It's been a week my friends. One that has certainly felt more like a month journeying between the hottest land in Africa to the most frozen part of Antartica. Chills, shakes, fevers, sweat. So disgusting. A head that wants to burst, a cough that won't stop and a horrible ear/throat/chest infection.
Today is the first day I could actually sit up and look at my netbook without wanting to be sick all over it. But I'll count that as progress. It's better than where I was. Now, back to sleep for me. I hope y'all are doing much better. Please share some happy stuff on on in your life to make me feel better.
Wednesday, May 16, 2012
Monday, May 7, 2012
It's So Cherry Super Spring Giveaway!
I'm excited to share with you a totally fun new store called It's So Cherry! They have the cutest accessories. And lucky you, I've been asked to participate in their giveaway for Mother's Day.
It's So Cherry Super
Spring Kickoff
The trees and flowers
are blooming, the sun is out (well, sometimes) and we here at It's So Cherry
are all about celebrating, so we're giving away gift bags to four lucky
winners, and a pair of barefoot sandals to 20 more. That’s right, you have
TWENTY-FOUR chances to win.
To enter, register
at www.itssocherry.com, and follow one (or more)
of the participating blogs, then fill out the form below.
Contest Rules:
- Must be 16 and over
- One prize per
household
- Must be registered @www.itssocherry.com
- Only valid for those
living within the continental US, or with a United States mailing
address
Each grand prize
goodie bag will contain (1) Flower necklace set (with earrings), (1) crochet
head wrap (color may vary), (1) scarf (color and style may vary), (1) package
nail wraps, and (1) black wrap bracelet. We will also give away 20 pairs
of barefoot sandals to 20 winners.
| Barefoot Sandals - Aren't they awesome? |
To enter, simply
register for an account with It's So Cherry (www.itssocherry.com)
and sign up for their email list. Entries will be accepted starting
Monday, May 7th, until midnight, mountain standard time, on Friday,
May 18th.
Prizes will be shipped
within 10 business days after contest winners have been announced. Winners will be selected using random.org,
and contacted using the email provided for registration on the It's So Cherry
website.
Names of the goodie
bag winners will be posted to participating blog sites as well as the blog for
It's So Cherry, www.itssocherry. blogspot.com.
Upon notification, winners will have 7 days to respond, after which another
winner will be chosen.
Monday, April 30, 2012
Motherhood & Autism
A week ago, my middle school son with autism came down with a bad case of bronchitis. The poor guy sounded like he was hacking up half his lung - and was absolutely miserable. He stayed home from school all last week. Which means mom got the pleasure of home schooling him. And it actually was nice. There's so much I miss while he's at school all day - his questions about context he's learning, interesting comments in science and social studies. By the time he comes home and I ask how his day was, all I get is a "It was great!". I enjoyed actually being on the discovery and working hard side for a change.
It also happened that last week was a mega deadline week. I had to make a lot of decision about how to schedule my time between meeting my family's needs, checking off my work to-do list, and stay mentally together. It was quite a challenge, but somehow it all came together.
One item on my to-do list actually helped me to freak out a tad bit less. I agreed to review Motherhood Matters by Connie E. Sokol. You may remember Connie from her Autism Celebration post earlier this month. I've enjoyed her books in the past and have reviewed them here on my blog. This time, her book is a short Mother's Day gift book. The chapters are tiny, but the messages have a powerful impact. Each day, I would read just one chapter - which took less than five minutes. I found I had one of two responses.
Which means I spent a lot of time this past month thinking about motherhood and autism. In Motherhood Matters, I was reminded that there is no "perfect" way of mothering. Each of our families has a different make up. Some people have large families, others just one or two kids. Some families don't have any special needs, some have a mixture of typical kids and special needs kids, and I even know a few families that each of their munchkins fall somewhere on the Autism Spectrum. Each family is unique and awesome.
Connie reminded me that we each get to be the best mother for our own families AND we should never compare ourselves to the whoever we perceive as the perfect neighborhood mom. I absolutely know that I'm the mom my kids need - yet, I still fall victim to looking at my friends and their awesome mothering skills and think "Man, I wish I could be more like her." It's refreshing to have someone else remind me that my goofy family and our way of working together is perfect for us - and my style of motherhood is awesome for our family.
