Monday, July 23, 2012

Busy Days of Summer

We had some very busy days last week! 

First we celebrated big events in the Einfeld family - Mom's birthday, Jeanne's visit out here from Illinois, the adoption of Lee and the birth of Carese!
 Next we celebrated Jeremy's 26th birthday on Tuesday:





What a goofball!  But he did like the shirts we gave him!

Next, we spent Thursday afternoon at the beach at our friend's home again.  Jeremy joined us this time!
Isn't she just the sweetest little thing???

Elizabeth gave Dayton a send off.
Elizabeth, our little fish!



Jessica with a happy baby, is there anything more normal?

Our wonderful hostess and her adorable little girl!


On our way home from the lake, we got to enjoy this beautiful sunset too:


Then on Saturday we went to Silver Lake in Everett for my side of the family's reunion (well, my father's mother's side of the family:








 

And yes, as you can see, Carese loves to laugh now!!!

I just LOVE baby feet!










Esther was taking lessons from Elizabeth!



 After the reunion we all walked onto the Edmonds' ferry to deliver Rebekah to my sister, who was taking her to stay with my mother this week.  Everyone enjoyed the ride and the dinner in the park.  We got surprised by the concert in the park - Daryl's favorite style of music, swing/bluegrass/ honkeytonk/ragtime stuff.  Then back across the ferry and home again. And I was on my crutches the entire time, but I made it!  I was a basket case on Sunday, but so glad to be able to do all those wonderful things with my family again! It was a super long day, but full of wonderful memories!

Counting the cars as they disembarked!

Is there anything better!


Time for warmer clothes!

Daryl enjoying daddy/hood and great music!

Man, I love this little girl!

The kids loved trying to stand up against the wind!


Beautiful!


Do you think she enjoyed the ride?
And then there's the "just having fun around our home" photos too: 

My Tweety Bird!


She prefers to ride facing forward now!






















We ha

Friday, July 20, 2012

This Breaks My Heart - But There Is Hope!

Yesterday I was checking on Alexandra's page on Reece's Rainbow and was soooo excited to see that she had been given an anonymous grant donation of $5,000!  Unbelievable!  I was so thankful to my Lord that He moved someone to donate to her adoption.

But today my heart is broken for her.  I also noticed yesterday that they mentioned that they had additional photos available of her so I requested the photos.  This is what I got today and it breaks my heart:

Do you see those precious little legs?  It says in her information "united multiple fractures of extremities, ribs" due to her "Brittle Bone Disease" and now you can see what that means!  Poor Alexandra needs her forever family to commit to adopting her and bring her home so she can have proper medical attention and nutrition to strengthen her bones!

Do you see her size?  I have no idea, but she looks to me like she weighs less than 20 pounds.  That's find for a baby, but Alexandra, IS FIVE YEARS OLD!

Do you see that smile?  In spite of everything she still gave a little smile for the camera.  She is in there, living this nightmare of inhumane care, but she has not mental retardation.  Just a physical disease that makes her bones weak.  

Please consider adopting Alexandra.

Please share this blog post. 

Please share her Reece's Rainbow Page

Please consider donating towards her adoption, even small donations will get her closer to being adopted.  

And Please Pray For Alexandra! - you can print this flyer (click on it to see it full size) and post it on your refrigerator:



Monday, July 16, 2012

What Can I Give Him....

Do you remember that sweet Sunday School song..."What can I give him, poor as I am?"  That kind of thought has been going through my mind over and over again throughout the past month of so...and here's why.

No, I am not poor, but I feel so unable to do something to help the helpless.  Over the last 22 months I have been following a family's journey through adoption and beyond.  This family was adopting internationally, like many other families I know.  But this was different.  First of all, I had never met this family, but I have a close connection to this mother going back ever farther.  Over two years ago, Susanna contacted me after she found this blog.  You see, she was expecting her 10th baby and had received a prenatal diagnosis of Down Syndrome.  When she was researching to prepare for her new little one, she found my blog and read about Esther . She sent me a message (which I found just weeks before her baby was due) and told me that my blog was a great help in preparing her for her little one, answering questions and dispelling fears.  I loved connecting with another mother-of-many  who would be mothering a precious child with Down Syndrome.  I followed via her blog, The Blessing of Verity, as she went down many of the same paths that we did...nursing difficulties, heart defects, open heart surgery, Occupational Therapy, Speech Therapy and more.

This precious little girl was born into an amazing family.  They loved her before they saw her.  They cared for her oh so carefully as she too, like Esther, had a hole in her heart.

But then, their journey began to take a new direction - adoption.  This was not something I could personally relate to, but was fascinated by.

I've known several families who had adopted internationally and have watched as they blessed children who had little opportunities to grow and develop in the nation of their birth.  Some were old enough to know the difference, others were not.  I always thought that it was wonderful that these parents would make such a huge sacrifice to help a child - to make a difference in the life of a child who has little hope in their future.

But Susanna's adoption showed me a whole new world.  Children who desperately needed to be adopted.  Babies and children left in their cribs all day.  Children with feeding problems who had a bottle propped up in their mouths and left to "deal with it".  Babies who had their diapers changed once a day.  Children who had never seen the light of day.

When I think back to the weeks we spend with Esther in the hospital I remember going days without stepping foot outdoors.  This was especially bad when she was in the Special Care Nursery in our local hospital as there were no windows to the outdoors, and in NICU at Seattle Children's Hospital as only some of the NICU rooms had windows but we never seemed to get a "room with a view" there.  I think it messes with your mind if you never get to breath fresh air, feel a breeze on your skin or the sun on your face (for that matter, the rain on your skin or the snow gently caressing your face - Esther's journey to her heart repair was mostly in the winter ;).  When I think of our Esther being deprived like that I just can't even stand the thought.  She had my love and tender care everyday, as well as  caring nurses, regular diaper changes and careful feedings even if I wasn't present.  But these precious little ones are never held, rarely talked to and hardly ever get out of their cribs.  My heart broke for these forgotten children.  There has been a program set up to give "Babbas" to these children, grandmas if you will, and this has helped tremendously, but it's not enough.  To read more about Pleven, the orphanage that Susanna was adopting from, Read This.

The really sad part to me is that children with Down Syndrome are so social.  They love to be around people, they love to smile, give hugs and kisses and are in tune to the emotional needs of those around them.  But these precious little ones at Katie's orphanage, on her floor,  could not do any of the these things, and to be aware of the great needs of those around them (even if only to be in tune to the suffering sounds around them), seems to me like the cruelest hell for someone with their special abilities.  Not all of the children on Reece's Rainbow are in these terrible institutions, but many of them are.  Even those that are in good orphanages or foster homes need the special care that only a lifetime family can give them.

Here is Katie without her family...take a good look at her calf and her wrist...
Susanna's blog posts told of these deprivations and more, but she also shared about a wonderful organization that was dedicated to finding these "hidden treasures" and getting them adopted.  It's called Reece's Rainbow.  They specialize in working to get orphans with Down Syndrome adopted into loving families, but they also have other "angels" who have other problems like Cerebral Palsey, Spina Bifida, Brittle Bone Disease and other birth defects.  I couldn't believe how many children there are in the world who had been rejected by their families because they had Trisomy 21 or some other birth defect.  I understand that some of them might have been unable to get their child the medical care that was needed, but by far the majority of these children had been abandoned at birth because they were not "perfect".  For many, the stigma of having an imperfect child was just too great, the sacrifice too much.  After about a year, Suzanne was able to visit their "Katie-bird", set up things for her care to prepare for going to her forever-home, and then return to bring her home.  This little girl may look like  she's a baby is in reality 9 years old in this photo.

I watched through her blog posts as Katie was able to come home to her forever family.  She flourished through both proper medical and physical care as well as the love of her new family.  She became active, started connecting with people, learning to love being held and caresses, and above all, growing!  She went from a child starving both physically and emotionally to a little girl thriving on good nutrition, proper medical care, lots of fresh air and timely diaper changes, and loads of love...these two photos are just 7 months apart!

But why am I telling you all of this?  No, we are not adopting (at least not yet, but who knows what God might do in the future).  Am I trying to get the word out about Katie?  Yes and No - this little girl has been saved out of that life, she's doing wonderful in her new home and new family, but that is not the real purpose.  I am telling you this story because it shows what a loving home and family can do for a child seemingly beyond hope.  Looking at Katie's photos in the orphanage you wonder if there's any hope that she could survive, let alone thrive...is the damage done too great?  Is it worth all the money and hard work to adopt a child from so far away?  Would she appreciate it?  Would she ever be healthy?   The answer is yes!  It is worth it all to get her into her forever family!  She will continue to have health repercussions and developmental delays due to the deprivations she experienced, but they are slight compared with the future she faced without adoption.  And she's not alone!  There have been several children adopted out of the institution where Katie came from and they too are thriving in their new homes, loved and cherished by their new families! And there are still over a hundred children (to the best of my knowledge) in that very institute, desperately needing to find their forever families.

I have been so challenged by all of this.  I've even looked into what it would take for us to personally adopt a child with special needs.  But at this time we can not do that (my knee is the biggest hurdle as I might be having surgery and laid up for a while this fall).  I'd love to be able to financially assist another family adopting, but we aren't in a position to do that right now either (but I hope to do this in the future).  But what I can do is get the word out - through my blog and through my business.  I can also become a Prayer Warrior, a Guardian Angel, a Family Sponsor and/or an Orphan Warrior.  I'm hoping to do all - I've even picked out which ones I want to feature here!!  

So, "what can I give Him?"  I'm giving my time, energy and my blog.  I can get the word out that these children need help.  Reece's Rainbow is dedicated to matching up families who are able to adopt, children with special needs who need to be adopted,  and those who can't adopt but can donate towards those adoptions.  It's a match made in heaven!

I've heard it said "but I can't help all those children!" No, but you can make all the difference in the world to one child.

Please take some time to pray about how God would have you help bring these precious little ones into homes where they will be loved and cared for.  It could be a simple as "sharing" this blog post, being a prayer warrior, "sharing" a little one as a timeline update on your Facebook account, sponsoring a little one or a family on your blog, or donating money towards a child or family.  Maybe for some of my readers God has grabbed a hold of you heart and challenged you to go further.  If so, I'd love to hear about it and work to help you bring your forever child home to your family!

Here are the precious little ones I have chosen to sponsor here on my blog:
Alexdra is a little girl who has Brittle Bone Disease.  She just turned 5 years old. She is in an Eastern European Orphanage. I hope to be her official Guardian Angel.  She needs to find her forever family!  Take a minute to check out her profile, and, if you can, send some money her way so her forever family can get the help they need once they find her!
Kimberly  is from Latin America.  She has Down Syndrome and a few other medical issues that we are familiar with like crossed eyes and hypothyroidism.  We have all marveled at how much she looks like Esther (hair color aside)!  I am going to be her Orphan Warrior.  Her forever family needs to find her! Please donate on her behalf - she doesn't have anything yet!

And the family we are sponsoring is Paul and Maria Brown of Washington State!  I picked them because they are here in Washington, and they are adopting a little girl named Gemma out of Pleven, the orphanage where Katie was adopted from.  I am looking forward to following their story as it unfolds, watching as God works His miracles in the life of another precious little one who has found her forever family!  You can too - check out their adoption blog, Carry Your Light.  Take a minute to check out their profile by clicking on the image below, and help them build their adoption fund - I'm sure it would be encouraging them as they are just starting out in this journey!


Wednesday, July 11, 2012

Carese, Camping, Cavities and Cartilage!

Carese is still little, but she's grown a lot!  This rose headband shows how much her head has grown!  She now weighs 11 1/2 pounds, and that means she's gained almost 8 pounds!



 We took her for her first camping trip this past weekend and she did great.  She loves to be outdoors so she was totally enjoying every minute of it.  She did great sleeping at night, and I had her sleeping in her car seat, so it felt a lot like her bed at home which has the bottom of the bed at an angle, like a wedge.



As you can see in this photo, she is enjoying some exercise time on an air mattress! As usual, we forgot a few things (like garbage bags), and ran into a few snags (like the trailer brake not being hooked up to the battery, and all but one air mattress going flat the first night).  We got to camp a lot later than I had planned, but it was better that way as I had planned to drive the kids up there by myself, but some of the problems I ran into required Daryl to fix them, so the nap I took was a great use of the time while we waited for Daryl to get off work.

I was having such a great time camping (in spite of crutches), that I didn't take any photos, sorry about that.  I did have some difficulty getting in and out of the trailer, but I worked it out and just didn't go in or out unless I really needed to!  But they would have been a bit boring as we mostly just relaxed and hung out with Daryl's work co-horts (it was his work's camp out at Silver Lake).
One surprise we had was that Rachel broke out with chicken pox the day before we left for camping (the day we went to the beach again), but we weren't sure it was CP until the end of the weekend.  Carese started showing signs of a mild cold the last night there, and she has been snuffly all week, with a little cough.  She's been wanting mama more than usual, and a little fussy in the evenings, but other than that she's doing really well for her first cold. Reuben seems to have the same cold only his cough is really bad.  Today he seems much better though, so that is a relief!  Rachel too this sweet photo of Carese sleeping at the beach in the shade. The camera had been set to "point and shoot" but the lighting worked well enough that the flash didn't come on and it turned out to be a nice, natural light photo after all!

