Tonight we spent time with our new friends, Hadiqa and Ayesha. These young women are international students from Pakistan, spending a semester in an exchange program at a local university.
Our pastor for missions connected us with them to be a "host family". He told us that 80% of international students never step foot in an American home during their time here in the U.S. We feel like it is such a unique opportunity for us and for our children to get to know these sweet ladies and broaden our worldview at the same time.
We shared a lovely "American" meal and lots of laughter at California Pizza Kitchen :) I feel honored that Hadiqa and Ayesha shared so honestly about their families, culture and Muslim faith and we were able to do the same. Our friend Rebecca joined us and it was so neat to listen to these young women relate to each other. They told me that as their host family I am their American Mom. I love that, what a privilege! I am happy to have children who know how to go potty by themselves. ;) ha! Our daughters thought they were so beautiful. Every time I looked up, they were staring and smiling at them.
Women like Rebecca, Hadiqa and Ayesha give me hope for the future. They have a passion to grow and learn about people, other cultures, and other points of view. It is a beautiful thing! I pray that God would be glorified in their lives and for generations to come.
Showing posts with label prayers of intercession. Show all posts
Showing posts with label prayers of intercession. Show all posts
10.30.2011
12.14.2008
On the 14th day of Christmas...
our little buddy Heath....received a NEW HEART!!!!!!!
We received a call last night at around 8:00 that Heath's dr.'s were going to "see about" a heart. That within 2 hours the Chris and Carrie would know if it was a possible "fit". We waited...heard from Pen again...and with good news "it's a fit", and the surgical team is going rest...surgery will hopefully begin at 3 AM and last until 8 AM. I'm thinking this sounds like a precisely planned military manuver...scary and exciting...went to bed around 11 (I don't think Dan slept at all) and then received a phone call at about 8:00ish, this time from Chris (Heath's daddy)...it's almost over and Heath's got the new heart he needed!! Lots of happy, sad, relieved tears for sweet friends...thank you, Lord.
***totally a random, insignificant piece of info...I was just looking at the little pre-made book I put together for the "December Daily, 25 days of Christmas" project and could not believe how I'd decorated Day 14 (2 weeks ago)...I'm thinking this will be a "heart for Heath" page!
We received a call last night at around 8:00 that Heath's dr.'s were going to "see about" a heart. That within 2 hours the Chris and Carrie would know if it was a possible "fit". We waited...heard from Pen again...and with good news "it's a fit", and the surgical team is going rest...surgery will hopefully begin at 3 AM and last until 8 AM. I'm thinking this sounds like a precisely planned military manuver...scary and exciting...went to bed around 11 (I don't think Dan slept at all) and then received a phone call at about 8:00ish, this time from Chris (Heath's daddy)...it's almost over and Heath's got the new heart he needed!! Lots of happy, sad, relieved tears for sweet friends...thank you, Lord.
***totally a random, insignificant piece of info...I was just looking at the little pre-made book I put together for the "December Daily, 25 days of Christmas" project and could not believe how I'd decorated Day 14 (2 weeks ago)...I'm thinking this will be a "heart for Heath" page!
As our pastor said this morning...advent is a season of waiting...waiting for the arrival of Christ...waiting in hope for delivery from sin and a life of despair...I think I'm beginning to understand just a tiny bit more what it means to wait...to hope...to REJOICE...for what God has done and the saving work he is doing to redeem his beloved creation, his children, from death...so that even after this life is over, we may live on with our savior in HEAVEN!
Please keep the prayers for Heath coming, that the heart will heal properly, and that his little body will make a good home for the heart. REJOICE!
12.03.2008
Baby Heath
Dan received an email tonight stating that Baby Heath had been taken to the emergency room, is on a machine to assist his breathing and is now at the top of the heart transplant list. Please pray for these dear friends.
11.14.2008
Heath update...
A friend of the family's created a blog to post updates...check it out...please keep praying for Heath!
11.10.2008
Please pray for baby Heath...
Some dear friends, Chris and Carrie just recieved news (Friday) that their son suffers from a heart condition that will require a heart transplant. We are very thankful for the opportunity to spend time with them this summer on our vacation.
We have had a special tradition for the last 6 years with the Tuttles and several other families to spend Labor Day week/weekend vacationing together. Our hearts are heavy and I hope you'll join us in prayer for this family. I don't usually post other people's personal stories on this blog. I'm sharing this information with you, because I trust that you, our friends and family will join us as we intercede in prayer for these friends, so needing God's strength to get through. I'm including some details so that we can pray specifically.

