Posts tagged ‘ibd’
Purple Challenge Day 5 Photos!
Day 5 of the challenge and we still have a whole lot of photos coming in (including a few from last night but I fell asleep to early to put them on the Day 4 post). I am so appreciative of everyone’s participation- it really shows how many people are touched by inflammatory bowel diseases!
Purple Challenge Day 4 Photos!
On the East Coast today it’s a bit grey and dreary but that isn’t stopping folks from sending in their #PurpleChallenge photos! Keep them coming all week long.
Debunking 10 IBD Myths
There are a lot of myths floating around about inflammatory bowel disease and I figured what better time than during Crohn’s & Colitis Awareness Week to clear some up!
Again, please note that I am not a doctor. All of the answers below are based on my knowledge of the disease and some external research. If any of this is incorrect, please let me know!
Purple Challenge Day 3 Photos!
Today is Day 3 of the Purple Challenge and folks are still going strong! I am so happy to see so many people not only in the U.S. but also internationally participating in the challenge.
Here are today’s photos- same drill as yesterday- I will continue updating as more photos come in.
Purple Challenge Day 2 Photos!
The photos keep coming in and I cannot express how excited I am that so many people are participating in the challenge!
That being said, here are some of today’s pictures. I’ll update throughout the day as more come in.
Purple Challenge Day 1 Photos!
Happy Crohn’s & Colitis Awareness Week everyone! I am SO excited for this week and to be participating in the #PurpleChallenge.
The photos are coming in on and I wanted to share some of them with you all of the fabulous folks participating in the challenge. I’ll be adding photos all day as they come in so check back frequently!
The ABC’s of Crohn’s & UC: “I”
Next up in the alphabet series is the letter I. I never thought I’d be saying that when 20 years ago I would run out of the room when the letter I came on during Sesame Street. But I digress.
There are a lot of really important I’s, so read up!

The Essential Hospital Bag
If you have IBD, it’s inevitable that at some point, you will wind up in the hospital. Some stays might be for a few hours, some a few days, and for the unlucky ones, a few weeks or months. Regardless of how long you are in the hospital, there are some essentials to take with you to ensure that your patient’s stay, and subsequently yours, is as pleasant as a stay in the hospital can be.

If only it were this simple…
I’ve come up with a list based off of what I’ve brought to the hospital the three times Dan has been hospitalized. Obviously, everyone has different interests so this list can be modified to fit anyone’s needs.
My Belated Gratitude Challenge
I found a blog recently written by a Crohnie called My Journey with Crohn’s. Sarah, the site’s author, recently did a week-long series on gratitude. I’m a little bummed that I didn’t find her blog sooner otherwise I totally would have participated.
Every day for one week, she posted five things that she is grateful for (in the spirit of Thanksgiving). On the last day, she also posted what some of her followers are grateful for. It’s such a great idea, given how unsettling and upsetting Crohn’s and UC can be, to think about gratitude and give thanks to the things that are good in your life.
That being said, while I won’t list 35 things that I am grateful for, I will do a short list here in the spirit of her series from last week.
Holiday Eating for IBD
With Thanksgiving tomorrow, I thought it would be appropriate to do a short write up about holiday eating for Crohnie’s and UC-ers.

Holidays mean food and lots of it. Some is good, some is bad, and some is all around delicious. But for those with IBD, eating the wrong thing or too much of the right thing can ruin the holiday and equal hours in the bathroom.






