Suvii
An old fart from North!
- Joined
- Dec 1, 2011
- Messages
- 115
I just joined the forum and wanted to share my story. Sorry for the spelling mistakes, try not to pay attention to them.
I was diagnosed with Crohn's in 1998 at age of 13. It all started when I was rushed to the emergency due to a difficult diarrhea and being sick a lot. I had a severe stomach ache. They ran lots of tests including colonoscopy and a MRI scan of my brain. My mom was terrified that they would found cancer etc. I was so tired that I couldn't even open my eyes when doctors came to examine me. Also I had anaemia back then, Hb 89. I was finally diagnosed with Crohn's disease and started eating Pentasa (12/1998). After 2002 I was medicine free and my disease stated to be in a remission.
In 2008 I was anaemic again, this time my Hb was only 60. I was in a gastroscopy what turned out to be normal. They wanted me to have also colonoscopy, but I was pregnant (♥) and decided to pass it later so I could get the premedication.
In the summer of 2009 I went to the emergency due to a very severe stomache pain. They checked my lower abdomen with ultrasound where they saw my ileum was thicken. I started Prednison and went home.
Finally I went to the colonoscopy in 6/2009. They found strictures and dilatated them.
In early of 2010 my small intestine was checked with MRI. In the terminal ileum they found a 10 cm long stricture and another that was 5 cm long. I started eating Entocort and Azamun + Pentasa. 4/2010 I had an iron injection because of my low Hb again.
Double Balloon Enteroscopy was made 9/2010 under anesthesia. They dilatated my obstructions/strictures.
11/2011 my small intestine was checked again with MRI. Still the 10 cm long stricture but now they saw that what earlier looked like a 5 cm long stricture was actually two separate strictures inside the 5 cm distance of my ileum. For the first time I was suggested surgery.
Now I'm waiting to meet my surgeon, I'm meeting him/her December 9th. Freaking out, naturally. I've had so much support from unknown people via email that I feel really lucky and cared! I've heard lots of stories and it really helps me to cope with this. So many people have recovered from surgeries and so will I. I just have to accept this.
Most of all I'm happy that my obstuction pains (they're so awful, I tell ya!) will hopefully be history after the surgery! They've been my biggest problem alongside anaemia. I haven't had to run in the toilet though so I think I'm really lucky in that way.
Thanks for reading! Feel free to comment!
You can visit my blog here, although I write it in finnish. You can always use a translator if you want
I was diagnosed with Crohn's in 1998 at age of 13. It all started when I was rushed to the emergency due to a difficult diarrhea and being sick a lot. I had a severe stomach ache. They ran lots of tests including colonoscopy and a MRI scan of my brain. My mom was terrified that they would found cancer etc. I was so tired that I couldn't even open my eyes when doctors came to examine me. Also I had anaemia back then, Hb 89. I was finally diagnosed with Crohn's disease and started eating Pentasa (12/1998). After 2002 I was medicine free and my disease stated to be in a remission.
In 2008 I was anaemic again, this time my Hb was only 60. I was in a gastroscopy what turned out to be normal. They wanted me to have also colonoscopy, but I was pregnant (♥) and decided to pass it later so I could get the premedication.
In the summer of 2009 I went to the emergency due to a very severe stomache pain. They checked my lower abdomen with ultrasound where they saw my ileum was thicken. I started Prednison and went home.
Finally I went to the colonoscopy in 6/2009. They found strictures and dilatated them.
In early of 2010 my small intestine was checked with MRI. In the terminal ileum they found a 10 cm long stricture and another that was 5 cm long. I started eating Entocort and Azamun + Pentasa. 4/2010 I had an iron injection because of my low Hb again.
Double Balloon Enteroscopy was made 9/2010 under anesthesia. They dilatated my obstructions/strictures.
11/2011 my small intestine was checked again with MRI. Still the 10 cm long stricture but now they saw that what earlier looked like a 5 cm long stricture was actually two separate strictures inside the 5 cm distance of my ileum. For the first time I was suggested surgery.
Now I'm waiting to meet my surgeon, I'm meeting him/her December 9th. Freaking out, naturally. I've had so much support from unknown people via email that I feel really lucky and cared! I've heard lots of stories and it really helps me to cope with this. So many people have recovered from surgeries and so will I. I just have to accept this.
Most of all I'm happy that my obstuction pains (they're so awful, I tell ya!) will hopefully be history after the surgery! They've been my biggest problem alongside anaemia. I haven't had to run in the toilet though so I think I'm really lucky in that way.
Thanks for reading! Feel free to comment!
You can visit my blog here, although I write it in finnish. You can always use a translator if you want
Last edited: