Showing posts with label encouragement. Show all posts
Showing posts with label encouragement. Show all posts

Friday, January 04, 2008

One Small Sparrow


I've just finished a book that I thought some of you would enjoy reading. It's called One Small Sparrow by Jeff Leeland and you can read my quick review over at my main blog, Up the Hill Gang. I have a hardback copy that I found in the free bin at our local book exchange place and I would love to pass it along to one of you! It's first come first serve...just make sure you leave me your e-mail or blog address so I can get in touch with you to get your mailing address!

Sunday, November 18, 2007

Words of Encouragement

As I was out and about visiting other blogs today, I came across a post over at The Not Quite Crunchy Parent blog which reminded me of all the words of encouragement we received and still do receive on Gus' Caringbridge site. MC Milker has written a post called "Caring Through CarePages" about how she has been lurking around one that has been set up for a child who has leukemia. This little guy goes to preschool with her child.

I can't even begin to tell you all how encouraging it was to us to find out that we had received comments. Some were short and to the point and others were long...all were refreshing and gave us so much love. Just that fact that someone had checked in on us was encouraging.

So, if you are ever at a CarePage or Caringbridge page, please be sure to leave a comment. It doesn't matter if you actually know the person or not. In fact, that is exactly how I met Judi, Grayson's mom...she had commented on Gus' page after he had died and we started corresponding. So, see...you don't have to really know the family to spread God's love and encourage one another.

I challenge you this week to find a Caringbridge or CarePage site and just leave a comment. Some pages are private, but there are plenty of ones out there that are not. Of course, you can always visit some of the kids we have listed in the sidebar.

You really can make a difference....

Wednesday, September 26, 2007

The Deaf Pilot...Cool!

I was avoiding any kind of responsibilities this morning and I came across a wonderful post that Lillie had written over at her blog A Writer's Words, An Editor's Eye. It's about two people who have overcome great obstacles. Of course, I focused in one the video of Stephen Hopson because he is deaf. Gus was profoundly deaf and I found that, while he was here with us, I developed a heart for the deaf. I am amazed at these people...what heroes they are. Can you imagine for even a minute what it would be like to hear absolutely nothing?? It blows my mind...

Here's a video about Stephen. I hope you enjoy it as much as I did and I hope that you are inspired by his "can do" attitude! I also hope you catch that there was one person, his elementary school teacher, that encouraged him...and I hope that instead of just looking at people who are "different" that we all reach out and encourage and embrace these people...and appreciate them for the wonderful gifts they are! Enjoy!



Stephen Hopson links:

Obstacle Illusions
Adversity University

Tuesday, September 25, 2007

Little Rooms...All the Cool Blind Babies Have One!

Really...I stole the post title from what the author of this neat site said because it completely cracked me up! It reminded me of how much it is necessary to have a sense of humor when you have a sick child...it's good therapy!

All that aside...if you have a blind baby or know someone else who has a blind baby, then you need to visit Wonderbaby support groups where you can meet with moms and dads who have "been there-done that"...it's . Not only will you find instructions for making your own "Little Room" but you will find a lot of resources for families with blind babies. Most importantly you can find severa moms and dads who have walked the path before...it's always comforting to know those who are farther along the path...

Sunday, July 29, 2007

Welcome To Holland


Emily Perl Kingsley is a writer for Sesame Street. In 1974, her son, Jason, was born with Down Syndrome. Her experience with her son inspired her to include people with disabilities in the Sesame Street cast.

Though Down Syndrome was not what we experienced, I really could relate to this story. I know a lot of other families do also.

by Emily Perl Kingsley.

c1987 by Emily Perl Kingsley. All rights reserved

I am often asked to describe the experience of raising a child with a disability - to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this......

When you're going to have a baby, it's like planning a fabulous vacation trip - to Italy. You buy a bunch of guide books and make your wonderful plans. The Coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It's all very exciting.

After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome to Holland."

"Holland?!?" you say. "What do you mean Holland?? I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy."

But there's been a change in the flight plan. They've landed in Holland and there you must stay.

The important thing is that they haven't taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.

So you must go out and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.

It's just a different place. It's slower-paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around.... and you begin to notice that Holland has windmills....and Holland has tulips. Holland even has Rembrandts.

But everyone you know is busy coming and going from Italy... and they're all bragging about what a wonderful time they had there. And for the rest of your life, you will say "Yes, that's where I was supposed to go. That's what I had planned."

And the pain of that will never, ever, ever, ever go away... because the loss of that dream is a very very significant loss.

But... if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things ... about Holland.

