Showing posts with label NKH Awareness Day. Show all posts
Showing posts with label NKH Awareness Day. Show all posts

Wednesday, April 29, 2015

NKH Awareness Day - Wear, Share, Give, Love



This Saturday, May 2nd is NKH Awareness Day across the globe.  This day has been created by NKH warrior-parents, fighting to draw awareness to the disease that affects their children, and in many cases, takes their lives at a very early age.  Mike and I, along with the rest of our NKH Family around the world, invite you to take part as we Wear, Share, Give, and Love to raise awareness. 

What does "raise awareness" really mean?  I've asked myself this question often.  It sounds silly, but you see things everywhere now, asking others to "raise awareness".  I can't speak for everyone, but I will share what the phrase means to me . . .

Raising NKH Awareness means that you are sharing information on this disorder which both of our daughters were born with.  It literally means telling others about NKH - what it is, what it does and how you can help; and how can you help?  You can help by giving to NKH research!  You can also help by loving, encouraging and praying for other NKH families.  Don't discount any of these things, Friends!  As an NKH parent, as a parent of children with rare diseases, I promise that love, encouragement and prayer are all things that I crave, that I need, and that I long for on this wild journey. 

For us, raising NKH awareness also means sharing Ellie Kate and Lucy's stories.  We long for our daughters' lives to leave a mark on this earth, and that includes having their names coincide with NKH research (thanks to you, research donations have already been made in their names!).  More importantly we want their names to coincide with "Reckless Love".  Our desire is that you will learn to love better, deeper, wider, and more unconditionally because of what you have seen and learned through Ellie Kate and Lucy Belle. 

You've shown great support on NKH Awareness Day in the past, making us extremely proud of the village of people who are along for our crazy roller-coaster ride!  For the last few years, we've asked you to wear gold and blue, the color of our NKH Crusaders (our NKH mascot).  You've also boldly written the Girls' names on your arms, hands, wrists, etc for all to see; the goal being that people stop and ask you about the "rough tattoos:)", and you get the chance to raise awareness!  This year, we are asking you to do the following on May 2nd in honor of Ellie Kate, in honor of Lucy Belle and in honor of our NKH Family around the world . . .

  • Wear Ellie Kate and Lucy's name (arms, sticky-notes, hands, etc)
  • Share Ellie Kate and Lucy's Stories with others
  • Give to NKH research which is going on now!
  • Love a special-needs individual in a reckless way
You can also change your FB profile picture to help us get the word out:
 
 


By raising awareness, you are helping us find better treatment for those suffering from NKH.  By celebrating this day, you are encouraging those in the trenches, fighting against NKH everyday.  Participating in the day lets us know that Ellie Kate's name will be used - that her story will be shared and that someone's heart will be touched by it.  As parents, May 2nd gives us hope for the future; for better treatment for those like Lucy, who are living with NKH.  By taking part on this day, you remind us that we aren't alone.
 
Thank you for standing with us, for fighting with us, for celebrating this day with us. Thank you for helping us raise awareness on May 2nd.  WEAR.SHARE.GIVE.LOVE.
 
--Ryan

Tuesday, May 6, 2014

Lucy Belle

We are home!  Thank you so much for praying for Lucy Belle.  She is doing so much better, although she still isn't back to her full, happy self.  We've upped a few seizure meds and have added a new rescue med for her long seizure episodes.

There is no way we could get through these things without your love and support.  This was such a scary time for us and for Lucy.  Your encouragement has meant the world to us.  Your prayers have lifted us up more than you could know.  We truly just couldn't do this without YOU.  YOU are a huge part of our journey!

Lucy did start running a fever tonight, and if it gets too high, we have to go back to the hospital; you can imagine how much we DO NOT want to do that!!  Please pray for her fever to go away completely.  Also, please pray that she will be back to her self again.  We are so ready to see our Bubbly Little Girl rolling around the house!

On a lighter note . . . we are SO grateful for all that you did to show us love on NKH Awareness Day!  Here are just a few fun pics that you posted and sent to us on May 2nd:







Thank you, Friends.  We are truly blessed by you in so many ways.  

With Love,
Ryan

Thursday, May 1, 2014

May 2nd - NKH Awareness Day



Tomorrow is NKH Awareness Day!  That's right, Friday, May 2nd is a day set aside to spread awareness for this disease which affects less than 500 people world-wide.  Last year we celebrated NKH Awareness Day in the hospital, but this year - THIS YEAR, WE ARE HOME!!  Wahoo!!  Lucy is home, and we are excited to celebrate our big NKH Day out of the hospital. 

We had such a great response last year from our friends and family.  There was so much support in raising awareness for Non-Ketotic Hyperglycenemia or Glycine Encephaloopathy .  Some of your support looked like this . . . 


















We are asking you again to spread the word on this disorder that has taken the life of so many, including Our Ellie Kate.  You can do this everyday, but in particularly, spread the word tomorrow!  Tell people about NKH.  Tell people about Ellie Kate.  Tell people about Lucy Belle.  Tell the world and raise awareness!  

Also, we ask that you mark yourself to spread awareness.  Yep - mark yourself!  Use your body to write special messages, like the ones seen above.  Undoubtedly, people will see your NKH markings and will ask you about it.  It will give you the perfect chance to tell the world about this disorder!  Also, post your pics on Facebook, Twitter and Instagram!  We want to see your NKH Love, so show it loud and proud!






Thank you for your prayers.  Thank you too for supporting our girls, our family, and our extended NKH Family around the world. 

For more information on NKH, please visit the following sites: 

NKH Family NetworkNKH Crusaders and Hope for NKH

With Hope,
Ryan

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