|My sweet love.|
I started this blog back in August of 2010 with the intentions of reaching out, sharing what works for us/Rachel, sharing how Rachel's clinic appointments go, providing a positive outlook in what can sometimes be a less than desirable situation, sharing how Rachel/we live in spite of CF, etc. I had one goal in mind when I created my blog and this is my thought; "If one person reads my blog and gets a tip.....then it's served it purpose."
About a week ago, I got an email from a fellow CF mom that I met on Facebook (I actually got to meet with her when Rachel and I went to Arizona.) The email really touched me and it was at that moment that I realized my blog had done it's job.
Here's the email (names removed) :
I just wanted to send a quick note to say hello. I recently showed my husband your blog to show him pictures of your daughter surfing. He has always been a fan of surfing and loves how surfers support the cf community. My daughter will definitely be doing a surfing experience day when she is old enough.
Your blog is very inspiring. I love seeing how much fun you have with your daughter! It shows me that you can take care of their cf, but still have a ton of fun, travel, and have fun adventures. I can't wait to do the same with my daughter!
I can't believe that my daughter will be 6 months in a few days. Time really does fly! She has been babbling up a storm lately and really likes hearing the sound of her own voice. She has been doing well with the pulmozyme, but she thinks her neb cup is a toy and tries to eat it the whole time. :) At least she likes it!
|Yes it is true.....we have no sense!|
Doing chest therapy/breathing treatments.