May 30, 2012
Special and Determined
I was born March 22, 2006 at 1:32pm in Naperville, IL by cesarean section. I weighed 7 pounds, 12 ounces, and was 20 1/2 inches long. The picture above was my christening picture in the hospital before my shunt surgery (16 days old). I was born with a congenital heart defect called Tetralogy of Fallot, which is a congenital heart defect consisting of four different abnormalities.
Tetralogy of Fallot involves four heart defects: A large ventricular septal defect (VSD) - a hole in the septum between the heart’s two lower chambers Pulmonary stenosis - involves narrowing of the pulmonary valve and the passage from the right ventricle to the pulmonary artery Right ventricular hypertrophy - the muscle of the right ventricle is thicker than usual An overriding aorta - the aorta is located between the left and right ventricles, directly over the VSD. As a result, oxygen-poor blood from the right ventricle flows directly into the aorta instead of into the pulmonary artery
Before I was born, my Mommy and Daddy wanted desperately to have a baby. They went through a year of infertility treatments until it got to be too much for Mommy. One unexpected day after Mommy stopped treatments, she found out she was pregnant.
Mommy’s pregnancy was considered “high risk” because of her age. The obstetrician recommended a few tests to make sure all was okay with the pregnancy. Mommy had a Level 1 ultrasound which is also called a “screening ultrasound” to check that there is normal growth of the baby and to look at the location of the placenta and to be sure there is enough amniotic fluid. During the ultrasound the Perinatologist discovered a hole in my heart. He told mommy that there may be a possibility of Down Syndrome because of this, and asked if she wanted to have an amniocentesis to confirm.
Mommy didn’t know how to feel about all this information except scared and overwhelmed and she didn’t know how to tell Daddy. After Daddy and Mommy talked and determined that they were happy to be having a baby and whatever God blessed them with they would handle it with a loving and open heart, they decided against the amniocentesis, and just had my heart monitored over the next 5 months to see how it was growing.
Mommy did all the things that expectant moms do. Started buying clothes, got the nursery together, tried mommy yoga (that didn’t go over that well) and had a baby shower. She wasn’t going to let anything ruin the excitement she was feeling as an expectant mom, she had waited far too long to be a mommy.
My Birthday: Well it was the day for me to come into this world and everyone was anxiously awaiting my arrival. Mommy and Daddy got prepped to go into the surgery for my delivery.
And here I was blue, as was told to Mommy & Daddy by the Pediatric Cardiologist before I was born. Mommy was eagerly awaiting the scream, after a couple of seconds there it was. Daddy never told mommy until just recently that I wasn’t breathing when I came out.
I got to see Mommy for only a few seconds before they rushed me off to the NICU to evaluate me. After what seemed forever, the Neonatologist came to the recovery room to tell Mommy and Daddy of the heartbreaking news…I might have Down Syndrome, but it won’t be confirmed until the karotyping (test to identify and evaluate the size, shape, and number of chromosomes in a sample of body cells) blood test came back from the lab. However there were other characteristics that would give them an indication I had Down Syndrome. The Simian Crease on my left hand (The presence of a single transverse palmar crease can be, but is not always, a symptom associated with abnormal medical conditions, such as fetal alcohol syndrome, or with genetic chromosomal abnormalities, including Down syndrome (chromosome 21), and a large gap between the big toe and the toe next to it on both feet.
Mommy and Daddy were quiet they didn’t know how to react to the news. Mommy was thinking it was her fault because of her age and Daddy just didn’t say anything, except “I’m going to call everyone to tell them the news.” Then the nurse brought a picture of me to Mommy. Mommy’s eyes started tearing up, she could see it in my eyes that I had Down Syndrome. Her heart started breaking.
It seemed like forever since Mommy and Daddy saw me so they wheeled Mommy down to the NICU to see me. I was hooked up to monitors and had an air bubble over my head to help me breathe, but Mommy wanted to hold me.
After two weeks in the NICU and several issues with my oxygen levels falling too low, I was transferred to another hospital were it would be determined if I would need surgery.
I had a Blalok-Taussig shunt put in at 16 days old to help with the flow of blood, so I could get stronger to have my complete heart surgery (open heart) when I was 6 months old.
Well finally 3 weeks and one day after I was born I was able to go home. My parents were so excited to get home and start living our lives as a family.
As I was getting stronger Mommy arranged for early intervention to start. I had a physical therapist come to my house to help me start to get stronger and help me to reach my milestones. I was scheduled to have my complete heart repair at 6 months old and they needed me to be strong to go through this major surgery.
Mommy would sit in on my therapies with Darla the physical therapist to learn all that she could to help me get stronger and help me reach my milestones. This is mommy helping me to stand with the encouragement of my pray bear. She used the step stool since this would help me to learn to grab on to something and pull myself up. She was very creative in what she used to help me reach my goals.
You can read more about my first six months in my book “Jacob’s Journal – My Journey Home”.
Follow me and my growth as I am now almost 6 years old.
Oct 10, 2011
Sweet Awareness
October is awareness month for a lot of things. For many moms, every day is awareness day. Here are a few things I've seen to help raise awareness.
I saw this on Parenting Special Needs' facebook page.
October is disability awareness month. Support our initiative to educate our communities about acceptance of people with Different Disabilities & Abilities.
Your Assignment:
♥ Start a Conversation ♥ Read a book to a group of children that emphasizes difference and fosters acceptance ♥ Share a personal story ♥ Pass on information about a disability ♥ Display our FREE poster ♥ Acceptance begins with a Smile : )
Rett Syndrome Awareness
from Brooklyn Ashleigh Butler...
Mitochondrial Disease Awareness
A touching post from Life With Jack...
A post about Mitochondrial Disease
and other awareness activities
by Mama Mia...
Spina Bifida Awareness
Daily photos & stories on the blog Beyond Measure....

