Newly Diagnosed with Crohns Disease or Ulcerative Colitis

I want to share some things I wish I knew with any of you who may be newly diagnosed with Crohns disease or ulcerative colitis or know someone who is:

1) There is no right or wrong way to treat Crohns disease or ulcerative colitis. Do what you feel is best for you, your body, your mind and your life. Things can always be adjusted.

2) Inflammatory bowel disease always plays with your emotions, always right in your face. The ups and downs are really challenging which is why a great support system is key and reaching out for help when you feel like you need is crucial. It is okay and healthy to ask for help. Crohns disease and ulcerative colitis are VERY difficult illnesses to live with.

3) Make friends with other people who have IBD…. Even if it just browsing through support pages on Facebook or Twitter, it allows you to see that you aren’t alone and that, for me personally, has been one of the greatest things for me to know with this incredibly isolating disease.

4) You didn’t develop IBD because; you didn’t eat the right foods growing up, you aren’t a person who doesn’t handle stress correctly, you aren’t harboring childhood trauma or have an inability to “let go” of the past. If someone that doesn’t have Crohns disease or ulcerative colitis says these things to you, they are placing blame on the patient which makes an already difficult illness even harder to cope with, much harder. There is NO REASON. It is NOT YOUR FAULT.

5) Listen to your body and trust yourself. Always. No exceptions.

A little over 5 years ago I was about to embark on the most physically and emotionally challenging experiences of my life. I had no idea what I was in store for but I know I couldn’t have made it this far without the support of my family and friends. I have met some of the most amazing people in person and online whom have become truly irreplaceable friends. They, along with my family, have made me realize that no one should have to go through this journey alone, no one.

From me Josh,

Months ago I found and saved this, I do not know who wrote it now (all credit due) and have changed it a little. This person’s advice is so true and something I wish I had had nearly six years ago.

joshuaerobinson@comcast.net

~my life is a work-in-progress….i’m perfectly content with that~

Advertisements

2 responses to “Newly Diagnosed with Crohns Disease or Ulcerative Colitis

  1. Reblogged this on Another Hope Entirely and commented:
    This post is perfect.

    I think it’s a helpful thing not just for IBD patients to read, but also for friends, loved ones, and even acquaintances of people with IBD to read. If more people knew this stuff, maybe IBD patients wouldn’t have to listen to infuriating, unhelpful, blame-y comments as frequently as we do.

Leave a Reply

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

WordPress.com Logo

You are commenting using your WordPress.com 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 )

Google+ photo

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

Connecting to %s