Whoever tells you this disease isn't progressive is full of it. Whoever tells you that there's no pain involved is full of it. I've been taking a medication called CellCept for 8 years now, and it's worked really well. I don't know if my body got acclimated to it or what. Although I WAS off it for 16 months with getting and being pregnant with Jacob. I think maybe that's part of it. Your body changes SO much when you're pregnant. Maybe what worked before won't work again. I don't think I'll ever get to the level of strength I had before having Jacob. I wouldn't change anything, because I can't IMAGINE my life without that child, but it was a huge physical sacrifice from which complete recovery is unlikely.
Plasmapheresis works well, but ideally I should probably have it once a week. Well, that's not practical when you have to drive 280 miles round trip, find someone to watch Jacob, etc. No hospital closer does in it my arm veins (peripherally), so I woud have to get a fistula, port, or quinton cath. to get it anywhere around here. I've had the quinton cath, and it's HORRIBLE. Ports and fistulas can easily get blocked or infected.
An easy solution is to go back up on the prednisone, and have my weight go up even more, have my bones thin even more, and give me more arthritis. But the MG might get better. There's a medication they just started using for MG called Rituxan. It's actually a chemo drug (you don't lose your hair) that they use for luekemia, non-Hodgkins lymphoma and rheumatoid arthritis. There are some crazy side effects though....like if you've ever been exposed to something horrendous (like TB, which I have been, shingles, etc.) it could come back en force. Or you could get some lovely new virus that your body is unable to fight off.
Don't you love my choices? I know, you really wish you could be me! One other option is to stop the CellCept and try Imuran. Been around forever. Kind of the Prozac of autoimmune drugs.
SO anywho. If you are a praying person, please keep me and this situation in your prayers, as well as my family. It's very difficult for Doug to be a full time boss, as well as a caregiver to me and parent to Jacob. Oh, and he's a husband. I completely get when he gets frustrated...I just don't think he gets my end of it sometimes. Like I told him the other day...it's not a lot of fun being me.
Fighting this disease called Myasthenia Gravis (MG) with a little humor, some good friends, and a lot of help from Above.
Showing posts with label quinton cath. Show all posts
Showing posts with label quinton cath. Show all posts
Wednesday, March 24, 2010
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