I get asked so often what I did to be almost 19 years post transplant. Here are some tips.
- I have never missed taking my transplant meds. Ok, maybe once or twice but it was because I had a flu bug and was vomiting
- I have kept all of my doctor appts and made sure I do all of the labs that were ordered. I am a "hard" stick so going to the lab at times was not always a pleasant experience. And yes after almost 19 years, I still "hold my breath" waiting to get the results. With a few glitches, my creatinine is consistently at 0.9.
- I know at first after a transplant they want you take your BP everyday. After almost 19 years I don't do that anymore, but I still take it weekly. I take it more often if I am dizzy, have a headache, or if I feel my pulse is high. I think it's important.
- I live in a state that does not have a transplant center in its boundaries, so I see a nephrologist here every 3 months. I write down questions that I might have for the next time I see him. If something serious comes up or if I have a question that can't wait till next appt., I make sure I "portal" ( medical system here email for DR) him.
- I live in a very dry & arid state, so dehydration is a problem for me. I never walk out the door without a bottle or 2 of water. I make sure to remember to drink.
- I have gained some weight since my transplant but try to stay active and walk everyday. Winters can be brutal here, so my husband joins me and we walk at the local mall.
- I think for a lot of things....moderation is the word. I eat a lot of chicken and fish but certainly eat BEEF, but not more than once a week. I live in a state that raises cattle afterall!
- Travel can sometimes be a challenge. Eating all of your meals in a restaurant can be a problem because they salt everything. I have found that more and more restaurants will skip the salt if you ask them.
- The one thing I cannot stress enough is to be your own advocate!! You know your body better than anyone. If you think something isn't right.....get on the phone and call your doctor or transplant center. This is your life and don't be afraid to ask questions.
- And most of all......Live Life!!! You didn't go through all of this for "fun"......you did it to live and that is exactly what you should do. After my transplant I saw both of my daughters marry and I now have 2 little buddies - my grandsons. My husband and I have traveled to Europe, the Caribbean, Mexico, hiked in the Rocky Mts in Glacier National Park, caught Salmon off Vancouver Island in Canada, retired and now live in WY. It was always our dream to move out West and so we did. I look upon my Transplant as a true Gift of Life!