So, today, as I wrap up this month of Autism Awareness, I wanted to share that message with each of my readers. No matter what your family is like, YOU are the mom your munchkins need. You work hard every single day to find balance between the joyful, mundane, and stressful moments. YOU are awesome. Take a deep, cleansing breath. And another one. Then repeat after me:
I want to end with a huge thank you to all the moms and dads who love their munchkins with autism so very much. Who celebrate their uniqueness, their talents and gifts, and their strengths. Who help their munchkins work on their challenges, help them take a step in the right direction . . . and never, ever give up. Each of you is an incredible blessing in your child's life. So, on behalf of your munchkins, I want to say thank you for your love and dedication to your families.
Happy Autism Awareness Month!
For more information about Motherhood Matters by Connie E. Sokol, please visit her website.
It also happened that last week was a mega deadline week. I had to make a lot of decision about how to schedule my time between meeting my family's needs, checking off my work to-do list, and stay mentally together. It was quite a challenge, but somehow it all came together.
One item on my to-do list actually helped me to freak out a tad bit less. I agreed to review Motherhood Matters by Connie E. Sokol. You may remember Connie from her Autism Celebration post earlier this month. I've enjoyed her books in the past and have reviewed them here on my blog. This time, her book is a short Mother's Day gift book. The chapters are tiny, but the messages have a powerful impact. Each day, I would read just one chapter - which took less than five minutes. I found I had one of two responses.
- "Amen! I've totally been there!" reaction, followed by a "It's so nice to have someone else admit to not being perfect, but who still enjoys being a mom." OR
- I found myself thinking about the chapter's topic throughout the day, wondering how I used it in my life, what my motherhood style was like, and how I work with Heavenly Father to care for my munchkins.
Which means I spent a lot of time this past month thinking about motherhood and autism. In Motherhood Matters, I was reminded that there is no "perfect" way of mothering. Each of our families has a different make up. Some people have large families, others just one or two kids. Some families don't have any special needs, some have a mixture of typical kids and special needs kids, and I even know a few families that each of their munchkins fall somewhere on the Autism Spectrum. Each family is unique and awesome.
Connie reminded me that we each get to be the best mother for our own families AND we should never compare ourselves to the whoever we perceive as the perfect neighborhood mom. I absolutely know that I'm the mom my kids need - yet, I still fall victim to looking at my friends and their awesome mothering skills and think "Man, I wish I could be more like her." It's refreshing to have someone else remind me that my goofy family and our way of working together is perfect for us - and my style of motherhood is awesome for our family.
So, today, as I wrap up this month of Autism Awareness, I wanted to share that message with each of my readers. No matter what your family is like, YOU are the mom your munchkins need. You work hard every single day to find balance between the joyful, mundane, and stressful moments. YOU are awesome. Take a deep, cleansing breath. And another one. Then repeat after me:
"I am a great mom!"
I want to end with a huge thank you to all the moms and dads who love their munchkins with autism so very much. Who celebrate their uniqueness, their talents and gifts, and their strengths. Who help their munchkins work on their challenges, help them take a step in the right direction . . . and never, ever give up. Each of you is an incredible blessing in your child's life. So, on behalf of your munchkins, I want to say thank you for your love and dedication to your families.
Happy Autism Awareness Month!
For more information about Motherhood Matters by Connie E. Sokol, please visit her website.
Friday, April 27, 2012
Why I Chose Autism by Katie Norman
People often ask “why” I chose to work with students with
Autism. My answer is: I didn’t choose autism it chose me.
As a student at the University of Kansas, I was studying
biology for pre-med. I always knew I
wanted to work with children and to somehow make a difference in their
lives. At the time, I had never heard
the word autism nor did I know anyone who had been diagnosed. All I knew was I wanted to work with children.
