Stay tuned

By -
We head to Shreveport tomorrow for Elijah's second wrist surgery (other wrist) on Wednesday morning. He will be checked into the hospital on Tuesday morning and hopefully discharged on Thursday. The docs at Shreveport probably call this routine, but my fears of infection are raw. Elijah's last arm rod made him very, very sick after two months. Please pray Elijah will make it through this straightening without any complications and complete success.

Pray for Sophia as she is again left behind. She will be well cared for by Auntie Lori and Uncle David and well played with by cousins Daniel and Makayla. She will be fine, but it is still hard on her.

Pray for our safe drive and smooth transactions along the way. We still don't know where we are staying while we are there.

Watch the blog, we'll update as we go.

Blessings to all.

Love,
Melissa

Comments

Anonymous said…
Praying for you as you go. If all goes well, we will probably be over on Saturday. We will talk about it later. Thanks for the update. Grandma Bobbie
March 1, 2009 at 3:47 PM
Anonymous said…
Will be checking the blog for updates. We are already praying for him a LLH and will continue to do so. Love you all...kisses to Eli from the Orange Class!
March 1, 2009 at 5:18 PM
Post a Comment

Popular posts from this blog

Elijah Will Be Represented at Boston Marathon 2014

By -
Our dear friends the Sperou family in Massachusetts recently asked if we'd be interested in seeing Elijah represented by a runner during the upcoming Boston Marathon in April 2014. Of course we said yes! What a fantastic opportunity, to know that someone has dedicated themselves to running 26.2 miles, thinking about Eli the entire time, working to raise money for children like Eli who are dealing with rare diseases. Kelsey Hoontis, our new superhero, is sponsoring Eli as part of an organization called "Running For Rare Diseases." They recently spoke with Christopher and Laurie Sperou about sponsoring their precious daughter, Shauna, who became a good friend of Eli's during our visit to the Rothmund-Thomsen Syndrome conference in Washington, D.C. Kelsey is one of three (for now) runners who will be representing RTS kids, and I'll tell you honestly, it feels so good to see Eli's syndrome garner more attention. We felt so alone in those early days when we had j
Read more

Tell us who you are

By -
Take a minute to sign into the blog, then reply to this post. Tell me, and everyone, who you are and what Elijah means to you. If you're the friend of a friend, then you're family now. Remember, the best blog strings go on for miles. As you view our list of friends, know that we keep each of you in our prayers just as you pray for Elijah. Dave
Read more

Seven...SEVEN!!

By -
Image
It's here. Eli's big day. Today, Eli turns 7 years old. The feelings and emotions I have for this day are overwhelming. It's been a long, long 7 years, but I can remember this day in 2006 like it was yesterday...and the months to follow. They are etched in my memory with Sharpie...never fading. Some of the memories, honestly, I wish I could erase. The hurtful ones. Some I've written about on this blog, but most I keep hidden. We hosted a birthday party for Eli on Saturday. He invited his entire regular class and his entire special needs class to his party. I began first thing in the day warning Eli that he might not have a lot of kids come. I wanted him to be prepared for the worst. Though Eli was confident his friends would come...I wasn't sure. When party time arrived, five precious kids came to celebrate Eli's birthday. I was relieved and Eli had a marvelous time with those five great kids. That same day, we had a family celebration where we all doted on El
Read more