Starting back on my methotrexate injections tonight after almost eight months off of it. My joints need the relief but my mind is in knots now. Just the word CHEMO is so off putting is it not? Whenever I accidentally mention the word people just stare, not sure what to say. If you ever want to shut someone up tell them you are on chemo FYI!
We've been getting this house clean as a whistle all weekend long. Now I am exhausted & so is Chris. Uggh, what a way to START the week ehh?
Peace, Love & STRENGTH be with you all <3
About Me
- Erin In The Sky With Lupus
- I am Erin & there were 31 candles on my cake October 2008. A few weeks later I was sent to a rheumatologist by a neurosurgeon (random?). After almost two years of being sick constantly & having ran every imaginable procedure & test possible, I was diagnosed with Systemic Lupus Erythematosus (more commonly called Lupus). There is currently no cure for Lupus & there hasn't been an FDA approved medication for it to come out in over 50 years. Most people can't even tell you what Lupus is. That's where I come in with this blog & hope to lessen the elusiveness surrounding Lupus. I love the beach & seashells & sea turtles & anything to do with the ocean really. I love taking pictures. I love my 3 cats, bunny Basil & new puppy Snoopy (aka "the zoo"). My faith. Family. Friends. Gardening. Music. Singing. Musicals. Painting. Scrapbooking. I just love to CREATE :) I love my husband Chris for the kind & patient man & care taker that he is. We've been married a little over four years now & I'm very lucky to have had him by my side through all of this :) Not everyone with Lupus has the support I have though & I realize this & want to help.
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