Showing posts with label Stellan. Show all posts
Showing posts with label Stellan. Show all posts

Tuesday, November 10, 2009

Big Changes!

This post is a bunch of mix & match thoughts. A little of everything!

Remember Stellan? Well, he finally went to Boston for that ablation. And I'm overjoyed to report, that it went GREAT. Read about it here. He & his family could still use prayers during his recovery. Again, I am in awe at what God can do.

In other news, this blog is going to be going through changes of its own. I am super excited & can't wait to see what's in store. You'll just have to wait & see with me. {:)

Also, for the last couple of days, I've been rethinking somethings. To be honest, I'm not done thinking things through. There have been some big changes in my life & the way I see things, which I will share in the coming days.

Tonight, I'm going to Mandy's house to have dinner with her mom. I'm super excited to get to see Momma Dawne, but it's bitter sweet - oh how I wish I was seeing Mandy too. I just miss her so much!

Jake has been working SO HARD, with long hours it is crazy. Then, on top of that, he has been working over mom's to help out, & helping with Dad & stuff. It's difficult to find time to spend together. I'm so proud of him though. He really does love his job & is a very hard worker.

The weather here is crazy & ever changing. It's been beautiful weather the past couple of days, but cold at times. Coupled with the fact that thanks to daylight savings time, it gets dark SO early - you got a picture of Maryland weather. Changes in the weather are always crazy for me as it makes me have to mange my pain better. However, the beautiful colors in the leaves make up for it all.

Enough randomness for now. What's changes are you facing? Do tell, I'm listening.

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Tuesday, August 4, 2009

Update: Stellan

I am over joyed to say that Stellan got released from the hospital yesterday. As the Lord would have it, he never went to Boston. It has been a long road, for MckMama & her family with lots of prayers a long the way. Stellan in SVT free, on a new drug plan that is actually working for him & they figured some things out along the way, such as Stellan metabolizes drugs differently than other little boys.

I think this entry will tell you some of where this journey has taken Stellan's family... And it's one of my favorite entries. This is also a great (& truthful) entry. All this is to say - beyond a doubt - that prayer works, & God can do not only good things but Great things. Just take a look:
From this:

To this:

Yes, He is Great, indeed.

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Monday, July 27, 2009

Not Me Monday: Praying for Stellan

This was supposed to be another Not Me! Monday post; however it is now:




It seems so fitting since Stellan & his charming family need our prayers, and his mom is the one who started Not Me Monday to begin with. I've been following Mckmama's updates on her blog, but the better way to get updated with the latest news is to follow her on twitter, which of course I'm doing.

My heart just breaks for Stellan. From what I can gather he is in heart failure and his kidney's are failing as well. But there is hope. There has to be. They are making plans to air lift him to Boston. I do not know what they are going to do with him there but, logic tells me they would not have moving him as a option if there was not some POSITIVE reason to do so.

I pray that Stellan's heart finds a normal beat again. I pray that Mckmama and the family get the answers, comfort, rest, & whatever else they need at this moment. I pray that the doctors & nurses have the wisdom to find the treatments and solutions they need to get Stellan and his family through this.

I also pray that those same people believe in prayer and miracles too, bc I know I believe.

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Sunday, July 26, 2009

Praying for Stellan

This sweet little boy is named Stellan. His I read his mom's blog, which you can find here. I do not know MckMama personally, but have come to care about her and her family, especially Stellan in the past couple of months, through the words she she shares with thousands of us. If you have not read her blog, I encourage you to do so. She has many talents (photography to name one - just look at that beautiful picture she took) & her gift for writing is another one of many.

All the talent she has, whatever gifts she possesses she still cannot heal Stellan. No one on earth can. Stellen has a heart condition called SVT. McMama can do a much better job at explaining Stellan & his medical condition than I can.

Right now, he is at the family's local hospital & in the PICU. Things are not looking good. They cannot get his heart at a normal level & his heartbeat has been pretty much at high levels (at one point I know it was at 224 per minute) for the last couple of days and the doctors seem out of options, for the night at least. Everything they have thrown at this little boy has failed - medicine, procedure, ect. I know for a fact, that his BP was 57/32 & they may have to vent him.

I'm asking that you pray for this sweet little boy & his wonderful family. I do not know what God has planned for Stellan, but I know he has touched the lives of thousands already. And I also know that with God, all things are possible.
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