T
thatgirl
Guest
doctor disclosure...thc
so i have been dealing with cd almost my whole life but i have just been diagnosed for good this month (i had a diagnosis for a couple of months but they took it back when i switched docs)...when i went to college i had what i now know to be mr first severe flare...i lost my appetite and would become overwhelmingly nauseous when i would smell food some of the time ( i thought it was just that the cafeteria food was bad)...i also started to experience the fatigue and arthritis pains at around the same time...like a lot of other college kids i was also starting to experiment with marijuana...i realized very early on that i was getting relief from the mj for the indigestion (that i again chalked up to the inferior food)...over the years i have found that the mj was the only thing that worked consistently and immediately...for the last 7 years i have been plagued with cvs (cyclic vomitting syndrome) and subsequently have learned during various er visits that i am allergic to ALL anti-emitics (zofran, raglan, compazine and the like) so that really only leaves me with mj to treat the nausea that plagues me eveytime i eat more than a mouthful...but it also relievs my pain (allowing me to function ) creates an appetite and helps me to combat the fullness factor (allowing me to maintain a healthy weight)...having said all of this i have yet to tell any of my docs about my mj use...as a young woman (28) i am aware that people my age are often seen as drug seeking because 1. mine is the rehab generation and 2. young people don't get sick or experience real pain...i have been labled as drug seeking on several occasions when my mom took me to the er explaining all of my gi problems (before and during the crohn's diagnosis)...however i'm getting tired of "hiding" and would like to be up front about my mj use...now that i have a definite diagnosis from a doc that i trust i would like to approach my condition differently as i am in it for the long haul...having said all this is there any one out there in the same situation and if you are a mj user who has disclosed to your doc how did you go about it...help please
so i have been dealing with cd almost my whole life but i have just been diagnosed for good this month (i had a diagnosis for a couple of months but they took it back when i switched docs)...when i went to college i had what i now know to be mr first severe flare...i lost my appetite and would become overwhelmingly nauseous when i would smell food some of the time ( i thought it was just that the cafeteria food was bad)...i also started to experience the fatigue and arthritis pains at around the same time...like a lot of other college kids i was also starting to experiment with marijuana...i realized very early on that i was getting relief from the mj for the indigestion (that i again chalked up to the inferior food)...over the years i have found that the mj was the only thing that worked consistently and immediately...for the last 7 years i have been plagued with cvs (cyclic vomitting syndrome) and subsequently have learned during various er visits that i am allergic to ALL anti-emitics (zofran, raglan, compazine and the like) so that really only leaves me with mj to treat the nausea that plagues me eveytime i eat more than a mouthful...but it also relievs my pain (allowing me to function ) creates an appetite and helps me to combat the fullness factor (allowing me to maintain a healthy weight)...having said all of this i have yet to tell any of my docs about my mj use...as a young woman (28) i am aware that people my age are often seen as drug seeking because 1. mine is the rehab generation and 2. young people don't get sick or experience real pain...i have been labled as drug seeking on several occasions when my mom took me to the er explaining all of my gi problems (before and during the crohn's diagnosis)...however i'm getting tired of "hiding" and would like to be up front about my mj use...now that i have a definite diagnosis from a doc that i trust i would like to approach my condition differently as i am in it for the long haul...having said all this is there any one out there in the same situation and if you are a mj user who has disclosed to your doc how did you go about it...help please