Thursday, August 16, 2012

Home...?

Last week, we got clearance from the doctor to return home to Connecticut.  We had mixed emotions about leaving the proximity and safety of the hospital.  There's comfort that the doctors who know Cole and his disease are only 30 seconds away.   It's surprising that there are no experts close to the NYC area - so we had to find a doctor willing to follow the protocol of our doctor's in Cincinnati.  There's also a lot of concern given that Cole's engraftment numbers continue to fall.  That means that Cole's bad marrow continues to take over Ryan's good marrow.  If the doctor's can't reverse that course, we will have to start over.  The doctor's are hoping to change medication and infuse Cole with more of Ryan's blood to stabilize engraftment and reverse it's course.  We remain optimistic and hopeful.      

After an overnight drive from Cincinnati, we were able to get Cole home early Saturday morning.  Janet will stay with Cole in the pool house while I try to spread myself between work, the house, the older two kids and helping Janet and Cole.  Thank God for family and friends who make this easier.  And mostly, thanks for Janet who is an iron willed advocate, nurse and protector of her youngest cub.  I couldn't imagine anyone trying to do this alone.  We're all trying to define our new "Normal" and find our way.  

For now, Cole can get outside occasionally with his mask, wave to the older kids and even hang out from a distance.  It's been a great spirit lifter for him and all of us.  Unfortunately, we have to take he and Ryan back Sunday for the next infusion in hopes of reversing the engraftment declines.  It's the first of many return trips to Cincinnati, but it beats the alternative of not being home at all.   

4 comments:

  1. So very happy that you are home. Those numbers will go up I am sure of it!!!

    Shannon

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  2. Hi Cole's family . . .one of my friends, and a marrow donor herself, met Cole's Aunt this weekend at the Be the One Run. I wanted to send a note to all of you that we have a group on Facebook to connect with other HLH families. Also, I just returned from Cincinnati last week as this is my 3rd year in attending the HLH Boot Camp/Family conference. I was hoping to have a chance to meet you all, but my guess is that you are back in Connecticut.

    I also have a child affected by HLH, and we brought her to Cincinnati in 2008. I'm happy to say that she just celebrated her 4 year transplant anniversary and is doing fabulous.

    Please reach out to the HLH group, there are tons of Cincy families in there, as well as families from all around the world affected with HLH. When I started the group in 2009, there were just a handful of families that joined, and now we have over 250. We are finding that it's not as rare as many originally thought, just rarely diagnosed correctly.

    https://www.facebook.com/groups/HLHSurvivors/

    Looking forward to hearing from you,

    Kelly Marsh & Family
    941-350-3767
    www.carepages.com/carepages/hannahmarsh

    Here is our daughter, Hannah's story . . . http://www.youtube.com/watch?v=anyMW9GHpZ4&feature=youtu.be


    P.S. We also have fellow HLH friends, also in Connecticut that maybe you guys would like to meet. There son is 5 years old now, and just celebrated his 5 year transplant anniversary, and they also went to Cincy.

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  3. Please know that continuous thoughts and prayers are with Cole. Let us know if we can do anything.

    Mondo

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  4. I hope he is progressing, please let us know how things are going! Prayers and love to you all, especially Cole...

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