No one is the same. We are all different. Know your symptoms. Know that your not alone.

[Rich6340]

recently just found this website. I really wish I knew about this way sooner than now. Now there's a lot of people that understand the things that are going on with me. I was diagnosed 3 years ago with stage two. Today I'm in a clinical trial. I've been there I'm doing it now. I put together my Primary doctor and the doctor's at the lover study. Everybody is working together. This is a crazy ride people. If you have a question for me, please don't hesitate and ask.

[nash2 Partner]

thanks Rich

We need more people willing to speak up about the details. Good for you to be in a trial. It is the only way we can get treatments.

[Jkf1]

Thank you for sharing your journey and good luck

[Cats2018]

Good luck to you Rich. Sounds like you’re on the right path. I was diagnosed just over a year ago with Nash stage 3 fibrosis. I’m just finishing a year long clinical trial. Had my final MRI 2 days ago, final blood tests and FibroScan yesterday and getting my 2nd liver biopsy to be compared with the 1 from May 2018, next week. My doctor is thinking she will have me apply for a 2nd clinical trial a couple months after I finish this trial. I’m hopeful because my FibroScan yesterday was much improved over the one done May 2018.