
Eventually, I will post the rest of the pictures either here or on facebook...maybe even both.
Please continue to include us in your prayers, thank you all so much!
My name is Catherine, and I am 28 years old. I have lived with Chronic Fatigue Immune Dysfunction Syndrome since I was 16. I have several inter-related diagnoses, and I am stronger than all of them...most days. Here I will chronicle my life as I continue my journey to become a counselor specializing in treating patients with chronic illnesses and disabilities. Masters in hand, all I need is the hours and license!

Eventually, I will post the rest of the pictures either here or on facebook...maybe even both.
Please continue to include us in your prayers, thank you all so much!

Or miss Emma's infectious giggle that has the ability to make me laugh uncontrolably over something as silly as trying on my dad's $2 pair of "cheater" reading glasses...



It's funny,... now that I have moved back home, I swear I think my friendship with one amazing friend (code shaft, lol)... has grown stronger because we are both making an attempt to call and chat whenever possible. I think it has helped me keep my sanity (shut up Sarah, I WAS sane at one time...stop laughing) now that I am back with my parents. Even though I miss her terribly, I think we talk more now than we had for awhile. We have grown so much closer, and I always enjoy making her laugh... we both seem to be really good at making the other laugh...especially when we aren't trying. Another incident of uncontrollable cackling....
Friends love you for who you are, not who you pretend to be, what you can give them, or how often you get to see them. I am blessed to have a select few "best" friends, whom I would not trade for all of the fake friends & aquaintences in the world. These friends know my heart, and I know theirs... and they know who they are.

