Princess Ky Background - The cutest blog on the block

Showing posts with label "fixing" Autism. Show all posts
Showing posts with label "fixing" Autism. Show all posts

Thursday, December 15, 2011

Interview with Author, Jolene Philo - Part I

Jolene's Son: Baby Allen
Just a few hours after birth

Yesterday, I introduced you to Jolene Philo: my friend and the author of two amazing books.

Jolene's newest book (just released) is

A Practical Guide to Raising a Child with Special Needs.


Jolene graciously agreed to an interview and she was very open, honest and candid with her answers.  The interview will be posted in two parts so find a cozy nook to settle in and get ready to meet a lady who is having a great impact on children, parents, teachers, social workers, hospital staff, caregivers, and many countless others.

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Q. What was the catalyst that made you decide to write the Different Dream books? 
I wrote Different Dream Parenting and my first book, A Different Dream for My Child, for one reason. Twenty-nine years after the birth of our son, the memories of his weeks in NICU are still fresh in my mind. I remember how alone we felt. We were 25 years old, 750 miles from home, clueless. If there’s anything I can do to help parents in similar circumstances know they are surrounded by people who care, I will do it. If I can make them understand they are God-appointed to advocate for their their children, I'll keep writing.


Q. Explain your son's diagnosis and what exactly made it life threatening.
At the time, the doctors called his birth anomaly a tracheo-esophageal fistula (TEF). These days they add "esophageal atresia" to the beginning of that, so it's alphabet soup name is EA/TEF. There are many versions, but in our son's case, his esophagus came down from the mouth several inches and formed a blind pouch. It came up from his stomach and hooked into his trachea. Many children who have EA/TEF have other birth anomalies, but Allen did not. As you can imagine, the condition requires medical care and early corrective surgery or the child dies.

NOTE: To learn more about EA/TEF click here


Q. Before your son, what were your experiences with children with special needs or crisis caregiving? (in other words, was this situation new to you?)
We had little experience caring for kids with special needs. But I had a minor in special education and had done several practicums in college in special education classrooms. Also, my father was diagnosed with multiple sclerosis when he was twenty-nine. I was two at the time and only remember him being in a wheelchair. He was in our home while my siblings and I grew up and we were actively involved in his care. So care giving was not new to me.


Q. Give us a peek into your pregnancy with your son. Did you have any thoughts and feelings during that time that you felt were "heaven sent" to prepare you for what you would soon face?
My pregnancy was quite normal though my blood pressure was always a little high and the further along I got, the more it looked like a basketball was stuck on my stomach and hard as a rock. And when the doc let us listen through his stethoscope during check ups, it sounded like Allen was crashing from one side of me to the other, yet I felt very little movement. (I didn't realize how odd that was until six years later during my second pregnancy with our daughter.) But we had no premonitions during the pregnancy that anything was wrong and ultrasounds were brand new and rarely used. I thought it was pretty cool that Allen was born a week early, the day after school got out, so I had one more week with him. That was in the early hours after his birth, before we knew anything was wrong, of course. Mostly, we were just glad to get to the hospital before he was born. My labor was only about 2 1/2 hours and we lived 90 miles from the hospital, with the first 55 miles a windy, scarcely populated gravel road.

Allen at 3.5 weeks: Coming home from the NICU

Q. Were you private or open about your son's diagnosis and needs?
Very open. Getting food stuck in the stricture where they rejoined the esophagus was a real danger. So we had to be open with day care providers, teachers, and babysitters. When he had a surgery at age 15 (2/3 of his lower esophagus was removed because of what they believed was pre-cancerous tissue), I emailed regular reports to his teachers. They read the reports to his classmates.


Q. Did you experience a period or varied periods of grieving? What did that look like for you?
Just a few days ago, I was looking at the trailer for my new book, Different Dream Parenting. It includes several pictures of Allen in NICU, and I felt so sad again about not being able to bring our baby home after he was born like other parents do. So grief lasts a long time. I remember grieving on his first Halloween because he was in the hospital and couldn't wear the little costume I'd made. Then I thought my feelings were wrong, but they were grief for a loss. And it's okay, even necessary, to grieve those losses.


Q. What benefits could someone who does not have or know a child with special needs take away from your books?
The books give others a glimpse into life as the caretaker of a child with special needs. Many people who read the first book, A Different Dream for My Child, have commented that they had no idea it was so complicated and difficult. It also helps them know how to begin a conversation with parents. The second book, Different Dream Parenting, is a valuable resource for anyone working with families who have kids with special needs - educators, health care workers, friends, church staff. It can help them help families tap into available resources.

Q.What is the one message you want to convey via your books:
Parents of kids with special needs often feel isolated. The one message I want to convey is that they are not alone. Many other parents have experienced similar trials and emotions and so did God when he sent his Son to earth.

