Thursday, November 29, 2012

Christmas Shoes for Sofi

Dear Life,

We are wracking our brains trying to come up with creative ways to fundraise money to fund our adoption to beautiful Sofi Rose. 

 The fees are crazy expensive...everything costs so much money.  But none of that matters to us...all that matters is bringing home our sweet girl...and having her be a part of our forever family.  I'm sure that some of  you are wondering what all of that money goes towards!  Well...here goes:




PROGRAM FEES PAID TO our adoption agency in the US

Application Fee (PAID) $700
Agency Fee $6500
P.A.R. (Refundable) Deposit – $500

FOUNDATION FEES: 3rd PARTY FEES PAID THROUGH agency – FEES DIFFER BY FOUNDATION

FOUNDATION “A”: 1000 EUR due at match, (PAID)  1000 EUR (PAID) due at dossier submission, 4000 EUR due prior to 1 st trip, (1000 PAID)
2000 EUR due prior to 2nd trip
 (We've had $3000 euro granted us in Europe thankfully, which goes towards this).


Additional Expenses incurred by family:

HOMESTUDY/DOSSIER EXPENSES:

Home Study Estimate $2250 (ALMOST PAID)
Post-adoption/Post-placement Report Estimate (requirements and cost varies from state to state) ($300-$1000)
Adoption Education Internet Courses ($30-$50 each)
CIS Filing fee $720
Fingerprint Charge (2 @ $85 each)
Passports (2 @ $170 each) (PAID)
Document notarization (cost varies) – estimate only $500

PRE-TRAVEL EXPENSES:

2 Trips - Round Trip airfare for 2 adults (@ approx $1000-$1500 per person, per trip) estimate
only $4000 +
Child’s one-way airfare (cost varies, estimate only) $500 +

IN-COUNTRY EXPENSES/FEES: Estimates will increase due to daily exchange rate for USD to EUR

Lodging and meals (2 people – 5-7 nights each trip) – estimate only $100 - $200/night $1000+
Medical for child’s Visa – estimate only $100
Child’s U.S. Visa $230
Incidentals (amount varies depending on family desires and tastes) varies

CRAZY, right?  That is why we appreciate all our friends, family, Spina Bifida friends, strangers, have done so far.  We have far to go...but we are confident we can do it.  Our big fundraiser at the moment is the collection of used shoes.  We are collecting gently used, wearable shoes.  They can be any shoes.....dressy, casual, flip flops, childrens, mens, womens, babies, cleats, etc.  They cannot have holes and they must match.  That is it.  We have seen a huge amount of people willing to clean out their closets and give us their shoes.  Many people are SHIPPING their shoes to us.  AMAZING.  IF we can get 5000 pairs of shoes, we can EARN 3000 dollars.  Awesome, right?   

Thank all of you....may your holiday season be amazingly beautiful.  



Sunday, November 25, 2012

Sunday Musings

Dear Life,

As I was in the hospital this weekend I was thinking a lot about Sofi.  


As I sat there I was SO grateful for Kumaka's AMAZING orthopedic surgeon who came to the hospital on Friday (Black Friday....you know...a four day weekend fora lot of surgeons) just to operate on Kumaka.  Just a few hours to work on MY BOY...that is not typical...at least not in our past medical experience.When he was out, and put in his room, we received excellent care.  They were going to put him in a shared room, but when I asked nicely, they put him in his own room.  They were so courteous, and so conscientious and LOVING to my little man.  Not only that, but when I was stressed at one in the morning because he was hurting, the nurse asked me if she could get me anything.  When I said "Not unless you can find some ice cream" (totally kidding by the way)...she said I will bring you chocolate and vanilla.  WOW, right?  While I pondered all of this on Saturday, watching my boy happily playing the Wii, watching his favorite shows, and playing games, I thought about Sofi.  I thought about the care she is NOT getting right now....and that no one is there...spending the night with her when she is hurting.  I thought about nurses doing bare minimums because that is the way it is there.  Then I thought about the nurse's tech who came in every so often, with his super hero shirt and his happy demeanor doing whatever he could to make Kumaka happy and I was sad for Sofi.  Sad that for three years she's known such a solitary existence.  Even though there are other children there, she is in a crib most of the day because she can't walk.  I thought about Kumaka's many years of physical therapy, of the AFO's he's received (a pair a year since he was less than a year old), his wheelchair, his walking equipment, his hand bike, the adaptive sports he will be doing, and I realized how very blessed he is.  And how blessed Sofi will be when she gets here.  She will be cared for and loved by so many....not just our friends and family but also the staff at CHOC, the community who have rallied behind her....everyone.  She will get a wheelchair, AFO's, physical therapy, occupational therapy, and speech to help her reach milestones. She will not be confined to a crib anymore.  She will see the beach, the park, Disneyland, she will go to church, and of course she will wear pretty dresses and bows (couldn't help putting that in).   