Heath is 9 months old. Chris very recently (in the last month) accepted a call as senior pastor at a church in Durham, NC. Carrie has very recently (in the last month) resigned from a full-time ministry position to devote herself to the needs of the family as a stay-at-home momma to their two children, Heath and Ella Brooks. Here's a portion of the email we recieved yesterday from Carrie's brother, Pete.
************************************************

"... our little Heath is a very sick little guy. Chris took him to his 9 month check up on Thursday afternoon where the Pediatrician heard some sort of heart murmur. He sent them immediately over to a Pediatric Cardiologist for further evaluation, who in turn sent them on to UNC Childrens hospital where Heath was admitted on Thursday night for testing and observation.
Heath was diagnosed with Restrictive Cardiomyopathy, which basically means that he has a thickening of the walls of his heart. This condition does not allow his heart muscle to relax and expand to fill with blood fully before it contracts again, which causes blood to build up in his lungs and into the rest of his system. For any of you that may understand medical terms, this condition mirrors the signs and symptoms of someone in congestive heart failure. I will put this in the words that the cardiologist said to the family last night, "none of this is or will be easy to deal with, but we don't sugar coat anything, it just makes it harder to deal with in the long run."
They are attempting to use medications to treat the symptoms of his sick heart, but the end result is that Heath needs a heart transplant very soon. After all of the testing is done he will be placed near or at the top of the national heart transplant list in the coming week.
Again, the TEAM of Cardiologists and other specialists are doing everything known to man in an effort to treat the little guy. They are going to continue to monitor him through the weekend and into early next week. They have a few more tests they would like to do on him the first of the week and then he will probably be discharged from the hospital so he can be at home with his family.
He is in a fantastic place and being cared for by an unbelievable group of people! True saints! As of right now, he is showing very few signs and symptoms that he is sick. This morning when we were there he was sitting up talking (baby talk of coarse) and playing with toys with big smiles for everyone! As I'm sure you can imagine Chris and Carrie are having a very rough time right now. They apprieciate everyone's thoughts, prayers, and offerings of help. They have asked for everyone to hold off on phone calls and emails for a fews days to let them work through this tradgedy together. The best thing we can all do is pray for Carrie, Chris, Ella and especially our little Heath."
We have had a special tradition for the last 6 years with the Tuttles and several other families to spend Labor Day week/weekend vacationing together. Our hearts are heavy and I hope you'll join us in prayer for this family. I don't usually post other people's personal stories on this blog. I'm sharing this information with you, because I trust that you, our friends and family will join us as we intercede in prayer for these friends, so needing God's strength to get through. I'm including some details so that we can pray specifically.

Heath is 9 months old. Chris very recently (in the last month) accepted a call as senior pastor at a church in Durham, NC. Carrie has very recently (in the last month) resigned from a full-time ministry position to devote herself to the needs of the family as a stay-at-home momma to their two children, Heath and Ella Brooks. Here's a portion of the email we recieved yesterday from Carrie's brother, Pete.************************************************

"... our little Heath is a very sick little guy. Chris took him to his 9 month check up on Thursday afternoon where the Pediatrician heard some sort of heart murmur. He sent them immediately over to a Pediatric Cardiologist for further evaluation, who in turn sent them on to UNC Childrens hospital where Heath was admitted on Thursday night for testing and observation.
Heath was diagnosed with Restrictive Cardiomyopathy, which basically means that he has a thickening of the walls of his heart. This condition does not allow his heart muscle to relax and expand to fill with blood fully before it contracts again, which causes blood to build up in his lungs and into the rest of his system. For any of you that may understand medical terms, this condition mirrors the signs and symptoms of someone in congestive heart failure. I will put this in the words that the cardiologist said to the family last night, "none of this is or will be easy to deal with, but we don't sugar coat anything, it just makes it harder to deal with in the long run."
They are attempting to use medications to treat the symptoms of his sick heart, but the end result is that Heath needs a heart transplant very soon. After all of the testing is done he will be placed near or at the top of the national heart transplant list in the coming week.
Again, the TEAM of Cardiologists and other specialists are doing everything known to man in an effort to treat the little guy. They are going to continue to monitor him through the weekend and into early next week. They have a few more tests they would like to do on him the first of the week and then he will probably be discharged from the hospital so he can be at home with his family.
He is in a fantastic place and being cared for by an unbelievable group of people! True saints! As of right now, he is showing very few signs and symptoms that he is sick. This morning when we were there he was sitting up talking (baby talk of coarse) and playing with toys with big smiles for everyone! As I'm sure you can imagine Chris and Carrie are having a very rough time right now. They apprieciate everyone's thoughts, prayers, and offerings of help. They have asked for everyone to hold off on phone calls and emails for a fews days to let them work through this tradgedy together. The best thing we can all do is pray for Carrie, Chris, Ella and especially our little Heath."
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