Baby Allen:
So alert to what is happening to him
First photo of Allen after surgery. He is three days old here.

Q. What is your faith/belief system founded on? What is your faith background?
My husband and I were both raised in church going families and became Christians as children. But our first real faith test came with Allen's birth and subsequent medical issues. Our pastor friend and his wife led us through the book of James. At least that's what Hiram says. The only thing I remember is that they cared enough to come. They were the hands of Christ to me. But whatever they said made a difference because my faith and Hiram's grew by leaps and bounds during those early years with our son.


Q. How did you and Hiram meet? When did you know he was "the one"?
Believe it or not, we met at the freshman orientation dance at college and the rest is history, At least it was history once we finally found each other again and started dating. Actually, I knew where he was, but it took him longer to find me. Mainly because he was so shy that he kept looking down at the sidewalk and didn't see me trying to catch his eye. He was such a nice guy and so sincerely trying to live his faith, I didn't need to look for anyone else.

Q. During this time of crisis and in the years that followed, what did you find that you "needed" from Hiram, your husband.
My husband Hiram gave me what I needed, though it wasn't always what I thought I needed. I thought I needed a husband who would make everything okay by doing big, dramatic things. But what I needed was a rock, and Hiram was always there for me and our son, Allen. He actively parented our son, rubbing his little cheek in NICU while I rested and recovered from childbirth. Once Allen was home, Hiram often slept in a recliner holding Allen and jiggling his tiny bottom all night long so I could sleep.  While I asked God why our son had this birth anomaly, Hiram accepted it and kept going. When I said we needed spiritual support, he asked a pastor in town to do a Bible study with us.

Q. What was most helpful to you when in a crisis situation?
Hiram was my biggest help. He is extremely calm in a crisis. He began EMT training during the year after Allen was born so that somebody in our house would be able to intervene medically (we both knew it wouldn't be me) if necessary. He enjoyed the training so much he eventually went back to school and became a nurse.



Q. Did the stress put a strain on your marriage? How did you work through that?
This was never an issue for us.


Q. Hiram's name sounds deliciously Amish. To me, his name sound so strong yet comforting.  I'd love to hear the story behind his name!  (guilty question that I have always wanted to ask.. ha! ha!)
You crack me up, Amy. Hiram is a twin. He and his brother are named after their mom's dad, Hayes, and her older brother, Harold whose nickname was Hiram. Why was his nickname Hiram? Because he was a preacher's kid with the last name Walker. They were a family of teetotalers, so his friends called him Hiram with a wink and a nod to Hiram Walker whiskey. So while his name sounds Amish, my teetotaler husband is named after whiskey.


Q. Did Hiram ever surprise you in a time when you REALLY needed "something" from him?
Does the year he gave me a toilet seat for Christmas count?

Q. Your advice to couples?
Don't give your wife a toilet seat for Christmas.

Q. What provided a source of strength for you in hard times? (any quotes, verses, songs, etc that particularly lifted you up?)
Knowing that people cared and were praying for us was my greatest source of strength.

Q. Did you have a "safe friend"? (someone you could say anything to - even yell it - and you felt perfectly safe in that relationship)
Again, that would be Hiram.
Q. Were friendships with other couples difficult to maintain? How did you handle this?
Because of the dynamics of the small town where we lived, that was not an issue. We had to make our own fun which usually consisted of hauling all our kids to each other's houses. The older kids would take care of Allen (he really was the town pet being the son of the school teacher) and we would all eat supper together and go home when the kids got tired.

Q. How did you balance parenting, teaching, being a wife and investing in yourself?
During the first school year after Allen was born, God blessed me with a wonderful group of students. The days were so busy with them, I didn't have time to worry about Allen, which was another blessing. When at home, I was quite a worrier that first year, until I finally realized that Allen was in God's hands whether our baby lived or died. At that point, I was able to enjoy being his mother. Really, there wasn't much time for myself for about three years, until Allen's health improved and the trips to the doctor let up. When we lived in South Dakota, doctor's appointments were a 240 mile round trip. Sometimes we would stay overnight in a motel with a pool. Often we went out to eat after appointments, just for a break. The most fun I had was in the summer when a neighboring town did a community theater production. Hiram stayed with Allen so I could be in the shows. It was nice to pretend to be someone else for awhile!

Q. Tell us a few things that most people don't know about you.
Every one of my elementary school report cards includes a comment along the lines of "Jolene needs to quit daydreaming and get her work done." I was very involved in drama in high school and college. Among other noteworthy roles, I have played a nymphomaniac, a hedgehog, and a deaf drunk in a nursing home. In another play, I wrestled with a priest in a straight jacket.