This morning, Kumaka woke up crying.  When we asked him  why he was crying he told us he had a dream that he had a new daddy.  Stuart held him and told him that he loved him and he would always be his daddy.  I asked him what happened in his dream when I realized what prompted the dream.  He asked me where Sofi's parents were a few days ago.  I told him her parents took her to the orphanage, so she needs new parents to take care of her, love her, and be her forever family.  That must have really stuck in his head.  So we explained that we would never leave him, that we love him so much...and that is why we want to bring Sofi here...to help her have a mommy and daddy too.  That made him happy.  







Tuesday, November 20, 2012

Mending hearts

Dear Life,


So grateful for girls time.  All I had to do was text this to Sarah:

"So in a funk".

She asked me why....in three sentences I tell her and in one sentence she says:

"Let's meet on Tuesday".

How grateful I was to go by the harbor....sit outside with my friend and drink our diet cokes...talking about life...our kids...and how to get through stuff.  Sometimes you just need a little pick me up to help you realize how blessed you are and how amazing life really is. 

Our conversation was like it always is...all over the place...from childhood to adulthood and beyond.  It's  crazy how many side conversations we have when we get together.  There is one thing Sarah shared with me that was so powerful....I just have to share it.  

After talking in length about something troubling my heart....Sarah shared with me how she gets through the things that really break her heart.  

"When my heart is so heavy I can't bear it one more moment, I close my eyes and envision a  box....and I put all of my heartache...all of my troubles in that box.  Then I wrap up that box, and give it to the Lord.  When I humble myself...and give my troubles over to Him...suddenly I am lighter and I know that He will help me and it's all in His hands." 

 I wept as  I felt the truthfulness of this statement.  I knew I needed to lay down my burdens to the Lord.

 28 Come unto me, all ye that labour and are heavy laden, and I will give you rest.
 29 Take my yoke upon you, and learn of me; for I am meek and lowly in heart: and ye shall find rest unto your souls.
 30 For my yoke is easy, and my burden is light.


And I know this to be true...as my heart was heavy I felt prompted to text Sarah.  It was Sunday night...at 10 pm.  We NEVER text that late.  She answered me.  And I was comforted.  My heart lightened.  As we talked to day...my heart lightened.  God knows my heart...and provides the way to hear the messages I need.  

So grateful for friendships that help mend my heart.




A break...and Sofi

Dear Life,

I woke up today to see Kumaka's right leg (the same leg he broke earlier this year) very swollen and warm to the touch.  Because he just came out of a cast, I was thinking maybe he had some sort of infection.  I made some phone calls trying to figure out where to take him, and finally decided to take him to the emergency room.  As I was driving to the hospital, I started to think about Sofi.  I was thinking how I would go about doing this with two children with severe needs.  I was wondering if I could take the stress of two children having to go to the emergency room for various things.  As I was searching in my heart...and really honestly contemplating these things...I thought about the reason I was stressed.  I was stressed because I love Kumaka so much, and it makes me so sad that he has to go through these things.  I don't ever begrudge my time going to the doctor or the hospital...it's just part of life.  I would do any of these things for ALL of my children.  Then I thought about Sofi.  Sweet Sofi....I would do any of these things gratefully for her too.  The thought came to me....she's alone.  All alone.  Yes there are workers at the orphanage, but none of them love her or care about her well being.  They make sure her very BASIC needs are met and that's it.  No one snuggles with her, or holds her hand.  No one strokes her hair and wipes her tears.  No one reads her books or sings her songs.  No one goes out of their way to give her anything extra.  That breaks my heart.  Of course I will do these things for Sofi...and I will do them gladly...grateful for her sweet spirit in our family.  Oh...and Kumaka has a broken leg.  Again.  Awesome. 