Down syndrome Awareness
31 for 21 from Unringing the Bell
Daily posts from lots of blogs!
Sweet message from Boston Clark Butler's blog
Dwarfism Awareness
Oct 8, 2011
Queen
Mar 21, 2011
Everyone is Different
by Lanny Sherwin
We’re all different colors, we wear different clothes,
We’re short, we’re tall, we’re fat, we’re thin,
We’re square pegs in round holes just trying to fit in.
Everyone is different, it’s really no big thing,
It’s the differences between us that make life interesting.
Those little quirks that make us work are Heaven-sent,
So give a little thanks
That we’re all different.
We’re wise, we’re weird, we’re cool, we’re geeks,
We’re pieces of a puzzle – strangely unique.
But put us together and what do you see?
The world is our home, and we’re one big family.
Everyone is different, it’s really no big thing,
It’s the differences between us that make life interesting.
Those little quirks that make us work are Heaven-sent,
So give a little thanks
That we’re all different.
Jan 15, 2011
God's Plan
From the moment you took your first breath,
I could tell that you had a special job to do
I could tell by the crease in your hand
And your eyes, oh they told a story too
I could see the look on their faces
They thought something was wrong
They didn't see what I saw before me
A perfect babe had been born
So don't tell me what you think he won't do
You gotta open your eyes to a better world
Give him a chance to do like the others
Give him some time to move right along
I'm not saying this job will be easy
You gotta understand
I think he was sent here to teach us a lesson
Don't mess with God's plan
He is part of the plan
Now you're growing up much too quickly
Trying hard to keep the pace, I know it's true
So your steps are a little slower
And your words, oh they take their time too
You were born with a love that's so pure
One touch and it shows
You are an angel sent here from heaven
And I'm sure that you know
Since the day you came into my life
I found the meaning of believing
And i know that miracles are real
Every
time that you smile
I know the meaning of belief
You gotta open your eyes to a better world
So don't tell me what you think he won't do
You gotta open your eyes to a better world
Give him a chance to do like the others
Give him some time to move right along
I'm not saying this job will be easy
You gotta understand
I think he was sent here to teach us a lesson
Don't mess with God's plan
He is part of the plan

Jan 6, 2011
Love is...

