Liver transplant - Let's support each other

I really appreciate the warm welcome from all. Thank you!
I was diagnosed with PSC when I started having the gallbladder issues. Technically it wasn't the gallbladder, but a duct cyst that would inflate with bile then whenever it felt like it he would rapidly drain into my stomach (approx 200cc) . I can only describe what would happen next by saying I would have given Linda Blair in the exorcist a run for her money on the projectile vomiting. That was sometime in the spring of '14 and had it all removed in December of '14 - Merry Christmas!! LOL
I have read that UC and PSC are buddies and generally come along at the same time. My UC started in March of 2010. It actually began because of a bout of food poisoning. I am told that an event can trigger it if it is already there but dormant. If they did start at a similar time then I have had it 10 years give or take.
As for my health it is good. My liver is asymptomatic. All my liver function tests have always been in the normal range. Since I dont have a colon my UC is cured. The only real issues I have are problems with skin, most notably around my ostomy, but I am slowly working out what works well and doesn't.
I dont know if anyone here is in Rochester, but I am in Dr Poterucha PSC surveillance group. He is a great guy and has a super bedside manor. I could chat with him all day.
I am so happy to have found this site. I wish I knew about you earlier, but I am here now. Thank you all again for welcoming me. This has been great so far!

Funny you would say foot powder Rosemary. My WOC nurse told me to use foot powder around my stoma when I get red bumps, like a heat rash. It does work very well. She told me she could get me a script for it or just go buy generic foot powder with 1% Miconazole and you will be good to go. I bet I use it every 4th or 5th wafer change. It is fantastic!

By the way “Raowdy Ramsey” is my dog. My name is Ramona. My dog ,Ramsey, is a collie and a present to me after surviving the transplant. He’s been at my side every minute since! WELCOME

Hello Jason! We are the same age. I’m a female though! Had a liver transplant in 2015,mid summer!. I was 47 yrs. old. I’m from Maryland so I got to choose between Johns Hopkins or University of Maryland. Kinda started at Hopkins and ended at University!! Welcome and feel free to “tag along”

Hi @msgtrebholtz. Jason, I'd like to add my welcome. It's so nice when people find Mayo Clinic Connect at the beginning of their journey to help prepare, ask questions and get support. I say beginning, but this is not really a beginning is it? It's just the beginning of learning about transplant. You have vast experience with ulcerative colitis, colon surgery, ostomy and more that I'm sure will benefit other members who are beginning those journeys. I invite you to also follow these support groups on Connect:
- Digestive Health https://connect.mayoclinic.org/group/digestive-gastrointestinal-problems/
- Ostomy https://connect.mayoclinic.org/group/ostomy/

Your knowledge and experience will be welcome.

Jason, when were you diagnosed with PSC? How is your health today?

@rowdyramsey, Tacrolimus is one of the medicines that I also take for my Liver and kidney transplant. In fact have taken it for 11 years now and have not noticed any rash or blisters as you describe. It sounds like this was in the past, -I sure hope so.

Unrelated to tacrolimus -I want to add that I am from a family who sweats alot when active, and I have developed an itchy redness after wearing my sun hat, and along areas lere my clothing fits snug and wet with sweat especially during summertime hiking. Scratching makes it more uncomfortable, and I didn't want to cause any open areas, so I (ready for this?) use a little bit of foot powder - the OTC powder for athletes foot care - and it works to cure the itch. A dermatologist suggested that I try it.

@msgtrebholtz, Jason, Welcome to Connect. I am happy to extend a virtual handshake to you. I am a PSCer. I am thrilled to meet you, because there are not many of "us". I actually joined Connect in 2011 to meet other PSCers after my transplant on 2009 at Mayo in Rochester. I transplanted at age 60 after having lived with PSC diagnosis for around 8 - 9 years. I did not have UC. My PSC (Primary Sclerosing Cholangitis) was discovered when my PCP observed abnormal liver functions in my routine annual labs. I am forever grateful that he immediately sent me to a GI who cared for me until it was time for me to have a consult and evaluation at transplant department.
Jason, I welcome any questions, anytime.

Here is a very special feature on Connect, that I want you to see! The PSC Page and Newsfeed - where Mayo Clinic investigators and their teams are making strides to better understand and treat PSC patients, with the ultimate goal of developing a cure for this disease. YI invite you to follow the PSC page and stay up-to-date as we post news about advances in PSC research, clinical trials, and available resources.
https://connect.mayoclinic.org/page/psc/

Hello all, I am posting here basically to say hi. I wanted to read from others what they have gone through so I am glad I found this site. I am a 52 year old white male that lives in MN. I had UC for many years and got to the point where my colon cancer threat was very high so in July of 2017 I had my colon, rectum and anus removed and a permanent Ileostomy made. That's just background info, not why I am here. Along with my UC there were issues with my gallbladder, a huge duct cyst and I found out I had PSC. I had my gallbladder and cyst removed and duct reconstructed. The PSC will progress to the point where I will need a liver transplant sometime in the (hopefully distant) future. I appreciate all your insight and thank you for letting me tag along. Jason

@contentandwell I can surely agree about wearing slippers instead of shoes. For about 2 years I could barely even get socks on lol...even in winter I could not get shoes to boots on. I also lost feeling in my feet and they were always tingling. Post transplant it took about a year to get the feeling back. The top of my right foot is still a bit numb and actually hurts at times. All in good time...

@gaylea1 My immunosuppressant is a generic and is supplied by a speciality CVS in Boston - they send it up to me via UPS. My transplant department wants me to always use the same generic so I have made sure that they do not substitute a different manufacturer. My feet were so swollen that I couldn't put any shoes on, I had slip-on slippers that I wore all of the time. I even went to my hairdresser in slippers!
JK