There are some wonderful people doing wonderful things to help Sofi....there are so many ways...please take a moment....look at the fundraisers....and if any appeal to you...please consider buying from one of these lovely friends trying to help bring home Sofi.  We are at 11% of our fundraising goals.  That is HUGE.  And it couldn't happen without all of you! :)  We only need 400 more dollars to be able to pay for our total homestudy.  That is HUGE..once it's paid for and completed we are that much closer to bringing home Sofi.  Please consider helping us reach our goals for Thanksgiving.  

My friend Sara is doing this:



Make a purchase at babysnazz.com using coupon code


sofi-rose


SAVE 25% off your order


+ 25% of the proceeds go to 


bring Sofi Rose home!


coupon valid until 12/31/12

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~


Tracy Wells and her family created a store called  ALL MY HEART AND SPINE.  They started it to raise money for their walk and roll.  
Nov 15 thru Dec 1st, All My Heart and Spine is going to give profits from all sales to the Jensen family to help bring Sofi Rose home.  


~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Amy, Kumaka's Wish Grantor (we call her wish fairy) from Make a Wish is a Creative Memories consultant and is offering this great deal with her Creative  Memories Digital Cards:  
Creative Memories cards are on sale 20% off until
 January 1. I am donating 15
% of all my sales

 between now and January 1 to Tracy Alexander

 Jensen to help bring Sofi Rose home. So you can get 

your beautiful christmas cards done, save money, 

and help the Jensen's. If you want to place an order, contact me or use my consultant number (12471736)

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
My friend Kathy is having a Thirty One Gifts party for Sofi.

 Remember that for every $35 you spend, you can order an exclusive Medium Utility Tote for just $5 - and for every Medium Utility Tote sold, Thirty-One will donate a Thermal Tote to Operation Homefront!  get to your party by Thirty One Gifts  then "locate my consultant" - my number is 176823




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Our normal 5 dollar Tuesdays (tomorrow).  We try to get as many people to donate at least five dollars.   Pack your lunch tomorrow....skip your latte.....don't buy your favorite treat....and donate it on Sofi's YouCaring Page.   It's been incredibly successful...and it's proof that just a small amount can make a huge difference.  





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Last but not least....David from Mimi's Jewelry in Fountain Valley is in the process of creating a diamond pendant I have fondly named "Sofi's Heart".  It will be worth $1800.  
It will be white gold with diamonds on the bigger heart and rose gold with pink sapphires for smaller heart.  It's going to be gorgeous!!  The raffle tickets are $10 each and the raffle will be going on until February.  What a great valentines gift~  Diamond Fundraiser

Thursday, November 15, 2012

Sexiest Man Alive

Dear Life,

People magazine...it's what people are talking about.  Who wouldn't want to pore over a magazine with a whole lot of hunky men in it?  But Channing Tatum, although you are a great looking man, I have to disagree with People Magazine.

19 years ago I met this amazingly good looking man. 


 One of the things I really loved about him was how kind he was.  He was a gentleman.  He didn't objectify me.  He was my friend.  We had a great time being together, having fun.  We both liked other people....but over time I started to have a crush on him.  So....I decided to make a bet with him.  Our bet?  I wouldn't call the boy I was "dating" (cause he just wasn't that into me) and he wouldn't call the girl he was "seeing" (cause she was just mean to him).  Whoever won would get an all expense paid for trip to Disneyland.  Well.....I won.....and let me tell you something....I had never in my whole life been treated like a princess before until that day.  He bought my ticket to the park, he paid for my food the WHOLE day, he bought be a pretzel and a balloon.  And that night I kissed him for the first time.  He had my heart after that day.  

Over time, this man became my best friend.  He was so respectful to other people, so patient, so loving, so giving.  How do you not fall in love with that? 


 Eventually he became my husband.  He became an amazing father of a boy....and then another boy....and another boy....and another boy....and yet another boy.  

He became a coach, a cub scout leader, a boy scout leader, and finally a caretaker.  He is loyal, faithful, and loving.  He works hard every day at work, and comes home and helps me with the household. 
 In his spare time he coaches basketball in the community and serves at our church.  He works on our cars, and sometimes the cars of our friends.   All of these things are the definition of the sexiest man alive.  So, sorry People Magazine...I beg to differ.






