When you care about someone and want the best for them even if it means putting your own needs last. Love is selfless. Love is when you see the best in a person even if others don’t care enough to take a good look. It is understanding their every word, even though they haven’t verbally said a single thing. It is believing in them, when others think things are out of reach. It is appreciating them for who they are and not wanting them to be someone they are not.
These are just a few of the things that define love to me, what is the meaning of love to you?

Mar 21, 2010
World Down Syndrome Day

Down Syndrome International (DSI) has officially earmarked 21 March as World Down Syndrome Day (WDSD). The date was chosen to signify the uniqueness of Down syndrome in the triplication (trisomy) of the 21st chromosome and is used synonymously with Down syndrome.

For ideas on how to celebrate WDSD, head to Down Syndrome NSW.
Feb 24, 2010
World Down Syndrome Day

Down Syndrome International (DSI) has officially earmarked 21 March as World Down Syndrome Day (WDSD). The date was chosen to signify the uniqueness of Down syndrome in the triplication (trisomy) of the 21st chromosome and is used synonymously with Down syndrome.

For ideas on how to celebrate WDSD, head to Down Syndrome NSW.
Oct 19, 2009
Jan 21, 2009
Healing Wisdom












Jan 14, 2009
Child of Love

A mom.
A medically fragile little boy with Down syndrome.
A story to tell.
We consider Parker to be an exceptional blessing in our lives. We are constantly amazed at how such a little guy has inspired so many people. But we believe that one of his callings in this life is to touch the hearts of others. Parker still has at least two extensive surgeries in his future.

His health issues include:
1. Pulmonary Hypertension - One of Parker’s doctors describes Parker’s PH as being caused by upper airway obstruction due to severe obstructive sleep apnea, combined with chronic lung disease due to Parker’s underdeveloped pulmonary system. This could cause heart failure, which requires Parker being on supplemental oxygen and medication. If we can keep Parker healthy enough for his lungs to grow, then new tissue will be generated to slowly heal his lungs. This will lead to his PH numbers receding.
2. Tethered Spinal Cord - Parker’s spinal cord was attached to his sacrum, which could cause paralysis as he grows. His cord was de-tethered in May of 2005, but vigilance is required to make sure that the cord does not re-tether.
3. Failure to Thrive - because Parker is constantly so sick, he hasn’t been growing very well. He weighs 23 pounds and is 2.5 years old.
What can I say? The kid is teeny. Really, really teeny.
But he’s HUGE in courage, smiles, spunk and love.
4. Bowel Obstruction - Parker will need two surgeries to create a functional tush, aka, his Teeny Tiny Designer Heiny. As of now has a colostomy until he becomes healthy enough to undergo such extensive surgeries.
5. To help with Parker’s severely obstructive sleep apnea, and his severe pulmonary hypertension, Parker was trached in October of 2007.

Because of these issues, Parker is on several expensive medications as well as using several items of durable medical equipment. Parker has already had two surgeries and many stays in the PICU at Primary Children’s Hospital in SLC, Utah.
To help us keep Parker healthy we have him in what we call our “Safe Room” This is a Parker and Mom and/or Dad room only, the kids can only come in one at a time after they have washed, sanitized and masked up.
Parker receives the following therapies and services:
Occupational Therapy
Through Alpine School District Parker receives one hour of OT a month. Parker is working on reaching across his baseline on a consistent basis and increasing his hand strength. We work with Parker to hold a crayon with the proper grip. We are teaching Parker how to insert small objects into even smaller openings. Parker is learning how to twist things on and off and flip switches. He has successfully mastered both throwing and catching a ball. Any ball. The kid loves balls. Parker has also mastered the fine art of stacking. They kid can stack anything…anywhere.
Physical Therapy
Through Alpine School District Parker receives physical therapy twice a week. He has mastered crawling (when he wants to), and pulling himself up to a stand. He is still learning the best way to get out of a stand. And we keep the faith that Parker will, indeed, walk. And run. And skip. And jump.
Speech Therapy
Through Alpine School District Parker receives one hour of speech therapy a week. Parker is learning how to express his needs through sign. He is working on two word sentences such as ‘Want Car.” Although “No! Mom!” still seems to be his all time favorite.
Feeding Therapist
Our school district will not provide any feeding therapies for Parker. So we have found an independent therapist to help Parker. It is fairly common for kids with g-tubes to no longer have a desire to eat by mouth. But since eating helps prepare a child for speaking, we feel that this therapy is something we need to provide for Parker. Plus, we hope that one day Parker will no longer need special feeds via a g-tube. When that time comes we don’t want him not to understand such basics as chewing, moving food around in his mouth, drinking from both a cup and straw and swallowing.
The whole eating thing is made even harder by Parker’s trach. Kids that have been trached can’t smell or taste. In order for Parker to smell or taste he has to be wearing his ’speaking valve’ on his trach. But because of Parker chronic lung disease he can’t wear the speaking valve for more than about an hour a week.

