Showing posts with label In Need Of Daily Prayer. Show all posts
Showing posts with label In Need Of Daily Prayer. Show all posts

Friday, December 25, 2009

Pink Glove Dance!


Emily (MacInnes) Somers, created, directed and choreographed this video in Portland last month for her Medline glove division as a fundraiser for breast cancer awareness. This was all her idea to help promote their new pink gloves. She was able to get so many employees, doctors and patients to participate, and it has really started to catch on. They clearly had a lot of fun doing it. I am told that when the video gets 1 million hits, Medline has promised to make a huge contribution to the hospital, as well as offering free mammograms for the community. Please check it out. It's an easy and great way to donate to a wonderful cause, and who hasn't been touched by breast cancer? Lets help them to get 1,000,000 hits. Dance on !!!
PINK GLOVE DANCE
http://www.youtube.com/watch?v=OEdVfyt-mLw

Thursday, November 26, 2009

My Cup Runneth Over!

I really have a lot of reasons to be thankful. Last year, one week before Thanksgiving, Randy was laid off. I remember sitting with my family at the table having a wonderful dinner...feeling really thankful and really scared! It was all I could do to smile, and with each bite of food I felt as if I were trying to swallow a rock. For the first time in many years we were without health insurance and I really wasn't sure what would happen. Would one of our children get sick? Would we lose our home? The year did bring quite a few rough spots...but we came together as a family and we made it through.

"As we express our gratitude, we must never forget that the highest appreciation is not to utter words, but to live by them." ~John Fitzgerald Kennedy

Today, my thoughts and prayers are with all who are still struggling through hard times and loss. Those who worked very hard... but lost their home anyway. Those who go to work sick or have a sick child and no health insurance. Those who fought with all they had...but lost their lives anyway.Those who would gladly give away their home and all of their belongings if only they could have their child/grandchild/or loved one back.

I am grateful for this past year...not only because we made it through...but because we made it through better and stronger than before. Our struggles this year reminded my family and ME just how much we have...the love of a family, treasured friends, support when times are rough, good health, a comfortable home.

We were also reminded of the many material things that we do not need. Just giving up eating out not only helped our budget, but also lead to cooking healthier meals, eating together as a family and....the six of us lost between 19-44 lbs.

I believe that everything happens for a reason. I believe that there is a lesson in everything that happens. Good things sometimes fall apart so better things can fall together. Things go wrong so that we learn to appreciate them when they're right.

Thank you Lord for always watching over this family... and for the countless ways you bless us everyday.

Happy Thanksgiving Everyone!

"For flowers that bloom about our feet;
For tender grass, so fresh, so sweet;
For song of bird, and hum of bee;
For all things fair we hear or see,
Father in heaven, we thank Thee!"
~Ralph Waldo Emerson

Tuesday, May 12, 2009

Rest In Peace Kayleigh Freeman

For those of you who have not yet heard....little Kayleigh Freeman has passed away.
Kayleigh was born on June 23rd 2008 3 months early due to IUGR and preeclampsia. A fragile 10 1/2 inches, 1 pound 1 oz she was the smallest baby to ever undergo open heart surgery. Kayleigh fought so hard for 11 months to get well and go home with her family...But the Lord has other plans for this special angel. She was such an amazing baby.My heart just aches for her loving family. Please click on her tag above to visit The Freemans blog and offer them support and prayer.

Saturday, April 25, 2009

An Update On Baby Sofi

beatingheartSofi's new heart is in, and it is beating, strong! She is ICU right now and so far so good. Thank you so much to anyone and everyone who has prayed for this precious baby. This could not have come at a better time...shortly after they opened her chest...her own heart gave out..stopped beating!She is not out of the woods yet...and there are things that could go wrong (but we're not going to think that way)...your continued prayers are appreciated! Also...if you could find it in your heart to stop by and visited her blog and leave a message of encouragement...that would be so great. I know her family would be so grateful to know that you are thinking of their little girl.

Sofi Needs A Heart





Friday, April 24, 2009

URGENT NEED OF PRAYER!

I have some amazing news! Sofi is getting a heart today! PRAISE GOD!
She’ll go in around 6 or 7 pm tonight and will likely be out by 3 or 4 am. It is unknown who gave has given this amazing gift....but I know her family is beside themselves...with joy and with fear.
Please keep their family in your prayers tonight during surgery and during the recovery process! You can find a link to their blog in the column on the right where it says "In need of daily prayer" Or just click on her picture below. I am so excited and happy that I am literally bouncing in my chair!

sofineedsheart74



Sofi has a condition called Hypoplastic Left Heart Syndrome...Which basically means is that the left side of her heart is under developed. Shortly after birth she underwent open heart surgery...the procedure is called Norwood Procedure. More than 25% of all babies who have this surgery, go to heaven...but she hung on. A few months later she had another surgery called Hemi-Fontan Operation. The doctors say that her heart will only last about 6 months to a year...She is in need of a transplant... 30% of babies on transplant list go to heaven while waiting. Please include Sofi in your prayers....click on her picture to visit Sofi and her sweet family




Tuesday, April 7, 2009

Baby Veiyah Is That Miracle!

