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Rheumatrex is what my rheumatologist has decided to do. I am choosing
injections as my hope is to get into remission and I don't want to add
more side effects than I need to...one day a week, I'm thinking Friday
nights so I can sleep a portion of it off and take it easy if need be
on the weekends. "Low dose chemotherapy" is what kind of reminds that
this is real...but not. The things we see are not, unseen...are! As I
know that until I'm better, I continue to follow doctor's orders,
believing that even thru new medicines, all testing, and trials (no
pun intended) Help is on the Way!
Thanks to very special people who lift me up along the way....
What does a room full of RA'ers on Prednisone look like? Moonies! I
officially look in the mirror and repeat, "it's not what's in the
outside that counts," until I can believe it. Ok I know the "power of
positive" is way overused & even marketed in a skewd manner... But I
assure you that positive things said are very powerful when it comes
to not buying into the negativity that comes with being sick! That's
my version and I'm sticking to it! And yes...the moon face is still
there...but there's hope ill get off of this horrific/helpful drug
soon and maybe get to lose weight soon! I've got an appt this next
week! Ever heard if rhupus? This is our next topic a la diagnosis di
jour....