I guess this is the part where the story gets a little more graphic/detailed, so I need to warn you all that there may be some “TMI” (Too much information) enclosed.
I haven’t fully decided just yet where I want to go with this blog. In a way, I am writing this to keep my friends updated about my ‘adventure’. I know that some people may feel uncomfortable asking questions or asking how I am doing. I mean, you never know what kind of answer you’ll get when you ask someone about how they’re feeling. I figured if I write it here, those of you who are curious but uncomfortable asking can just read about it here anonymously. That’s fine with me!
I’ve also been thinking about people I don’t know…. If they manage to find their way to this blog, and they’re about to go through chemo themselves or have a family member or friend who is, it might be nice to read about someone else’s experience, so they’ll know what to expect. In the latter case, these extra details would be very beneficial. Not all my side effects, thus far, have been terribly unpleasant… but some are just not fun to hear about (or experience them, but, yeah.).
So, this is my ‘disclaimer’…. If you think you’d rather not deal with the personal details of my experience because that would be too awkward, I’d understand if you stop reading here. But for the rest of you… here we go!
No comments:
Post a Comment