I was diagnosed with Crohn's in 2007 (even though I've had the symptoms and was being misdiagnosed for 18 years). By 2009, after many surgeries and procedures, I was given a permanent ostomy. Before then, I was a full-time case manager with a company for 20 years. I decided to resign before I was fired for all the lost time I had. Anyway, it has been two years, and I am ready to work again. I don't think I am able to work full-time due to stress, but would like part-time. My question is, is there a place where you can work that the hours are flexible to meet my needs? I have periods of flare-ups and chronic fatigue, and I need to work for someone who is understanding. Any suggestions or ideas? I tried working from home through the internet, but that was a joke. Thanks.
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Hi gang,
I was thinking what a great resource this site has been for me since I found it. It would have been really helpful, but maybe a bit scary, to have found it before my ostomy, but that's water under the bridge. But I got thinking about it, and now I'm questioning why doctors and hospitals don't provide this site's contact info to any patient even considering an ostomy today. And how can we change that so potential ostomates can learn about the road ahead for them by getting on here and asking questions before the docs go chop-chop. How exactly do you get all hospitals to provide their patients specific information, like this website?
I just happened to find this site something like 4 years after my ostomy when I Googled "ostomy forum" or something like that. But I never found it during previous searches.....so I found this site pretty much by pure luck. We need to find a way to make this site available to new or soon-to-be ostomates......as that's when we really need to commiserate with fellow ostomates. Anybody have any thoughts on how we do this?
Thanks,
Bob
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