Wednesday, November 5, 2008

Windemuller's new blog


ourkids-ourangels.blogspot.com is Curt and Carla's new blog site.

I had the privilege of being able to spend a couple of hours with Carla today and it was so nice to be able to do that. During those couple of hours, we worked on her new family blog. Carla hopes this blog will highlight the joys and sorrows of what their family is going through.

Thanks Carla! It was a fun two hours, with lots of laughter! We will continue to pray for you guys and be with you every step of the way! Just remember..... our Lord, will not walk ahead of you or behind you, but beside you! God Bless you guys!

Tuesday, November 4, 2008

So..... who are the Windemullers??

I've been so busy with just getting prayer requests out, that it was brought to my attention that people would like a little history of the family. So, with Carla's approval.....here we go! I can't even tell you how many years I have known Curt and Carla. I guess if I wanted to add it all up, it has been close to 20 years - wow time flies when you are being goofy! I guess goofy is the word that comes to mind when we are with them or when we think of them! I have been through the joys and the sorrows with them. I have had the pleasure of witnessing the birth of Josh, the day we celebrated Josh's new life with Christ, Caleb's birth, Zach's arrival into the family by adoption, many birthday parties for Ashley, sporting events for Ashley, observing what Curt and Carla went through when diagnosing Zach's autism, and MANY MANY more that I can't even begin to list. Brandon and I have had the honor of being Ashley's youth group sponser back when she was in junior high and then the honor of being at her wedding. Brandon and I hold this family near and dear to our hearts. The Windemullers have had many mountains to over come and Satan has sure made his presence in this family, but they have held on to their love for each other(as husband and wife) and their Savior. Both Josh and Caleb have been diagnosed with Leigh's Syndrome. This is a very uncommon disease that really no one can predict what will come next, only the Great Physican can. The disease is terminal and basically it impairs bodily functions, including organ functions. Both Josh and Caleb suffer from continous seizures that the doctors try to control with medication. As for Josh, he entered the gates of Heaven when he was only three years old and is now enjoying life to the fullest. Then there is Caleb...... I still remember visiting Carla when she was pregnant and then the many visits after Caleb was born. He was my healthy chunky buddy, until about 3 months of age. I still remember that day as if it was yesterday. I remember getting the call, from Carla, and she then told me that Caleb suffered a seizure which was the start of the disease. From that day, the doctors jumped on treating him with meds to control the seizures and I am sure that is why Caleb is still alive today. Caleb is now 14 years old and we had the honor of watching him grow and the priviledge of being at his birthday party about a month ago. What a special little - big guy :)! As things are taking a turn for the worse and Caleb's days on earth are number, prayer is the only thing that matters right now.

Here are some prayer requests:
1.)Pray for comfort. Lately Caleb has been more fussy and things are obviously wrong and he can't vocally express things and fears.
2.) Pray for peace. Between now and the time when God calls him home. May they all feel the love of God wrapping His arms around them.
3.) Strength... There have been many sleepless nights or a few hours here and a few hours there. I pray that God will give them strength. They not only have Caleb, but they have Zach too. He is in Junior High and he has needs also.
4.) Frustration. Pray that God will continue to bless and strengthen their marriage. Satan wants to use Caleb to put a wedge in the family, but as Christians, Satan will never win!
5.) We know that we can't pray for healing, God has much bigger plans for Caleb! What a wonderful day it will be for everyone when we meet our Savior. I'm sure we are all anxious for that day and to see our loved ones that have been having the joy of rejoicing with the Lord day after day after day.....

I hope that this will give everyone a little understanding why I have been keeping them in my blog. This family is very important to us amd what an honor that we have had the priviledge of walking with them step by step.

Psalm 121:1,2 I lift up my eyes to the hills - where does my help come from? My help comes from the Lord, the Maker of heaven and earth.

Monday, November 3, 2008

Trick or Treat!

Everytime at Halloween, I make a point to get to most of my family members. Even though it means having to break it up into two days. This year, on Friday night we went to see Brandon's parents and grandma - then headed off to church for our trunk or treat. I would've gotten pictures of that, but somehow I ended up getting stuck sitting on our tailgate handing out candy. On Saturday, I was able to get to my side of the family and to my best friend for some priceless pictures!

Sisterly/Brotherly love? Hmmm, let's give that a year or two :)!


My parents, can you tell that the kids are getting sick of pictures?


Uncle Jeff and Aunt Helene


Abbie, Ben Nykamp, Bryce


My grandparents


Brandon's grandma

Caleb

As of this morning, Caleb took a nose dive. His heart rate and breathing was quite high so hospice has now put him on oxygen full time and upped(sp?) his valium and morphine. Carla said that he is quite fussy today so she is not quite sure what is going on in his precious little body. This is another downfall so we ask that you continue your prayers for peace and comfort for Caleb and his family.

Saturday, November 1, 2008

Update on Caleb

Thanks to everyone for their many prayers! Curt and Carla have sure felt them over that last couple of days! Caleb has been resting more lately, which is a HUGE answer to prayers. Carla has now been able to get some more sleep during the night. Caleb has been a little more fussy, when he is awake, which is making Carla wonder if maybe his seizure activity is picking up. That is just a guess though, they have no way of really knowing. Caleb is still VERY critical and so they ask that you continue to pray for peace, comfort, and rest. Sometime next week, hopefully, I am going to help Carla set up some type of blog or carepage. She is leaning more towards a blog so she can also highlight the good that their family is experiencing. I will keep you all posted when the blog is up and running. Once again, Curt and Carla are very grateful for the many prayers and everyone's act of kindness.