Feb 29, 2012

Wonder Baby

Ivan Kapi'i Bobnar was born June 11th, 2005. Soon after birth, Ivan was having trouble breathing, and, after hooking him up to monitors, we discovered that his blood oxygen saturation was very low.

We spent the first week of Ivan's life in the hospital, then we were sent home with monitors, oxygen canisters, and medication. The doctors were confused but assured us that he would grow out of these respiratory problems (which included apnea and reflux) as his system matured. We were very anxious but also very happy to have Ivan home.

His breathing problems did pass, but by the time he was 2 months old and not focusing on objects we were worried about his eyes. We were told to wait until he was 3 months old. He still wasn't focusing and that's when the crazy stream of doctors' appointments began. Most of his doctors assumed Ivan had LCA (Leber's Congenital Amaurosis), and that was confirmed with an ERG in July, 2006. (You can read more about our ERG and Ivan's LCA diagnosis here.)



Ivan is happy! In the summer of 2008 we attended an LCA conference and felt that Ivan, then three years old, just wasn't keeping up with his peers. So we began scheduling more doctors' appointments and tests and by late 2008 Ivan was diagnosed with Joubert Syndrome along with the already diagnosed LCA. Ivan began seeing a geneticist at Children's Hospital Boston and we soon discovered that he had a mutation on the CEP290 gene that is often associated with both LCA and JS.

But Ivan's trials weren't over. When he was about three and a half years old he began losing his speech and by the time he was four he was completely nonverbal. Ivan had gone from a boy who had over 100 words and was beginning to put two- and three-word sentences together to a boy with no language at all in about six months.

More doctors' appointments led us to a diagnosis of Landau Kleffner Syndrome, a language processing disorder caused by sub clinical seizures in the language center of the brain. Of all the diagnoses Ivan has received, this one was the hardest to take. LKS took Ivan's speech away from him, along with much of his physical and cognitive skills. Seizures are nasty, nasty things.

In 2010 Ivan had his first sustained tonic-clonic seizure and we knew his epilepsy was getting worse. It was a frightening day, and we are still playing the medication game trying to find the right combination and dosage. I'm happy to report that his last 24-hour EEG was spike free!

Through it all I've learned that regression is a bad word, but that it often comes hand in hand with disability and that we should appreciate everything we have now because life is fleeting. I'm also impressed everyday with the grace and strength with which Ivan faces his challenges and I am determined to help Ivan be the best Ivan he can be!

WonderBaby.org, a project funded by Perkins School for the Blind, is dedicated to helping parents of young children with vision impairments as well as children with multiple disabilities. Here you'll find a database of articles written by parents who want to share with others what they've learned about playing with and teaching a blind child, as well as links to meaningful resources and ways to connect with other families.

WonderBaby.org: Resources for Parents of Blind Children


If you would like to link to WonderBaby, please click here.

I began this site in 2006 when my son, Ivan, was only one year old. He had just been diagnosed with LCA, a rare retinal disorder, and we were desperately searching for support and answers. At the time I thought it might be a good idea to gather everything I found into one place.



In 2011 WonderBaby teamed up with Perkins in order to provide more features and support for families through the internet. My original intent for the site was just to link to resources I found on the web, but before I knew it I was writing more and more about Ivan and all he had to teach us! I soon learned that other parents were experiencing this too... we all know that our children are full of wonder and they amaze us every day. As we focus on teaching our children all they need to learn in order to be as independent as possible we are often surprised to find out that we are learning so much from them!

If you want to share your story or have any ideas or advice for other parents, we'd love to hear it! Please contact us!

Rare But Strong Together


Feb 28, 2012

Try This Fresh Perspective On Your Strengths & Emotions

Photobucket
I went to a women's conference a few weeks ago and I keep thinking about one of the talks. It really resonated with me and I wanted to share it with all my kidz readers. I hesitated to do so, though, but it just keeps nagging at me and I cannot put it off any longer. I hope you can be touched by this like I was. It really helped me accept and understand some of my feelings about a lot of things! I'm just doing a re-cap from my notes about the talk given by Julie Hanks, a clinical social worker/therapist as well as a singer/songwriter. If you've ever wondered where your miracle is and can relate to the lyrics of her song, then the message of her talk is for you!

