pattercat
pattercat
I had a revision from RNY to BPD-DS June 2018. My highest weight (pre-RNY) was about 450 and at the time of my revision I hovered between 275 and 300. I just couldn't lose below 275 though and consulted a surgeon in Indiana. He was great, and even though I've had some issues, I would still do the revision again. Honestly, I wish I had fought for BPD-DS the first time around, I just was younger and didn't advocate for myself then as much as I do now. Today I'm hovering between 180-185.
I have normal malabsorption issues and really depend on my vitamin supplements. However, this past year I started having some major issues that I kept attributing to my BPD-DS and didn't discuss with my doctor when I should have. Long story short, after months of multiple yucky GI issues, feeling very weak and losing weight without trying, I saw my doctor. What really started to scare me was losing a lot of muscle mass. In the end, I've been diagnoses with EPI (Exocrine Pancreatic Insufficiency) and that causes even more malabsorption issues and I was super low on my ADEK vitamins.
I've started taking Creon with every meal and it has really helped, along with doubling my already high vitamin supplements, I'm slowly starting to feel better. What sucks is that the Creon looks like it will be a lifetime commitment since the pancreas does not heal. I can certainly tell when I don't take my Creon.
I'm really curious how many others who had a Duodenal Switch have ended up with pancreas issues. I did some research and while it is rare for a WLS patient to develop EPI, there is evidence that 5 years + post-op for DS that the risk level of having pancreas issues increases.
I have normal malabsorption issues and really depend on my vitamin supplements. However, this past year I started having some major issues that I kept attributing to my BPD-DS and didn't discuss with my doctor when I should have. Long story short, after months of multiple yucky GI issues, feeling very weak and losing weight without trying, I saw my doctor. What really started to scare me was losing a lot of muscle mass. In the end, I've been diagnoses with EPI (Exocrine Pancreatic Insufficiency) and that causes even more malabsorption issues and I was super low on my ADEK vitamins.
I've started taking Creon with every meal and it has really helped, along with doubling my already high vitamin supplements, I'm slowly starting to feel better. What sucks is that the Creon looks like it will be a lifetime commitment since the pancreas does not heal. I can certainly tell when I don't take my Creon.
I'm really curious how many others who had a Duodenal Switch have ended up with pancreas issues. I did some research and while it is rare for a WLS patient to develop EPI, there is evidence that 5 years + post-op for DS that the risk level of having pancreas issues increases.