Thursday, April 24, 2014

Like Si on Facebook!

The Life of Si

I was off of Facebook for a long time... but I want to do all I can to spread awareness for my little guy and all his friends...so I'm on.  Like him and keep liking him... post and share to help spread the word!  I'll also update the page whenever I have a new post on here!  So.... See you there!!!

Tuesday, April 22, 2014

He answers Prayers.

I know this because.... I prayed for Si.  I didn't remember it right away, but as I was watching him this morning.. and when I watch him, I also feel God, so I remembered about 2 years ago.

A friend and I were driving home from somewhere. (I don't recall where) We were talking about other friends and their God given mission for their life.  We were wondering where our "mission" was.  We were envious (in a good way) of their passions in life.  They had a "calling", I guess you might say.  God had placed something on their heart or in their life.  Anyway, we wanted one.  I remember us both deciding to pray for it.  I did.  I prayed for several weeks.  I knew were I had been passionate all my life, but I didn't know how to make it a "calling".  I began to want one desperately.  One of my closest friends had adopted and I had prayed with her before even starting the first adoption for weeks that her path would lead to adopting.  We prayed, with others, that God would put a little girl in her family.  He was faithful.  He was faithful and second time.  She continues in her passion to make adoption a way of life in His Church.  I have other friends that are passionate about caring for the grieving.  They have lost and are passionate for bringing hope to others.

So, I knew my loves and my passions.  I have always had something inside me that has a love for other cultures and races.  I believe God put that in me.  So, I got involved in the ministries that bring me in contact with my loves.  My brother has lived with HIV for many years.  I have a desire to bring understanding and a love for people with AIDS.  Homosexuality and HIV is something I have been a part of since I was a child and I have a strong desire to show love and hope to people in that area.

So I have not been passionless.... I just have lacked ... well, something... I know, now, it was someone.

Those 2 years ago I prayed and prayed.  I was pregnant.  I was devastated by the loss of that baby.  Even more so than the 2 other losses before.  Then I was pregnant again.  I didn't pray for this one.  I prayed, selfishly, for me. Other's prayed for him.  When I finally started praying for him, I was praying out of guilt and fear that God was going to take him from me.  I thought something was wrong with him almost the whole time.  We had tests done...I called them the old lady tests to make sure he was ok...No health problems associated with trisomy 18, 21 or whatever else.  We came out relieved with a positive ultrasound that showed he was good... no health problems.  I remember sitting in my friends house and feeling so nervous.  I told her that I couldn't shake this feeling that something was wrong.  I felt like God was going to punish my baby because of my feelings of not wanting to be pregnant.  She assured me that she was pretty sure God did not work that way.

God was working.  He had been working and preparing me.

9 years before, Ian's ultrasound had shown a marker for Down Syndrome on his heart.  The doctor had told me we could do an amnio to be sure or we could just wait to see if it disappeared in the next ultrasound.  I waited.  While we waited, we had our Small Group pray for our baby.  We prayed that the hole would be gone by the next time and that we would have a perfect, healthy baby boy.  I remember Rob and I talking  a little about the possibilities.  I had told him that I felt like God wanted me to have a baby with Down Syndrome.  I didn't know much about it then.  I did have this deep feeling about it.  By the time the next ultrasound rolled around, the marker was gone and we were pleased, several months later, to have my sweet baby Ian in our arms. :)

The labor and excitement of having this baby, 9 years later, and not being pregnant anymore over took any uneasiness that I had been having all 9 months.  He was delivered and they laid him on me.  The first thing I saw was his little hand.  I squinted and was briefly confused.  His hands didn't look like the 3 previous tiny hands that had been laid on my in the very same way.  He had short stubby fingers.  I said something out loud, but Rob, I think, thought that was a funny thing to notice.  Why did that matter?  They took him and cleaned him up... but his oxygen level was down.  This wasn't unusual for me... Seth was the same way and they had flopped Seth on my skin to skin and his heart and oxygen went right back to normal.  God is awesome that way, making mothers 
a healing spirit to their babies.  But when they put Si back on me, it did not help.  They took him and worked on him some more.  The doctor, that was on call, not my own... came over to me and put his hand on my arms and I saw him praying over me.  I looked an wondered what was wrong.  I new something wasn't right... just by... something...I guess you just know after having four babies.  The nurses decided to take him to the Nurse practitioner to see what needed to be done to help him.  I was without him for hours.  When Rob went to find out about him... that's a story he can tell.... he came back to my room and looked as white as a sheet.  He was scared but I didn't know why.  He told me that the nurse had told him that Si looked as if he had down syndrome, failing kidneys, heart problems, etc... I don't even remember the list.  I asked if he would live through the night and she said he was stable but he would need to stay in the NICU.

