Showing posts with label CHOP. Show all posts
Showing posts with label CHOP. Show all posts

Friday, August 9, 2013

Feeding School

Sometimes kids don’t eat.  I’m not referring to picky eaters who hate lima beans. (Doesn’t everyone?)  I’m talking about kids that for one reason or another have serious eating problems not caused by lax parenting or strong wills.  Some kids require being fed through a g-tube.  Others like Sophie and Alexander start out eating a wider variety of foods only to narrow their preferences down and then subsist on these same few foods every.single.day.

Sophie and Alexander both eat a small variety of crackers and chips.  Sophie’s favorite is baby goldfish crackers from Pepperidge Farm, (must be baby goldfish as she gags on the regular size), but no broken crackers.  Alexander prefers BBQ Pringles.  They both love popcorn and chocolate milk, though Alexander must have his slightly warmed up.  Cold drinks bother him.  They also both refuse nearly all fruits, vegetables, and meats.  The only exceptions I can think of are the smooth fruit medleys that come in squeezable pouches that Sophie occasionally eats.  We call them squeezies.  Alexander will eat hotdogs or chicken McNuggets (must be McNuggets) from time to time, but mostly he eats peanut butter sandwiches (no jelly) on wheat with the crusts cut off.  He doesn’t like meat now that he knows it comes from animals and complains that it makes his tongue feel funny.

Sophie had her first appointment with the children’s hospital Feeding and Swallowing specialists in September of 2012.  Yada yada yada, it’s now August 2013.  Alexander and Helena are enjoying an extended visit with the family in Iowa so that Mark and I can focus on Sophie.  She began an intensive outpatient program at the children’s hospital on Tuesday, 8/6.  For the month, Monday through Friday from 9am-5pm we will be at the Day hospital participating in the feeding program.  We hope that Sophie can learn to eat and that we can learn how to help Alexander as well. 

Sophie is allowed only 4 ounces of chocolate milk in the morning at home.  Then at 10am, 1pm, and 4pm she is with a feeding therapist while we watch behind a two way mirror.  During week 4 Mark and I will begin training to feed her ourselves.  In the evenings at home she can eat anything as long as we log it and she must drink a specific amount of liquids.  The plan is extremely regimented, time consuming, and exhausting.  It is also extremely successful.

1 watermarked Tuesday was Day 1.  The lead feeding therapist (we’ll call him P.)  and I observed as Mark attempted to feed Sophie.  This gave P. an insight into her food avoidance behaviors.  The rest of the day was mostly meet and greet with tours, a session (for us as parents) with the psychologist, a vitals check and physical exam.  Soph will be weighed weekly and her calorie requirements while at home adjusted based on her consumption at the hospital.  Her team consists of a lead feeding therapist, a team of feeding therapists, a social worker, psychologist, nutritionist, physician, an occupational therapist, and medical and psychology students.

2 watermarked

On Day 2 P.  introduced the rules to Sophie, which are pretty simple.  Eat your bite = get to play with your preferred toys and receive praise.  Don’t eat = you will be helped to eat.  Keep rejecting food = no play.  There’s more to it of course, but it focuses on lots of praise for compliance while ignoring noncompliance at first.  If noncompliance continues, then they might use hand over hand to get the food in.  If that doesn’t work, then blocking her hands or even techniques to open her mouth may be used.  All of these techniques are discussed with us before they are implemented.  It is hard work for our little girl.

3 watermarkedHer meals consist of a few different foods that are in Styrofoam cups off to the side of the therapist.  She is presented only one bite at a time so that she is not overwhelmed by the sight of the entire meal.  Sometimes the spoon or fork will have food on it and presented on a plate.  This minimizes the work she has to do so she can focus on eating.  Other times she must get the bite from the plate to the utensil herself.  A lot goes into good wrist movement, hand control, and coordination.  Sophie still struggles with this. 

4 watermarked

For the first few days Sophie was presented her preferred foods.  She was given her favorite toys and bubbles when she complied.  This allowed the therapists to earn her trust.  Then, slowly, food she used to eat but has lately refused (such as macaroni and cheese & hotdogs) were added.  To our shock and great happiness, she complied easily.  5 watermarkedToday is the last day of week 1 and my first day alone with her without Mark.  He prefers to drive into the city despite the heavy traffic.  I prefer the trains, so off we went!  I appreciated so much the kindness of strangers who held doors, carried our bags, and engaged her in conversations. 

At her first feeding P. introduced bananas, which is something she has NEVER eaten.  She ate the first bite and I fell off my chair.  Then it got real.

These are only a few of Soph’s avoidance techniques.

