Monday, November 18, 2013

Hearing Aid Bill Vote Today!

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

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

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.
Laila described the picture of my lobsters on Facebook as follows:
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.