This guest post is from the masterminds behind Let Georgia Hear-- Kelly Jenkins and Sara Kogan.
I am pulling for them today and the Commission (see below) is voting on HB74. They have been tireless in their efforts and I could not be more proud of all they have done, but today will be a long day for them. Keeping them in my thoughts. From Kelly and Sara:
In 2011, we started Let Georgia Hear with a group of parents of children with hearing loss. We started Let Georgia Hear because hearing aids for children are not covered in our the state of Georgia even though 20 other states have passed bills requiring coverage. Upon the formation of Let Georgia Hear, we launched a website, started an online petition, began approaching non-profits and other organizations for support and we started building relationships with legislators and influencers within our state legislature.
Since our inception, it has been a whirlwind. Let Georgia Hear has been featured in both the local and national news. At this point in time, we are at a crossroads with the legislation (House Bill 74). The Special Advisory Commission for Mandated Health Insurance will vote on our bill on November 18th. Though the Commission's position on the bill will be non-binding, it will be incredibly difficult for us to gain any traction within the legislature during the upcoming session without the Commission's support.
It has been wonderful working on Let Georgia Hear with so many talented and passionate parents and we are committed to staying the course until this bill is passed!
Respectfully,
Kelly Jenkins and Sara Kogon, Co-founders of Let Georgia Hear
Monday, November 18, 2013
Saturday, November 9, 2013
Lobsters
Remember that Friends episode when Phoebe told Ross that of course he and Rachel were going to end up together because she was his lobster?
The theory was that lobsters mate for life. Everyone has that one true life companion and
no matter what might separate you temporarily from your lobster, it is fleeting
because you will eventually end up with them for all of eternity. I always thought this idea was reserved for
romantic relationships. And back in the
90’s before I met my husband, I hoped that I had a lobster and that we would
end up together. I had theories about my
‘soul mate’ and who that person was and whether we would “end up together”
because it was “meant to be”. The thing
about your lobster is that you really do not know who yours is until you find
them.
I imagine that this person, like Phoebe says, would
metaphorically walk around the lobster tank with you, holding your claw for the rest of your life. You would never be alone and you would know
that you belonged somewhere. What I
never predicted was that circumstances beyond my control, after my marriage and
after two out of three of my kids were born; I would find a whole tank full of
extraordinary lobsters. Maybe not the
kind of lobsters I had planned for, but arguably better. And here they are. Well some of them, anyway.
These ladies are my Moms of the Ear…my Speech School moms. They are mine because I know them intimately,
I know and love their kids, and they “get” me and my journey better than any
other people on earth. Hearing loss
brought me my lobsters.
Let me be clear that we are not exactly alike by any means—we
all come from different income brackets, marital statuses, careers, educational
institutions, etc. but the thread
between us (raising a child with hearing loss) is unique. Also, since hearing loss does not
discriminate, our differences are completely irrelevant. Having this experience leveled our playing
field. When we get together there is a
lot of fun and there is sharing about our kids’ progress or our latest worry or
our plans for next school year. We are
all cheering each other on and routing for each other’s kids. We accept each
other without judgment. Our personalities are different but we never really clash.
We express concern for the others in the group and we think through solutions
together. Like soul mates, we have a
magnetic pull back to one another and having each other is a matter of physical,
mental and emotional survival.
I wish that everyone reading this blog could 1) know these particular
women and 2) have a group of women just like them in their own lives.
In lieu of introducing you to your own network of lobsters,
let me tell you about some of mine:
Kelly and Sara have three kids each, yet what they are known for is being amazing advocates for all of the kids
with hearing loss in our state. They are working tirelessly to make sure
that hearing aids are covered by every child’s insurance company. It is hard work and they are not sure how
long it will take, but they are never deterred. They solve problems together
brilliantly and impress me every day with how savvy they have become on GA
legislation and how to get things done without being obnoxious about it. They are the co-founders of Let Georgia Hear…if you get a chance check out their website and sign the
petition no matter what state you are in. All children deserve access to
hearing aids to learn language if they need them. Period. Kelly just won the Atlanta Business Chronicle 40 Leaders Under 40 Award. These two inspire me to do more every
day.
Julia is a single mom who unfairly described herself as
“letting everyone down” the other night.