I am married to the sexiest man alive. 



















Sunday, November 11, 2012

The gift of life


Dear Life,

Today I feel prompted to talk about something that is a little sensitive. The topic is life...the gift of life.  It's a hot topic...people are very passionate about their position.  I don't want to take away someone else's opinion....just share mine and why I feel so strongly about it.


I want to talk about how a woman feels when she is pregnant....and has happily carried that baby to second trimester....and is waiting to find out if they are having a boy or a girl.  It's an exciting time...you may or may not have bought some clothes....if it's your first child you may have started putting the baby's room together.  Everyone in your life knows you are having a baby.  And then it happens.  You go to your ultrasound....grasping your husband's hand excitedly....and suddenly there's a knot in your stomach as you watch the tech's face drop...or the doctor doesn't talk for awhile as he's looking at the ultrasound pictures.  Suddenly the happy, beautiful, sunshine day has turned dark, dreary and so very sad.  You are told your child has Spina Bifida.  You are blown away.  You don't even know what that means.  You  cry and you ask what it all means.  You are told things like: your child might not walk, might be cognitively delayed, might have bowel and bladder problems, might have brain damage, might not live.  You are told that your child will not live a productive life.  You are told you have a small window to terminate your pregnancy.  In our case we were 19 weeks pregnant.  Almost half our pregnancy.  When you see ultrasound pictures, the "fetus" looks like a baby.  In your heart this is a baby.  And how do you process all of the doom and gloom the doctors tell you?  How do you figure out which path to take when someone from the medical field that you trust tells you it's okay to terminate your pregnancy?  When you are told worst cast scenarios, but in reality the doctor can't tell you exactly what to expect until the child is born.  How can we think about doing something so permanent to a child who has no voice?  Aren't we, as parents, supposed to be their voice from the very beginning?  And shouldn't the medical field support that notion?  No one told us that our child would have such a sparkly personality....that he would have the strongest disposition and not let anything stop him....no one told us that he would melt our hearts every day.  Why?  Because they can't....but they also can't determine what kind of challenges the child will have from an ultrasound. So what does a parent do with that?  Where do they turn?  Who do they trust?  They go to the internet....they search day and night...for hope...for a sign of joy in a scary land.  If they are lucky, they will find some pretty amazing parents who are willing to share their life with them to give them the strength to go through the hardest thing they have ever been through.  If they are lucky they see some pretty amazing children LIVE.  And if they are lucky....they realize that life is a gift...and just because their child has a diagnosis....it doesn't mean that is who they are.  All of the children I know that have Spina Bifida are first and foremost children.  They are people....they do amazing things...yes...some things take longer for them....or maybe they won't do some things that other kids do....but that is just a small part of who they are.  They have smiles that brighten a room....they have strength that you never thought a child could have....they are the hardest workers...and they love their life.  Their life is a gift.



 I feel so blessed to have an amazing group of women around me who are willing to put themselves out there, share their innermost feelings to help other soon to be mothers.  I am so blessed to have mothers who share their daily struggles and joys...so that we can all get through the highs and lows and know that we are all going to be ok.  There are scary moments...we've all had them...and been there for each other.  We've also rejoiced together...these women make my little world complete.  They laugh with me and they cry with me.  When I have questions...they are there with answers.  Not one of us regrets this gift we've been given...it's actually the opposite.  We feel humble, blessed, and incredibly happy that these children are in our homes. 

I feel strongly that it is my responsibility to talk about this....to share these feelings with all of you.  You see, there might be a mother...a scared, confused mother.....who doesn't know what to do.  They might read this and feel a little hope...they might ask me for more information.  And then they can enter this circle of mothers...this strong group of amazing people.....and KNOW that they can handle anything....and that this life is a gift.

Thursday, November 8, 2012

What? We're adopting? How?


Dear Life,

Adoption.  My husband and I always thought adoption was an amazing thing.  For other people.  We have five beautiful boys, and our plate is full.  Our oldest is eighteen and our youngest is almost six.  We have battled ADD with our oldest son and are currently on quite a journey with our youngest son who has Spina Bifida.  You can read about him HERE.  