I went through several thought processes that night.  Lots of prayers.  Lots of fear.  Lots of guilt.  All I wanted was God to let me keep this baby that I only was able to hold for about 1 minute.  I had really only laid eyes on him for a minute or 2.  I prayed for his life.  Then the following days, I prayed for Rob and my kids.  I knew that I was ready to take on this baby whether the genetic testing said he had Down Syndrome or not.  But I wanted Rob to be ready.  My worry that I had never considered before was how that would affect the other kids.  So what do you do when you need to know something badly???  I Googled it.  Search: how will my other kids be affected with a baby with down syndrome?  :) :)  That was an easy answer.  All around, the sites told me that siblings of a baby with Down Syndrome is ... more loving, more accepting, more compassionate, more likely to go into the field of Special Education as adults.  PERFECT! I'm good.  I just needed God to take care of these  health issues and feel like Rob was comfortable with this, and I was good to go.

God answered both of these prayers.  He is Faithful.  This isn't the only answered prayers.... if you've actually made it through this long-winded post, you'll know he answered FAR more than those last 2 prayers.  He has been answering my prayers for 10 years.  He had been preparing me for this time in my life for, probably, much much longer than 10 years.  My love the persecuted and different, for lack of better words, was all moving me forward toward this Calling.  He gave me the passion that I prayed for 2 years ago.  It's strong... it made me join a group that made me uncomfortable to begin with, because I lacked understanding... it made me control my competitive nature because Si is going to develop at his own rate... it's made me not shy from people looking at me, but long for it so I can show Si's humanity...it's even made me write these crazy serious and seriously long blog posts.  All to say that people with down syndrome are incredibly awesome.  Si is going to change many people in his life.  He has already done it.  I will be watching along beside him.  I will help when I can.  I will encourage him to tell his story.  I will help him to know he is special and different and that God made him this way so he can show people God's power.  I will try to help him understand why people stare at him and how to smile and show them Jesus's nature.  I will encourage him to talk to people about what Trisomy 21 is and how he is just as valuable in God's Kingdom.  I will pray for his every move toward God and in God's plan for him.

So this is what God has given me.  It's what I asked for.  He not only answered my prayer... He changed my life in the process.  My prayer, now, is to not squander this gift and passion.  But pray every day to be aware of His Presence and what He wants me to do to show His Passion each day.
I pray that my new passion will show His True Passion.

pas·sion
ˈpaSHən/
noun
  1. 1.
    strong and barely controllable emotion.


    2.  the suffering and death of Jesus.
    "meditations on the Passion of Christ"
    synonyms:crucifixion, suffering, agony, martyrdom More

Monday, March 24, 2014

It's not just that I wouldn't change him....It's more that I'm sad if I think that he could have been ordinary.

I've been reading blogs and posts about how they wouldn't "change their baby with down syndrome for anything".   I want to agree with that, but it's more than that for me.  I have a very active daydreaming imagination.  I can think about someone dying and be crying in 10 minutes like it really happened.  So as I started imagining Si not having Down Syndrome, I was so sad.  It felt like I was being robbed of my future with him.  Like all my dreams I have dreamed for him and our future was lost.  I have a dream that Si and I will someday own a Toyota Tacoma truck and he and I will drive around town together in this truck that we will both love.  I think about teaching him to drive it.  When I imagined him not having DS.... well, that would be crazy.  He wouldn't want to hang out with me and spend time riding around in a dumb truck with his mom.  That's just one of things I see in our future.  I dream about what God will do with Si's life... of how He will use him to change people to change His world.  I have these dreams about all my kids, but I love how with Si, I can count on being a big part of it.  I'll have this front row seat to it.

I know parents go through a "mourning" for the child that he dreamed of, when they find out about a DS diagnosis.  I must have done the same thing to some extent, but I wish I could convey how incredible it is to have had this unexpected awesomeness thrown our way.  So now, I have this reverse "mourning" for a child I'm so thankful I don't have.  That's cheesy, right?  But it's also truth.  Like I've written before....  I thank God, literally, every time I pick Si up.