She said she told her trainer to suck it up because she was a mom and
her kid has special needs and she has a job and therefore she was not going to
let him shame her because she ate some things she should not eat last
weekend. She was basically trying to say
, “Get in line, dude.” We Moms of the Ear are always feeling like we are
letting people down, but in truth we are shining like diamonds every day. Unfortunately,
it never feels like that to us. We
always think we should be doing more. Julia is also generous and easy going and
gorgeous and has a beautiful home and I have never seen her down in the dumps
about her son and his challenges. She
says unequivocally that she never measures her son against other kids or his
chronological age or any other societal expectations because he is who he is
and as long as he makes progress, she is happy.
She is incredible. She never lets me down.
Scarlett is a former teacher who is married to a school
principal, but she is at home with her kids now. She has to be because her youngest daughter
is attending the Speech School and it takes her two hours to drive there and back every
day. She does that two hour commute, day
in and day out, without a single complaint.
In spite of it all, she is always the life of the party. She could easily feel sorry for herself, but
she chooses to find ways to lift herself up and to lift up others as well. It
has been four years now that she has made this commitment to her daughter. She knows it means sacrifice for her and even
her other kids, but she never waivers. She
is the strongest voice in the Let Georgia Hear movement other than Kelly and
Sara and she is willing to share her own family’s story of struggle to purchase
hearing aids in order to help all kids in GA.
She somehow finds it in her heart to cry with me about my own family
because she is deeply empathetic.
Mostly, she is a fighter.
Laila has a daughter with the same condition as my Wyatt who was diagnosed
later than most of our kids. Her
daughter has made amazing progress in the last couple of years, especially
since she received the cochlear implant.
Laila was very brave in making that decision to implant her daughter and
like me, doubted it every step of the way, but she pushed through because she
knew it was the right thing for her. She
has a demanding job and now is awaiting the birth of her twin boys! Even on bed rest, she still finds time to be
the co-President of the Parent Teacher Committee at the Hamm Center. Lately when I see her, she is planning the
next event or working on donations of treats for the cookie decorating party
coming up in December. She is also
worried about her twins and whether they will have the same condition as her
daughter. However, it will not matter to
her at all because she knows how much of a blessing her kids are and she will
celebrate each one of them every day.
She is an angel.
I could gush about these ladies all day long and each of the
others pictured (and not pictured) in the photo above. But that is not really the point. They all
have their story and each of their stories touch my heart and keep me going.
The point is, I seriously, could not survive this Profound Life, and frankly,
one single Profound Day without these moms.
Lately, in my work, I have been thinking and planning ways
to increase and infuse parent to parent support (like the support I get from my
group of moms) into every state early hearing detection system in the U.S. What are the elements of successful support? Is it just friendship or, as my intuition
tells me, is it friendship plus informational support, plus leading by example?
How do you seamlessly fold in new members of the network? How do you create a lasting commitment and
sacred love for one another’s kids? Can
it be cultivated or does it have to happen naturally?
My gut tells me that you can cultivate it. I am lucky enough to have a group of women at
church who have been meeting on about two Thursdays a month for close to four
years. We all were invited to the group
by a role model—a person whom we all want to be. Because of this woman’s deep faith, her
ability to make us feel comfortable, and her authenticity and concern for the
spiritual nature of our lives, we were all pulled in easily. Who would not want to spend more time with
this woman and grow in spirituality at the same time? No brainer.
Then we leaned in with a fierce commitment to showing up, to sharing with
each other and to keeping a sacred trust and confidentiality. Now I absolutely hate to miss the meetings of that group. So, over the past four years, I have been
fortunate enough to see that people can certainly create an environment of deep
support that we will always return to.
The primary difference is that these women at church chose their faith
and executed free will to be a part of the group. With hearing loss, you are hit with the
diagnosis and you are typically dragged in kicking and screaming and crying the
whole way.
That has to change. It does not have to be so terrible in
the beginning. We need to shorten the
path out of despair for moms of children with hearing loss.
I feel particularly responsible to solve this problem because
I like to share my good fortune. I think
that may stem from a feeling that I am undeserving of anything unless everyone
else can have it too. I believe that Moms of the Ear need each other for
survival and I have found my people and want others to find theirs too. No one should have to endure the path of
their life without their lobster.
Maybe once you discover the power of this type of support, you just naturally want to pay it forward. That is why one Mom of the Ear feels compelled to mentor another as soon as they have the capacity to do so. Lobsters helping baby lobsters. It is how we make meaning out of our Profound lives. I read this blog the other day that describes the mentoring of other families as a purpose in life in direct rebellion to the hard work and the heartache that also lies within the journey. It is exactly what I have been ruminating about ...
http://ardinger.typepad.com/bliss/2013/11/a-purpose-we-found-it.html
Maybe once you discover the power of this type of support, you just naturally want to pay it forward. That is why one Mom of the Ear feels compelled to mentor another as soon as they have the capacity to do so. Lobsters helping baby lobsters. It is how we make meaning out of our Profound lives. I read this blog the other day that describes the mentoring of other families as a purpose in life in direct rebellion to the hard work and the heartache that also lies within the journey. It is exactly what I have been ruminating about ...