She successfully avoided or spit out pieces of banana many times during meals 1-2.  The bites got smaller and smaller and P. mushed them up to the consistency of pudding to make it as easy to eat as possible.  The first time he took her toys away she did not cry, but she was shocked.  She didn’t say a word but she looked at him as if to say, “What the heck is going on here?”  At this point, if a bite got in regardless if she spit it out, she was praised and the spitting was ignored.

6 watermarked

Using her IEP as a guide, Sophie will have two hours of OT/week.  I watched this morning as the OT sprayed shaving cream over a foam alphabet.  As I could have predicted, when presented with it, Soph flipped it over.  She does NOT like getting her hands dirty.  They moved from the picnic table to the floor and tried again.  Sophie resisted at first but eventually used her fingers to push out the messy letters, one by one.  Her OT is challenging her to work through her sensory issues.

By her last meal with a therapist for the week, Soph showed remarkable improvement towards accepting the first new food.  As the bites of banana went in easily, they got bigger and bigger.

The first bite (above) was banana.  Her only trouble was handling the spoon.  SHE’S EATING BANANA!!!  This was followed by play and a bite of mac-n-cheese.  We are exhausted and happy.

Friday, May 24, 2013

Our New/Old Normal, part 2

continued from part 1

eval photo blackenedIt took a couple of months to finish and the final report itself is 21 pages long.  The school psychologist had Alexander self report, she had his teacher, OT and ST therapists complete evaluations, she conducted classroom observations, and Mark and I complete questionnaire after questionnaire.  The tests bore out what we already knew.  His IQ is 111 or above average.  He has a superior vocabulary but delayed processing speed.  Areas of significance include emotional control, initiation, working memory, planning/organizing, organizing materials, and monitoring.  ADHD was ruled out but attention problems were highlighted as well as adaptability, functional communication, attitude towards school, and activities of daily living. 

Perplexed by his speech pattern, his ST called a stuttering expert at CHOP who indicated he has seen the same pattern in people with Autism.  This was about the same time that the latest series of parent questionnaires started to scare me.  His pediatrician did not think it was ADHD and began asking questions that scared me.  We were headed in a direction that I was desperate to stop.

That’s when we got a phone call from the school psychologist and speech therapist.  They didn’t want to send home the parent questionnaire for Asperger’s without giving us a heads up, which was a good move.  Three days later the reports were completed and we were told that “results of the social-emotional and behavioral assessments along with the testing results, the data from the questionnaires, as well as the observations indicates that Alexander demonstrates behaviors that are consistent with the characteristics of children with Asperger’s Syndrome.”  

I spent the weekend alternating between crying, raging, drinking wine, cursing God, painting my kitchen blue, researching Asperger’s, bargaining with God, searching for ways to blame myself, and then landed firmly in denial.  Mark was unfazed and that fazed me.

How could this possibly go unnoticed for so long?  Taken separately each of the traits that I now suspect are tied to Asperger’s could be explained away.  Much of them were exactly how Mark was as a child.  The trains obsession, the picky eater, the meltdowns and on and on.  I became depressed and felt like such a failure.  Still I dragged my butt to work and commiserated with my colleagues who also work in the disability field. 

It was a miserable few days and I was so disappointed in myself that I couldn’t stop looking at my son differently.  Not negatively per se, but with eyes that know too well the struggles that go along with disabilities and the immense load of work that had just landed on my shoulders to ensure he will have everything he will need.

continued HERE

Tuesday, January 1, 2013

Prayers for Alex & Sophie

Meet our good buddies Nancy and little Alex.  I met Nancy within the first couple of weeks of moving out here and we have become great friends.  On Thursday, January 3, 2013 Alex will be having his tonsils and adenoids removed, otherwise known as T&A surgery.  It is fairly common for people with Down syndrome to have T&A surgery and many in our community have reported excellent results.  Alex has been having seizures recently and is on medication to treat them.  His mama hopes that the T&A surgery will mean he can get more oxygen as he is breathing so he can stop taking the medicine.  Alex will also have surgery on one of his testicles.

Alex and Nancy watermarked Nancy and I did not plan it this way, but on the very same day, Sophie will also be having T&A surgery and she will be getting a new set of tubes in her ears.  Especially as she has floppy airways (tracheomalacia and laryngomalacia), her Anesthesiologist has back up plans ready to go if her airways become compromised.  We have high hopes for this tune up.  With new tubes, the fluid that has built up can drain which should lead to better hearing and improved speech.  Once the tonsils and adenoids are gone, we hope she will be much healthier and able to fight off viruses that lead to infections.  Currently she catches every cold and flu virus that she comes into contact with.  Also, Sophie is not a good eater, (understatement of the year).  We hope that as the T&A surgery will create more space in her throat, that she will start eating more foods.

