Experiences with

Graves' disease

Atypical Parkinsonisms (www.pcla.org) Date & Time July 12 11am PST // GMT - 8 https://pcla.us13.list-manage.com/track/click?u=f98a2ddbff31f952712a71bf0&id=60a1a1735e&e=b75464422e Description from the advert : Atypical Parkinsonisms present with some of the signs and symptoms of Parkinson's

Hi everyone, I haven't posted in quite some time, but I'm back because I need input from all the wonderful people on this platform. More than five years ago, my mom had a fall and was put on hospice care. They gave up on us too quickly, and she ended up with an NG tube down her throat for months

While we wait for the next generation PARP inhibitors to become available (I have written about it few weeks ago and I will soon have some first hand data), here are the results of Olaparib +Abiraterone It actually has decent effect also for people with no HRR mutations, but it works at its best with

finally got to talk to a very knowledgeable liver specialist having been trying to get some answers for months. He understood why I wanted to know and given some idea how long I can expect too live. He went into a lot of detail fully explaining all the scenarios, which is exactly what my wife and I wanted

It is with sadness that I report that My "vacation" may come to an abrupt end . After cruising along with an Undetectable PSA for a little over 2+ years, my recent test results indicate a PSA of 0.03 and my Testosterone jumped from <7 to 13. The good news is my T is coming back but it looks like

Hi all, I'm new to this board but would love some feedback. My father, 80, has been dealing with prostate cancer for a few years. He had initially had radiation plus Lupron injections. His PSA started rising again a few years ago and he wound up on Lupron regularly. His PSA has been slowly rising

And suddenly yestarday, can't explain why, my ebook becomes a bestseller on Amazon brain diseases category.😃 I wrote this book with the intent to help others, specially more recent diagnosed people, trying to leave some clues and to show that we can still have a fullfiled life with Parkinson's. This

I'm so sorry to bother everyone again. I promise this will be my last post for quite some time [hopefully]. I'm taking some advice from a couple of lovely members from this forum who have advised me to try and not worry so much over every detail of my condition, and live each day to its fullest. Just

Did some blood tests for day today The last blood tests were done on 2nd May - PSA 18 Alk Phos 180 which led to the prostate cancer diagnosis. Was diagnosed with bone mets to a few bones. Initially the plan was to do lupron and he was started on bicalutamide which he took for 3 weeks uptil 7th

My Dad was diagnosed with Prostate Cancer back in 2011. Here is his history (sorry if this is too much information). PROBLEM LIST Prostate cancer, status post prostatectomy, Gleason 4 + 5 = 9, March 2011. Pathology: ypT3b pN1 cM0, stage IV with positive obturator node. Adjuvant Lupron for 2 years

Interesting....see the fourth (4th) paragraph... MALVERN, Pa., June 26, 2024 (GLOBE NEWSWIRE) -- via IBN – Annovis Bio Inc. (NYSE: ANVS) (“Annovis” or the “Company”), a late-stage clinical drug platform company pioneering transformative therapies for neurodegenerative disorders such as Alzheimer’s

Hey everyone, I have a Liver Biopsy next week, as my blood tests have shown that my body is attacking my liver as it thinks it's "Foreign". I'm going under general for it. Does anyone know why my body is attacking my liver? Thanks,

Hello, it's me [again]. Only one more day until I go for my endoscopy as they picked up varices on my cat scan. May [or most definitely will, according to my gastroenterologist] have to band them. This whole procedure has got me thinking again, and I inevitably then end up with more questions [sorry]

I turned 87 just 3 days' ago. My QOL is still good: no pain, and a lot of physical activity. Fatigue is mostly annoying, but I generally can work through it. The issue is my concern with a slowly rising PSA. Today's blood test showed a PSA of 1.5. How concerned should I be, and are there steps to

Links now open Opening remarks by Dr. Elster and Darryl Mitteldorf, LCSW https://youtu.be/zFRCXKByqH0 https://youtu.be/atjTsMIkV2Q Dr. Callen Baker discusses the importance of creating inclusive healthcare environments for LGBTQ+ patients. https://youtu.be/6k0JNFofwUs Tom shares his personal journey

Hi all, I'm due for repeat liver enzyme tests next week for slightly elevated GGT and ALT, I've stopped drinking since Feb ( apart from a beer last weekend) and I've started weight training at the gym. I'm starting to lose weight but I've read weight training can cause elevated liver enzymes and to not

Fri 25 oct Cardio Respiratory investigation Echocardiogram Friday 1st November. Chest high resolution At 1 40pm Ct chest high resolution at 1 40 CT Angiogram Pulmonary at 1 40 All on Friday 01 November 2024 Not too shore what they all

For those who may be interested... MALVERN, Pa., June 25, 2024 (GLOBE NEWSWIRE) -- via IBN – Annovis Bio Inc. (NYSE: ANVS) (“Annovis” or the “Company”), a late-stage clinical drug platform company pioneering transformative therapies for neurodegenerative disorders such as Alzheimer’s Disease (AD)

My MO recommends taking PET CT F18 -DCFPYL in case I want to go intermittent after two years of Lupron and Erleada. My PSA is still less than 0.2. I had one PSMA in March 2022 when PSA was rising to 1.03. Scan show 3 preaortic lymph nodes and two spot on ribs. Then 6 weeks RT and ADT (Lupron, Erleada

Hoping for some advice. My wife has HCM and has had an ablation a few years ago. Her Afib seemed to calm down but recently it has increased dramatically. The ablation was carried out in London and appointments were not too difficult to obtain. We now live in Gloucestershire and it seems that getting