After Anya’s path became clear, and after she was born, I
stopped looking for a while. I was too involved in my child’s story to think
about anyone else’s. Now that we are home I find myself looking again. I have
liked several pages on Facebook that routinely ask for prayers of support for
families affected by CDH. Prayers for babies to fight, babies who are
undergoing surgery, or other complex issues. Sometimes babies that are being
discharged home to thankful families.
More recently though there have been more and more prayers
for healing of broken hearts. So many CDH’ers have recently died. More frightening
to me is that some of these children were not infants, but toddlers, well past
the age they should be ‘out of the woods.’ Over and over, like an unhealing
sore I wonder why. What happened to that child? I watch Anya and feel a mixture
of pride and dread. She is doing so well, gaining weight, reaching milestones,
weaning off meds. Still there is no guarantee that she may need to be
hospitalized at some point, and I fear that it could be our family that needs
those prayers.
So I lurk on websites, on Facebook pages, trying to glean
some snippet of information that will make me feel better. At the same time I know
I will never find anything that will reassure me. I have had too many
experiences in my life that have demonstrated how frail life is, how quick to
change. Ever since my mother died I have been waiting for my life to be ‘normal’.
I suffered through depression, infertility, balancing caring for my father and
caring for a young child, Dad’s death, a miscarriage, and now a life
threatening condition in my second child. I spent 100 days away from home and
my preschooler to give that child a chance at life, and have now put my career
on hold to give her the best shot at developing on track.
I need to quit lurking, and I need to quit waiting. It is
obvious my life is not meant to be ‘normal,’ at least not the way I have
defined it. For better or worse, this is what my life is. Worrying what might
happen tomorrow is taking away from today.
My little Supergirl! I have had my heart set on dressing her up as Supergirl since I called her that in the blog! |
Hi Kelly,
ReplyDeleteI have just come across your site through another CDH mama's blog. My survivor is Lincoln and we are also in STL. I'm glad you were able to find the right care for Anya with Dr. Kays. I've heard such wonderful things about him. I'm so happy that Anya is doing so well and hope that you find her care at Children's and with First Steps to be great as well. We love both MoFS and SLCH!
i understand your lurking feelings. It is hard to go through this journey, and all the kids are so different and statistics are unknown or not consistent. All you can do is live day to day, soaking in your little one and know she has the strength to overcome. She has already.
I wish your family the best,
Dorothy
Kelly, I so understand your feelings, and I totally get how heart-breaking it is each time you watch one of our CDH children pass. Erin who just died was the same age as my Samuel and it hit hard. Yes.
ReplyDeleteSamuel had 22.5% fetal lung volume on his MRI at 22 weeks. He was considered among the "most severe of the severe range" and not expected to live. I *did* memorize those numbers. And I have found that they don't mean all that the doctors say they mean. Samuel spent 148 days in hospital before we brought him home and he's had 2 reherniations. But he's okay - awesome, really. And our family is okay too.
As you've already found out in your previous hardships, you can do amazing things. Normal doesn't mean smooth sailing, I guess. :) Anya just came home and so you are in a rough transition place. Be gentle. There will be lulls in the worrying, and then surges. And you can do this.
Thanks for sharing these thoughts. I'm with you all the way, CDH mama.
Corinne
www.samuelslight.blogspot.com
I totally relate to all you are feeling. It is a daily struggle for me to remember to enjoy TODAY instead of worrying about tomorrow.
ReplyDeleteI'm with you. Keep taking each day one step at a time. And rest. Keep resting. CDH mommies never get enough rest.
Rose
babymorrison2.blogspot.com