The Liebster Award
I have recently connected with another blogger who is the mom of a sweet boy with special needs named Silas. You can check out her blog at A Boy Named Silas. She is truly an amazing mom, and I just ordered her book which is an account of the time they spent in the NICU with Silas. She just nominated me for The Liebster Award - Special Needs Edition. Thanks, Alana Terry! I was very surprised, humbled and honored all at the same time.
The Liebster award comes with certain rules, one of which is sharing 11 facts about myself:
2. Who is your favorite doctor, specialist, or therapist for your child and why?
3. What symptom of your child's disability breaks your heart the most?
6. In three words, describe how you have changed after becoming a special-needs parent.
8. Would you take away your child's disability if you could? Why or why not?
10. "One thing I wish more people realized about my child is ..."
The Liebster award comes with certain rules, one of which is sharing 11 facts about myself:
1. I took piano lessons for eight years
2. I would love to have two Doberman Pinschers
someday
3. I work for a health insurance company
4. I have only colored my hair once in my life
5. I’ve never had a massage (by a
professional)
6. My all-time favorite movie is still
Footloose
7. I’ve had a pacemaker since the age of 25
8. Along with my journalism degree, I
also have minors in speech communications and animal and range sciences
9. I can drive a 5-speed and prefer driving a stick to an automatic
10. I successfully gave up drinking caffeine
11. I was born on an Indian reservation in Wolf
Point, Montana. We lived in Luster at the time where my dad worked as a
ranch-hand.
I was asked 11 questions by the blogger who nominated me for the award and here are those questions and answer:
1. Think of the day your child received her diagnosis. What is the first word that comes to mind?
BROKENHEARTED
2. Who is your favorite doctor, specialist, or therapist for your child and why?
Faith has had so many wonderful people working with her, so this is a hard
question. I would have to say though it would be her pediatrician, Dr. Ocejo
who oversaw Faith’s care in the NICU. He and Faith have a very strong bond and
when she is sick, she looks forward going to the doctor because she knows she is
going to see him. They spend the first 10 minutes of the appointment talking
and laughing with each other (no matter how bad she feels, she always has a smile for him). He always takes extra time with us and even if our appointment is at 4:30 and he is supposed to be done at 5 o’clock, he stays afterwards just to make sure all
of our questions are answered.
3. What symptom of your child's disability breaks your heart the most?
There are a few of them that are pretty
heartbreaking but the one that tops the list is her inability to go to the
bathroom on her own and still being in diapers. There are times at school that
she accidentally wets through her pants, and she has to leave in the middle of
what she is doing and get changed. It’s not lost on the other kids what is
going on and I think she is very embarrassed when this happens. Her inability
to read is also very heartbreaking.
4. What symptom of your child's disability
is actually somewhat endearing?
When she tries to get a teddy graham out of the
bowl all by herself and ends up dumping teddy grahams everywhere. At least
she’s trying!
5. What is something your child is REALLY good at?
She has really good
memorization skills. When we read her a story, she wants to have it read to her
over and over again until she has it memorized. Then, we’ll ask her to recite
it and she’ll tell the whole story word for word on her own (without even looking
at the pictures.) The first book she memorized was an Amelia Bedelia book.
6. In three words, describe how you have changed after becoming a special-needs parent.
Having more faith.
7. How has having a special-needs child
impacted your spiritual life?
I am working on a blog post on this exact question.
Being a special-needs parent is making me aware of the Christ-like qualities
that God wants to instill in me – many of these qualities centering around
being a servant. My prayer life has certainly increased as well as I have
prayed for Faith more than anyone I have ever prayed for in my life.
8. Would you take away your child's disability if you could? Why or why not?
Yes, I would take it away in an instant. I want her to be completely well and
whole and I know God wants that for her too. I believe that sickness and
disease come from the enemy and one of the benefits of being a Christian
is to have healing from sickness and disease. (Psalm 103).
9. What is the most disrespectful thing
anyone has ever said to you or your child?
Thankfully, we have not had anyone
(that I know of) say anything disrespectful to or about Faith. What bothers me
is when people, especially other kids, blatantly stare at her. This is
unnerving to me, even though I know they are probably just curious.
10. "One thing I wish more people realized about my child is ..."
that
she just wants what every other child wants – to feel loved, appreciated,
secure, confident, protected and supported.
11. If you were to articulate all the wishes you have for your child, what
would they be?
My wish for my child is that no matter what her struggles or challenges she faces on a day-to-day basis is that she knows in her heart how much she is loved, accepted and cherished by her family, friends, caretakers and most of all by Jesus.
And now 11 questions I would like to ask 11 other nominees who have a special needs child:
1. What has been your best resource as a
special-needs parent?
2. How did your extended family react to the
news of your child’s diagnosis?
3. Is there anything you wished you knew now
that you didn’t know in the early stages of your child’s diagnosis?
4. What prayers do you feel God has answered
for your child?
5. How do you REALLY feel about being a
special-needs parent?
6. What or who has been your biggest source of
support/encouragement?
7. What do you do for fun?
8. How has being a special-needs parent
affected your marriage (or other significant relationships?)
9. What hopes do you have for your child’s
future?
10. What is something you wish your child can
do that he/she can’t do?
11. What is something good that has come out of
having a child with special needs?
Rules of the Liebster Award: The Liebster Award is designed specifically for small blogs (less than 200
followers) and is a fun way to get to know other bloggers. First you
post 11 random facts about yourself. Then you answer then 11 questions
your nominator asked you. Then you nominate 11 other people and ask them
11 new questions. In your response, you make sure to personally thank
(and link) the person who nominated you. Also, be sure to insert the pink Liebster Award image somewhere in your post!
I would like to nominate the 11 following blogs/bloggers for the Liebster Award. If you participate in the Liebster Award, please leave a link in my comments section for this post. I would love to know more about you!
So I've also colored my hair exactly once. I have had one professional massage as a gift from a friend when I was pregnant. And your doctor sounds wonderful! I'm sorry about Faith's getting embarrassed about needing to be changed. I think it's so hard when our kids are able enough to understand what's going on but not yet able to do something about it. Thanks for your answers. I enjoyed them all!
ReplyDeleteThank you so much for nominating me. I am so excited. I can't wait to participate. I love you blog.
ReplyDeleteErin
I meant to say I love YOUR blog, lol!! Can you tell I'm in a hurry with Raygen crying at my feet and gotta go get Zoie from school, lol. Crazy day.
ReplyDeleteHi.
ReplyDeleteI'm fairly new to blogging and had never heard of the Liebster award. We have two blogs. One focuses on inspiration and encouragement through posts about life, music, discipleship, worship, and ministry. It's at http://www.worshipsounds.wordpress.com
Our other blog is called Family Song. It's all about family and the Christian home. Our post categories include "Encouragement for Families," "Harmony helpers", "Family fun", and "Special needs, special blessings". That blog is at http://www.familysong.wordpress.com
You question about how one really feels about being the parent of a child with special needs reminded me of a recent post that I called, "The Secret Life of a Special Needs Parent". Maybe the thoughts that I shared would be helpful to you and your readers, so I am sharing the post URL. http://familysong.wordpress.com/2013/03/07/the-secret-life-of-a-special-needs-parent/
Blessings to you,
Cynthia