Early in my college education, I realized biology and chemistry were not for
me. Half way through my second year of
college, I enrolled in a child development class and absolutely fell in
love. From there I started exploring
some psychology classes. It wasn’t until
I changed majors from Biology to Human Development and Family Life/Psychology
that I found my true calling. I enrolled
in some behavior modification classes and then had to pick an emphasis within
my major. I chose “Working with Students
with Autism”. I took courses that primarily
focused on the autism spectrum. I
excelled in these courses and loved them. I enjoyed the readings, the
assignments, and didn’t dread the tests. This was what I was supposed to be
studying.
It was then that I met my first student.
| Katie Norman with my son Isaac & his Autism Specialist, Mr. Todd. |
A foster grandmother had approached me in one
of my classes. She needed some home support for her grandson with autism. She asked me to meet him and work with him at
home as well as take him into the community.
I had read about students with autism and ways to teach them but this
was going to be a new challenge. From
the time we first met, I became a part of his family. I worked with him several days a week after school. Don’t get me wrong, he was a challenge for me
and for his grandparents - both behaviorally and academically. However to watch
the progress he made over time, made it all worth it. It reinforced my belief that I was in a field
I loved. I worked with him in the home setting from the time he was 8. He’s now
21 and I still keep in touch with his family.
Although I taught this student a lot, he and his family
taught me even more. They taught me to
love unconditionally, compassion, patience, and to never give up.
I graduated college, obtained my teaching certificate and a
master’s degree. Then I started my career as an Early Childhood Autism
Teacher. I was in for what I thought of
as the challenge of my life (up to that point).
I was a first year teacher opening up a new program with 6 students with
autism and 3 peer models. I knew how to
do 1:1, but what was I going to do with 6?
It was also my first time managing classroom paras. Yes, it was difficult at first, but it was one
of the most rewarding times in my career.
I built a program for these students and got to watch them flourish
first hand. I was there writing their
initial IEP‘s and talking their parents through what it would be like to send
their babies to school for the first time.
I had to build trust and confidence with these parents. I also had to be a shoulder for them to cry
on for parents who recently received the diagnoses – and sometimes I cried
to.
There isn’t anything was more exciting than hearing a student’s
first word or witnessing a first sign. I
videotaped these milestones so the parents wouldn’t miss out. I witnessed many other first milestones - students
using the potty for the first time, a student who could no more than sit for a
portion of circle time could now lead circle time, a student who wouldn’t touch
paint was now a master in art center.
These were the times that made smile.
Our moto was “Tiny steps to giant victories” and that is exactly what it
was in my classroom. We celebrated each and every “tiny step”.
When I made the choice to leave the
classroom—one of the hardest decisions ever—I put on a preschool graduation for
my students. At that time there were 8
identified students and 4 peer models.
The students participated in a circle time session with their parents
and then was followed by a slide show of my class and students over the last
two years. There was not a dry eye in
the room. I was the worst. I was saying goodbye to many of my first
students who had come so far. Goodbye to my classroom and para educators. Each and everyone one of these students,
parents, and staff were a blessing to myself, to each other and together we
learned a ton. I will never forget my
first students. I still see some of them
today as they are get ready to transition to middle school. They have come so far. I am so proud of each
and every one of them.
If you could work with people with disabilities, what area would you choose?
Katie Norman is an Autism Specialist for Olathe School District. She taught an autism preschool prior to
becoming an autism specialist. She studied at University of Kansas for
both her undergraduate degree and Master of Science in Special
Education. She is currently taking course work
through Florida Institute of Technology in Behavior Analysis. She loves her job, the students she work with, and the families she is able to support!
Wednesday, April 25, 2012
Autism Celebration 2012: My Experience with Autism by Sarah Anderson
| Sarah and her son. |
When I was in college, I needed to volunteer in a special
needs classroom for a day as a class assignment. I was a little apprehensive
because I had pretty much zero experience with non-typical kids. On the day of
my assignment I parked my old Honda Accord on the street next to a worn two
story building across the street from campus. I really didn’t know what to
expect. The sign next to the road read Oakridge high school. I met up with
others members from an art education class and headed for
the main office. The secretary sent us to different classes as volunteers for
the day.
