you’re part of this as well.

I’ve found through this whole thing, that it’s not only myself that is battling Crohns, but my family and friends also. My family have suffered every time I have, they have sat beside me in hospital and felt my pain. I somehow feel that it was worse for them that it was for me. Okay, I’m the one that has had to go through the operations and live with a stoma, but my family and friends are the one’s that feel completely and utterly helpless. When I was away in fairy land all doped up on Morphine, my family had to sit, helplessly at my side. They had to watch me writhing in pain and have my veins punctured multiple times. When I publicly showed my pain, it was watching my parents faces that frightened me more than the crippling agony. I understand now, that with a good support network the healing time almost halves. My family and friends have been there through every step of this process, from ushering me to a quiet corner of the shopping centres so I can catch my breathe, rubbing my back on the ski trip when I didn’t understand why I was throwing up my juice, to bending over with me in the middle of the street (what I did to try and combat the pain) just so I didn’t look odd on my own. This is as much your illness as it is mine, and I want to thank every single person that has struggled along with me. As a very lovely nurse once said to me; “the body won’t heal unless the heart is content.” – he couldn’t have been more correct and I think this is the reason why I am healing so well. Thank you all very, very much for your patience, love and friendships.

I also found this article that brilliantly explains a few things that some of my family and friends may have been wondering. I know it’s just as hard for you lot as it is for me, because you want to be there for me, but don’t know how to or don’t want to upset me. I don’t get upset very easily, and believe me! I wouldn’t get offended if anyone said one of these things to me, but I found it to be quite a good article to give you an insight in to how to act when discussing someone’s chronic illness;

11 Things Not to Say to Someone with Crohn’s Disease or Ulcerative Colitis

Living with an inflammatory bowel disease (IBD), such as Crohn’s disease or ulcerative colitis, is a challenge.
People with these serious conditions can lose weight during a flare-up and gain it all back—and then some—if they need to take corticosteroids to get symptoms under control. And it can be hard to find food that’s OK to eat, because the conditions differ for everyone.
For all these reasons, certain comments—such as those that focus on looks, weight, and diet—can be more harmful than helpful. Here’s what not to say.

You don’t look sick
“That’s one of the hardest things about having colitis—people can look OK on the outside,” says Leigh Stein, 35, a fourth-grade teacher in Pittsburgh who was first diagnosed with the condition at 23.

People don’t realize that it may have taken that person’s last ounce of effort to get showered, dressed, groomed, and out the door, says Stein’s friend Gina Lynn, who also has ulcerative colitis (UC).

I know what you’re going through

When people with IBD tell someone about their condition, they often get an earful about that person’s digestive problems.

But it’s probably better to keep details of your upset stomach, diarrhea, or irritable bowel syndrome (an unrelated condition) to yourself.

“Don’t say you understand what they’re going through, because unless you have it you don’t know what they’re going through,” says Julie Novack, 44, a senior credit underwriter for Wells Fargo in Charlotte, N.C., who was diagnosed with UC at 22.

You’ve lost weight! You look great!
“My biggest pet peeve is comments about my weight—anything weight-related,” says Marge McDonald, 46, who runs a council on aging and senior center in Chelmsford, Mass., and was first diagnosed with ulcerative colitis 10 years ago. She recalls that when her mother, who also has UC, lost about 50 pounds, people kept saying how great she looked.

McDonald says she would think, “No, she doesn’t. Her skin is hanging off her; she looks gray.”

“We’re so focused on weight we don’t notice anything else,” she says.

You’re so lucky; you can eat anything and stay skinny
Well, not really. Weight loss is often due to flare-ups that cause severe abdominal pain and bloody diarrhea that can mean spending most of the time in the bathroom.

And during a flare-up, a person may need to choose food very carefully so they don’t make symptoms worse.

“Stop, stop, stop telling people that they are lucky to be thin,” says Denise Lindberg. “I have to work to stay not malnourished.”

You’ve really put on weight!
Prednisone, one of the most effective short-term medicines for quickly quelling a severe flare-up, has several side effects, including weight gain. Another side effect is “moon face,” in which the cheeks get rounded, making for a chipmunk-like look that can give the impression that a person is heavy even when his or her body is rail-thin.

Fortunately, this effect tends to go away when the person stops taking corticosteroids. Until then, the best approach to commenting on weight or looks to a person with IBD is not to comment at all.

Is it OK for you to eat that?
There’s no one-size-fits-all diet for people with an inflammatory bowel disease. Fruits and vegetables may be no-nos, but some people do just fine with spicy foods.

“Different foods affect different people differently,” Stein says. “It’s a trial-and-error thing, and each individual figures out what’s OK and what agrees with them. Crohn’s and colitis patients know what they can eat, and when someone’s looking over your shoulder and commenting, that’s kind of bizarre.”

come on, try a bite!

By the same token, many people with ulcerative colitis and Crohn’s disease are by necessity very familiar with what foods they should avoid. John G. says he gets annoyed when people ask him why he eats the same thing every time they go out.

“Definitely listen to your body,” says Kristine Fulco, 29, a graphic designer in Brooklyn, N.Y., who was diagnosed with ulcerative colitis at 21 and says she’s fared much better by figuring out what foods are OK for her to eat rather than listening to generic advice. “Don’t let everyone else bully you.”

You must have a lot of stress in your life
Many people mistakenly believe stress causes inflammatory bowel diseases. There’s absolutely no evidence that stress or tension cause Crohn’s or colitis, although it can make symptoms worse for people who have the diseases.

A rogue immune attack on the digestive tract appears to be the cause, and the result is symptoms such as abdominal pain and chronic, bloody diarrhea.

Damage from inflammatory bowel diseases can be so severe it requires surgical removal of portions of the colon.

Can you wait until the next exit?
Assume the answer is no.

If you’re in the car with a person with ulcerative colitis or Crohn’s disease and they tell you they need to go, listen to them, Novack says.

“One of the biggest fears of probably anyone with ulcerative colitis or Crohn’s is getting stuck in traffic,” she says. Just help them find the closest bathroom, and get them there as soon as possible. Another question not to ask: “Why can’t you just hold it?”

Why are you so tired?
“People need to understand that ulcerative colitis is a serious disease,” says Novack. “If you can’t go to an event or you have to stay home from work, it’s not because you’re slacking—it’s because you really are sick.”

Jill Plevinsky hates when her friends and family try to get her to do things she’s not up for by saying, “Oh, come on. You can’t be that tired.” She likes to answer them by saying, “If you lost as much blood as I do with each bowel movement, you’d be pretty wiped out too.”

You need to change your diet
Krystle Carbone says she often gets unsolicited advice on her eating habits, such as, “Maybe if you ate better you wouldn’t have that problem.” And, “Why are you sick all the time? Maybe you should take vitamins and supplements.”

Although the food a person eats can affect their symptoms during a flare-up, there’s no evidence that diet causes inflammatory bowel diseases or brings on flare-ups. It is important, however, for people with colitis and Crohn’s to eat as healthy and balanced a diet as possible—which they most likely know already.

By Anne Harding /


3 thoughts on “you’re part of this as well.

  1. Doesn’t this sum it up nicely?? I wish all my coworkers could take a peak at this post…might spur some understanding?? maybe? 🙂

Leave a Reply

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out /  Change )

Google+ photo

You are commenting using your Google+ account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )


Connecting to %s