Right then so I am going to start off by taking the big
positive from today after my scare this morning my right foot is not hurting.
Now because it is not hurting doesn’t mean that the lump that I felt has gone
away because it hasn’t but at the same time it is a huge relief as I thought
that when it hurt this morning that was it and it was going to be as painful as
my left foot.
It is fair to say that right now I am feeling a bit stupid
because my left foot took a few years before it was hurting all of the time and
another 6 months of more or less constant pain before it reached anywhere near
the level of pain that I am in now. On top of that today I managed to do a lot
more lab work sitting down and this did help the pain in my left foot, still
hurts a lot when I stand but that’s nothing new.
Now that I am writing lots of science posts for the blog I
am wanting to write something a little less hard and so was wondering what I
could do that would still be related to my foot and also raise awareness. I
have always wanted to write a book, sure I was figuring that it would be a
crime-thriller book as I love all the books by Jeffery Deaver and James
Patterson and many other authors like that but I do not have the knowledge to
be able to write that sort of thing. I was then thinking I could write a sort
of short story type thing (see how good I am with words) that is partly based
on real-life in which a kid finds out he has Ledderhose and the story through
that. Not sure whether I can make it interesting enough to be a decent read but
I don’t think it is going to hurt me trying, I mean stick in a love interest
here (thinking of 14/15 when I say kid and not 4/5) a few bullies there and
maybe it can be interesting. Then all I have to do is put it on the internet for
free and watch it sell in its millions and soon everyone will now about
Ledderhose disease muahahahaha.
Still the odds of that happening are very unlikely as for
one I have to write the book and for two I have to make it interesting and for
three I have to actually get it online and the list goes on. Still I think that
it would be a really cool way of spreading the word about both Dupuytren’s
disease and Ledderhose disease, I mean I could easily make a diary and science
mix by just compiling my different blogs post together but I am not sure that I
want to do that.
Anyway...
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