When  we were in the beginning stages of this journey called Spina Bifida, we were often overwhelmed, and felt grateful that Kumaka came at the end of our little family because there were times we felt like we never would have had any other kids had he been first.  As he gets older, we have become wiser, we have learned to be patient, to deal with the fact that we are not in control of his health.  We have learned to roll with the punches.  Although we never ever like seeing our baby in pain or suffering in any way, there are times when we feel like we have been truly blessed because of Spina Bifida.
`
We have seen miracles, we have met amazing people, and our little man brings us so much joy every single day.  His smile brightens even the gloomiest day.
 One day I asked my husband if he would ever consider adoption.  He looked at me and said of course.  I was a little surprised he so readily agreed that he would consider it.  Still, we never really thought we even qualified for being adoptive parents.  Hello, my husband is 52, we have five kids, and let’s face it….we are not wealthy people.  So yes, we both felt like it was something we would do, but it wasn’t something we felt we would be able to do.  One day I was looking at an agency, at some of the kiddos , and I thought I would just contact them and find out what the criteria was to adopt a little girl with Spina Bifida.  It wouldn’t hurt to ask, right?  The agency was so nice, and the lady I spoke with sent me pictures of a few girls that had Spina Bifida.   (Here is where I confess this ISN’T the first time I had perused various websites,  saddened by these children in orphanages all over the world.)  As I clicked open to look at the pictures, one sweet little girl with huge brown eyes and brown hair stared out at me and I literally bawled. 

 I showed my husband her picture and he too fell in love.  When we looked at other websites, we felt saddened but never felt pulled like we were at that moment.  I emailed our contact person and asked what exactly the criteria were…and told her all of our “issues” (age, amount of kids, etc.).  After I listed my concerns, she told me that we still qualified.  We were over the moon excited…and terrified at once.  We felt very strongly that we were prompted to find this sweet girl.  We both feel like we have been blessed with knowledge, love, and the ability to help another child living with Spina Bifida live  life to the fullest.  We felt so strongly that although Spina Bifida is the hardest challenge our family has ever been through, it has also been a blessing in many ways.  How could we be so blessed and not help another child who just needs a family, love, and support?  The only way we can show Heavenly Father how grateful we are for His love, for the blessings He has given us is to help at least one of His children.  Kumaka was born into a family while Sofi was taken to the orphanage.   It is heartbreaking to think about these children wasting away…because in other countries children with disabilities are not considered worth living.  This sweet girl has the right to be loved, to have a forever family. She has the right to have the best medical care available to her.  She has the right to have five big brothers love her and adore her. Sofi hasn’t smiled yet, she hasn’t spoken yet and she’s three years old.  We decided we could help Sofi smile, we could be her forever family.
 We decided to go forward with the adoption.  We sent papers to the country in August…and every single day for a month we held our breath to see if the court would find us a worthy family…and allow us to be her parents.  They gave us the green light.   Now we are in the crazy busy fundraising madness.  It costs approximately $30,000 with travel fees.  We don’t have that kind of money lying around…so we are trying to be creative about raising money.  We have raised a little over $1000.  We look at each thousand as a goal.  We only have 30 goals.  We have met one.  So we are basically 1/30th of the way done.  We have sent $700 to our agency for the initial paperwork fees.  We are now officially in the program.  Now we need to come up with $9000 to cover the various fees that come up while filing papers as well as pay for our Home Study.  Although it’s stressful to think about the money…and how we’re going to come up with it all, we have already seen miracles.  People have stepped up to become angels to help us bring home Sofi.  We have seen people donate money and we don’t even know who they are.  Our community has rallied behind our little Sofi.  An article was written on our local magazine, Fountain Valley Living, and three fundraisers have been planned, one of them being an $1800 diamond heart pendant that was CREATED for this event by one of the local jewelers to raffle off.  A dear friend who is a photographer is doing mini sessions next week and 100% of the proceeds are going towards Sofi’s adoption.  Who does that?  I am so in awe by the amount of people who have come together, and shown us LOVE.  That’s what the world needs to see more of….that is what will change the world.  We love Sofi, and we truly cannot wait to bring her home. 
Our boys are excited to have a sister (of course after their initial chagrin about the fact that she was a girl…they are so used to it being a boys world).  We talk about Sofi a lot, and we ask them questions all the time.  We asked Kumaka the other day where Sofi will sleep.  He said she will sleep in her bed…in his room. 
 Kumaka likes “sandwich” hugs.  I asked him where Sofi would be in the hug sandwich.  He said “I will be on this side by daddy, and she will be on that side by mommy, and then we make a sandwich”.  Adorable, right?   Kumaka told me he would teach her how to talk, and he would take her to physical therapy with him.  He told me he would take care of her when she has to go to the hospital.  I love the fact that he is so willing to take care of her. 