Saturday, July 28, 2007

The Prayer Chain

This is the Prayer Chain I made while Gus was in the hospital before he died. I keep it on our mantle as a reminder to me of God's answered prayers...He answered them all. Sometimes, He didn't answer in the way I wanted Him to but He did answer. If I had started this chain when we checked in the hospital the last time, I would have a much bigger heap of chain. I only thought about this toward the end of Gus' life. I had it taped to the wall and the nurses knew that when I came into Gus' room that I would want to know which links I could add to the chain. They were great and so understanding....I miss those gals!


Here's a link that says "Dopamine Down"...when Gus' Dopamine level was lowered, I added this strip of paper to the chain. I had a good twenty strips with specific prayer requests written on them. A lot of times, prayer requests were duplicated because his need for meds would be different hourly...I really wish that he could have gotten a transplant....

Sponsor me...please.

G.U.S. Boxes

Shortly after Gus died, I received a care package with several books of encouragement. I was so touched by this that we decided to create our own package to send to families who are suffering the loss of a child. Linda, the TEIS coordinator for our area, called to my attention that Gus stood for "God Understands Suffering"....and she was absolutely correct! Who knows better than God who sent his only son to die on the cross so our sins would be covered...and so we could have an eternal relationship with Him!! We have seen firsthand, the comfort and love that He pours out on his children who are suffering and missing their own little ones.

It is our desire to send these boxes out to anyone who needs them...free of charge. If you know of someone who you think would be encouraged to receive a G.U.S. Box, please e-mail me with the address. I will keep all addresses private.


Contents:

Tuesday, July 03, 2007

Noah Moves Up the List!

I’ve just read that Noah has been bumped up on the transplant list! This news is really good but also not so good…ahhhh….life on the transplant list. You see, the sicker Noah gets then the higher he goes up the list. Right now he is listed as a 1A…I’m not sure how the heart list is set up but that’s as high as you can be on the liver list. Also, Noah may need to have another surgery that would help protect his lungs.

So, all you prayer warriors out there, let’s all pray that his mom gets the “call” really soon and that this potential upcoming surgery will be successful.

Also, Noah’s mom has been meeting people at the Ronald McDonald House who are post-transplant. What a huge encouragement this is to her…I thank God for places like the RMH and I thank Him too that he has brought these people across Crystal’s path. I love how God works!

Be sure to zip on over to Noah’s blog for all the details!

Sunday, May 06, 2007

Devastation


I saw this photo over at CNN and all I can do is shake my head...I can't even begin to imagine what this is like...what it is like to live through something like this. When I see natural disasters like these, I can't help but wonder about all the people who are dependent on medical equipment such as TPN pumps, oxygen, nutrition pumps, etc....most pumps have a battery back-up but sheesh...who wants to worry about a battery dying in the midst of all of this??? And TPN needs to be in the fridge...and what if your fridge has been blown away...and what if your meds have been blown away....too much, too much....
... though he stumble, he will not fall, for the LORD upholds him with his hand.
Psalm 37:24

Tuesday, March 27, 2007

Cry Babies!


This is what my nurse practitioner and I did today at my appointment!! I went in for my six week after-delivery check up....several years late! lol!! The FNP was so sweet...she told me there were no words she could say to me to make any difference...and then her eyes welled up with tears...and we cried. Ahhh...but she did make a difference! She didn't need words...just the fact that she would cry with me and allow me to share with her a few memories of Gus. I consider my visit with her a "hug from God"....she truly blessed and encouraged me today!

Wednesday, February 14, 2007

Valentines ...to Heaven



Valentines...... To Heaven



This Valentine is not of the ordinary kind,

Its still filled with love...and blessings inside;

But mine has to be sent on the wings of love...

You see its destination is the Heavens above.


Its not being sent to my parents so dear,

For they are still with me each day of the year;

Its being sent to my child...who left earth so soon,

Who's now in the Heavens with the stars and the moon.


The message is the same as your valentine,

"I love you...my sweet precious child of mine;

My love is still deeper than the ocean is blue,

And its sent with hugs and kisses...from me to you."


"I know you are with me each and every day,

You listen as I talk to you...and hear what I say;

For that is one thing that disease cannot do......

you'll always be apart of me...and me a part of you."


"I know God did not give you the awful disease,

Thank Him for His comfort He gives me...would you please?

I dont know what I would do without His undying love...

Sent to bereaved parents from the Heavens above."


"I know you are in the best of care,

But it's so hard for us left on earth to bear;

Could you put in a request from us left behind...

For God to send the knowledge..so a cure we can find."


"So that no other family has to go through this pain,

Our lives without you will never be the same;

When I get lonely I will look to the sky at night...

And see you shining down your big bright light."


"Happy Valentines day sunshine...I miss you so much,

I know you know how many lives you have touched;

You'll always be mine...I love you with all my heart,

I know we be together again...and then we'll never part."


So you see the meaning is still the same...

The method of delivery is the only change;

Mine must be sent by a little white dove...

On the wings of Love.