The class I was sent to had five students. Their ages ranged
from 14-17. They all had normal names and wore normal clothes. At first glance
they looked like a group of normal American teenagers sitting around a large
table. But they were anything but normal. They rocked back and forth, some hit
their heads while others muttered strands of unintelligible words. All of them had
a faraway look in their eye as though their souls we’re trapped deep inside. They were autistic. Not high on the spectrum
but so deep they hardly acknowledged my existence. The day ended with a school
wide sock hop that consisted of a gathering of kids with a variety of
syndromes. Teachers rocked wheel chairs back and forth, and I jumped up and
down over exerting myself trying to get just one kid to move.
The next day my classmates spoke about how sad it was, how
hard it was to look at some of the student deformities, and even how they would
not want to teach them. But I couldn’t
wait to go back. I started volunteering on a regular basis, and then moved to a
different class room as a part-time TA. I met a kid who could organize
anything. I’m even guilty of deliberately messing up stuff just to keep him
busy. I spent mornings taking kids out in the community. I even went to
McDonald’s and helped the kids clean tables as part of work program. At the end
of the year, I was on a committee to decorate their prom.
A lot of the kids didn’t
recognize me from day to day but I kept coming back. It was hard but I felt I
needed to be there. I wanted to see them smile back at me. I wanted a sign that
I was helping but I got nothing in return. I went back and forth about changing
my major, even though I was almost done. I left on church service mission, but
when I returned, I jumped back in. Nothing in the classrooms fit my schedule,
so I became a lunch aide just a few hours a week, but it was enough. I loved
these kids who could not reciprocate. I worked there until the school changed
locations and I could not follow.
On the last day, I remember leaving the parking lot and
thinking there had to be a reason I was pulled toward these kids, given three
years of my life to them. I felt certain I would draw on the experience that it
hadn’t been for nothing.
Two years later I gave birth to a child with
Neurofibromatosis. It’s not Autism, but I use a lot of skills and patience I
learned from my time at the special need high school. I draw on my experience
to get through therapy sessions and IEP meetings. My son goes to a special needs preschool
where his best friends are kids on the spectrum because they don’t seem to
notice he is different.
Autism has touched my life. Serving those with autism has
made me a better person. And autism has given back to me through my son. I will always have a special place in my heart
for those who are a little different.
Have you had a teaching or volunteer experience with someone with autism? If so, how did they touch your life?
You can learn more about Sarah on her blog.
Monday, April 23, 2012
Autism Celebration: How to Use Technology to Help Our Kids with Autism by Victoria Holt
In just the three short years since our daughter
Tessa’s diagnosis of ASD, the availability of knowledge, information and
resources has boomed. Books, local special education services, Smartphones and
iPads, and especially the Internet have expanded the help that is available to
families touched by the disorder.
| Victoria and her daughter, Tessa. |
Recently, we were preparing for a trip to the
dentist, and I felt prompted to bring my digital camera. I thought I could take
photos of the waiting room, the dentist, the exam table and so on, and use them
at a later visit to the dentist for a social story. The visit to the dentist
went even better than expected, in large part because my daughter Tessa was
determined to make it so. She told me before we arrived that she did not want
to cry! I took photos of everything: big sister brushing, Tessa smiling, the
hygienist working on big sister’s teeth and so on. The staff was extremely
accommodating, and allowed Tessa to sit during the exam, rather than lie back
on the chair. I recorded it all, feeling such pride and accomplishment on
Tessa’s behalf. She was working so hard to not let her anxiety take over, that
I had to blink back tears. After a
successful exam and many accolades, we came home, and I had these remarkable
photographs of something I thought I would never see. Tessa at the dentist,
happy.
It occurred to me that I could upload the photos to
our computer and look at them often to boost my daughter’s morale. As I was
uploading, I thought about my blog and how neat it would be to put them on
there. But my blog is about food and cooking…not really the best venue for such
momentous pictures! That’s when it all snapped into place. I would create asocial stories blog for Tessa to review photos of events that she participated
in, and to remember what it was like, and how she reacted, all in vivid Technicolor!
As I recorded the dentist appointment, it occurred
to me that other parents and kids might benefit from such a blog. I made the
executive decision to open the blog for public viewing. I hadn’t seen anything
like that in cyberspace.