Q.How did your personal upbringing (the parenting of your parents or life lessons you learned) prepare you for the life you have led?
My parents were an example of perseverance and commitment. Mom cared for Dad in our home from 1959 until 1983 when he went into a nursing home. From then until his death in 1997, she visited him every day. She honored the "in sickness and in health" vow to Dad's last breath. Though she has never been comfortable saying "I love you" she taught me what love is. She was also a very good money manager and taught me to always live within my means and save as much as possible. My dad was an incredibly funny man, and my sense of humor comes from him. No matter how bad things get, I always look for the humor in what's happening and think of Dad.

Q. Do you have an example of a time where ... while going through something, it made no sense or didn't feel fair, but later - much later, saw the purpose in it or were able to help someone because of it?
Hmmm...basically my entire life has been an example of that idea. Everything I write comes from what seemed unfair at the time, but resulted in experience through which I can help others.




Q. Tell us about your blog
http://www.differentdream.com/ features resources and products for parents of kids with special needs. Several guest bloggers (including Amy) share stories of their lives parenting kids with a variety of special needs, too. Reading comments from those who visit the blog is a highlight of my day. I love to connect with them and point them to resources. If readers click on the "buy the books" tab, they can watch book trailers, download excerpts from both books, and follow the links to their Amazon pages. Or people can email me and order signed copies.


***Stop in tomorrow to read Part 2 of my interview with Jolene Philo***


Monday, October 31, 2011

File Folder Games for Fall (Halloween Too)


This was one crazy busy weekend for our family.  Before it was over, Kylie had been in her Halloween costume no less than 6 times.  We had a blast as a family! 

I will be sharing pics as I get them cropped and formatted, but here is a sneak peak.



However, in addition to all the Holiday Happenings this weekend, My fabulous hubby gave me some time to put together 5 Fall themed File folder Games for Kylie.  November starts THIS WEEK and I am trying to pull everything together for my November themes.

These ideas are not original with me.  Most of them come from Preschool Printables, Learning Center World and File Folder Fun.

I was unaware of how much TIME it takes to put these together.  It looked so easy (well, it IS easy, but they take a long time to make - especially if you make them to last by laminating everything)

Here's a few pics of our Fall File Folder Fun in action.

Halloween Number Game:
The Ghosts have the numbers written on them alphabetically.  You match those to the numeral on each pumpkin stem.



This one is called "Halloween Number Names" (from Learning Center World)



"Pumpkin Alphabet" by File Folder Fun
Pumpkin Alphabet was a real draw for Kylie.  I modified this one so that you fill in the missing letters, but then also so you can match all the letters to their pumpkins.




Scarecrow Colors:
This one, I also modified so that not only do you match the colors, but I also made a color free set with just the alphabetical wording on them so she matches the color words to their colors.

"Scarecrow Colors" by Preschool Printables
Here she is matching the colors



And, of course, it wouldn't be a good day if we didn't line them all up...
But notice they are not lined up in the order of the color of the rainbow... Progress in being flexible!!
Here she is matching the all white scarecrows with their colored matches

 Turkey Lurkey:
I made her two Turkey Lurkey games - one for colors and one for numbers/counting.  She is boycotting the number one because you have to "work" to count the dots on the Turkey's chest and then match the correct number.  She will do it with prompting only. 

However, she loves the color one. This isn't just solid colors either.  The Turkeys are very colorful making it a bit more challenging


"Turkey Lurkey Number Match" and "Turkey Lurkey Color Match"  by Preschool Printables
This one is "work" for Kylie. 
She is really smart and can do it, she just doesn't want to take the time to do it.
I love that they are so colorful and appealing to the eye.

We have had a really productive weekend and Kylie has really enjoyed this addition to her learning/therapy tools.  She gets them out as she wants them and she has been really good about putting the pieces back into their bags. 

However... This pic better sums up our weekend.... Very little work and a whole lot of SILLY!!



More pics to come and

Happy Halloween!!

Friday, October 28, 2011

Center Grove Orchard Fun - A great way to celebrate fall!

Center Grove Orchard - Fall 2011

I wrote yesterday about Kylie's Sound Sensitivity and how it impacted our visit to Center Grove Orchard.

We did manage to have a good time (when we could dodge people and find a few semi-quiet places)

Enjoy sharing in our day...


