Tag Archives: communication disorders

Let the Joy Begin

Joy 2015

It has started, and this year it is already so much more. More joy.  More dresses.  More excitment.  Joy Prom is seven weeks away.

Our church, the creator and host of Joy Prom, has dresses and tuxes at no cost for the honored guests. So, on a joyful Tuesday evening, Savannah and I met up with Ms B and Ms D.  Ms B is the large-hearted woman who co-ordinates not only Joy Prom but the special needs ministry at our church, and Ms D is Savannah’s personal angel who makes personalized lessons every Sunday just for Savannah to learn the greatness of God. They are our blessings.

We arrived at the church for Savannah’s personal fitting. Like some upscale store catering to a movie star, dresses were brought in and shoes were laid out and accessories were bountiful and pop-tarts and VeggieTales were there on demand.

For over an hour, Savannah was Joan Crawford, Grace Kelly, Betty Davis. She tried on purple dresses, black dresses, pink dresses of one shade and then another, Dresses with sequences. Dresses with layers. Dresses with many colours. The child with sensory issues wore bracelettes and rings. Eventually, she settled on an off-red, one-strapped dress with flowing scarf, accented by silver sparkly three-inch heels. Her first pair of heels. She chose, out of all of the shoes showered at her feet, her first pair of heels. I took my little girl to try on dresses and an hour later left with a beautiful excited young lady.

Savannah left that evening with a new dress, a purse, jewelry and of course shoes. More importantly, she left happy, confident and feeling both beautiful and loved.

Seven weeks before prom: let the Joy begin.

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Too Many Miles

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Joseph and I were driving down the street, on our way to CVS, then to pick up Savannah, then to horseback riding, then to occupational therapy. It was an incredibly busy, typical Wednesday. Savannah had allowed me about four hours of sleep, and so I had picked up a toxic 20 ounce vice if classic Coke, hoping the sugar rush and caffeine might keep me awake. Besides, I was fighting off the back-to-school muck Savannah had brought home and knew the carbonated water would soothe the sandpaper coating my throat.

As we hurried down the road toward CVS, I opened the coke, releasing a sticky caffeinated geiser. It spewed over me, drenching the driver’s seat, morphing the steering wheel into a sticky mess. Joseph stared at me wide-eyed. I looked at him, his large eyes waiting for my reaction, uncertain and stunned by the carbonation that still trickled down the bottle, over my fingers, staining my thigh. I couldn’t help but laugh. Joseph began to laugh, forcing me to laugh harder and him to laugh harder, and it cyclically continued.

Since then, I’ve been reminded of our Mayo visit. Somehow, in Minnesota, every meal I managed to spill something. I don’t know if it had to do with the fact that Minnesota has amazing food or the fact I was suffocating in apprehension or just that I was food-clumsy, but every meal created more mid-west laundry.

Our Minnesota week was hard. The air was filled with the fear of what we might find. We carried the burden of entertaining the kids in a hotel room that was much too small. We lived surrounded by needles and tests and sterilization. We also lived surrounded by doctors, waiters, and strangers who were full of compassion and respect. We held the blessing of new friends and fellow patients and magic book-men. We breathed in the knowledge of some of the world’s greatest specialists.

We were trapped in a great freedom.

It is impossibly hard to be miles away from the only people searching for your answers. And yet all there is to do, is wait. Wait and take selfish advantage of every moment. The dual mitochondrial genome analysis takes six to eight weeks. I thought it was difficult to wait the few weeks for the NPC, now there are weeks more to wait. The tests can’t even be run at Mayo and have been sent off to Baylor. There’s nothing else to be done. Still, even though it’s only waiting, even though the tests aren’t even there, it’s too many miles away.


Squeals of Friendship

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Madeline was born six months after Savannah. My best friend, Elizabeth, and I were thrilled that our little girls would grow up together and would also be best friends.  They would roll a ball together, play tag, go to school, keep secrets, whisper about boys and first kisses and in decades sit on the couch and hold their daughters together.  They would have the benefit of having a sister, even if we had no more children, the same way we were.  Best friends, best sisters, and they would get to experience it from infancy.

