One night, at home, in bed, I insisted on being left alone. I had an out-of-body experience and realized that I was going to die. I was in bed, yet my spirit had sunk below the bed through the floor of the house and was looking up towards my body. The realization of imminent death took over and I decided that I was not going to let this disease take my life! A flush of energy took over my body and, even though I was still very sick, I knew I was going to be OK. I had come to the realization that I had to be accepting the hospital as the only thing I could do now.
Earlier, I had booked into an alternative bowel treatment center, and tried many treatments. That clinic was just learning about oxygen therapy, which I did, along with colonics, wheat grass juice, and many other treatments. Having never taken any steroids or medication for my Crohns’ I had done these kinds of treatment off and on for years. This time it was different. There was no response and I was deteriorating.
It was time for trying something drastic. Although scared about the idea of surgery, realistically this was the only option left. I had lost all control over my bowels and vomited anything by mouth.
Fortunately, by the time I was this sick, I was in Toronto, and Toronto is the home of Mount Sinai Hospital which is considered the best one in Canada for bowel problems. At 82 lbs, having lost most of my vision due to dehydration, and not being able to stand, I consented to going to the hospital. My sister got a cab and off we went. When we got there my hemoglobin was so low from bleeding that they could not understand why I had not died. In my opinion, the oxygen therapy, and my earlier decision to not die was what was keeping me alive.
Once in the hospital, on some steroids, and TPN, my mind started to come back and I began to become aware of my surroundings again. Being in the hospital was quite an experience for me because I had only been in a hospital once or twice in my life for a quick visit. I was in shock. Mount Sinai Hospital has a whole wing dedicated to bowel surgery, the biggest in Canada. And the saddest place I had ever been.
Most hospital stays for people are a few days, maybe a week. Well, not here. Here the stays are more likely a few months, maybe a year, and the average age was under 30. Most of you with an ostomy know what I’m talking about. The despair that one gets when they are admitted to hospital with no idea of when they will be able to go home, and it looks like it will be months, is terrible. I was defiantly not staying; I would be out of here next week!
Well… the weeks turned into months and I did not get to go home. But, after a while, I insisted on being transferred to a hospital closer to my family.
Love, Sheri
[Editor’s note: Sheri’s writings are spread out over time so they’re not strictly a follow-on from the previous writing. I’m sure you will find them most interesting and, hopefully, find her experiences and positive messages helpful. Below are links to Sheri’s personal journey experience writings and thoughts. You can also access these links from the side menu, or the “About Me” menu on the top-right of the page. ]
- About Me — My “Pull Through” Journey — Introductions
- Controlling Crohn’s Disease? Anorexia worked! Until it didn’t.
- [Current Page] Accepting the Hospital ~ No other choice left.
- Transferring Closer to Home
- Yesterday I Cried ~ With an agenda.
- It’s OK to Cry
- My Prescription Drug Addiction — Good or Bad?
- Leaving the Poor Me Stage
- My Journey of Pulling Through — Final Thoughts