Below is a link to a Veiyah Karg update...Thanks to everyone who have prayed for this beautiful little miracle.

Veiyah Karg Video Update


On March 17th Veiyah began throwing up and on the 27th was admitted into the hospital due to severe dehydration...But is doing much better.

Please stop by the Karg Family Blog "Dirty Knee's" for more updates and some pretty cute pictures! Be sure and say hello! Just knowing that you guys are out there praying for them helps A LOT!


Please Visit All The Precious Angels Who Are
In My Daily Prayers!

Monday, March 2, 2009

Please Include Them In Your Daily Prayers

These amazing, and beautiful children and their families are in need of your daily prayers. I can think of nothing worse than watching your child fighting for their life. But I know for certain that prayer works !
Click on pictures to visit them!

"We cannot do great things on this earth. We can only do small things with great love." ~Mother Teresa


The Karg Family found out 13 weeks in the pregnancy that they were having twins, and then at 18 weeks both are girls! Aderah Psalm (the heathier of the two) passed away 2 weeks before they were birthed at just 30 weeks. She developed SVT and her heart rate stayed at 320 bpm for 5 days straight which caused heart failure.Veiyah thrived even though she was the one diagnosed with the heart defect and her organs on the wrong side of her body. Veiyah has fought through several serious surgeries. She is one tough baby!...But she and her family need your prayer. Please of you have a moment...Click on their picture above and pay them a visit.
If you would like to send a card or letter to Veiyah and her family the address is:
Veiyah Karg
University of Iowa Childrens Hospital
200 Hawkins Dr
Iowa City, IA 52245
Attn: PICU - 7JPP


Photobucket
Let me tell you first off that you can't have this little cutie...I've already asked! LOL Zoey is child number 6 and she is absolutely adored by her family!
Zoey was born with a cardiac issue and because of the type of defect, AV Canal Complete, she was born with Down syndrome. She also arrived with Transient Myeloproliferative Disorder, a rare transient form of leukemia. In February 2008, she was diagnosedwith a catastrophic form of epilepsy referred to as Infantile Spasms or West Syndrome....and if that were not enough October the 29th 2008, Zoey was diagnosed with AML M7, Acute Myelogenous Leukemia. Stop by and meet Zoey and her family today and offer your support!


Kayleigh was born on June 23rd 2008 3 months early due to IUGR and preeclamsia. A fragile 10 1/2 inches, 1 pound 1 oz she is the smallest baby to ever undergo open heart surgery. Kaylee is now 8 months old and has just hit the 7 pound mark...She has been very close to going home with her parents a couple of times...and also very close to going home to be with the Lord. She is an amazing baby! Please click on her picture to visit her blog and offer support and prayer.


Abby was adopted from Guatemala. At three years old, she was diagnosed with a high-risk, aggressive form of Leukemia. Certain genetic complications have put her chance of surviving the treatment at about 20%. She is now 4 and desperately needs your prayers. Please stop by and offer Abby and her family your support!


Isn't she precious? One minute you're going through life like everyone else...then in the blink of an eye..your whole life can change...On October 2nd, 2008 Abigail was diagnosed with Acute Lymphocytic Leukemia (A.L.L.)lease stop by the Colberts blog and meet sweet Abbey and family....Your support and prayers would be appreciated!

sofineedsheart74
Sofi has a condition called Hypoplastic Left Heart Syndrome...Which basically means is that the left side of her heart is under developed. Shortly after birth she underwent open heart surgery...the procedure is called Norwood Procedure. More than 25% of all babies who have this surgery, go to heaven...but she hung on. A few months later she had another surgery caled Hemi-Fontan Operation. The doctors say that her heart will only last about 6 months to a year...She is in need of a transplant... 30% of babies on transplant list go to heaven while waiting. Please include Sofi in your prayers....click on her picture to visit Sofi and her sweet family

Prayers for Stellan
In the womb, he was diagnosed with heart failure: premature atrial contractions at 20 weeks; supraventricular tachycardia, hydrops, and intermittent advanced secondary heart block at 23 weeks; and enlargement of the heart at 32 weeks. When the doctors told them at 24 weeks that their very ill baby would surely die, they chose to give Stellan completely to God, for He alone knows best.
Stellans Story