Pre-school
Because of Parker’s health issues he is unable to attend school. And after lots of discussion and prayer both Reed and I feel that Parker needs would best be met in a home schooling setting. In a few years we may re-evaluate this decision, but I doubt it. Through Alpine School District Parker is visited once a week by a special needs pre-school teacher.
This year Parker will continue to work on colors and sorting and identifying animals. I have also created almost 25 lesson plans that will cover topics from bugs to trucks to gingerbread men. I want Parker to explore the world around him to the best of his ability.
I am so grateful for the degrees I have in Early Childhood and Elementary Education. These have served me well with all of my kids. But they are even more of a blessing with Parker.

We absolutely believe that with the love, prayers, and support of family and friends Parker will be able to overcome his health setbacks and will be a much loved and needed member of our family.
Sincerely,

If you could keep our Brave Hero in your prayers for his pain to be manageable and that he can heal and return home, that would be so very appreciated.
Child of Love
Child of love, our love's expression
Jan 12, 2009
Good News & Good Idea

What a great way to start out the new week.... Good news!

Our friend, Dallyn, who had open heart surgery just last Wednesday, is home (early) and doing amazingly well!!! His mom Shellie said he loved the blanket in the hospital, and now that he's home, he has been enjoying the music and books. Thank you, thank you for everyone's thoughts, prayers, and gifts sent for Dallyn and Shellie.
Wow. Doesn't that just put a big smile on your face? I know it does for me!
If you need another reason to smile, and you missed this week's kidz feature, go meet Mercede and Cheyenne.... they and their mom will teach you to live, love and laugh!
I could end the post there, and I'm sure you would all feel fulfilled, but I wanted to share this fabulous idea to do with your children while it's still the beginning of a new year....

Their list of questions for the interview includes....
cereal
vegetable
drink
toy
TV Show
game
book
restaurant
holiday
animal
If you could change your name, what would you choose?
What do you love about each person in our family?
Where would you like to go on vacation this year?
What are some of your wishes for this year?
Oh, I just think this is such a simple, easy and great idea! Enjoy doing this with the kiddos starting this year!
I just wanted to remind you that the kick-off party will be here before we know it. There will be three grand prizes (and boy oh boy are they grand)! There will also be daily giveaways. I would like the daily giveaways to be something handmade, to support the many mom-preneurs out there. I'm eyeing a few things on etsy, but I wanted to ask everyone's opinions. Do you have a suggestion for the daily handmade giveaway (under $40)? Let me know if there is an on-line boutique or etsy vendor you'd like me to consider.
Remember to spread the word....

Copy & paste the following code into your blog or website
Jan 7, 2009
Live, Love and Laugh

When I found out I was pregnant for the first time, I was very excited but very fearful of having a still birth. After I found out I was pregnant, I didn't buy any clothing for my baby and didn't get anything ready until the last minute. I was afraid to jinx things.
I got pregnant 4 months after my 21st birthday. I was young and had a 6 year old step son I was raising. I was excited to have a baby of my own to love and care for. I had a normal pregnancy and only one sonogram (they didn't call them ultrasounds like they do now) when I was 6 months along. It didn't show any problems but they couldn't even tell me the sex of my baby either.



