EVEROLIMUS vs TACROLIMUS EXTENDED-RELEASE CAPSULES

I share this for the benefit of others looking for hope in treatment for metastatic RCC. As we know, everyone's case is different and my experience is my own. I (48,M) am about 22 months following diagnosis with RCC, 21 months post radical nephrectomy (left). I was diagnosed with metastatic lesions

´´Long COVID is frequently discussed in this subreddit so I thought this is probably a good place with knowledgable people to ask this question. I recently stumbled on this article: [My Long.COVID Prevention Protocol.](https://desmolysium.com/covid/) The author notes that his friend who has long CO

I tried rapamycin after reading [this article](https://www.healthrising.org/blog/2022/07/06/apamycin-resurgence-doctor-chronic-fatigue-syndrome/) on health rising blog, but it made no difference to my symptoms. Many people believe CFS involves neuro-inflammation so I decided to try the closely rela

Hi, I just found an article and the author claims to have been on rapamycin for 4.5 years. This is probably the longest time I have heard of anyone being on rapamycin in an uninterrupted fashio. It is highly informative so I recommend to check it out: [**My Experience With Rapamycin**](https://desmo

I am 7 weeks post liver transplant. My team asked me to join a clinical study which would take me off Tarc and replace it with a medication called Everolimus. This medication is supposedly just as effective as Tarc but less stressful on the kidneys. Does anyone have any experience with this medicati

I graduated in March as an LVN. I started my new and first nursing job about a month ago. I work at a SNF… I love my job so much and enjoy seeing my patients. I would go deeper into everything, i’ll keep it short. I don’t think i was properly trained, was taught a lot of short cuts and tricks for me

Got a message from my transplant hospital today informing me that I’ll be covered through June but no guarantees after that. I didn’t even know they were in negotiations! My meds will be available through June but no idea what July will look like. I can’t afford my meds without insurance. I could a

I work at a kinda big pharma plant, and deal with some unpleasant stuff. Our latest batches are mostly bound for the USA, and a minor amount is for other markets. If you happen to use, or have used some of these medications, i'd like to hear if they really help. These aren't all the meds we make, ju