Friday, February 21, 2014

A Bad Word

CF is a deadly disease. That may sound trite, but honestly, I was surprised to learn the other day that in the medical community, Cystic Fibrosis is classified as terminal.

I've written about it before, but seeing the word terminal to describe the disease that my baby boy has, is just almost too much for my Momma Heart to bear.

Terminal literally means "predicted to lead to death." What a bad word.

Some may argue that we are all, indeed, terminal. And, while it's true that we all have a start and end date in our lives here on Earth, does that fact make it any easier to bear that my baby has something that cannot be cured or adequately treated (for now) and that is "reasonably expected to result in the death of the patient"?  

CF is not going away for us, for Crosby. That fact is a long road to acceptance. Acceptance of the word terminal is even harder. He is healthy now, but that ugly, bad word is an ever present black cloud.

So, forgive me when I annoy you by constantly posting about CF fundraisers. But trust me, if your baby was helpless to gross, cruel disease like CF and there was a way that a possible cure could be sought, you too would ask for donations from your friends and family again and again and again. Forgive me when you come to our house and I bark orders at you immediately to wash your hands and use sanitizer (I'll hug you after, I promise). Forgive me if my blog posts aren't always hopeful, lighthearted and just full of pictures. Most days I can be the glass-half-full kind of girl or if I'm not, Lance can gently remind me to relax. But some days, a bad word like terminal can cause the panic and anxiety to creep up within me. Seeing the word terminal can ruin your day.

A word like terminal forces you to stare at the possibility of loss. And the possibility of losing something that you love so fiercely and so dearly, well, it can shatter you. Terminal. Such an ugly, bad word. A constant reminder of what all you have to lose. 

Facing a word like terminal forces me to love him differently. Better. Because it forces me to remember that life is fragile. But, I do know that no matter how long or short his life may be, I do know that it's a gift. And I'm trying to treasure every second.

Ah, I'd love to wear a rainbow every day,
And tell the world that everything's OK,
But I'll try to carry off a little darkness on my back,
'Till things are brighter, I'm the Man In Black
-Johnny Cash





To donate to the CF Foundation, click here.

To donate to Great Strides in honor of Crosby, click here.

Love,

Carmen


Tuesday, February 18, 2014

Crosby @ 5 Months

Dear Crozzie Bear:

You are 5 Months Old Today!



A few things we love about you...



You are so happy in the mornings. Even at 5am.



Your smiles and giggles melt my heart.



You are so inquisitive and want to hold everything in your hands. And then you want to put whatever it is in your mouth!



Now when I hold you, you hold me right back. Sweetest. Thing. Ever.


You are a cuddle bug and just want to be held all day. You are content and fit perfectly in my arms. We are so thankful to have you with us and we praise God for you.






A whole bag of breast milk for me?! Happy Valentines Day, Crozzie. He grabbed the whole bag from Lance while he was making bottles! 










Love,

Momma and Daddy

Friday, February 14, 2014

65 Roses






Happy Valentines Day to the Fans of The Crosby Show!

Being that today is all about hearts, love, and roses, I think Valentines Day is a perfect day to share about what a rose symbolizes to us now. Roses use to mean romance and beauty. I'm right there with most gals who swoon a little over receiving roses from her guy. Remember the movie Bed of Roses? Christian Slater anyone?  Please! I think Natalie and I pretty much had that entire movie memorized circa 1996! 

But for thousands of patients with CF, a rose is the symbol of their daily struggle to breath. It's a symbol of their battle against the horrific disease that shadows their life. 

"65 Roses" sounds a lot like "Cystic Fibrosis."

"65 Roses" is what many CF kids call their disease because the words are much easier for them to pronounce.

In 1965, a 4 year old boy named Richard Weiss, overheard his mother, Mary Weiss, who started the Palm Beach County chapter of the Cystic Fibrosis Foundation out of their Palm Beach home, making constant phone calls in an attempt to raise money and awareness for a disease few people had heard about in the 1960s. 

Cystic Fibrosis sounded like 65 Roses to Richard. That innocent observation would go on to become the slogan and symbol for all those who suffer the devastating effects of CF.






Since 1965, the term "65 Roses" has been used by children of all ages to describe their disease. But, making it easier to say does not make CF any easier to live with. The "65 Roses" story has captured hearts and emotions. 

The rose, appropriately the ancient symbol of love, has become a symbol of the Cystic Fibrosis Foundation. And the rose means so much more to us, than it did before.










{Sorry for the blurry pictures. My little Indian Chief is a wiggle worm!}

We hope everyone has a wonderful Valentine's Day. Crosby sends each of you his XOXO.

Love,

Carmen

Friday, February 7, 2014

A Day For Hearts

Today, February 7th, is Wear Red Day to raise awareness and draw attention to heart disease and it's remedies.

February is National Heart Awareness Month.

February 7-14, is Congenital Heart Defect Awareness Week.


We are wearing our red today in memory of our Pappy.

We are wearing our red today in honor of our friend, Emma Wasson. 







More on American Heart Month: http://www.cdc.gov/features/heartmonth/

More on Wear Red Day: http://www.goredforwomen.org/wearredday/

More on Congenital Heart Defects: http://www.tchin.org/aware/



Love,

Carmen
 
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