Here is a crazy story about this spiritual vocation of mine…to mentor and serve. Last weekend, I was exhibiting for GA Hands & Voices at the Atlanta Area School for the Deaf Fall Festival. Hands & Voices exists in most every state in the US as a parent-to-parent peer support agency . We actively partner with professionals in the state to shepherd families from despair to determination on their journey through childhood deafness. In GA, we are working on creating a Guide By Your Side program that will hopefully create paid positions for moms and dads to mentor other families with children who are deaf or hard of hearing. We do this support activity without bias toward communication modality—ASL, Listening and Spoken Language, Total Communication, etc.
I admit I was a bit out of my element and wondering if I was
going to be able to get additional members for our Hands &Voices Chapter
at this particular event because we use no sign language in my family and
almost all of the folks at the event were signers or had kids who used ASL to
communicate.
Then, in walked my newest lobster. I met a mom who was like me, but not. She had
the same configuration of children with hearing loss in her family as me: her
oldest daughter was hearing, her middle
daughter is profoundly deaf, and her youngest, a son, is hard of hearing. Sound
familiar?
There were a couple of differences between us though. Her son wore bilateral hearing aids and mine
is unilateral. Her daughter does not
have implants and she attends the Atlanta Area School for the Deaf. The major
difference was that she was a child of deaf parents and had grown up culturally
Deaf—her first language was ASL, even though she could hear. Her sister and dad were also Deaf. She had married a Deaf man who was an oral
communicator with good speech, but needed ASL receptively. In spite of our language choices, we had a
ton in common.
She and I bonded immediately over our kids. We bonded not only because we had a similar
kid configuration, but because we both had some kind of genetic deafness on our
dad’s side and because we both were struggling with getting the right kind of
educational support for our kids. Her
middle daughter was doing great at AASD and reading two grades above grade
level, but her younger son had been placed in a mainstream setting and was
struggling in his classroom. For this little boy, whose family was always using
fluent sign language all around him, he depended on that visual support to fill
in the gaps. Yet, because of a dumb decision by the school system, he had no
interpreter in his classroom.
In my case, Ella is also struggling intermittently because
of her teacher’s lack of consistent use of her FM system. Because my family had more progressive loss
and had never had any profound deafness before my daughter was born, my family
of origin had never learned sign language.
Unlike this mom’s family, we really needed the FM system to fill in the
gaps for Ella. Different needs, but yet the same.
Truthfully, I felt a little self-conscious around her at
first because I was afraid she would disapprove of my choice to get Ella
implanted. I explained to her that I
felt inadequate to be able to be fluent in ASL fast enough for Ella to learn
the level of language that her daughter and son were privy to in her
household. Surprisingly, she understood immediately
and never made me feel bad about my choice.
That’s what lobsters do- they support without judgment. In turn, I would go to the ends of the earth
to find a solution for this mom. I
wanted her son to have what he needed as much as I want my child to have the
perfect scenario. I promised to reconnect with her after the event and I have
not stopped talking about her story to anyone in the field who will listen. I am forever changed by the struggle she has
had with the school system to get them to see her family as bilingual. Her son deserves better.
At Laila’s baby shower, pictured above, we welcomed another
lobster into our midst. This mom has a young
baby, only 8 months old. Not that much
older than Wyatt. I can see her still
coming to terms with her daughter’s hearing loss and her worries that she may
need an implant someday. I thought
afterward that with Ella we had the blessing of really never having any hearing
to lose. However, I get her struggle a
little more now, as I watch Wyatt’s left ear decline in increments toward a
unilateral deafness situation. I think
it is harder to watch it go slowly than it is to just rip the band aid off and
get all of your mourning done in the beginning. In spite of the challenges she
will face and the ups and downs of it all, I know this mom will be just
fine. I know that because she has now
been lucky enough to land in the presence of my lobsters and we are now holding
her claw and walking around our tank with her.In my church group that I mentioned above we are reading a wonderful book called "The Gifts of Imperfection" by one of my favorite authors, thinkers and writers, Brene Brown. Today, While I was waiting for a conference call to come in, I randomly opened the book to a page to see what messages God might be trying to send me through Brene this time. The first full paragraph on the left side page started with this sentence:
"Whether we're overcoming adversity, surviving trauma, or dealing with stress and anxiety, having a sense of purpose, meaning, and perspective in our lives allows us to develop understanding and move forward."
