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Crohn's Disease Forum

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Sep 5, 2007
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Didn't know anything about this site until recently. I have been reading a few stories and I am sooo relieved to find I am not the only one suffering through the
pain, discomfort, embarassment and humiliation that comes with this cruel and merciless disease. I was diagnosed with Crohn's 30 yrs ago and had 2 bowel re-sections during the first 10 yrs. I took Salazopyrene during that time but the side effects were terrible i.e. major dental problems. I had a major "flare up" 9 years ago which lasted 2-3 years. I am now taking Pentasa (8 a day) and numerous vitamin pills. Also getting a B12 shot every month. Like everyone else food and sleep are the most important things in my life. Food is more like an enemy. I try to pace myself by eating lightly during the day and nothing after 8 p.m. Seems to work fine until my boyfriend visits and then you know what happens.....all nighter in the bathroom, sometimes I don't make it in time. Then there is the hassle of explaining to people why you are not hungry at normal mealtimes, why you are dropping off to sleep at 11 a.m. after being awake since 8 a.m., why you are in the bathroom 5 times in one hour, why you can't dine out in the evening and then "dance it off", etc., etc. I might have rambled on a bit and I don't want to bore you any more than I have. I'm sure all of you know the drill by now.
 
Hi Maryp.. Welcome to the forum. Don't worry about rambling on, there's one ol fart on here who never shuts up. It's true, theres a lot of things we can't do after IBD. I try to do as many of them as I can, whenever I can, just to spite this damned disease. The rest of the time, I admit to my post illness restrictions, give into them, and go take a nap... On the upside, having a legitimate excuse for a nap isn't so bad
 
For now I just want to welcome you Mary to the forum! :)

Please don't feel as though you are rambling..
we're here to listen and try to help one another.

We cry with them through the rough times,
pray for them during real bad times...
and laugh with them when things are going well.

You see, we're all in the same boat...so, we understand.

Please feel free to vent away, or throw in a comment wherever you please.

Once again...welcome.

Healing hugs~Nancy
 
maryp said:
Didn't know anything about this site until recently. I have been reading a few stories and I am sooo relieved to find I am not the only one suffering through the
pain, discomfort, embarassment and humiliation that comes with this cruel and merciless disease. I was diagnosed with Crohn's 30 yrs ago and had 2 bowel re-sections during the first 10 yrs. I took Salazopyrene during that time but the side effects were terrible i.e. major dental problems. I had a major "flare up" 9 years ago which lasted 2-3 years. I am now taking Pentasa (8 a day) and numerous vitamin pills. Also getting a B12 shot every month. Like everyone else food and sleep are the most important things in my life. Food is more like an enemy. I try to pace myself by eating lightly during the day and nothing after 8 p.m. Seems to work fine until my boyfriend visits and then you know what happens.....all nighter in the bathroom, sometimes I don't make it in time. Then there is the hassle of explaining to people why you are not hungry at normal mealtimes, why you are dropping off to sleep at 11 a.m. after being awake since 8 a.m., why you are in the bathroom 5 times in one hour, why you can't dine out in the evening and then "dance it off", etc., etc. I might have rambled on a bit and I don't want to bore you any more than I have. I'm sure all of you know the drill by now.
i think i am doing this right.i have only had my computer for a month.
hello my name is nikki. you have just described my life. it is really comforting to be able to talk about things very honestly and without making a joke of it or smeone else making a joke.
 
Yeah Nikki, you are doing this right. This site allows us to rant N rave, to cry, to offer help, advice, comfort and solace to each other. Someone who doesn't have this just isn't allowed to joke about it. Period! We, on the other hand can, and often do. It's not that this isn't a serious disease, and this a serious site; it's just that laughter is the best medicine... and sometimes it feels better to laugh at something than to cry.
 
Welcome maryp! This place is for whatever will make us feel better, so your post is definately what you are supposed to do :).

You will see that many of us suffer many similar symptoms, so hopefully you see you are not really alone.
 

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