When I was in my teens I thought I never wanted to marry, have a family, and do all the traditional 'llife' stuff. I had good reason too. I knew I would likely not live to see my 30th birthday or possibly even my 20th birthday. I felt like it would be wrong to let someone love me and have to lose me. I knew a family would pretty much be impossible due to infertility and risk of pregnancy. I thought I was happy being alone, living "MY" life. I am glad I am wrong, I am glad that GOD has a plan for me and that he knew I needed Bryan. I met Bryan when I was just 19. I wasnt' looking for someone to love or to love me back, but that's what happened. I felt guilty sometimes, like I was cheating him from being with someone who could give him things I couldn't (like kids and growing old together). I know nothing in life is a guarantee. . .but I knew I had an expiration date much sooner than most. I just know that I would have never made it through life and living with CF as an adult if I hadn't had him by my side the whole time. Love can make us stronger than we think we can be. I pushed myself through the sick times to get healthy to have more time with him. He spent countless nights with my in the hospital because I couldn't stand to watch him leave. He was my motivator to do my meds and treatments. He wouldn't give up on me and wouldn't allow me to give up on myself. I thought I needed a life alone to accomplish my Dream of Acting. . .when I really needed loved, 100% undying, dedicated, unconditionally loved.
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4 comments:
I love reading about how happy you are with you husband. *squish*
You guys are the perfect couple...seriously! We love having you in our family and wouldn't trade it for anything...except for maybe that crossed eyed Bec, oh I mean,....ha ha...just kidding...we love ya!
Love ya Jamie!
Happy LOVE day! Xo
Jamie,
Thanks for that post. It helped me realize that it's not just my husband being odd by not allowing people in his life. I never could really grasp why he felt that way but seeing that other CF'ers are the same way helps me understand him much more. I am learning so much about the psychological impacts of CF even more by reading your posts and I thank you again for that. Your post-transplant change is uplifting and I dream about the day Jim has his new lungs and all the things (no matter how small) we will be able to do. Thank you again! Denise (wife of Another Outlet).
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