just a thought...

luckycolon:

Here are some things i have learned about college and ibd. 

1. REST when you need to.

2. Don’t be embarrassed of your ibd. 

3. Tell the people that need to know. 

-Teachers, roommates, etc.  

4. Don’t forget to talk to your school’s disability center and reap the benefits.  They can help notify your professors why you might be late or why you rush out of the classroom in a hurry.  They can allow extra time for tests if you have to use the restroom, etc.  If you fall behind because you spent a few weeks in the hospital, they can help you find a tutor to get caught up again.  If your living on campus they can help with dietary restrictions and put you in a room near a bathroom.  I highly advise this.

5. Let the little things slide and manage your stress.

6. Have a support system.  Check in with your parents, friends, whoever your support system is on a regular basis.  Find a friend on campus that can understand and keep you positive.  Keep a journal.  Even try to find a support group in the area.

7. Let your doctors know.  They can give great advice and make sure your meds are good and ready to go.  Find doctors in the area.  

8. Stay Positive. Not only is this good for your mental health, but you’re in college! You got there, despite your health, good or bad, you got there! 

9. Enjoy it. Have fun.

sooo true!

(via crohns-sucks)