Another big even last week was Esther's first dentist appointment with a new pediatric dentist, Dr Apple.  Dr Apple is working out of Dr Yeh's office, he's our orthodontist, when Dr Yeh is in his other offices.  This means that all our dentists and the orthodontist appointments are all within three blocks of each other!  Esther did much better at this dentist appointment.  Esther doesn't not like to have her teeth brushed, and oral sensitivity can be a problem with children who have Trisomy 12.  Overall Esther does not have oral sensitivity, so I think it's more of a toddler thing of not wanting anyone messing with her mouth.  The dentist was very upbeat and encouraging to Esther, plus she didn't seem to be in a rush.  She did find two watch spots, but no cavities - Yay!  The fact that the dentist is a woman was reassuring as well, I believe.  She did so well (she did cry, but she wasn't hysterical) that she got to pick out a sticker.  She picked out a very appropriate sticker don't you think?

A little information about my knee  - here's an excellent image of the knee, and if you look at the work cartilage on the left side, there's an arrow pointing to the Medial Condyle Cartilage.  My defect is approximately 1 cm around, going through the cartilage to the bone.  The defect is on the weight bearing surface, probably right where that arrow is pointing.  Only it's my right knee, not the left as show in the image.  Today I went in for another appointment,  since it hasn't improved much he wants me to keep on crutches, icing it 3 - 4 time a day,  for the next 5 weeks, hoping that it will find a new normal (cartilage does not heal).  If needed, at my next appointment I am expecting to get a different injection, and I hope it will do the trick for me.  This injection will be of Hyaluronic Acid, and it's usually used for osteoarthritis (which I had the early signs of on the edges of the cartilage) and can also be helpful with cartilage injuries.  It basically coats the inside of the knee covering defects with a smooth, slippery gel like coating, covering a multitude of sins, so to speak.

Now for some more Photoshop fun!  I learned how to dark the edges, or surround a focal point with a darker version of the image.  This is great to bringing the object of the photo into sharp focus, drawing attention to what you want looked at!  This can be done just around the edges of the image too, but I haven't done that yet.

 I used that technique on the photo of the butterfly below, giving the impression that the light source was through an opening in the leaves above the butterfly, and then I also used the dark space to add scripture.  I am going to frame this one for my kitchen as my kitchen is in blue, black and white!  If you click on the image (or any image on my blog) you can see the full size version!


Monday, July 9, 2012

A Day at the Lake

A week and a half ago I got to spend the afternoon at a friend's house which just happens to have a beach at the end of their back yard.  We had a great time in spite of a cloudy day that even rained quite a bit.  I even had the privilege of  using our host's telephoto lens on my camera!

For those of my readers following my photo learning journey, these were all shot with the Manual setting and in RAW, and edited with Photoshop CS3 - no special effects, but learned a lot with every photo about lighting, focus, shutter speed, "noise" and more.  I love shooting in RAW - now it seems easier than it should be!  I've also learned to delete bad photos (RAW images are huge), save the original image in RAW for good images, save a large version of the image and one that is sized for the blog (800 pixels wide).

Here are some of the highlights of the day:



This was in quite low light, but with PS I was able to brighten it up.

All I can say is "WOW" - a great portrait of my serious man.
See how the background is all out of focus?
This was a very low aperture (4) and a very awesome lens!

He was about 30 feet off the shore.  Does this kids ever smile?
Yes he does - he was beaming from ear to ear after going tubing!

Esther hamming it up at the alfresco dinner.

Our host taking his cat out for a leisurely row...
never seen that before but it was great!

A sweet portrait of Rachel soothing Carese.

Jonathan and Rachel canoeing - about 150 feet from shore.

This is Rachel, sitting in the canoe about 60 feet from shore
I sure hope I can get a lens like this one someday!

Rebekah keeping Esther warm and happy!

Heading out for tubing...all the kids had a great time,
 but they were too far away for any good  photos.

Jonathan helping Dayton learn to paddle 
and finally Bocce Ball to finish off the evening.

Monday, July 2, 2012

Photoshop is Awesome!

I have been learning to use Photoshop like crazy!  I haven't even received my copy of "Photoshop for Dummies" yet (picking it up from the library today!).

Here's some things I've been learning:

Original photo:
Here's the original photo with it only re-sized to fit here.

Here's the photo as I originally edited it by some basic adjustments like cropping, gamma correction and light.

Here I took the edited photo and pulled it into Photoshop and applied a filter of noise reduction and hue adjustment 

Then we had some fun and applied another filter called "poster edge"

And another cool filter was "dark stroke"
Daryl and I also worked all day Saturday creating new graphics for my website, the most awesome of which is the new graphic which started with this photo:

and ended like this:


I can't wait to do some more, but first I need to finish my website overhaul...we are very close, but need to tweak a few things and update all the pages...