When my son was three, we were told he was of age to get a formal diagnosis. We went to a developmental center where he was given extensive tests by specialists. One of his diagnosis was Developmental Coordination Disorder.
Developmental Coordination Disorder also known as DCD is a neurological disorder. It is common in Sensory Processing Disorder and affects motor planning and coordination. One big struggle he had was putting movements together. For example, he could kick a ball if he was standing still, but struggle with running to kick a ball. He would trip when running or he would miss the target. When he went after a ball, it would remind me of Charlie Brown running to kick a football. My son had bad timing, poor balance, trouble coordinating steps together, and trouble with spatial awareness.
Upon getting this diagnosis, we increased his time in Physical Therapy. For three years he worked hard developing strength, coordination, and balance. Recently, he tested out of Physical Therapy. Even though he still struggled with some tasks, he has shown amazing improvement.
Today when I picked him up at school, his class was finishing PE. The task was running a mile. I got to watch my son in perfect running form cross the finish line first. Yes, you heard me right, FIRST! I was in tears. I was just so proud. What a testimony this little miracle boy is! He certainly is an overcomer destined for greatness.
I hope my blog will give therapy parents help, hope, and encouragement as I share what I have learned, and what I am learning now. Let us go on this journey together!
Friday, September 25, 2015
Wednesday, July 1, 2015
Try Something New Everyday
One thing that my children
struggle with is change. Change is what causes their anxiety and meltdowns. One
thing that our family has done to help our children with change or newness is
adopting a saying at our house, “Try something new every day.” Last week my son’s
speech therapist said that during feeding therapy, my son encouraged another
child to try something new with the saying, “Try something new every day.” It
made me smile. Here is a list that we have gone over with our children to
encourage them to try a change or new thing:
·
Meet
a new friend
·
Say
hi or talk to a new person
·
Try
a new food
·
Go
to a new place
·
Explore
a new activity
·
Try
a new hobby
·
Watch
a new show
·
Play
with a new toy
·
Try
on different types of clothes
·
Read
a new book
·
Add
something new or take something out of your schedule
Encouraging our kids to try new
things has helped us explore the word change in a positive light. I hope this
idea will help your child too.
Friday, June 19, 2015
Sometimes, We Just Need a Change of Environment
When most kids hear summer break,
they get super excited. For my son, it is scary. Summer break means a new
schedule with new activities and new people. The change is too much. Last
summer, it took him a full month to lower his anxiety, stimming, and meltdowns.
By the time he loved summer, we had to prepare for school to start. Too bad he
can’t be in year round school.
The hard part about summer time
is that people are coming and going due to vacations and most activities are
flexible with different kids each week. For a child that struggles with change
this is a nightmare.
This week, we walked into
gymnastics and my son immediately was covering his ears and yelling too loud. I
asked him what was too loud. He couldn’t tell me. All I heard was some people
talking. I took off his shoes and socks. Then he said, “Too many people. “
There were only five kids in the gym, so I think he meant too many new people
since we did not know any of them. He then ran under and chair, started making
noises and rocking. I pulled him out, and told him I would go into the gym with
him. I could feel his little heart racing.
We went into the gym and my
almost six year old sat on my lap. I gave him deep pressure hugs. The teacher
asked him to say his name and do a trick. All he could do was make humming noises.
It is like the language won’t come out when he has reached this stage of
anxiety. He couldn’t move either. After all the kids introduced themselves, the
coach got my son to sit with him. I went out to the observation room. About a
minute later, my son was next to me. I asked him if it was too much. I told him
that we could go home. We said he wanted to stay, but then he curled up in
fetal position and started rocking and humming. I could tell that this was
escalating fast. I gave him a choice to go into the gym or go home. When he
couldn’t choose, we headed home.
This was the hardest day this
summer. Most of the time, he will warm up after ten to fifteen minutes and
start participating. I look back on the situation and start doubting myself: I
should have stayed in the gym with him longer, it is because he is tired from
too many activities, I should have let him stim until he was ready (although
that might have led to a meltdown if the stimming didn’t calm him). His anxiety
did finally calm after crying it out at home. He really needed a new environment
where he wouldn’t be over-stimulated.
Yesterday I went over the scenario
with our occupational therapist. She gave me a great idea. She said, "Instead of
going home to calm him, take him to the bathroom. It is usually quiet there. You
wet a paper towel, and put it on his face and arms to give him some calming
sensory input. You can also hold him and give him deep pressure. This will
help calm him and prepare him for his class."
I loved this idea. Next week, we
are going to try it, and see if it helps lower his anxiety. I have also started
putting a citrus blend of essential oils on his feel to help with transitioning
into summer. Hopefully, our summer will become easier soon.
Wednesday, June 3, 2015
Self Monitoring: How is Your Engine Running
One thing we work on with our
children is self monitoring how they are feeling. This helps them learn how to
gain control of their feelings to prevent meltdowns. The self monitoring
program we use at home is an ABA tool called “How is your engine running?”
This tool compares your body and
the way it is feeling to an engine in a car. When the child’s engine is running
low, the child may feel tired, sad, or lonely. When the engine is just right,
the child is happy and their body feels good. When the engine is running high,
the child might be excited, angry, anxious, scared, or overwhelmed.
To help my kids self monitor with
this tool, we made a visual. You can find several examples of these visuals
online. It looks like a gauge with a moveable arrow (green- low, yellow- just
right, and red- high).
Once the child is able to
recognize their feelings, they can learn how to get in the middle of the gauge
to feeling just right. For example, if the child’s engine is low, they might
need a nap, hug, crunchy or sour snack, or movement activity to get them to
just right. If the child’s engine is high, they might need a break, deep
pressure (weighted blanket/ vest), hug, calming music, fidget, or movement.