As you all know, life is hectic and at times,
overwhelming. I don’t update the social stories blog as often as I would like,
but it is a resource that is always there when we need it. We recently viewed
the famous dentist appointment visit again, as it was time to return for a
check-up. Tessa remembered the hygienist’s name, the general routine, and her
younger brother enjoyed looking at the photos as well: it was an unexpected
benefit because he had a check-up also.
When I have time and the inclination, I like to
photograph simple events in our lives and put them on the social stories blog
so that Tessa can prepare herself for upcoming situations. It is a somewhat
simple solution that has great dividends for our family. I have also used
photographs to create a hands-on social story by printing them out and making
laminated books that Tessa could look at again and again. In a pinch, I have
simply carried my camera with me, and recorded events as they happened, and
shown the photos on my camera to Tessa during the outing. It has the ability to
calm her down because it gives her a slightly different perspective on the
situation. Additionally, Tessa’s school teacher uses an iPad and other hi-tech
devices to aid Tessa’s learning in the classroom.
I am thankful
for the prompting I received to bring my camera along to the dentist that day,
because it turned out to have lasting positive consequences. I encourage other
parents to think outside the usual routine and attempt to use some of the
technology that is out there to provide better experiences for their child with
Autism. Everyone who views the photographs, from the child with Autism to her
parents, siblings and grandparents, will enjoy this alternate perspective on
situations, and has the potential to bring happy memories alive again, and put
a positive spin on an otherwise stressful event.
Notes from Danyelle: Here are some additional recommended apps to use on your android tablets, phones or iPads. Enjoy!
Notes from Danyelle: Here are some additional recommended apps to use on your android tablets, phones or iPads. Enjoy!
- Model Me Going Places ($24.99) - Social videos
- Easy Kid Tokens (FREE) - Cute token economy. I personally love it!
- Easy Kid Timer (.99) - Transition timer w/ pics of next activity
- AAC Speech Buddy ($27.99) - An interactive PECS system for Android, iPhone, iPad, MAC, or your personal computer
- iPrompts ($49.99) - iPad version transition timer w/ picture choices
- ABA Flash Cards: Emotions (FREE) - iPad emotion flash cards
- Pictello ($18.99) - Create talking books for social stories on your iPhone or iPad
What types of technology have you discovered to help your child with Autism?
Victoria Holt is the mom of 5.33 kids. She has had a handful of short
fiction stories published in literary journals you've never heard of,
and also an essay in Segullah, which you may have heard of. She loves to
scrapbook and read outside in warm weather. Her daughter's ASD
diagnosis actually came as a relief after two years of genetic testing
and other false starts. Autism has brought her family closer together
and closer to God. For some low-key social stories, check out her social
stories blog http://asdsocialstories. wordpress.com/ . For some low-key recipes, you can check out her other blog: Whats4Dinner?." http://v1ct0r1a.wordpress.com/
Friday, April 20, 2012
Autism Celebration 2012: Girls Scouts & Autism by Dena Millet
My 11 year old daughter with Asperger’s Syndrome has been active with the Girl Scouts since she
was five years old. While she struggles
with meetings and the social aspect of Scouts (especially as she has gotten
older and the friendships in the Troop have become more complex), she adores
activities, field trips, and going to camp.
I have noticed through the years that she blossoms in Scouting, she
dives into service projects with both feet and finds her voice in public when
she wears her Girl Scout Vest. The same
child that struggles to answer simple social questions from a person she does
not know, wears her Girl Scout Vest, and has confidence, handling social
situations with less difficulty. She is
able to work with many members of the community in setting up, managing, and
following up on various service projects.
In 2011, we tried doing Cookie Booths for the first time,
as when she was younger, I was unsure how she would handle working with the
public in such a hectic environment. She
did very well with the booth sales and she and her younger sister earned enough
through their cookie sales to pay for a weekend at camp. We went as the only members of our troop, and
I stayed with the girls. My daughters
both had been having challenges with night terrors, and the Camp Director (“Chipmunk”)
was very helpful in making accommodations for the girls, putting us in the
health center in the lodge so that the girls would be able to experience camp
without added social stresses (and to prevent their sleepless nights from
keeping other campers awake). I was so
pleased to see how much assistance we received to make camp a memorable
experience for her.
