The night of August 16th was probably the most painful night of my life. Starting at 5pm and finally at 4am on the 17th, I let my wife call 911. I was brought to the hospital and diagnosed as having a perforated colon from diverticulitis. If I wasn't on so much morphine, I probably would have flipped out. Finally, that afternoon they found air floating around my chest area and decided I had to have surgery. I was well prepped for it as far as info goes, so I knew I would wake up with a bag. My last words before going out in the OR were "Where is the music? There is always music on TV." They put on the hard rock I asked for. After the surgery, I couldn't even look at the bag for 5 days. I wanted to go home, so on the 6th day, the stoma nurse taught me how to manage it and I went home. Over the next ten weeks, I can't even describe the emotion, but I must say I think I handled it well. I went back to work for a few hours a day, even while I was in the hospital (laptop and phone). Ten weeks later, I had the reversal. I am now almost 5 weeks post-reversal and am doing well and have been back to work for three weeks (light duty and 4-5 hours a day, I am in sales so it's easy to drive around and visit accounts).
While I had the bag, I told everyone I was involved with and was amazed how many people told me about their experience with someone in the family that had a similar situation. I even went on a four-day golf trip with the bag on and it worked out OK as well. So besides the ugly scars on my belly, I think I am going to be OK. By the way, I am 59 years old and in good health besides this.
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Hi All, If you have an " old" or recent ostomy, this is the place for you. I think I've been a member for more than 15 years, but I have had my surgery, since I was a kid of 15 ( do the math-that's more than 60 years ago). As a teen, with a new ostomy ( for Ulcerative colitis) my parents dragged me off to my first ostomy association meeting. I wasn't happy, but in the long run, it's the best thing that happened to me. I met others, older, and teens like me, adjusting to the changes. A group of us started a Young adult group, and helped each other, and even visited kids who were new to the world of ostomies. But soon I married, and moved out of state, and although made some connections with other NJ ostomates, I became pretty much isolated. Until I discovered MaO. By then, I was having a myriad of other medical issues, and my aging stoma " wasn't doing well". I received a lot of help and support from members! I was pleased that I was also back to supporting others. I met a gal on line (from Papua New Guinea) who was trying to help ostomates in her country. There is a scarcity of supplies in some other countries, and unlike the US, insurance to pay for supplies isn't available. When my son followed his "love" twenty years ago, and moved to Australia I took advantage of an opportunity to help other ostomates. On one of my first visits to Oz, I brought a suitcase full of Ostomy supplies, handed them off to an Ostomy assoc. On the Gold Coast, who then had a friend take them to PNG. They were grateful for the help, and Janet and I still write.. This is the place to be, if you need help, and it also gives you the opportunity to provide help and support to others. Feel free to write, if you'd like to chat, about things ostomy, or life in general. Best REgards to all.. Marsha
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