Overwhelmed and underpaid
Morning comes too soon
Running late and on my plate
A million things to do

Got a baby cryin'
Another trying to find the other shoe
When I open my eyes the dam will break
Their need will flood my room

My mother's sick
And I'm late to pick up kids at school
I need to clean, can't fit in my jeans
The fridge gives no comfort food

You made wine from water
And raised up Jairus' daughter from her bed
Filled the empty fishing nets
And with some loaves and fishes fed a hungry crowd
Make enough of me to go around

Multiply and magnify this tiny little life of mine
Enlarge me and expand this heart and fill it with divine
My heart is cold, nothing grows but thistles and some thorns
They choke the light and shrink the vine, I need to be reborn

You made wine from water
And told a scarlet daughter, 'Sin no more.'
Surrendered to the garden,
Through thorns and nails you pardoned the angry crowd
Make enough of me to go around


 Many women live by several myths:
  • Taking care of myself is selfish
  • I should always be happy and perpetually sweet
  • Acknowledging my strengths is prideful
These things are NOT true! This is truth:
  • We have to take care of ourselves first so we can take care of others.  (Think of the oxygen mask in an airplane).
  • We need to acknowledge all of our emotions so we can identify the source of those emotions, manage them, and use them for good purposes.
  • It is ultimate humility to acknowledge the good of God in yourself. Understanding and owning your divine attributes and divine purposes is one of the highest levels of gratitude. Here's a short clip from Julie Hanks talking about accepting your strengths and improving your confidence:



Start to think of emotions as E-MOTION ---> energy in motion. Emotions are to be used as a guide in our lives and to help us understand our true, authentic self. We don't have to feel better, but get better at feeling and understanding those feelings. Don't suppress your emotions. Instead, ponder on them, then use them to direct your actions and interactions so you can be a source of joy as well as find joy for yourself! What brings you joy is information about your life's mission, so prioritize the things that bring you JOY!


Oftentimes our to-do list doesn't get checked off because we spend time taking care of other things that come up, like talking to a friend who is going through a hard time, doing a craft with our child, or going on a walk because the weather was so nice and it made us happy. Then we beat ourselves up when we look at the unchecked items on our list. Stop that!!! Instead, make a "Ta-Da!" list at the end of each day. This is a list of good things you did, those things that really are most important. Acknowledge your accomplishments, do not dismiss them because you didn't achieve the trivial tasks around the house. See and appreciate the good within yourself and all the good that you do each day!

I hope these concepts touched even one other person as much as they touched me. As I have applied this fresh perspective on my emotions and strengths, I have seen a tremendous difference in my life -- an increase in happiness! And you special needs mamas definitely deserve a little more happiness!

  Photobucket

Feb 27, 2012

Love That Binds

Photobucket
Love Quilts is a great organization that creates quilts for critically ill children. All that is required is a page such as a blog or Caring Bridge that keeps the association or quilt maker updated on child's progress. Here is a little more about how it started.


Hi!