I coped by learning all I could, getting my hands on anything I could read. I didn't have internet until about 10 years later. I couldn't find much information before that about Translocation Trisomy 21. I'm one who gets over things quick and moves on. I didn't grieve long, less than a few weeks. So I really didn't need help with coping about her having Down syndrome. The heart issues were another story. They scared me for years.
Almost two years after Mercede's birth. I gave birth to another daughter with DS. Cheyenne also had the same heart defect as Mercede. We discovered her heart defect in my 8th month of pregnancy. It was an AVCanal defect. The same heart defect her sister had, and one that is very common in babies with DS. We then knew she had DS too, we had declined any testing, except for sonograms and fetal echoes.


Mercede was hospitalized a lot as a child but now is doing well. She still has to have more heart surgery in the future to replace her mitral valve and she will always be on heart meds. But you would never know it to look at her. She loves to dance, she loves working out to Richard Simmons video's. She is active in pottery class also....


Mercede, while my most annoying child (trust me, she is, lol) is also the one that doesn't take others for granted. Mercede loves to be around other people that she can help. Mercede has fed the sick and the dying and also cared for them. She has laid beside her great-grandmother (whom had colon cancer) and rubbed her head and spoken softly (which is a feat , if you know Mercede) to her during her Grandmothers last days. She will often tell you about feeding her Aunt Mary (whom passed of Alzheimer’s last year) and what her Aunt didn't like to eat. She will also tell you they are with Jesus now. Mercede had a best bud for years that she liked to sing to and dance with. Her friend had CP and was 20 years older than Mercede. Her friend could not talk but could smile and laugh. She smiled and laughed alot when Mercede was around. Then a year ago her friend passed on, it was very hard for Mercede. But soon there was someone else to take her place. A woman with Down syndrome whom also had Alzheimer's. Mercede could make her smile and laugh. There would be a light in her eyes when Mercede was around. A few months ago, Mercede also lost this new buddy. But Mercede moves on, as she knows they are with Jesus now. When Mercede stays with my mom, her favorite thing to do (besides eating potatos) is visiting the nursing home with my mom. When she talks on the phone to my mom she will often asked how someone is that she is worried about. She is also getting frustrated with me, because I keep promising her that I will take her here to visit some church friends in the nursing home and I haven't done it yet. She is also very spiritual. She will often raise her hands in praise in church and also cry when the mood hits her. I don't know how much she understands about God, but it is obvious she feels his presence. At the same time, she can spell t-r-o-u-b-l-e!! At home, she is obsessed with the bathroom and can't stand to have stuff on the sink. She is always hiding the hand soap and hand towels. She hides shoes all the time. You can fine one, but not the other. I will find them in my bookcase, out in our fishing boat. It took me a year to find the match to my favorite pair of shoes. She will argue about anything. If I give her something to eat, she will say "I don't want it, I'm full", So I take it away and then she says "Nooooooooooooo, I want to eat!" So I give it back and then it goes on and on this way til I am pulling out my hair. At school she behaves herself, but on the school bus....................oh my. She has a collection of bus tickets. Just a few weeks ago, she choked the bus driver with his seat belt while he was driving. Now she didn't actually choke him, but she did have it pulled around his neck and he couldn't get it off. Course she giggles like crazy thinking it is funny. She also threw his jacket out the bus window. This is one of her favorite bad things to do on the bus, throw things out the window. She is like the character from the "Problem Child" movies, when she gets on the bus. She will be 18 this year and is only 4'5". Since her open heart surgery (mechanical mitral valve put in) she has gained like 10 pounds and now weighs 82 lbs which is fat for her!! lol When we go out to eat, they still give her childrens menu's and "Hey, you can't complain about a cheaper meal". Now her big thing is scratch off lottery tickets. She loves scratching them off.