Author~ Laura/Heavenly Lights Childrens Memorial
Love~ Claire (Mommy to Laken in heaven)

Sunday, January 07, 2007

Holland


Red Tulip Field in Lisse, Amsterdam, North Holland, Netherlands Izzet Keribar




I know that quite a few of you are already familiar with the story "Welcome to Holland" by Emily Perl Kingsley. If you are not, please take the time to read it here. It is one of my favorites!




Tuesday, December 19, 2006

The Brave Little Soul



The Brave Little Soul

By: John Alessi





Not too long ago in Heaven there was a little soul who took wonder in observing the world. She especially enjoyed the love she saw there and often expressed this joy with God. One day however the little soul was sad, for on this day she saw suffering in the world. She approached God and sadly asked, “Why do bad things happen; why is there suffering in the world?” God paused for a moment and replied, "Little soul, do not be sad, for the suffering you see, unlocks the love in people’s hearts.” The little soul was confused. “What do you mean,” she asked.” God replied, “Have you not noticed the goodness and love that is the offspring of that suffering? Look at how people come together, drop their differences and show their love and compassion for those who suffer. All their other motivations disappear and they become motivated by love alone.” The little soul began to understand and listened attentively as God continued, “The suffering soul unlocks the love in people’s hearts much like the sun and the rain unlock the flower within the seed. I created everyone with endless love in their heart, but unfortunately most people keep it locked up and hardly share it with anyone. They are afraid to let their love shine freely, because they are afraid of being hurt. But a suffering soul unlocks that love. I tell you this - it is the greatest miracle of all. Many souls have bravely chosen to go into the world and suffer - to unlock this love – to create this miracle - for the good of all humanity."



Just then the little soul got a wonderful idea and could hardly contain herself. With her wings fluttering, bouncing up and down, the little soul excitedly replied, "I am brave; let me go! I would like to go into the world and suffer so that I can unlock the goodness and love in people’s hearts! I want to create that miracle!" God smiled and said, "You are a brave soul I know, and thus I will grant your request. But even though you are very brave you will not be able to do this alone. I have known since the beginning of time that you would ask for this and so I have carefully selected many souls to care for you on your journey. Those souls will help you create your miracle; however they will also share in your suffering. Two of these souls are most special and will care for you, help you and suffer along with you, far beyond the others. They have already chosen a name for you. God and the brave little soul shared a smile, and then embraced.



In parting, God said, “Do not forget little soul that I will be with you always. Although you have agreed to bear the pain, you will do so through my strength. And if the time should come when you feel that you have suffered enough, just say the word, think the thought, and you will be healed.” Thus at that moment the brave little soul was born into the world, and through her suffering and God’s strength, she unlocked the goodness and love in people’s hearts. For so many people dropped their differences and came together to show their love. Priorities became properly aligned. People gave from their hearts. Those that were always too busy found time. Many began new spiritual journeys – some regained lost faith – many came back to God. Parents hugged their children tighter. Friends and family grew closer. Old friends got together and new friendships were made. Distant family reunited, and every family spent more time together. Everyone prayed. Peace and love reigned. Lives changed forever. It was good. The world was a better place. The miracle had happened. God was pleased.




I found this wonderful story over at Molly Grace's Caringbridge site.


Wednesday, January 18, 2006

The Strength of an Egg

I found this story over at Lisa's CB site.




The Strength of an Egg


by Juliet Freitag




Parents of children with cancer, or really any serious condition, are often referred to or viewed as having strength "like a rock." Albiet flattering,it isn't quite true. It is more like the strength of an egg. An egg, you ask? Yes!



If you'll think about it, you'll see my point. An egg has a polished, smooth outer appearance, with no cracks or weak spots visible. It seems almost inconceivable that the inside might not be so smooth or solid.



Most children, at some point are shown the famous egg trick. An egg set at just the right angle can withstand enormous amounts of pressure and cannot be cracked or broken. Yet the same egg, tapped gently at an ever slightly different angle, will break. The contents, once so neatly concealed, will come spilling out. The no longer perfect shell will be crushed. It looks so fragile that it seems inconceivable that it ever held any strength.



A rock, on the other hand, is solid all the way through. To break it is almost impossible. If you succeed, you will find that there is nothing inside but more rock.



It takes a lot more than pure hardness to hold the hand of hope. Parents of [medically fragile] children are not solid all the way through. We hurt, we fear, we cry, we hope. It takes a very careful balancing act to keep the shell from being shattered. "Balancing an egg" while running a household, going for doctors' visits and hospital stays, keeping the family together, and holding on to the constantly unraveling ties of your sanity can be very tricky indeed! Occasionally, the angle will be off and the shell will break, shattering hope and all the neatly secured appearances of a truly fragile existence.



Unlike Humpty Dumpty, though, parents of [medically fragile] kids will pick themselves up and put themselves back together again.