The day Madeline was born, Savannah sat patiently with us in the hospital for hours. She had spent the last three months lying on Elizabeth’s stomach, feeling Madeline move. Squiggling on top of her stomach, while Madeline would squiggle below.  Reaching for Elizabeth’s bulging belly each time she saw her.  Finally, a man covered in blue scrubs headed our way. He pushed a small sterile cradle with one nicely wrapped blanket. Savannah squealed and screamed and tried to climb out of my arms toward the bundle he pushed. A little bundle of Madeline. Savannah banged on the glass and laughed, as we watched Madeline be cleaned and measured and weighed. She was re-swaddled and returned to her rectangular crib, but Savannah’s banging and giggling and striving to reach her continued.  The thrilling squeals of friendship didn’t stop until she was held next to the sleeping swaddled bundle. Savannah’s excitement was unbelievable and undeniable.

When Madeline was about two months old and Savannah eight months old, Savannah and I had our first visit to their home. Savannah tried to play with Madeline, but Madeline was only confused by her. Savannah tried to help Madeline take off her socks and gloves. Those horrible, suffocating socks and mitts that Savannah couldn’t stand to inhibit her senses. Madeline, however, loved the comfort and coziness they provided and kicked and cried each time Savannah tried to help her out of them. That evening, the girls feel asleep in our arms, as we sat and watched a movie. Elizabeth and I laughed at the irony. We had known each other for a decade, through high school parties, college parties, first kisses and late night dates. We had fought and loved together.  We had seen each other through broken hearts, marriages and home ownership.  What a different world we had entered into together. The night was perfect, as we held our daughters, drinking hot tea instead of beer. We thought it would be the first of many, but it was the first of few.

There were a few times we went to the arboretum or relaxed and played at each others houses, and of course there were birthday parties. But it wasn’t near what it should have been. We were busy with life. The life we hoped to share together began to keep us apart.

Savannah didn’t develop like Madeline.  At seventeen months, Savannah stopped talking and refused to eat.  By twenty-two months she was receiving services.  At that time Madeline was sixteen months old.  Madeline was playing tag and rolling balls and eating everything she could reach.  Savannah spent her mornings in therapies.  Madeline spent her mornings making friends at day care.

Elizabeth and I have known each other over two decades.  We live worlds apart, but have never been closer.  Living in different states, we text multiple times a week, keeping regular conversations. We do visit, but not as much as we would like. We have been through divorces and affairs and family deaths together. We love each other’s children, life family, and our children have learned that love from us.  We are family, despite blood and distance.  But Savannah can’t play with Madeline the way she once could. The desire is there, but so is the disability. Madeline can talk and cook and bathe herself.  She enjoys music and TV shows that aren’t preschool motivated. There is a world of difference between them. A world that’s hard to explain to a ten year old. A world that is hard to explain to anyone. Honestly, Madeline is confused by Savannah and understandably so. Fortunately, Savannah has yet to notice. She has only noticed the love.

Even though the girls adore each other, and a vibrating excitement drips from Savannah each time Madeline visits, it isn’t like we thought. It isn’t picnics and lipgloss and cupcakes. I dream about that distant idealistic night, watching a movie and holding our sleeping daughters, and I know for one moment, it was perfect.


Breathing Deeply

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Week three came and went. Week four came and went. We sat in the middle of week five.

Dr. R had carefully explained the NPC test. It takes roughly three weeks for the biopsied cells to be ready for the test. The test itself doesn’t take long. The cells are put through a machine, and then run through again. It would be three to four weeks for us to receive results. If there were any “red flags,” then the test could take longer. Each red flag would be run again by hand, twice, and that would take more time. Everything with NPC is tested twice. They must always be certain before they give an answer.

The biopsy was taken June 24th. July 10th, we received notice that the test had begun. On July 31st, the middle of week five, we were still waiting. Visions of red flags haunted us all. Friends had sent texts. Family had called and called again. Everyone was anxious. Everyone knew the answer should be back, unless there were red flags.

Tonight, we checked the portal, as has become the evening ritual. The letters were solid and blue and firm. I was afraid they’d fade before me. A paragraph of medical jargon, summed up with, “These observations are not consistent with a diagnosis of Niemann-Pick Type C disease.”

I waited, and when the letters didn’t fade, I breathed. I took a deep breath, letting the air fill me. It tasted sweet and crisp and light. It tasted of relief, and I took another breath.


the Pity, the Sorrow, the Realization

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Yesterday, we headed out to Jefferson City. It’s always a big trip, even if it isn’t. Jefferson City is about an hour and a half away, which means we have to leave two hours before the appointment. There may be traffic. There may be construction. There is always McDonald’s. McDonald’s is right next to the hospital that holds our regular appointment, and if it isn’t visited beforehand, then the visit is a constant explanation that we will visit McDonalds after our appointment, which makes for a very long hour. The appointment isn’t an hour. The appointment is fifteen minutes, but let’s be honest, we are the patients that always go over. Then of course there is the wait. We aren’t the only patients that go over.