This journey will take a year, and I’m sure we will face challenges along the way.  But bringing home this sweet angel is well worth it.  Once she is here, we will have another set of challenges.  We know that we will be okay….that God has brought us here and He will be there for us throughout the journey. 
  



Am I enough?


Normally I start my posts with Dear Life....but today I am writing to parents all over the world.

Dear Parents,

Parenting is the hardest job in the world.  It's also the most fulfilling job in the world.  

 It's beautiful when your newborn is placed in your arms, wrapped up and content.  It's amazing when your toddler grasps your finger to walk for the first time.  It's hilarious to hear first words and sentences.  All of these and many many more milestones will make your heart leap for joy and your mind will remember those times with great fondness.

It's so hard when your kids hit the teen years.  One moment you'd like to strangle them (or lay them across your lap and spank them even when they are four inches taller than you!) ...another you're confused as to why they are choosing to completely ignore you and not speak to you....another sweet small moment they open up their hearts and ask questions about what they are going through.  Some days the teen years make me gray, and others are the most amazing, fulfilling times.  

It's devastating as a parent to hear your child will be born or was just born with a disability, or your child has had an accident and their life will be forever changed or they get some kind of illness that will completely take over their life and possibly shorten it.  This is the hardest part of being a parent in my opinion.  What do you do when you find out a diagnosis, or hear your child is injured?  I am going to admit there are times when I would like to go in my room, pull the covers over my head, and go fetal.  (There are times I have actually done that.)  But then I have to get up, put on my big girl pants, and get on with life.  I get on my knees, I beg and plead for the strength to get up and do what my kids need me to do, and then I move forward with the hand of God on my shoulder to strengthen me in my weaknesses.   

The gift of life is amazing.  I have been blessed....by a Father in Heaven who trusts me enough to mother five wonderful children.  That is so humbling.  Occasionally I question my ability to parent these boys up to the standard that God would have.  I question myself, my patience, my understanding.  Am I enough?  Do I give enough?  Do I love them enough?  Do I teach them enough?  Are they growing up knowing the gospel?  Are they growing up knowing how to love others?  Are they growing up knowing how to love themselves?  And are they growing up knowing how to be GREAT men?  I hope so.  I pray so.  I believe so.   

How, as parents, can we hold all of these emotions?  Having five children, I sometimes feel like I have to have multiple personalities in the same day to help every child.  But I truly treasure each child for their individuality, their strengths, and even their weaknesses.  My children amaze me every day.  And when I'm weak, when I make mistakes, when I'm so tired I just don't do what I'm supposed to do, I gather my brood and I talk to them.  I tell them how I'm feeling, I tell them I love them, and I tell them I'm sorry when I could have done a better job.  I'm not perfect, they're not perfect.  None of us are perfect, and we are not expected to be perfect.  We are here to learn, grow, make mistakes, and grow from those mistakes.  We are here to receive hardships, and to learn to rely on a loving Heavenly Father to get us through them.  We are also here to learn to serve others, to not get so wrapped up in our own problems that we forget that the friend around the corner may need to talk, or get some help with a ride for their kids, or someone may need babysitting, etc.  As we serve, we strengthen....ourselves and others.  It's a beautiful thing.   

So, am I enough?  Yes.  Are you enough?  Yes.  Can we get through these crazy, amazing, wonderful years of parenting and survive?  Yes!!!!!  

I am so grateful for my husband who lifts me up when I am down and is always a source of strength in our family.  I am grateful for each and every one of my children.  They amaze me every single day.  Sometimes it's a great kind of amazement...and others...well....we all have those kind of days.  But I wouldn't change one of them....they all have different strengths, different weaknesses, but they all have amazing hearts.  I am grateful for my God, who I know has a plan for me, my family, and for this world.  I am grateful for the gospel that has taught me so many correct principles...that allow me to live my life knowing that I will be with my family for eternity.....that allow me to find a strength I never knew I had....that reminds me that when I am low, when I am down, God has got me...and He will always be there.  I am grateful for amazing, wonderful friends.  I am grateful for challenges, and for the ability we all have to get through them.  I am grateful for life....
I was featured HERE today talking about how we started our adoption journey.

