- Joined
- Aug 30, 2012
- Messages
- 19
Hi everyone,
Well I am new here and I guess I'll just jump into it.
I'm 22 years old and was, I suppose, technically diagnosed in 2008 with Crohn's. The reason I was brought into the doctors to begin with was a sharp pain in my lower right abdominal area (near my hip bone) that I was experiencing for a few days.
I went in to see my primary doctor and they set me up with a CAT scan (might have been something other than CAT, I can't remember). Anyways, after that ordeal I went back to my primary doctor's office and according to my results from the scan I had Crohn's. Now, I was utterly shocked because my only knowledge of Crohn's was a family friend who was recently hospitalized for Crohn's. Needless to say, I was terrified. They gave me a shot to ease the pain.
Anyways, I was referred to a GI doctor and had a colonoscopy. The only thing he could tell me was that it "looked like crohn's." I was put on medication and I didn't experience a symptom since.
Shortly after I moved out of my parents house to go to college and for various reasons (in retrospect, stupidity), I stopped taking my medication and seeing my GI doctor. I didn't experience any symptoms until about 6 months ago. I started having the same sharp pain I had experienced before so I went to my new primary doctor (we had changed insurance). Based on my history they referred me to GI. For many different reasons I was unable to have a colonoscopy until last week and by then the pain had spread across my lower abdomen and at some points became completely intolerable.
The results of the recent colonoscopy were consistent with Crohn's (according to my GI doc). I guess I was hoping for better news but I figured as much. I was put on the same medication again (Pentasa) and now I am waiting until next week for a follow up appointment with my GI. Also, might I add, that the colonoscopy was a miserable experience. I was too nervous to fall asleep during the procedure and it hurt sooo much. The pain is still there (the results of the colonoscopy showed many ulcers and a lot of inflammation) and the pain killers I received from urgent care this past Sunday are no longer working.
I'm so tired of this pain, I'm so mad at myself for ever having stopped that medication. I'm mad at everyone else who isn't in pain all the time and can eat whatever they want because whenever I eat I feel like I'm dying from the intestines out. Not to mention that a blood test shows that I might also have Celiac disease. Fun. :|
Well I am new here and I guess I'll just jump into it.
I'm 22 years old and was, I suppose, technically diagnosed in 2008 with Crohn's. The reason I was brought into the doctors to begin with was a sharp pain in my lower right abdominal area (near my hip bone) that I was experiencing for a few days.
I went in to see my primary doctor and they set me up with a CAT scan (might have been something other than CAT, I can't remember). Anyways, after that ordeal I went back to my primary doctor's office and according to my results from the scan I had Crohn's. Now, I was utterly shocked because my only knowledge of Crohn's was a family friend who was recently hospitalized for Crohn's. Needless to say, I was terrified. They gave me a shot to ease the pain.
Anyways, I was referred to a GI doctor and had a colonoscopy. The only thing he could tell me was that it "looked like crohn's." I was put on medication and I didn't experience a symptom since.
Shortly after I moved out of my parents house to go to college and for various reasons (in retrospect, stupidity), I stopped taking my medication and seeing my GI doctor. I didn't experience any symptoms until about 6 months ago. I started having the same sharp pain I had experienced before so I went to my new primary doctor (we had changed insurance). Based on my history they referred me to GI. For many different reasons I was unable to have a colonoscopy until last week and by then the pain had spread across my lower abdomen and at some points became completely intolerable.
The results of the recent colonoscopy were consistent with Crohn's (according to my GI doc). I guess I was hoping for better news but I figured as much. I was put on the same medication again (Pentasa) and now I am waiting until next week for a follow up appointment with my GI. Also, might I add, that the colonoscopy was a miserable experience. I was too nervous to fall asleep during the procedure and it hurt sooo much. The pain is still there (the results of the colonoscopy showed many ulcers and a lot of inflammation) and the pain killers I received from urgent care this past Sunday are no longer working.
I'm so tired of this pain, I'm so mad at myself for ever having stopped that medication. I'm mad at everyone else who isn't in pain all the time and can eat whatever they want because whenever I eat I feel like I'm dying from the intestines out. Not to mention that a blood test shows that I might also have Celiac disease. Fun. :|