Dr. H is our pediatric psychiatrist in Jefferson City. We went through two psychiatrists before settling on Dr. H and weighing the travel as worth while.

Yesterday was our usual med-review visit, but it was also our post-Mayo update visit. I brought copies of all our Mayo labs and Dr. R’s notes. I explained the degenerative outlook and the disappointing neurological autoimmune results. I explained how the NPC results were still not in, and how at this point, everything waits on that. I relayed Dr. O’s warning on changing medications before having the NPC results and his honesty that medication won’t make much difference if the test is positive.

Dr. H took it all in. We talked about our Mayo visit. We talked about Savannah’s progress since our last Jefferson City visit. We talked about our next visit. As we left, with promises to notify the office as soon as the NPC results come in, Dr. H’s demeanor changed. Dr. H is always the same, always reserved, always professional. Yesterday, Dr. H’s demeanor broke. Behind it was the apologetic expression that we frequently saw at the Mayo Clinic. The pity. The sorrow. The realization. It had followed us back to Tennessee.


Deep Breaths of Laughter

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This next week is the moment of truth. In theory, this next week will bring us the test results for NPC. It means I will have to register my Skype account.

It all seems so far away. As much as I didn’t want to leave the Mayo Clinic, it now seems distant. It seems like a hazy dream from another life. A few weeks ago, John was giving Savannah a piggyback. They rounded the banister at the bottom of the stairs. For a moment, a brief moment, they paused. Savannah looked at me. Her smile was massive and her laughter vivacious. The words flittered through my mind before I could stop them. “This is not the smile of a dying child. It is not the laugh of one. It can’t be.” By the time the words had left me, John and Savannah had vanished up the stairs.

Two test results have come in that open wider the possibility that we are not looking at NCP. If the NCP test comes back negative, then Mayo-grown DNA will be sent to Baylor for advanced mitochondrial testing. The various types of mitochondrial diseases are expansive.

While test results were flooding in negative, we were settling back into normalcy: church, speech camp, sprinklers. We’ve played and fought and tickled. Normal family life. The difference is in the hugs. I hug her more. I hug her tighter. I inhale deeper. I want to breathe her in. I want to keep her inside me: her breath, her scent, her skin, her laughter.

It took two weeks for me to find the nerve to download Skype to my phone. Now that time has run out, I will have to create an account and wait for Dr. R’s message to set up a time to virtually meet and receive what news she brings.


a Summer Specialty

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A few years ago the local college had a wonderful program, Kid Swim. Graduate students from the speech-language program, and sometimes from the physical therapy program, would volunteer their time and help special needs kids swim at the university pool for one hour each week. Of course, I use the term “swim” loosely. Some kids splashed, some floated, some swam but most played. All enjoyed. Graduate students helped kids with socialization, movement, word-prompting, but none of the kids realized it was work. They were too busy having fun.

Unfortunately, graduate students graduate, and after a few years the volunteers were too low for the program to continue. Today, however, there was Kid Swim. A summer speciality.

Savannah was hesitant to get in. The water was predictably too cold, and the ladder too confusing. After a few attempts to figure out the ladder, we gave up and sat on the side of the pool. She kicked her feet and splashed and squealed. Little by little, she lowered herself in, tugging me in after her. She jumped and splashed and yelled and laughed and splashed and jumped. I tried to help her float on her back, but she wrapped her arms around my neck and giggled. I tried to get her to lean against me and kick her feet, but the kicks were sloppy and weak, not strong and concentrated like years before.

Over and over, with her arms around my neck, she would jump at me giggling. I thought she wanted to pull me under. After all, she had pulled me in. Eventually, she succeeded, and I realized I was wrong. She wanted me to hold her. I haven’t been able to carry Savannah in over two years, when her medication increased her weight more than my strength. It is an impossible concept to explain to 115 pound, eleven year old little girl, who considers herself to still be a small girl. But today, in the pool, she wrapped her arms and legs around me, and I carried my little giggling girl with bright blue eyes around the pool.


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