Monday, November 5, 2012

A letter of thanks

Dear Life,

Whew!  After a post every single day in October I am pooped!  I have some things that I will be posting in the next few days, but I today I just want to take the time to share some thanks in the form of a letter to Sofi.

Dear Sofi,

Going into this adoption, we knew it would be tough.  There are a lot of steps, a lot of things we are responsible for getting done.  All of these things cost money.  What we think about more than the money though, is Sofi.  We are going to share a bit of you right now Sofi girl:

Sofi is three years old.
She is a beautiful brown haired, brown eyed baby girl.
She has Spina Bifida and Hydrocephalus.  
She lives in Eastern Europe in an orphanage. 
Her days are very regimented...and she spends most of her time in her crib day in and day outT.
She is not held, sung to, or kissed.
She is alone.
No one has ever even wanted to adopt her.
No one.
Until we came along.
Until we looked at her beautiful brown eyes and fell in love.
Now she has a family of boys that are anxiously awaiting her arrival.
A mommy and a daddy who are praying every night that you stay healthy...that you can somehow feel their love from miles away...and hang on.

We're coming Sofi.  We're working hard.  Other people are working hard.  People have heard our story, you're story Sofi, and they have been touched.  They want you to come home...to have an eternal family. First a friend from church shared their cupcake store....had a day for you.  It was so fun to see them sell out of cupcakes!  Then our local community put an article in the local magazine.  They also put together a few fundraisers.  Tonight we had the first one....and it was amazing. A local jeweler is making a diamond heart pendant in your honor...it's going to be beautiful. He is raffling it off to help pay to bring you home.  The generosity of these people warms my heart....reminds me of a time long gone when community mattered.  And then over the weekend a dear friend (who I know online but have never met in person) decided to put together a weekend of photography sessions and donate 100% of the proceeds towards bringing you home.  In fifteen minutes the sessions were booked.  Her heart is so big....and we are so touched by all of this.  It's overwhelming in some ways to see God working so hard to bring you here.  We can see He wants you to have a chance...to have a family.  It's humbling to see His hand in this work.  We  know that we are so blessed...and that if we could help just one of His children, we would be giving back just a little to He who has given us everything.  And we are able to see His hand in it all.  Sofi, we can't wait to meet you...to hug you...to bring you home.  And when you're ready we will be having a party!

Love you so much Sofi!


Thursday, November 1, 2012

Living Beyond the Diagnosis

Dear Life,

I have introduced you to just a very small amount of families that are living with Spina Bifida.  In sharing these stories, I hope you have seen what these families have gone through (in a small way)....from devastation when finding out the news to living beyond the diagnosis.  That is a HUGE phrase.  LIVING BEYOND THE DIAGNOSIS.  LIVING.  That's what it's all about.  And that can be said for any person dealing with a medical diagnosis.  It's just that.  A diagnosis.  Yes, in this case these people have Spina Bifida.  But Spina Bifida does not have them.  It does not define them.  How they live their lives defines them.  Who they are as people (even little kiddos) defines them.  Their spirit defines them.  Sometimes, with surgeries or illnesses, they regress, and sometimes it would be easier to stay home and not make the effort of going out, and living their life.  But that is why we are here....to live life.  And all these families and thousands others are living their lives and living it well.  It can be hard, and we cry sometimes.  We laugh more, we live more.  You can see that in their smiles.  Thank you for taking the time to read about these families.   I would like to thank all of the people who shared their hearts with me, and allowed me to share their stories with you.  You may not know it, but it is really hard to relive some of the experiences we have shared.  I am really grateful to all of my wonderful friends for opening up a window into their lives.  I also want to thank all of my readers for always being so supportive of my family, Kumaka, and little Sofi.  This is has been an amazing month for me.  A reaffirming month....a month of strength, courage, endurance and love.

If you missed any stories, look below and you will find a link to that post. 


Nathaniel's Story  




















Brendan's Story 
















     






                        



























Halle's Story
















Taylor's Story



















Jet's Story
 














Keely's Story





















Neveah's Story










Yordanka's Story




















Micah's Story




















Tanner's story