Experiences with

Phosphate test

Has anyone had a blood test showing low phosphate levels please ?

Hi everyone , Father , 56 age ,completed 6 docetaxel 3 weekly cycles (dose75mg/m2 , his total dose -135mg ), his blood reports are HB-8.7 , Platlets - 160, Alkaline Phosphate - 865 , PSA - 2.287 All other test like liver ,kidney profile , glucose within normal range .

I have just been through something quite strange and frightening. I had a CT scan of abdomen with contrast on Monday for assessment for an NHS trial. (EMBIO) About 6 hours later I felt a little queasy. I woke up at 230 am with abdominal pain which I thought was indigestion. This quickly became non

Has anyone had allergy/intolerance testing to get a reason to what is causing the constipation? My doctors keep telling us she will grow out of it and to keep giving her laxido sodium phosphate and senikot which is no longer working

My bloodwork shows that I am high in B6 yet I dont supplement with B6. Normal is 3.4 - 65.20 and mine is 121.3 To decrease B6 it says to stop taking it.... so I am stumped. Any info would be appreciated

hello all. Husband dx in 2017 with 489 PSA. So far we’ve done Docetaxel, Xgeva, Zytiga. Currently on Xofigo (Ra 223) it knocked the Alk Ph way down then after the third treatment it went up a few points. Has this happened to anyone? RO suggests doing 4th treatment then PSMA scan to see if there’s

Hi, I have recently been diagnosed with CKD Stage 2. I am also scheduled to have a colonoscopy in December. I am scared that the laxative solution and the phosphate enema that I have to take as part of preparing for the colonoscopy will damage my kidneys even more than they already are. I am also worried

Hi All, If anyone was adversely affected by the FDA's shock decision to reject Tenapanor as a treatment option for hyperphosphatemia, please use the link below to send your comments to the advisory committee that will be reviewing Tenapanor on November 16th. A lot of patients can't take phosphate

Hi, hope you're all doing well! Since getting covid in March of last year I have had a whole bunch of symptoms like fatigue and joint pain and fevers, also butterfly rash and some photosensitive rashes so my GP did an ANA and dsDNA for lupus which both came back negative and the rest of my blood were

I had kidney transplant 3 months ago and it has been a living hell.I have ibs to begin with and for three months my intestines have been getting destroyed from meds.I have chronic watery diarrhea to the point that i cant leave my home for more then 2 hours and if i do i need to have a bathroom close

https://youtu.be/_PNWmaV81F4

Hi all, I've just asked for a print out of my FBC, Dr Says all tests are fine, but I've come across my phosphate level and in the comments it says "below the recommended range" 0.79 (0.8 - 1.5) I know it's only just under,but does anyone know much about this? thank you.

Does any of you had a problem with low parahormon? Diagnosed with tetany. Phosphate and calcium and magnesium economic not in level. Neurological problem occured

£3!! and rather annoyingly really nice... heck I'm worth it! I only went in for a sneaky sushi treat 😏 Edit... actually cheaper in Waitrose as they sell the 500g where as the other only sell 250g £1.85 Oat Base (Water, Gluten-Free Oats (11%), Sunflower Oil, Salt), Coconut Cream, Stabilisers (Tapioca

I have just written to my Local MP about this as I think time is of the essence to stop it happening. I have read that it can impact thyroid function? I believe the type of fluoride to be used is hexafluorosilicic acid which is an industrial waste product from the pollution-scrubbing operations of the

Hi folks My question is about side effects with Venetoclax and Obinituzumab. I wonder if anyone out there has any insights. I'm 66, was diagnosed in July 2020. Watch & wait until July 2022. Started Venetoclax and Obinituzumab in New York at Sloan Kettering. I’ve completed the Obinituzumab, and

Hello Everyone, I hope you are all well I had a Liver Function Test last week. I was asked to take the test 2 weeks after starting Atorvastatin 40mg. I spoke to the Cardiac Nurse today and she said my Alkaline phosphatase level is at 142 (normal range 30-130). She mentioned the last

Hi all, I wrote back a month ago worried about my lowering platelets and the doctor taking me off Besremi. My last injection was early November 500 mcg. My platelets got down to 53! They are coming up, now at 87, 2 weeks after the 53 reading. The Besremi is still having a lowering effect on my white

I was diagnosed with MBC in the liver in March of 2019 and have been on Faslodex only since that time with stable scans and lab work. I fell 10/1 and fractured my femur near the hip. On 10/2 I had a partial left hip replacement. I missed my October oncology appointment and Faslodex shots. I saw the doctor

I’m worried.. I’ve been on Urso for 3 months, my ALT and AST came back normal but my Alkaline Phosphatase increased from 220 to 240….really confusing. Any advice or information would be appreciated.