 I know these little people feel the same way.  
What would we do if we weren't teaching this little guy how to crawl, hug and say "more".  
Si and his best Friend.


Thursday, March 13, 2014

Getting' Ready for The Big Day!

I'm getting excited for our first DS Day where we are not in a daze.  I'm prepared with these handy dandy post cards to help spread the word and the cuteness.  Pin and Post to help bring awareness and acceptance to all the individuals with Down Syndrome.  Si is Loved, Respected and We are striving to bring him Full Inclusion in his Community.













Saturday, February 22, 2014

"Special Ability"

We were blessed to go to the Near His Heart dinner the other night in Auburn. It is a yearly dinner for families with children with special needs. We had an incredible time and were overwhelmed by the hospitality and love that was displayed by these volunteers.  All 4 kids went to their own childcare. I had talked to Ian and lily before hand, like I always do when we go to these events, to remember their manners and to be patient and kind to everyone.  They affirmed my request and ran off excitedly.   Rob and I attended the dinner and listened to the speaker, who has a son with Down syndrome.  I really can't put into words our experience.  It was amazing and doubly amazing that Rob only tried to cry 3 times. So after picking the kids up from their 3 hour vbs type experience, we piled in the car and I asked Ian first, "Did you meet any kids with special needs? And tell me about it".  He said yes and told about a boy  he hung out with and for what I could put together, he was autistic.  So Ian had a good time.

Lily was next. She said "Well, I did play with some kids but I don't know what their Special Ability was!"  That did it.  The show Glee used the phrase "handicapable" and I loved that. But this is it!  We now refer to it as "Special Ability" or maybe even "Super Ability" :)  Leave it to Lily to teach us again.


Friday, February 21, 2014

Just some quickies....

Just a few little pictures that I had to post.  

 So, we are new to an intergenerational Life Group at church.  I love it because the kids are studying with us.  His is Si and one of the Elders of our church and Life Group Leader, praying.  Just about the most precious thing I've seen.

 My oldest and youngest.  They are so handsome and so sweet.  They love each other so very much too.

 Si's first time to pull up to his knees in the crib!  I was, literally, jumping for joy. :)  Now for crawling....

 Lily and Si.  He is the ONLY person she will cuddle with. :)

One of my favorite pictures of my newest favorite guy and my original favorite guy.  This is my brother and Si at his birthday party.  Ever since we have been in Montgomery, my brother has made a point to come to every birthday party we have for the kids.  As we have added to our number, that is no small feat.  He is at every party and if we don't have a party, he comes bearing gifts.... not only for the birthday kid, but for ALL of the kids.  So he has requested that we quit having kids. :)  I love him so much and I love how he loves my babies.  He always spoiled me so I guess it's only right for the spoiling to continue.

 Our buddy, Addi, and Si playing at her house.
Poor red cheeks when the weather was so cold and windy. :(

Friday, January 31, 2014

We'd try to love him.

We were all in the car coming home from school.  So, every once in a while it comes up about Si having Down Syndrome.  I'm not sure the exact conversation train, but I ended up saying...

"What if Si didn't have Down Syndrome?"

Ian and Lily:  (almost the exact words and timing)  "Oh! I'd still love him anyway!"

I wasn't expecting that... Lily is always in disbelief when she remembers me telling her that 90% of people who find out their baby has down syndrome abort them.  She usually bluntly says, "The people kill their babies, just because they have down syndrome?!"  I am a little more tactful and politically correct than that...  I always tell her not to speak so harsh about people "killing" babies.... that all we are responsible for is showing people how cool it is to have a baby with Down Syndrome.  We can show people that Si is just like any other baby, but just..... well... cuter.  She loved that.  She usually is the one that brings us back to reality that Si isn't the cutest baby in the world.  She says, "mom, some people in other countries have cute babies and they think their baby is the cutest.... they haven't seen Si before, so they say the same thing about their baby."
She's very logical.

So I thought when I asked that question... What is Si didn't have Down Syndrome?  that I would get something like.... well I don't know... I guess something.  The more I try to think of an answer, the dumber the question seems.

Anyway, My point is.... my kids are so awesome.  That's all I wanted to say with this post.

And, we would all still love Si, even if he didn't have Down Syndrome.  We'd try to love him, anyway....