Topic: RE: PLEASE READ BEFORE YOU HAVE GB Brian-thanks for your post. I empathize with you. I had BPDDS (bilio-pancreatic diversion with duodenal switch) in 2002 at age 34. The psychiatric test didn't rule me out, & I was diagnosed with bipolar disorder at age 18 & had spent 2 separate stints in hospital lockdown between ages 18 & 34. I am 5'2", my weight at surgery was 286. Health wise, no diabetes, just hypertension, back pain, knee pain, foot pain, headaches... Other than bipolar, that's all. According to doc, a perfect surgical candidate. He even recommended the BPDDS! I had open surgery, not laparoscopic, so very hard recovery. 2 surgeries within a year post-op for hernia repairs. Tummy-tuck with 2nd repair. Slowly I started having issues with the malabsorption of my medications (doc mentioned the procedure would result some malabsorption of nutrients, he never mentioned it would do the same to medications and I was too starry-eyed to realize that!). I have been on disability now for 4 years because I cannot get my psych meds stabilized. I take about 50 pills daily ( there is 1med alone that I must take 9 pills of a day to get the proper amt into my bloodstream), its extremely hard for me to get them all in properly. In addition, the fact that I have only 4 feet of functioning small intestine has resulted in severe digestive issues (painful abdominal cramping & bloating, uncontrollable flatulence and daily diarrhea) for the past ELEVAN YEARS! At least I know now the digestive issues can be controlled by not eating wheat, or Gluten, products. Thank goodness! But my psychiatrist has no answers for the meds. 4 hospital stays in the past 4 years. Hypertension has returned. I've gained about 40 lbs, and my body looks strange. No, not just in my mind. My lower abdomen (tummy tuck area) is still flat as a fritter and always will be. The weight gain starts at my belly button and I have a true barrel upper abdomen. Actually hard to breathe because of the weight pressing on my lungs and diaphragm, and clothes fit improperly. All of these issues have made me say more than once that I would never have had the surgery if I knew then what I know now. It's so hard to tell others of the bad parts of WLS as they are so starry-eyed. I know I was. But I was a pioneer. In 2002 there weren't a lot of people 11 years post-op to advise me. And, like you, I agree that each individual's experience is just that-an individual . I wouldn't wish this experience on anyone.