- Joined
- Nov 10, 2008
- Messages
- 85
This will be just one major vent, I dont expect people to read or respond to it. Just need to vent out all my frustrations...:depressed:
I'm so annoyed with this disease, for months I had symptoms and just pushed them aside. It got to a point where I forced myself to drive to the emergency room, crying in pain I asked my boyfriend of whom I live with (of 3 years) to come and his response is "i don't like hospitals" ..who the hell does?! I sat in a hospital with him for 7 hours when he had severe mono. Now, after a proper diagnosis and meds that don't work he thinks that I use this disease to my advantage. Yes, because I love moaning. when abdominal pain hurts, and going to the bathroom 8 times a day, and having no energy to do anything anymore. But yet I treat him as if he has the disease and he never has to lift a finger.
I hate the fact that my brother and sister gang up on me. My brother believe its just all in my head and that I am aneroxic. My sister, who is a 27 year old woman thinks crohns is just a tummy ache, and she gets those all the time so there is no reason for me to be on medication. I would expect my own blood to understand out of anyone.
The fact that I have lost friends has bothered me to. Since I don't tell them I have a disease they just assume I don't want to go out anymore and have become anti-social. I refuse to go out with people who are going to drink all night, and then ask why I haven't picked up one, or why I'm so pale and skinny now.
I am lucky to still have my best friend. Without her I would go insane and I wish that everyone had someone like her in their life. We talk everyday and because she lives literally 6 blocks from my house thats about the only person I hang out with. She asks how I'm feeling when I don't look so hot, and makes sure I always have a bottle of water with me. She even showed up in the emergency room when she found out I was there alone. We finally went out to the city for a change of enviorment and she was sure to ask every hour is I needed a break, need to go to the bathroom, and how my stomach was feeling. So I can't be completely pissed off.
I wish there was some sort of machine people could get hooked up to and it would pass sypmtoms of this disease through their body so that could really understand what we go through.
I cryed all night yesterday because everything has just gotten to me. Thats all I have to write.
I'm so annoyed with this disease, for months I had symptoms and just pushed them aside. It got to a point where I forced myself to drive to the emergency room, crying in pain I asked my boyfriend of whom I live with (of 3 years) to come and his response is "i don't like hospitals" ..who the hell does?! I sat in a hospital with him for 7 hours when he had severe mono. Now, after a proper diagnosis and meds that don't work he thinks that I use this disease to my advantage. Yes, because I love moaning. when abdominal pain hurts, and going to the bathroom 8 times a day, and having no energy to do anything anymore. But yet I treat him as if he has the disease and he never has to lift a finger.
I hate the fact that my brother and sister gang up on me. My brother believe its just all in my head and that I am aneroxic. My sister, who is a 27 year old woman thinks crohns is just a tummy ache, and she gets those all the time so there is no reason for me to be on medication. I would expect my own blood to understand out of anyone.
The fact that I have lost friends has bothered me to. Since I don't tell them I have a disease they just assume I don't want to go out anymore and have become anti-social. I refuse to go out with people who are going to drink all night, and then ask why I haven't picked up one, or why I'm so pale and skinny now.
I am lucky to still have my best friend. Without her I would go insane and I wish that everyone had someone like her in their life. We talk everyday and because she lives literally 6 blocks from my house thats about the only person I hang out with. She asks how I'm feeling when I don't look so hot, and makes sure I always have a bottle of water with me. She even showed up in the emergency room when she found out I was there alone. We finally went out to the city for a change of enviorment and she was sure to ask every hour is I needed a break, need to go to the bathroom, and how my stomach was feeling. So I can't be completely pissed off.
I wish there was some sort of machine people could get hooked up to and it would pass sypmtoms of this disease through their body so that could really understand what we go through.
I cryed all night yesterday because everything has just gotten to me. Thats all I have to write.