Sophie and Jen watermarked*Alex is due to the hospital at 10am and Sophie at 11:15am.  They are going to be hungry as they aren’t allowed to eat after 11pm.  The surgeries are fairly routine for the good folks at CHOP.  Both little ones will be staying overnight for a minimum of one night and both with their mamas by their side.

Please send good thoughts and prayers on Thursday, January 3rd that my baby girl Sophie and our dear friend Alex have successful surgeries, good pain management, and quick recoveries.  If you could spare a thought of support for those of us in the waiting/hang wringing room, we would appreciate it.

Monday, October 1, 2012

Villanova Buddy Walk 2012


Please join Team Sophie on Sunday, October 7, 2012, at Villanova University Stadium for The Children’s Hospital of Philadelphia 11th Annual Buddy Walk® and Family Fun Day. In addition to the Walk®, the day will be filled with great activities for the whole family. We would really like to see as many of our friends as possible walk with Team Sophie!

In just ten years, this Buddy Walk®has raised over $2.1 million for the (Down syndrome) Trisomy 21 Program at The Children's Hospital of Philadelphia. By working together we can make this wonderful event even more successful.

To Register to Walk with Team Sophie, visit our page at: http://giving.chop.edu/goto/Team_Sophie
Scroll down to Team Sophie and click Join Team and follow the instructions.

To Donate without Walking, visit our page at: http://giving.chop.edu/goto/Team_Sophie
Scroll down under the photo of Sophie and click, Donate to Team Sophie! 
 

On behalf of our family and Team Sophie, we thank you for your support.

Gratefully,

Mark, Jen, Alexander, Sophie, & Helena

Friday, December 10, 2010

Curve Ball

Sophie had her first appointment with CHOP today (Children's Hospital of Philadelphia). They have a satellite office closer to our house than the big hospital in Philly, so we went there. The visit was to establish a relationship with her new ENT (Ear, Nose and Throat doctor). She had tubes inserted into her ears in March of 2009 and recently her pediatrician couldn't see them during an exam (no big surprise there as most docs can't). We needed to see if they were actually still there.

Like many people with Down syndrome, Sophie's ear canals are very narrow making it difficult to visualize the ear drum without a trained eye and special equipment. Dr. W took a look after clearing out a lot of wax and her tubes are still in place and look good. He surprised me by sending us off to audiology for a behavioral hearing test right there and then. During the last two auditory tests at St. Louis Children's Hospital the audiologists said her hearing appeared normal in the conversational level but showed a mild loss in the lower decibels. (in these tests the audiologist trains the child to turn to a stimulus - a light and toy that makes noise when they hear a sound. Then the audiologist just plays the sound to see if the child will turn to it for the reward of seeing the toy, etc.)

Today the tympanogram showed that the tubes were clear (a good thing) especially as she has a cold though it hasn't migrated to her ears (knock on wood). However the behavioral hearing test showed mild hearing loss in both ears (more loss in the right than the left). The loss is in the conversation range and the higher tones which is different from what the last two tests showed at St. Louis Children's Hospital. Of course, this was done through a behavior test with a little girl with few words and a developmental delay so they can't be certain about the accuracy of the level of loss without further testing.

In February we will head to Philly to CHOP for a sedated ABR to confirm or rule the loss out and to find out about each ear specifically. If the loss is confirmed, hearing aids may be the next step. However, I don't want to get ahead of myself, so I'm trying to reign my thoughts in about that until we know for certain.

My blog has been quiet lately. Writing daily in October really burned me out and I have been working through a lot of old and new personal ~stuff~. I've written posts I haven't published. It's always a trick to know what to share in such a public venue. Blogging has been my outlet and not feeling motivated to write or comfortable in sharing has been something I've been trying to work through.

A recent development is that Helena (who is 18 months old) has surpassed Sophia in vocabulary. While I knew it would happen eventually, adjusting has been...interesting. Mark and I have also both been very homesick. We are saving to buy a house, so we decided not to travel back to the midwest for the holidays. Thankfully family is coming to us. Mark's cousin Greg is staying with us for a while until his new place and job are ready in Jersey. Mark's parents are coming up in the next few days and later next week his little bother will be here. It will be a blow up air mattress slumber party and we're very excited.

So, tonight as I digest the latest curve ball that we've been thrown, I'm trying to keep it all in perspective. Hearing loss is something that we can work with. It is not completely out of left field given Sophie's DS, though it did take me by surprise. I will try and focus on being thankful for our awesome health care and doctors. I am thankful for the opportunity to catch it early, for those with DS who have come before us who have taught us to screen for things like hearing loss at such an early age, and for the amazing technology to help if her hearing loss is confirmed.

our home as taken by iPhone

an avalanche of Christmas bears (2 from 1987!)

Speedy, our hotly debated Elf on the Shelf (but that's another post)

Decorating the tree as captured by the iPhone

MY NEW SEASONAL ANTHEM!