Experiences with

Graves' disease

After surgery PSA should be undetectable. What does it mean. Once the lab give 0.03, once 0.04. I guess it s the lab (standard error of the machine), but what is the limit of the lab and when should i consider that THERE IS a PSA. Why is PSA still detectable after surgery should nt it be 0.00 ?

This video talks about ivermectin and prostate cancer. FWIW https://www.bitchute.com/video/3RFTIHS6CUC8/

I know this forum is primarily for those with advanced PCA, yet I regularly see posts by those who've only recently discovered the disease and are not in such adavanced stages, being treated only with 1st-generation ADT. Thus, as a nearly 20-year survivor of PCa (first discovered in 2005) and 10-year

I'm 83, prostate cancer(PSA 30) with negative bone scan, negative MRI, but PET shows multiple small mets throughout both lungs and multiple lymph nodes throughout the chest. Started with 600 mgm bid of Nubeqa, and Orgovyx 120 mgm once a day. I also received radiation to the prostate approx. 6 months

"[i]We've been doing a lot of work at Johns Hopkins using high-dose testosterone therapies to treat patients with metastatic prostate cancer, " says Mark C Markowski, MD, PhD.[/i] This comprehensive overview of bipolar androgen therapy (BAT), by Mark Markowski, MD, PhD, associate professor of oncology

UroToday.com) The Society of Nuclear Medicine & Molecular Imaging (SNMMI) 2024 Annual Meeting held in Toronto, ON between June 8th and June 11th, 2024 was host to a prostate cancer therapy session. Dr. Fuad Novruzov presented the results of a prospective phase 3 randomized study from Azerbaijan evaluating

Diagnosed end of April, 2 days of intravenous pred @ 500, 1 day at intravenous @ 1mg and then onto 60, 50, 40, 35 - just started on 30 today. Bloods from 3rd June came back with liver and kidney markers out of range ....... steroids 🤷‍♀️ Have a slot to discuss the results with the surgery pharmacy

My husband was diagnosed about 7 years ago. we delayed medication (trying endless supplements and life changes) as long as we could but a couple of years ago tried c/l he did not have any success and it made him nauseous ... tried Rytary about 6 months ago and since has been having depression

Hello. I am trying to find some information for a family member. He took a break last August and left his job as long dustance HGV1 driver. 6 months later, went back to old job, lasted a week and his boss said, you're not well, sort your health issue out. So in March I took him to A&E and what we

Curious if anyone experiences random liver area discomfort. Not pain, just a tender discomfort. Last usually 7 or so hours, then its good. Causes? PBC since 2020ish Urso 3x a day. 250 Osteoporosis TanGram =)

Hi. I started Hydreasin two years ago one capsule a day. Last year it was found I had obstruction of ureteroreanal junction. out of the blue. I suffered much pain and in two days I am having surgery. I read somewhere that Hydroxy does that. Any idea about it? I am thinking of changing to Besremi as

After 4 .5 weeks of radiation PSA dropped from 6.6 to 3.46 but on 6/3 went up to 5.88. I have MO appt 6/11 and he has previously indicated that docetaxel could be the next step. Following last PSA increase switched from Zytiga to Xtandi. I am guessing that a PET scan is in order and maybe SBRT prior

After 5.5 years on Lupron (no Zytiga, Xtandi, Daro, etc.), my PSA hit its highest points ever (1.92), although I'm still not 2 points above my lowest reading of 0.5 (only one of those). I'm metastatic and was at diagnosis, so still have prostate. I've been researching Provenge a bit, and understand that

Hi. I'm so glad I stumbled on this site and I'm hoping that someone could be kind enough to reach out to me? I'm so very, very scared, and it's all my own fault. I have suffered from an anxiety disorder for 15 - 20 years and used wine to cope....and lots of it. I was diagnosed with compensated cirrhosis

I was wondering if anybody with ALD/AMN in the UK was using Dalfampridine (Ampyra) to help with walking? I believe that it was initially an MS drug but it is now being used around the world. As I understand it, it is approved for Wales and Scotland but not for England.

Hey all, Having an MRI in 2 weeks time for my pituitary. I am unable to be on thyroid replacement I used to be on, raising doses seem to increase my cortisol further. Any helpful info would be amazing! Thanks x

Hi there, I’m Liz and this is my first post. I have recently had an ELF score of 9.9. My GP didn’t request this test - I requested it myself because I just wanted to know if my liver was in good condition and healthy. I have had an ELF test In the past which was raised but not unduly so and over the

Hi This is my first post since being diagnosed with the above condition. I have now stopped drinking. I am confused with the staging element. I would be grateful for clarification in layman terms. I am awaiting an MRI of my liver and heart. I have also recently been diagnosed with dilated cardiomyopathy

Hi all, My 17 year old daughter has just had her follow up post op appointment following a laparoscopy which she had last October. She has confirmed Endometriosis and all the surface (that they could see) Endo was removed. Unfortunately her pain has not improved and she says it's the same as before the

[i]Two of the common conditions associated with PBC are thyroid conditions and with those that cause anemia. This is because they both have shared genetic factors that affect our immune response. [/i] [i]An underactive thyroid is caused by an autoimmune response to the gland itself.[