Yes, okay. I hear you loud and clear.
“We
are missing a few folks...but looking at this pic brings to mind words like:
inspiration, strength, courage, unconditional love, perseverance, fate, and
hope. Thank you ladies for being my rock, and thank you for an unforgettable
night! Love you all!”
Could
not have said it better myself. I would
only add the word commitment. We belong
to each other. And we take it seriously.
Do
not mess with my lobsters or you will get pinched.A couple of years ago we adopted a toast that goes something like this, “Here’s to the hard road because it led me to you.”
Amen!
Love
you, Lobsters! Thank God we ended up together. It was meant to be.Monday, November 4, 2013
The Day I Barely Made It- September 11, 2013
In order to end Sibling Week, I am posting this journal entry about this past September 11. It was actually a crazy day for us, but not because of the anniversary of the terrorist attacks, but because my family was being challenged. I was racing against time and the school bus and I only partially succeeded. And Avery noticed, as she always does....
At 2:47 pm, I pulled up to my house in the minivan stuffed
with my two youngest kids, supplies for an entire day, and my mom. And waiting for me at the bottom of my
driveway was my oldest child’s school bus.
I felt a wave of relief, confusion and shame wash over me at the same
time. We made it three minutes later
than her afternoon bus stop time. It was perfectly timed in a way because the
bus driver let her off at the end of the driveway, and we did not have to
proceed four houses down to the corner to meet it at the normal stop. It was serendipitous because if we had been
just a few minutes (or seconds) later, she would have had to go all the way
back to school, most likely in tears, because there was no one there to meet
her at the stop.
Picking her up there, at the afterschool program, would have
been awful—it would have caused such a pit of guilt in my stomach, and so much anger
was likely to come from her for having to endure such parental neglect. It was
confusing, though, because I had quickly arranged with a neighbor just a few
minutes before to get her off the bus because we were almost there, but might
not quite make it. Somehow that didn’t
happen. It was shameful because it
looked to Avery and to the driver that I had NOT made such an arrangement and
it really did look neglectful. I was
feeling like a bad mom—my plans gone awry.
In truth, we had just barely made it—late enough to miss the
actual stop, but early enough to catch it before it left the neighborhood. As I look back on the
day, it is clear that I had packed too much in—lots of important stuff, of
course, but none the less, too much of it. Yet again, because of my
overscheduling, Avery was going to feel like she was last on the list and she
was going to let me know it.
So. Much.
Guilt.
So it really did not matter that we had timed it perfectly,
really, because in Avery’s mind a deviation from her normal bus stop with the
threat of having to be the kid who had to do a ride of shame back to school
feeling quite unloved and forgotten was unforgivable. I agreed with her, but it was too late. I barely made it and it was obvious to
everyone involved.
Failure.
Deep Sigh.
Back when I worked in an office in an important-looking
building in the middle of the important-looking downtown, I had lots of
important things to do that interfered with where I wanted to be. I needed a haircut, and I couldn’t go because
I had a meeting with a client. I had a
meeting with my boss, and so I could not make it home for dinner with my
husband. Then I had kids and my important things doubled, tripled, quadrupled,
and balancing it all (without beating myself up all the time) became a daily
decision: What is most important today relative to the rest of my week so that
by Friday everyone is content? Maybe not happy with me, but content. This was
my standard—mediocrity spread thin.
This daily prioritizing was exhausting but I was totally
committed to succeeding with my “have it all plan”: Keep the downtown office
job and manage my kiddos. Here is what I
did not count on: HEARING LOSS. Totally unexpected. Totally outside of my neat, little plan. And in most ways, it was more important than
anything I had ever done before. Talk
about imbalance! The scales were tipping
in favor of my second child (Ella) every day because I had a small window of
time to help her succeed for life— I knew it was much less evenly spread out
because of brain
plasticity and the science of early intervention. We
were racing against the clock and we had only three short years to get there on
time. Oh the Pressure!
To add fuel to the fire, I was still responsible for more
than half of my family’s income and I had another child (Avery) to boot. Here is where the rub is—and I’m being very
honest here. In some ways, the first
three years of Ella’s life were so critical to the rest of her life that I felt
like even my other child would have to sacrifice in the process. True, but terrible and unfair to a 2.5 year
old whose baby sister was diagnosed at birth.
