Living with UC? Tell us about your experience. Take our survey here.

caret icon Back to all discussions

Has anyone had to go on TPN?

Has anyone had to go on TPN (Total parenteral nutrition)? Doc wants me to go on this week. I’m scared.


Have a question? Ask it here!

  1. Hello there , we are glad you've reached out. I hope that others may chime in with their own personal experiences on TPN, as I know that you are not alone in being recommended to go on it. One of our team members, Paul, has been put on TPN and written about it quite a few times in some articles that I will go ahead and share with you here: https://inflammatoryboweldisease.net/living/low-numbers/ It's okay to be scared, and we want you to know that we are here for you. Have you been able to bring up your fears/concerns with your doctor? Please do keep us updated, and know we are thinking of you. Warmly, Ashley (InflammatoryBowelDisease.net Team Member)

    1. Hey . I dont have personal experience, but I know many others in the community who do.

      It'd only natural that this would be a worrying time for you! I see Ashley has already shared some useful links with you, so that's good 😀 I do hope they help!

      Another useful article is this one: https://inflammatoryboweldisease.net/symptoms/complications/malnutrition/

      Here's hoping it helps you!

      - Sahara (team member)

      1. TPN is a handy thing to safely and effectively nurture your body. I’ve had it twice but only when I believe I really need it. Remember you have the right to refuse it. Only I can say my opinion is you know ur body the best, if u can’t eat, and are fading away, you know u need nutrition then obviously don’t do that to yourself, take the TPN and get healthy! Know it’s scary thinking of them inserting it, look the other way and then have fun keeping track of ur weight gain daily! Plus u feel human again when ur nourished!!!!!

        Please read our rules before posting.