I was sad to learn that Dr. Jackson died on Thursday afternoon, we were her last cohort selected during her life. Such an honor to carry on her legacy through the generations to come. I learned A LOT at this conference, and I am still learning! I am learning how tough this life is going to be with RA/Lupus/Fibro….I was amazed at how much energy a conference takes!!! Seriously so much pain and now sickness!
This choice of career is rewarding, amazing, but wow gosh….someone said they would rather do a residency (MD) that go for the PhD/EdD! While I do not know how true that is (and I doubt we can compare) I was shocked!
It is so tough living with an invisible disease, from the side effects of the drugs, to the fatigue, exhaustion, pain and frustration of limitations…it is like WOW! We have a different life! Our new normal…is tough but I am THANKFUL that for today…I can still do what I love.
Honestly, I have more than many I know! I can still walk, and go to work! I can still go to class and work in my research. I treasure those blessings because one day I might not be able to do that, and so I def. treasure these days!
I am THANKFUL for what I do have despite my RA/Lupus and Fibro! Thankful for the Affordable Care Act that is giving me hope of insurance (cards should be here any day!). I cannot wait for 12/01! Making appointments SOON! 🙂
Here is a link to learn more about Dr. Jackson (http://www.ucea.org/home/2012/11/19/honoring-the-memory-of-barbara-l-jackson.html)