We were in the middle of the dinner line on our first night
when my heart sank into my toes. We were
in the cafeteria and out of the corner of my eye, I saw a girl staring at my
daughters. Immediately, I spun around
and took a good look at her, recognizing her as the girl that had been a bully
to my daughter for two years. I hurried
the girls into the cafeteria and to a table, my mind racing to determine my
next action. My first thoughts centered
around making a quick escape and taking them home. Not wanting to do so, I decided that I would
keep my daughter so busy that she would not know that this girl was also at
camp. I felt very tired all of a
sudden, realizing that this proposition was going to require a lot of work and
quick thinking. I decided to enlist the
assistance of my 8 year old to help me.
She is very protective of her sister and I knew I could count on her.
We went through this for the first evening’s activities
as well as the activities for the next morning, and through lunch of the second
day. Any time for Mom to relax in the
mountains was rapidly disappearing into the time and energy that was spent
staying one step ahead of my daughter.
This was not fun for me nor my younger daughter, and my older daughter
was happily oblivious. This was not
going to work for the remainder of the weekend.
I talked to “Chipmunk,” explained the situation, and the other girl’s
Troop Leader was given a head’s up as well.
That evening at dinner, I made my move, informing my
daughter that the girl was at camp and that I had a plan to help her feel
better. She immediately began to exhibit
anxiety and worry. I gave her a hug,
told her that she was going to be ok and that we were going to handle this
together. I had hatched a plan that
would hopefully put this to rest and bring resolution to my daughter so that
this experience would be memorable and meaningful to her and give her added
self confidence.
The ritual at camp for meals was to have small pieces of
plastic fruit that were distributed from table to table allowing the girls at
that table to visit the salad bar. When
our table had completed our round at the salad bar, I handed the plastic banana
to my daughter and we walked to the table across the room, her with much trepidation
as she was rapidly breathing, knowing we were going to the table at which sat
the girl who had, in a nutshell, made her life very difficult. I held her hand and encouraged her the entire
way. When we got to the table, she
reached out, her hand shaking, and held the banana for the girl to take. She uttered a tentative, “Here,” and the girl
reached out, smiled and thanked her. The
exchange was complete; the ice had been broken.
My daughter sighed, and practically flew back to our table.
During a SWAPS exchange, the girls bring pins, etc. that
they have made and exchange them with their new friends. I had made one the night before to give to
the girl and planned on visiting with her at the exchange and telling her of
her strengths and challenging her to always use her dynamic personality to the
betterment of others, rather than to try and control them. This exchange went well, and my daughters saw
the interaction (but did not hear it). When
it came time to do the SWAPS exchange, I sent my daughter to exchange with the
girl (she was able to approach her on her own without my support) and stood by,
watching her countenance change. Within a
few seconds, she turned, with a huge smile on her face, and walked a little bit
taller that day.
I am so proud of how she did in facing the fears which
had troubled her for so long. I’d expected
to bring home memories from Girl Scout Camp, but had no idea that the memories
which she would be bringing home would involve such a life-changing experience,
especially since she has not mentioned this girl and her bullying since.
Have you had a Boy or Girl Scout experience with someone with special needs?
~~~~~~~~~~~~~~~~~
Dena
Wootton Millet is a wife, mom of 2 girls and step-mom of 4 girls - the
six range in age from 8 to 20. Dena and her husband spend a vast amount
to time trying to keep track of all the ins and outs of 6 girls and
their busy schedules, not to mention their own! One of Dena's daughters
was diagnosed with Asperger's Syndrome at the age of 7. Dena works
raising awareness of Asperger's Syndrome as well as her work to increase
awareness of and advocating for adult and child victims of Domestic
Violence and Abuse. She co-authored Cheaper, Greener, Cleaner - Ceiling to Floor Savings and regularly blogs at: http://www. cheapergreenercleaner.com/ blog-every-day-the-cheaper- greener-cleaner-way/
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Review Disclaimer: Sometimes a book I review has been sent to me for free by a publisher or an author. This in no way effects my review, which is my own opinion about whether the book was a good read for me, fit my tastes, and if I would recommend it to others. Other than possibly a free book, I am not compensated in any way for posting a review.

