Monday, January 3, 2011

Project 365: Day 3

(sorry for the bad picture; it is hard to catch a quick shot of the TV screen sometimes)
A girl can dream, right?   I have it in my head that winning the lottery is now my only path to happiness.   Why you ask?   Well, the cost of a round of PGD/IVF or private adoption is so far out of our reach that it feels like it would take millions to make us parents.    I know it isn't as drastic as that, but most days it does feel that way.    I guess we learned the hard way how unfair life can be in that aspect.  It is frustrating to see others struggle to provide basic needs for the kids when we have so much to give.   More frustrating are the news stories about babies found dead in dumpsters or shaken/beaten to death.   We'd gladly take those babies; there is no need for them to be killed or hurt.

I do miss living in the world most others live in.   I'd love to try to get pregnant, be excited for months, and give birth to a healthy baby that grows up to give me grandchildren.  No matter what path we chose now, pregnancy would never be a happy or exciting time for us.   It would be stressful time that would only end when we saw our child move normally for the first time.  No amount of testing would ever be enough for me; I'd have to see normal movement, normal development to ever be able to believe that everything was okay and even I'm not sure that would be enough.  

Dealing with bad genes and lack of insurance coverage/money has really put a strain on our relationship over the past couple of years, but we are still hanging in there.   It is not an easy path to navigate, but we hope that in this instance, love IS enough.

Sunday, January 2, 2011

Project 365: Day 2





It rarely gets cold enough to use the fireplace, so we normally only burn one on Christmas Eve and/or Christmas Day.    It was a little chilly today and we still had a starter log that my parents brought us, so Jason fired it up tonight.   It is nice and relaxing to just sit and watch it, but I took it a step further tonight and did some aperture practice with the camera.
When I sat down to upload my pictures, my sweet boy just looked too adorable so I had to snap one of him as well.

Saturday, January 1, 2011

Happy New Year: Project 365

Okay...so I decided to try to do Project 365 this year.   Don't know what that is?   You can read more about it at 365project.org.  Basically you take a photo a day to both improve your photography skills and document your life for that year.    Sounds fun, right?  

My first picture is of one of our cats, Bailey.   She HATES when the camera comes out and most of our pictures of her remind us of Jim Brewer after a few joints.    I am determined to get some good shots of her this year so I started off with her.  

I love my kitties.  They have always been "my kids", but even more so after losing Eli.    I get angry when they wake me up scratching at the door at 4 or 5 am, but I guess I should be glad that they love me so much that they just need to see me.   :)    They bring us much laughter and always seem to know when we need a little snuggle.  

Wednesday, December 29, 2010

Two years ago today we first heard those three words.   Spinal Muscular Atrophy.    

We had no idea our beautiful son would die less than three weeks later.

Sunday, December 19, 2010

Birthday!





I had to share some pictures of my amazing birthday present.   My friend Sara makes the most wonderful cakes and she stopped by today with this lovely creation.   I thought she was making me one of the ugly cakes from Cake Wrecks, but nope, I got the prettiest Barbie EVER!    I never got a Barbie cake as a little girl and I must say, this cake made it worth the wait!   :)

I'm sure she has no idea how much it really means to me.   For most of my life, I have been the giver.   I am the person who always makes sure everyone else has a cake or a gift or is thought of on their special day.   Usually that means that on my day, I get a bunch of apologies that people didn't have time or something came up and they didn't get to do anything.    But, every now and then a special friend or family member surprises me and does something that really puts some sunshine into my day.   Sara has been that special person not only on my birthday, but over and over again day in and day out.  She only met Eli once and we only worked together a few months, but she truly loves me and does so much for me and for SMA.   I don't know how many hours she worked on this cake, but I know she didn't get much sleep last night.    She is awesome and I am so very lucky to get to call her my friend. 

Thursday, November 25, 2010

The Holidays are Here!

 Our new Christmas tree.   After years of fighting with the lights and each other OVER the lights, we broke down and bought a new pre-lit tree this year.   It is also self-shaping, so it was up and ready to decorate in about 15 minutes.   It felt strange, but I don't miss the hours of putting on lights!
 This year I am attempting to make my own dressing.  I even dried and cubed the bread!   It was a labor of love, so I hope our guests like it.  I used this recipe from Allrecipes.com because of all the great reviews. 
 Here's Eli's crab ornament from last year.    I found 3 new ones this year at Hobby Lobby and will try to post pictures later.   
 This is our first ornament as a couple.   I sent it to Jason while we were living miles and miles apart.    
I was playing around with the camera today and here's one shot of some of the shiny glass balls.    I love trying to photograph the Christmas tree.   Hopefully my pictures will get better with practice.  

Happy Thanksgiving.

Thursday, November 11, 2010

Great News!!!!!

I know, I know.   I'm horrible at updating over here.   I've been so focused on my Stampin' Up! projects and upcoming craft fairs that I've mainly been posting on my card blog and Facebook business page.    I do have a few things to share though!

First, Through Eli's Eyes is now officially TAX-EXEMPT!    We are thrilled to have that designation now because it allows us much more freedom to do fundraisers.   I am forever thankful to Robin and Wade, our awesome friends who donated their time to get the application together for us.   They ROCK!    