Using this tool in our house has
been a huge blessing. It has helped my children express their feelings/ needs
and learn tool on how to self regulate. I hope this tool can help your child
too.
Monday, June 1, 2015
Reflecting on Therapeutic Riding
Last Month, while driving,
my two year old daughter yelled, "Pretty horse, I want horse." My son
immediately looked at her, and said, "Sissy, a horse is lots of work. They
have big poop that you have to shovel. You have to get them dressed and
undressed. You have to brush them. You have to clean their shoes. You have to
walk them. You have to give them food and water. You have to fix their boo boo
and give them a treat. It is a lot of work to have a pretty horse."
I was amazed at what he said. He has learned so much about responsibility and has gained so much confidence through Horses for Healing. It is such an incredible program. It is neat to look back and see how far he has come.
I was amazed at what he said. He has learned so much about responsibility and has gained so much confidence through Horses for Healing. It is such an incredible program. It is neat to look back and see how far he has come.
When my son was almost
two, he lost his language and began to withdraw after being sick for a couple
weeks with high fevers. After speech therapy for a year, he started speaking in
phrases again, although, it was hard to understand what he was saying.
It was during this time
that we started therapeutic riding. Now, after a little more than two years, he
is speaking in conversation and his words are clearer. The movement of the
horse helps him pace himself while talking. He is making better eye contact and
feels more confident engaging with others after spending time here engaging
with the volunteers and other riders.
I am so thankful for this
program and the strides the horses are making in the kids lives. With every
lesson, my son is getting physically and mentally stronger. The things the kids are
learning here, such as, responsibility, confidence, and engaging with others
will not just help them today, but throughout their lifetime.
Sunday, May 17, 2015
Needing Oral Input Can Be Dangerous
This week has been a scary week
for our family. On Mother’s Day Night, my son started having projectile vomit.
Throughout the night, he threw up 16 times. The next morning we ended up in the
ER. He had to have an IV due to dehydration. The doctor then gave him zofran to
stop the vomit. The vomit stopped, but then he had explosive diarrhea. After
having 12 episodes of diarrhea in 8 hours with no urine, he had to have another
IV. After three days, it still wasn’t slowing down. He was x-rayed, given a CT
scan, had 5 blood tests, a urine sample, and two stool cultures. The doctors
finally concluded that it was the rotavirus. Because it is a virus, my son has
to let it run its course with no antibiotic. The doctors have been actively
monitoring his blood count, hydration levels, and kidney function now for six
days. It has been very scary.
So how did he get it, and how can
you prevent your child from getting it?
The virus lives in the infected
person’s stool. It is spread by people not washing their hands properly, and
then touching things that you might touch or eat. The virus actually lives on a
surface for ten days. If you touch the virus or if an object touches the virus,
and it is placed in your mouth, within 48 hours you will start showing
symptoms.
You can prevent it from spreading
by:
·
Keeping
the infected person at home until they have normal stools for 48 hours.
·
Practice
good hygiene with hand washing before preparing food, eating meals and after
using the restroom.
·
Spray
your toilet with Lysol after someone has diarrhea.
·
Do
not let your child eat food that has fallen off the floor. People walk in the
bathroom and then walk all over the floor spreading germs.
·
If
your child needs oral input, have things your child can safely chew on, and
store them properly.
·
Keep
your child’s hands out of their mouth.
For a child that needs oral
input, I am shocked that we haven’t got it sooner. My son loves to mouth tables,
chairs, and playground equipment. From now on, I am going to be more cautious
and remind him to chew on his chewy only. I just wanted to inform other parents
about this in case you also have a child that seeks oral input on objects out
in public.
After seven days of this horrible
virus, I can say that my son is feeling better. Even though we are not in the
48 hour period yet, he is finally having less stomach issues in a day.
If you have a baby, I also
learned that there is a vaccine to help decrease the effects of this virus. IT
IS WORTH LOOKING INTO.
Every Child Matters
Recently, I
made a choice to tutor a group of special needs children in reading. When I
came to this choice, a friend asked me, “Why are you going to do this?”
She asked a great question. I can also think of several reasons why not to do this.
I mean, I have never taught beginner readers how to read, let alone special
needs children. Even though I am a reading specialist, I am used to helping children that already have the basics
down. It will take a lot of research and time working with younger
children to find good resources. But, these kids are worth it, and I believe I
can make a difference. Even if it is only three kids, I will do it one child at
a time because everyone of them matters. I plan to just meet them where they are, and send them soaring as far as they can go.
The only way I can truly describe my decision is found in the story of the starfish:
Once upon a time, there was an old man
who used to go to the ocean to do his writing. He had a habit of walking on the beach every morning before he
began his work. Early one morning, he was walking along the shore after
a big storm had passed and found the vast beach littered with
starfish as far as the eye could see, stretching in both directions.
Off in the distance, the old
man noticed a small boy approaching. As the boy walked, he paused
every so often and as he grew closer, the man could see that he was
occasionally bending down to pick up an object and throw it into the
sea. The boy came closer still and the man called out, “Good
morning! May I ask what it is that you are doing?”
The young boy paused, looked up, and replied “Throwing starfish
into the ocean. The tide has washed them up onto the beach and they can’t
return to the sea by themselves,” the youth replied. “When the sun gets high,
they will die, unless I throw them back into the water.”
The old man replied, “But there must be tens of thousands
of starfish on this beach. I’m afraid you won’t really be able to
make much of a difference.”
The boy bent down, picked up yet another starfish and threw
it as far as he could into the ocean. Then he turned, smiled and said, “It made
a difference to that one!”
Subscribe to:
Posts (Atom)