Mercede was a huge Barney fan while growing up. Needless to say, a mom can only take so much. So I banned her from Barney. Mercede was so upset that she went thru all my videos looking for something she liked. Then in the corner cabinet, under five inches of dust, she found Dancing to the Oldies. For the next few years Mercede worked out with Richard every single day. During the summer she worked out 3 hours a day, while I laid on the sofa eating chocolate and cheese curls shouting "Go Mercede! Go Mercede!" She was his biggest fan........well okay, probably his smallest (wink, wink). To cut a long story short. I pulled Mercede from school so she could attend a Woman's Conference in our home town that Richard Simmons was going to be at. Surrounded by hundreds of large women (me being one of them), little, tiny, skinny Mercede worked out with them/us. She was near the front of the stage and Richard called her up on stage. Mercede was so happy to meet him! When she does that mouth open, eyes rolled up toward heaven look, you know that she is on super excitement mode. He pulled her to the front of the stage, and then Mercede lost it. She slapped him away. While we didn't get THAT photo, we did get the priceless look on his face after it happened.
Richard Simmons with Mercede & other adoring fans

Cheyenne, 2008
Cheyenne is currently not on any meds and doing great. I was so excited to give birth to her. Mercede was such a joy that I actually wanted Cheyenne to have DS too, and was granted that wish.
She watches a lot of TV. She can stay at home by herself. She is such a flirt and has been for some time. At times it is funny and other times disturbing. lol She comes home every day from school with a story about either "her boyfriend" or the boy she can't stand. Of course these are the same boy. Sometimes she will be so mad she will go into her room and slam the door and throw a book at it. My husband has been worried especially when she said this boy had pushed her, he told me I needed to talk to his mother. I have known this boy since he was a baby (he is a year younger than Cheyenne) and he like her, has Down syndrome. His mother started laughing, when I told her my husband says I should talk to her about it. She was like, "Has he seen my son?" Nope he hasn't. Her son is tiny compared to my girl. She is much taller and much heavier. Like she said, my daughter could beat her son up!! lol ( I do know that he hasn't hurt my daughter, as the bus driver keeps me informed).
Every year she attends a summer camp and there is always a "summer crush", it is normally one of her camp councilors also. I didn't get a picture the first time but did the next two times. She will keep the picture until the next one. lol Well his and Brad Pitt’s picture, and Omar Epps (from House MD). In the past she had a crush on my husband. Boy this was a rough one. My husband is her stepfather and when we were dating, you could tell she had a big crush on him. When we got married, then she was horrid to him. She wasn't very nice for the longest time. Then she had, wait has, a crush on my sister’s husband. That is quite funny, because she all but ignores my sister and everything is "Hi Matt", ""What you doing Matt" etc…. Now, the most embarrassing crush has now developed. Last week, I couldn't find her at church, then I turned around and there she was. I can read her smile and see her giggle. Darn it, if she isn't flirting with our minister. I have to look back on my crushes. There were several teachers and even a cousin! YIKES, but NEVER a minister, of course mine were all in their 70's.
In 2004, I gave birth to Aysha, my first child without DS....
Aysha, 2008
Aysha is a translocation carrier like I am, she will have the same chances to have a child with DS too. She has been a handful since her birth. She isn't anything like my other two babies were. I think the next time I have a child, I'll be hoping for another one with DS.
Mercede will probably never be able to have alone time, she is too trusting of strangers and also doesn't react to danger appropriately. Both she and I are hoping that we can find funding to get her placement with one of the organizations here in town where she could live in an home with a few roommates. I didn't know how she would do with a workshop but she is working in one in a work program at school and liking it. I know she will spend time volunteering in nursing homes, as that is one of her favorite places to visit.
Cheyenne I can see working doing cleaning work, she loves to clean. I see her living semi-independent, as she can now stay home hours by herself. I see her one day getting married (if she could settle on one guy, lol).
My advice to other parents is to live, love and laugh....
If that doesn't work, Xanax and Paxil are great!
I work for an organization that supports people with disabilities and have ran across so many wonderful people with Down syndrome. I think everyone has a special talent, you just have to look for their abilities not disabilities....
Bernadette Resha
One of my favorite artists is Bernadette Resha . She is a married woman whom has Down syndrome and is an incredible artist, among other things.
The Tulip, by Bernadette Resha
Her display of Art can be found here.
For more information about Down syndrome, go here.