Second, there is an awesome new fundraiser going on that was brought about by some of my local friends.   Houston photographer Debi Gomez does an amazing calendar each year and chooses a children's charity to donate the proceeds.  My friends at Merry-Go-Round nominated one of our SMA organizations so this year's recipient is the Gwendolyn Strong Foundation!   You can check out the beautiful Hope Calendar here!   Please consider picking up a few of them as Christmas gifts to help support GSF and Debi's effort to fight SMA!

Saturday, September 25, 2010

Nothing new to report...just wanted to share a funny picture.   He's had a rough day today following me around, so he is VERY tired.  :)

Sunday, September 19, 2010

Please VOTE!

Gwendolyn Strong Foundation has a chance to win $20,000 for SMA through YOUR daily votes! Yep, we need your super awesome voting fingers to get to work again!


Twelve children’s charities from around the country, including the Gwendolyn Strong Foundation, were selected by the Jimmie Johnson Foundation for the Samsung Helmet of Hope that NASCAR champion Jimmie Johnson will wear in the upcoming Pepsi 400 race in October 2010. The Jimmie Johnson Foundation has already been incredibly generous, awarding a $10,000 grant to each of the twelve charities and increasing awareness about each of our missions. We are incredibly honored to be among these important causes. And we are equally honored to now have the opportunity for additional awareness and funding to help further our passion — an END to SMA!!!
WE. CAN. DO. THIS! Together we can END SMA — one vote at a time!!!
PLEASE VOTE: It’s really this simple –>
  • You can vote once EVERY DAY from now until September 29th at 5 PM EDT
  • Go to VoteForSMA.com, select the Gwendolyn Strong Foundation, enter the two security words, check the Official Rules box, and then click “Vote Now!”
  • That’s it!
  • And…don’t stop there — SHARE!

Saturday, September 11, 2010

Eli's Quilt


We received Eli's quilt from Cole's Quilts this week.   If you haven't read about the quilts, go check our their website.  (if you cross-stitch, please consider volunteering!)  It is something we will be able to treasure forever.   Two of the squares are extra special because they were made by members of my SMA family.   The 3 giraffes in the car was done by MJ and Brenda.   If you've been a frequent reader of my blog, you should know all about MJ by now, but if not, you should spend a little time reading her story.   She is one of the most amazing people I've "met" and I hope I can give her a huge hug in person one day.  
Another square was made by my fellow SMA mom, Marla.   Marla lost her son Jay to SMA and has been one of the people I've come to lean on because she gets it.   I hope to make it up her way to visit her one day and get some cuddles from her amazing twins who are SMA free!   She made the Through Eli's Eyes square  for the quilt and I love it.   It is so nice to have the foundation name on there.
Here are some close ups of the other squares on the quilt.  I'll try to post better pictures when I have someone around to hold it up or when we figure out where to hang it.   I'm trying not to lay down and cry on it, but it is hard...    I sure miss that boy of mine.  

Monday, August 23, 2010

BBQ Chicken Pizza


How yummy does that look?   We tried this awesome new recipe tonight and it was delicious to say the least!

I finally got back to counting my Weight Watcher points last week and lost 2.8 pounds.  I feel a little better mentally, so hopefully I can stay on track.   We figure we have about $3500-4000 more to save up for IVF and I want to lose at least 30 pounds.   Crossing my fingers that I can do that and we can save the money and try around the first of the year.   I am working part-time right now and trying to get my Stampin' Up! business going as well.   This month has been tough, but getting out of the house has helped some I think.   The holidays will all be coming up soon and that's always a whole other hell we have to go through too.  

Tuesday, August 17, 2010

A few pics of the kids...

Bella
Bailey
So cute, but don't let her fool you.  Touch the wrong spot and she'll get you!
My sweet boy.    He is so bad when we have company, but is always the perfect companion when it is just the two of us.   

Sorry I don't have much to post lately.   I finally went back to work and am trying to get my Stampin' Up! business off the ground.   It is hard to get back in the groove of things!

Eli's walk went great, but I forgot the camera!   We raised about $450 and sent it all to the Gwendolyn Strong Foundation for the 200K for SMA campaign.   They were nice enough to write up a very sweet post about Eli today, so go check it out here.

Monday, August 2, 2010

Happy Birthday Eli


Not sure if we had posted his wind chime before.   It was placed one year ago today and is still playing music...
Dragonfly solar light we found at Target.   I wanted to know there was some light near him at all times.
We took out some sunflowers today to place on his grave.  

And finally, the balloons...


Sunday, August 1, 2010


During the week that we were told Eli probably had SMA, a postcard appeared on Post Secret  that led many people to sign the petition and raised some serious awareness of SMA.   Today, I found this postcard.   As we go into yet another difficult anniversary, I find it fitting that one of my frequent complaints shows up on PS.   I wish people could understand how the words they *think* are comforting really just piss me off and make me want to slap them.   If I told you I planned to go out and kill someone or if I saw a man dying my plan would be to do NOTHING to help, would you think that was a good plan?   A plan that that person's family would find comforting?  No.   So your god planning for my son to die or doing nothing to cure him is NOT comforting.   Please think before you speak, especially when dealing with grieving families.  

Now they just need something to deal with the other stupid line of "everything happens for a reason".