On Monday, Wednesday and Friday, this is one day's worth of medication. All other days, I take two less than this. Once a week, I have one additional shot to take. It's a lot of meds, but soooo much better than nebulizers, IV's and oxygen (life before transplant).
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2 comments:
Wow, unbelievable. Thanks for your joyous spirit.
I've been following your blog a little. I have a 3 year old with CF. You have an amazing story! Just out of curiousity, what are the needles for? Is that CF related, or transplant related?
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