He started having pain recently

Super interesting N=1 case study from the PSMA experts in Germany. Like me, you've probably never heard of transketolase or why you would even want to inhibit it. Turns out transketolase is a thiamine-dependent enzyme that serves as the rate-limiting enzyme in the non-oxidative branch of the Pentose

hello all So I had an Iron IV (first ever) on Tuesday morning and then went to the boxing club Thursday evening and literally when I finished I ended up having body aches and mild shivers felt like a flu coming on however no flu came just these body aches they have now cleared and som dizziness remains

Hello, Just wanted to ask if I am entitled to request the ELF test from my GP? I was diagnosed with NAFLD 3 years ago and NICE guidelines say you should have the ELF test every 3 years to check for fibrosis. I've had 2 sets of blood tests done in the last 5 weeks, which show worsening liver function

My father was diagnosed in April 2021 with advanced prostate cancer . His PSA was 6491 and 4 out of 12 cores were tested positive Gleason score 8. MRI dscovered 4 pelvic enlarged lymph nodes and two masses in prostate . He started Eligard in May 2021 and biculatamide for 30 days ; in June 2021 his PSA

My father was diagnosed in April 2021 with advanced prostate cancer . His PSA was 6491 and 4 out of 12 cores were tested positive Gleason score 8. MRI dscovered 4 pelvic enlarged lymph nodes and two masses in prostate . He started Eligard in May 2021 and biculatamide for 30 days ; in June 2021 his PSA

I was diagnosed with PBC and 2017. My alkaline phosphate levels were 277. I was told I was gonna go in the liver transplant list or I was going to die. I was prescribed URSODIOL and Oclavia. My levels started to go down, but I was starting to have a reaction from the Oclavia, causing me to have eczema

Hi This post isn’t about me (a recovering alcoholic, sober 3.5yrs!) but my completely normal, low level of alcohol intake, partner! He had some bloods run as part of a routine check up for his age (46) and they’ve had him back in for full LFTs / scan next week as his ALP was 139.. When I say normal