So, I live in a state where medical marijuana is legal. I’d never thought much about it before, always assuming treatments would work for me, and also because, well, I’m not the marijuana type. I’ve never smoked it, not even during college, when many people tried it. I don’t drink or use any recreational drugs. Not that I have anything against either; they’re just not my thing.
But my friend, who lives in the same state as I do, has decided to try marijuana for relief from her multiple sclerosis. She’s in the process now of getting cleared. It seems like a very long process of going to various doctors, obtaining a license, choosing from among many varieties, etc. It’s also quite costly as insurance won’t pick up the cost. She’s started a GoFundMe page to help with her expenses. This is after years and years of treatment for her disease, with constant relapses. I admire her ability to look confidently in another direction.
It got me thinking. Would it help me? In the past, I’ve kind of laughed when people suggested it. My mother-in-law used Marinol, the prescription version of cannabis in a pill, during the last months of her life. It made her incredibly high, unaware and sleepy. She didn’t like what it did to her, and I didn’t either. I remember going to her house one day when we couldn’t get her on the phone and finding her basically incoherent and passed out on the couch. I rushed her to the hospital, and she was fine by the end of the day as the drug eased out of her system.
These days, when I’m in pain, I take Percocet, a drug prescribed to me by my gastroenterologist. Not all GIs will prescribe pain medication for Crohn’s, which really bothers me. We’re not all going to become addicted to it. I use mine only when the pain becomes unbearable, at the height of my flare-ups, and I use a quarter of a pill at a time, doling it out to myself like I’m rationing my favorite food, chocolate.
When I mentioned medical marijuana to my doctor, he was against it. That seems to be the stance of many doctors. My doctor said it won’t do anything to abate my symptoms; it will just make me high enough to not care. But I’ve read articles that show that if you get the right mix — a certain kind of compound — you can avoid getting high from it.
I’ve done all of the medications we can think and none of them have worked. They’ve caused a lot of pain and expense and time and energy and I can’t seem to get into a remission unless I’m taking prednisone, which has been a staple of my medical diet for the past four years. I cringe when I think of what I’ve done to my body with prednisone. And though it’s a drug with a whole lot of issues, it’s prescribed over things like Percocet and, obviously, medical marijuana. Yet, according to the Mayo Clinic, Crohn’s is one of the diseases medical marijuana can help.
I don’t think I’ll act on it just yet, but my husband said he didn’t blame me for thinking about it. I’m now coming off another two-week flare, after getting down to a 5 mgs. dose of prednisone. I’m back up to 30 mgs and now we’re questioning the ability of Stelara to put me in remission. My doctor wonders if I should — if my insurance will let me — increase it to every four weeks instead of every eight, or do another IV infusion of it. But the insurance will never agree.
So, I’m enjoying time on my prednisone, while I have decent energy, want to eat, and all is well in the bathroom, only to know that in a few weeks, that will likely all end.
Would medical marijuana be better? I really don’t know.
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