I’m back from my blog break. I had planned on taking off some more time, but there is simply too much fodder that keeps lapping at the heels of my writerly itch. My short but much needed respite has me recharged and ready to roll again.
As my faithful readers know, one of the things I continue to stand behind are the needs of children. I write and volunteer and speak out extensively about issues like education, health care, child abuse, and hunger.
I’ve used this space over the years to share my experiences as a pediatric bone marrow transplant volunteer. Those ten years have moved me and shaped me in ways only second to motherhood. I’ve written about some very special patients and stories that will tear your heart to shreds. I’ve written about the magic of the Ronald McDonald House. I have been so very fortunate and believe volunteering in my community is but one way to show my gratitude. Call it paying my dues, paying it forward, call it what you will. I lead a charmed life. And I promise you I don’t take it for granted.
It’s easy to write about issues that blaze my spirit toward action. It’s easy to be motivated by media stories and chance encounters. It is another thing entirely to write about people I know personally, especially children. My friend’s young daughter has been diagnosed with Severe Aplastic Anemia. She is a first grader at my sons’ school, and she has eyes that will melt the coldest of hearts. She needs a bone marrow transplant. As a mother, I cannot wrap my head around what it must have been like for my friend to hear these words. I shut down the part of my brain that likes to play the What If? game.
Lucia is a typical little six-year old girl. She likes fairies, horses, and American Girl dolls. She loves playing with her big sister and her aptly named dog Wonderful. Lucia will go through quite a journey on her road to recovery. In a nutshell, her bone marrow has stopped working. This means that Lucia’s little body is not producing red or white blood cells or platelets. Yet another thing we all take for granted…When’s the last time you paid any attention to your platelets?
As Lady Luck can be cruel, Lucia’s sister is not a match. This is where you come in. We can do our part as a community to help.
Please join us on Saturday, September 8 10:00 – 1:00 at Wiley Elementary School at 301 St. Mary’s Street in Raleigh, NC for a bone marrow drive.
We need everyone age 18 – 60 to come get tested. Ages 18-44 are urgently needed! Did you know that you are ten times more likely to be called as a match between the ages of 18-44 years of age? I’m about to turn 44 and will be there! If you aren’t a match for Lucia, you just might be someone else’s life saver.
To be tested requires a simple, painless cheek swab. No pain but lots to gain.
It costs $100 to test bone marrow donors and add them to the national registry. You do not have to pay to be tested! Patients like my friend’s daughter rely on all sorts of support to get through this ordeal. If you can’t join us for the bone marrow drive, you can still help. Check out the Love for Lucia page and donate what you can, help spread the word, get tested in your own home town, share Lucia’s story.
You have the power to save a life. That trumps all super heroes.
In closing, here’s something to give you a nudge. Talk about moxie…
Erin says
I’ll bring the whole family and maybe even my parents and mother-in-law!
Andrea says
Shared on FB and on TriangleMommies for you, I will continue to get the word out. I do not know that I am eligible to be tested but will check the info and criteria on health restrictions. I will keep her in my thoughts and heart.
Jen a.k.a Jael Custom Designs says
Shared via Twitter! I’ll share on FB also and mark my calendar! The family is is my thoughts & prayers.
magpie says
I sent in my swab a couple of months ago, because: http://www.magpiemusing.com/2012/05/get-swabbed.html
Natalie P. says
Shared on my facebook fan page and twitter! I WISH I could help, but I have ankylosing spondylitis, and can’t “be the match”. 🙁
Amanda says
Sharing. Sharing. Sharing!
Amy says
It’s on my calendar and shared on my FB page…we’ll keep this brave little girl and her family in our thoughts and prayers!
thedoseofreality says
I just shared this on my FB page, and I have been on the marrow registry as a donor since I turned 18. I will re-confirm on Monday that I am still up to date. Please know that your friends are in my thoughts and prayers. I am just so sorry.
Erin Lane says
I’ve already been tested but will absolutely spread the word.
Elena says
As the survivor of a bone marrow transplant, I cannot even begin to describe how important this is. While I cannot be a donor, I will share with others.
Speciality Hospitals in Pune says
It is easy to say ‘I understand your pain’ but it is very difficult to really understand that pain. The true realization of suffering occurs only when we undergo the same situation ourselves.
One of the worst moments is when we want to help our relatives but can not because of medical constraints.
Some of the most severe medical conditions are caused due to such activities in the body to which we hardly pay any heed to. The absence of enough platelets resulting in need for bone marrow transplantation is one such example.
More and more people should come forward to help people who are suffering from any disease.
Best Hospital in pune says
God bless the little girl lots of strength. If she get donor then her chances to recover very soon.