Avery is what some would call a high need child—not to put
labels on her, but I say all the time that she started out with colic as a baby
and has always required attention at levels outside of the norm. She is also fiercely independent and wants to
do things herself. However, she really wants
you to sit next to her and watch and praise her every move while she
independently does things. She gets emotional when she is not perfect, in spite
of our urging that we do not care if she is perfect. We, like one of my
favorite bloggers, Glennon Melton
told her children, we do not want her to be perfect, we want her to be kind and
happy. At her core she is always both,
but she does demand and command more day-to-day, minute-to-minute, parenting
than most kids. And I may not have
minded it, but in my head, I thought—how can I give you my all every day when
you are my HEARING child. You have to
get with the program, kid. Suck it up.
You have a deaf sister and she needs me now more than she will at any
other time in her life. Sorry, but we
are all sacrificing here. Nobody asked
for it, but it is what it is.
How do you explain such a concept to a little one? You can’t.
It is a steep learning curve for everyone and I realized that her life
as a high need sibling of a deaf child was going to be exponentially harder and
possibly charged with more than the average sibling rivalry. And I was totally unprepared to handle that.
On Valentine’s Day 2011, when Avery was five and in private
kindergarten at her wonderful full-time preschool that she attended from four
months old on, it all came crashing down.
Ella had a Valentine’s Day party at the Atlanta Speech School and
Avery had a dance performance and party later that day. I could do both, I told myself. It would take some driving around and some
effort, but it was only one day and I could do both. How could I NOT do both? They both needed me to be there.
Did I mention that I also had a high-need client at the
time?
She needed me desperately that day as well, and I knew that
in my work world, there was no snubbing this lady. She held very important, very large purse
strings and preschool parties or not, I had to jump when she said jump. So in between the 10am party at Ella’s school
and the 3 pm party at Avery’s school, I needed to be at the client site for a
very important meeting, which was in a third impossibly traffic-ridden part of
town. Recipe for disaster. Do you see it coming?
Ella’s party was delightful and full of language-rich
activities, arts and crafts, sweet treats and homemade Valentines. Oh, I forgot to tell you that I started a
tradition when Avery was 2 that we would make our Valentines from scratch for
each child in the class as a fun project.
Trying to win the Pinterest Mom-of-the-Year
award, I guess. Therefore, on the days leading up to the big day I am covered
in red paint and pink glitter and glue and doilies, bits of construction paper
and stickers and marker from the late nights of crafting each tiny greeting,
usually largely by myself. Not only
really smart of me, but also a hot look for the office.
Anyway, I may have been bleary-eyed from
putting finishing touches on sweet treats and cards the night before, but it
was easy to get to Ella's party on time because I simply stuck around after
dropping her off and there were no issues.
After the party, I made my way to the client meeting and
also made it just in time. However, the
client was late getting there and wanted more time than I had planned for. So, at 2:30, I finally hopped into my car to
make the 30 minute trek to Avery’s school to see the dance performance that she
had been working on all week. Just
enough time.
Not, of course factoring in the horrendous traffic jam on
the highway that kindly extended my drive by an extra 15 minutes. Oh, I told myself, not to worry, I always get
there on time and these little performances never truly go off on time. We end
up standing around waiting for every parent to get there before they start, so
surely I would not miss the dance.
Wrong. Very Wrong.
I got to the school at 3:15.
I high-tailed it to the classroom with the hope that I could still make
it, only to find a completely hysterical Avery in the arms of a teacher.
I had missed it. And she noticed. Big time.
My heart sank and then shattered into tiny pieces. I ran over to my precious girl and led her
outside and we had a big long cry together on the playground. I hated this for me and for her and I could
not take it back. I apologized and she
forgave me, but I knew this would be an indelible memory punctuated with the
fact that I had made it on time for Ella’s entire party. Which she asked me about,
and I admitted out of lie-guilt. Great!
More proof that I loved and cared about her sister more than her. Yes, at five she was that analytical.
When we came back in, the most magical thing happened. A sweet teacher (who dedicated her life to
wiping away the tears of kids whose parents had to work and had to miss things)
found deep compassion for me and my little girl in her heart. She asked the kids to come back up to the
front of the room and do a repeat performance of the dance.
I got a do over!
It was not the same as having made it to the original
performance. I would have liked to have
skipped the tears, but I got to see it, Avery felt like she got to perform for
me and all had been made just a little better.
