- Joined
- Jul 17, 2015
- Messages
- 14
Well. I finally got into see a new GI doctor. It took me 4 trips to the ER this past month (2 of them were ambulenced) in order for my primary doctor to crack down and find me one that takes my insurance. They had previously diagnosed me with Crohn's due to intestinal inflammation, joint pain, severe rectal bleeding, extreme abdominal pain, vomiting / nausea ect ect you get the point. And I know for a fact my GI problems are due to at least a form of IBD but this new GI I saw (whom everyone seems to say is "the best in the state" **rolling eyes**) barely listened to my complaints, noticed I had mental disabilities (PTSD being one of them) and straight away began to just treat me as though I just have IBS. It seemed very descrimative & possibly sexist (I'm a 24 year old women & I've noticed that doctors tend to take men more seriously when it comes to their health problems & pain than women. Maybe it's just the state I live in or maybe I'm just "imagining things"). Either way, since I've had severe GI problems for the past 2 years and have seen a numerous amount of doctors, I don't take their s#1+ anymore. I demanded him to do a blood test for IBD and also to perform another colonoscopy to see if my ulcers have healed or not / check up on my tumors & hemorrhoids / take as many biopsies as possible to test for IBD (Crohn's). The doctor seemed very annoyed & honestly I found it amusing. Doctors should help us who are in pain, not just tell us it's all in our head. I highly doubt I have IBS because this GI condition I have has basically ruined my way of living. I'm scared to eat / drink, constantly in pain, constantly tired, and I pass out / black out due to the weakness and joint pain and dehydration from consistent vomiting and diarrhea. My bowel movements are rarely ever normal, they're always either NON EXISTANT, hard & covered in mucous, black tarry and loose, bloody, or straight liquid.
**end of cr@ppy doctor rant**
Anyways. I was wondering if any of you who have Crohn's or any other form of IBD has experience with the medication hyoscyamine? I begged the doctor to switch me off the norco's I've been on for 2 weeks now because 1.) pain meds make me just WEIRD / crazy 2.) they constipate me really bad and 3.) they're addictive. The doctor said that hyoscyamine will help with the abdominal cramping but unfortunately not that severe joint pain I have (that is the worst in my legs). I started it last night & it made me extremely tired & I zonked out so that's a good sign I guess. Usually I don't get sleep at night due to GI disturbances. Only side effect I have is a sore throat.
I would really like to know your experience with this medication because I honestly question this doctor's professionalism considering he immediately wanted to diagnose me with IBS.
**end of cr@ppy doctor rant**
Anyways. I was wondering if any of you who have Crohn's or any other form of IBD has experience with the medication hyoscyamine? I begged the doctor to switch me off the norco's I've been on for 2 weeks now because 1.) pain meds make me just WEIRD / crazy 2.) they constipate me really bad and 3.) they're addictive. The doctor said that hyoscyamine will help with the abdominal cramping but unfortunately not that severe joint pain I have (that is the worst in my legs). I started it last night & it made me extremely tired & I zonked out so that's a good sign I guess. Usually I don't get sleep at night due to GI disturbances. Only side effect I have is a sore throat.
I would really like to know your experience with this medication because I honestly question this doctor's professionalism considering he immediately wanted to diagnose me with IBS.