A stolen moment in the old fashioned school house

We skipped the "official" orchard sign (and the huge line of people that went with it) and found a simple pot of fall flowers.  (You can tell the sound is starting to get to her.  It was shortly after this pic that she started putting her hands over her ears)
She loves to have her picture taken with mannequins (and scarecrows) - maybe because they don't talk??  =0)
Kylie LOVES animals.  Even stinky goats!
Kylie and the White Rabbit.  (Have I mentioned she has a "thing" for Alice in Wonderland? Both "Alice" and "Henry" (we don't know where he came from) live at our house and are Kylie's imaginary friends.)
Playing at the Mad Hatter's Tea Table
Pouring Tea... one of her favorite things.  We could have stayed under this tree all day.
In the old fashioned school house - What a student!
Can you say "detention"??
Bored in school??
(actually, she started to see a group of people enter the school house)
Watching Daddy be silly. 
We figured out we can make her smile if we sing "How much is that doggy in the window" (she starts to laugh and tells us to "turn that off" - so funny!)
Favorite thing: Jumping Pillow
She jumped so high!! She was loving it!
more jumping
The corn ocean: Kylie normally LOVES this, but she couldn't take it this year with all the kids screaming.
She pretty much was attached to our legs and begged to leave. (not-like-her-at-all)
The end of our fun day - and ready to go to ....
PIZZA RANCH (Kylie's favorite place to eat)

It was a fun day - though a difficult one for our precious girl.  We might try to go back in November and see if she doesn't do better with less people around.  We'll see.

Thursday, October 27, 2011

When Hearing Hurts - A Sensitivity to Sound

Does anyone notice a theme to these pictures?

We tried to go to the Center Grove Orchard on Saturday.  We absolutely LOVE it there and have made many great memories there in years past.  We love the corn ocean, jumping pillow, tractor ride, corn maze, animals, and all the other great attractions, but for some reason, Kylie had a REALLY hard time this year: The sound was just too much for her.

Sensitivity to Sound (light, texture, motion, smells and so many other sensory things) is extremely common for children and adults who experience Autism (in any form).  It impacts their daily living in ways we cannot fathom. 
Things have gotten a little easier for us since Kylie has gotten older and has learned some coping strategies (putting her hands over her ears, saying or signing to us that it is "too loud" or that she "needs a break").  But, it is still VERY difficult to interact socially when you suffer so much from the sensitivity of your senses. 

If we are with other children and they squeal with delight over something fun and exciting, that puts Kylie in a tail-spin, she cannot duck, cower and cover her ears fast enough.  Her anxiety elevates and she wants nothing more than to vacate the premises.  If we are with adults, and they give a round of applause to a performer - the same is true.  These common, everyday occurrences cause physical pain for our girl.

It breaks my heart to know how these things impact her.  I can see her face visibly change when people enter a room.  She knows it is coming- the pain, the discomfort.  She scoots closer to me and many times hides behind my leg or squats in a corner trying to "block out" the world. 

We can't "turn off" the world, so how do we help our girl navigate through it?

We avoid crowded and chaotic areas as much as possible.  We spend much of our time with our hands over Kylie's ears, or with one hand over one ear and her other ear pressed into our leg to muffle the sound.  We warn her when we know sound is coming and let her know that it is "ok" to put her hands over her ears if she needs to.
It is a marvel to us.  Some days she does just fine and other days even the swish of a grocery sack is too much for her to bear. She enjoys music, but cannot handle the cry of a baby. She can hear a train from miles and miles away several minutes before Dan or I can hear it.

Our girl is made in an amazing way and she has talents that go beyond anything I can imagine.  I wonder a lot what her "thing" will be.  Will she be an artist? an engineer? a writer? a caregiver? How is God planning to use that super sensitive hearing?

There is a perfect plan prepared for my girl.  I am excited to learn what that will be.  Until then, we will do our best to cultivate her talents, guard her from the things that hurt her and do our best to integrate her into society as painlessly as we can.

If you think of it, whisper a prayer for a little girl who feels pain every time she exits her front door.  The world is a scary and painful place for her. 

This mommy and daddy would be so grateful!!

Friday, October 21, 2011

MORE Icky Sticky Halloween Sensory Box Play

We are having SO MUCH FUN with our Icky Sticky Sensory Box (see my original post HERE) and things are just getting better!  Take a look at what I found at Dollar Tree today!!  Kylie and I were in Icky Sticky Sensory Box Heaven!!



They only had three packages in stock and we grabbed all three.  These stretchy body parts will go GREAT with the items we already have!!


I was really impressed with the quality of these little guys (ahem... items).  They are so detailed! 




We especially love the tongues.  They are incredibly squishy and life-like!  They have bumpy taste buds and even look shiny like they are wet!!  Really creepy but also fabulous additions to our sensory box.  We could hardly wait to get home to play.


Kylie thought she would try on the nose.  It was pretty funny!



Then she went for the eyes.


I hope you all are saying ...

Cause that will mean that we did good!  =0)

Here is the final product with the new additions.



Just can't get enough of that tongue!!  ha! ha!

Maybe the Icky Sticky Sensory Box is too much for you or your little ones.  If so, be sure to check out our other Halloween Sensory Bin.  It is great fun too!

Happy Playing!!
Amy