We got a metaphorical band-aid that particular day.
But on this day, I hearkened back to that Valentine’s
day. My important things that day were
to achieve five appointments spread across two kids at the Children’s Hospital
complex between the morning school bus time and the afternoon school bus
time. It was going to be a challenge, I
knew to get to the afternoon stop, and I had a backup plan if we were cutting
it too close. After a double ENT
appointment with prescription writing (Ella) and ear cleaning (Wyatt), we
headed to the audiologist who determined that we had a broken hearing aid and
needed a new ear mold for Wyatt.
Then we crossed the street to the main hospital building and
headed to the phlebotomy lab to get some blood taken for Ella’s Allergist. However, the orders for the bloodwork had
been mailed to my house instead of faxed to the hospital and were, unbeknownst
to me, sitting in a pile of papers on my kitchen counter instead of being the
least bit useful.
We headed to the cafeteria where I promptly called the
pediatrician and asked them to resend the blood work orders by fax. After two transfers, I finally got the right
person. I stuffed down a cafeteria
cheeseburger and lamented over the fact that my daughter was not going to eat
anything on her plate but her potato chips.
I played with my baby a little while he sat in his dreaded car seat,
took a call from a colleague at work and then headed back downstairs to the
lobby of the hospital to register for Wyatt’s hip scan.
All of my kids have to have hip scans for dysplasia because
Avery had it so the family history makes them all at risk. It was Wyatt’s turn. We went through the three step process (give
your name, wait, give your insurance and registration information), then we got
his paper work and his little ankle band.
We jetted down the hall to the phlebotomy lab to see if the orders from
the pediatrician had arrived via fax.
They had! So Ella received the
very awesome and helpful numbing cream on her arms over the veins they might stick
for the blood draw.
A storyteller with a
wagon of books and stuffed animals then entertained her while she waited 30
minutes for the numbing cream to work.
At 1:35, my mom took her back to get her blood drawn. Meanwhile, Wyatt and I were already back in
radiology in a dark room with soothing music playing (Did I mention how much I
love Children’s Hospital of Atlanta
because of all of the warm embraces they give you on days like this? Please if
I ever fall ill, pretend I’m under 21 and send me to a top notch children’s
hospital—so much better than the adult version.) Wyatt had his diaper off, a loincloth
covering parts that might squirt the technician and an ultrasound probe was
being used to scan his little hip joints to see if they were healthy. He was
delightfully smiling at the technicians and cooing as he also snacked on a
breast milk bottle I pumped for him before we left, per hospital instructions.
T-minus one hour until the bus arrives. When the technicians leave the room to “check
with the Radiologist to see if they need more pictures,” I text my neighbor to see
if she could grab my daughter off the bus should we be unwillingly
detained. “Sure” was the text I got
back. Deep breath. Mantra begins: It is ok to ask for help. It is ok to ask for help. Dark side of the brain enters the
conversation: Avery is going to kill you for not being the one to pick her up
from the bus. Avery will kill you. Avery will kill you. Possibly only emotionally with her dirty
look, possibly in your sleep when you are defenseless. (Exaggeration, here… she is not the murderous
type, but you get the gist.)
It is ok to ask for help.
Although, Avery may kill you.
Image of the Valentine’s Day scene from 2011 flashes before
my eyes. Another reminder that I am not
the perfect parent she craves and I mentally add a tick mark to the running
total in her head that says “She loves my brother and sister more than
me.” Not true, sweet girl, and I would
do anything to eliminate that thought from your pretty strawberry blonde head. But I have to show you, not tell you, don’t
I. Cue more knots.
The “check” with the radiologist takes over 20 minutes. Sigh, and cue nausea. I quickly make the exec decision to dress my
son and prepare for departure. I
practice the line to the technician in my head should she need more pictures,
“Sorry, we will have to reschedule. We
have been here since 9:15 this morning and we need to pick up his big sister
from the school bus.” Planned sacrifice
for baby girl #1 that she will never see- a return visit to the hospital on
another day.
Luckily, the technician reports that we are all done and we
speed race in with the stroller to the main lobby, pick up Ella and my mom and
head to the parking deck. We leave at
2:18 pm. And well, you know the rest.
I barely made it. The tears from Miss A only lasted 2 minutes
when she heard that we had been at the hospital all day. She softens, and I realize she gets it. She knows it is hard for all of us, but she
wants to make sure I won’t forget her.
I won’t forget
her. I re-promise that I will always
be there for her. Even when I’m
not there for her.
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