I am Cathy, I run the online group Love Quilts. If you have been a part of Love Quilts for a while I know what you are thinking, "Wow, I now have a face with all the emails!". I know how nice it is to finally see a picture of someone I have been corresponding with for a while, but they never look like I thought... I am sure it is the same with me! :-)
I am creating this page because so many have asked about me and how Love Quilts began. I thought this would be a good way for everyone to get to know me a little better.
First I will start with a bit about me. My name is Cathy, I am 41 and I have been married for 20 years to Jeff. We have two children, Curt is 19 and Kayte is 16. We live in Michigan and for 3 1/2 years we lived in the house my husband grew up in, we bought the house in October 1999. We moved into our brand
new home in June 2003 and we just love it! Both my husband and I are Christians and have been since we were children. We attend a wonderful church in our area and we just love it! I am a stay at home mom and the full time coordinator for Love Quilts. I enjoy cross stitch (obviously! LOL), crocheting, genealogy, history, lighthouses, my computer, cats, camping and more! We also enjoying having exchange students. In 2007 we had Marlene from Mexico and Jenny (Eun-A) from S. Korea. Marlene was with us for 10 months, Jenny for 5. In August 2007 we were joined by Pia from Norway, but she only stayed 2 months and moved back home. This year we had Tabea from Germany for 4 months and we had a welcome student, Sophie from Belgium. Sophie was with us for 2 weeks before she went to her permanent home. This past summer (2008) Marlene came back for a visit for 5 weeks and it was wonderful!! We miss her so much! The organization we used for our exchange students is PAX - http://www.pax.org/. We have enjoyed going through this organization.
Well, lots of people want to know how and why Love Quilts began. LQ began in February 1999 and was started because of some things that had happened in my family. In April of 1998 my first cousin's daughter, Kelsey, was diagnosed with a massive brain tumor. She was a very sick little girl and they didn't know if she would live through the operation. The sad thing is her mom had been taking her to her family doctor since she was about 3 (she was 5 by then) with complaints of headaches that made her throw up. The doctor said she had allergies at first and then said she was faking it! Finally her mom had had enough and took her to another doctor and was immediately diagnosed with a massive brain tumor that was wrapped around her optic nerve. They did the surgery in the middle of April (1998) and she had another surgery in July of the same year to remove the remaining tumor missed in the first surgery. These surgery's left her with a number of problems including the fact she has lost all of the hormone part of her brain. Your hormones control so much, including your sleep, the hormones tell you to go to sleep and when to wake up and she couldn't do that. There was the risk that she would go to sleep and never wake up because her brain wouldn't tell her too. She is now 16 years old and she is doing ok, but the effects of the tumor will last her a lifetime.

In May/June of 1998, 2 months after Kelsey's diagnosis, my nephew Justin (my oldest sisters second child) was diagnosed with bone cancer in his left leg at the age of 16. He had been doing cross country racing in high school and during a race his calf area of his left leg began to hurt. It hurt for a couple of weeks and they finally took him in to a walk in clinic and they did x-rays. The determined that he had broken the small non weight bearing bone in his leg. Because there wasn't any major trauma and he was young and healthy they looked into it more. The cancer in the bone had weakened the bone causing it to break and allowing the cancer to spread out. He started chemo right away but the leg grew bigger and bigger and he could no longer walk on it. Chemo was hard on Justin and he suffered a lot because of it. Just 2 months after he turned 17, on September 30, 1998, they removed his left leg above the knee. They tried to continue chemo, he was scheduled for about 2 years more, but his bone marrow was failing and they felt the chemo was killing him. He is continually checked and scanned for cancer, but so far is doing great and he married his long time girlfriend Becky on March 4, 2005!
When Kelsey was first diagnosed I started a prayer page for her to keep everyone updated on her progress. An online cross stitch group got in contact with me and they wanted to make a quilt for her. She received her quilt in July of 1998, see this link to view her beautiful quilt - Kelsey's Quilt - isn't it great?! When this group found out about Justin as well they decided to make a quilt for him too (our grandfather/greatgrandfather also had cancer at the time, sadly my grandfather passed away on April 30, 2003). Click here to see his wonderful quilt - Justin's Quilt - I know you will love his as well! My aunt Sharon was diagnosed with cancer in the fall of 2004 and sadly, she passed away on September 10, 2005. This is the daughter of my grandfather that passed in 2003. She was the youngest sister of my father Harlin, Justin's grandfather, and of my uncle Don who is Kelsey's grandfather.
After Justin received his quilt I decided I wanted to give back to another child what these wonderful stitchers had given to the children in my family. I decided to coordinate a quilt for a child from the Make A Child Smile page, Kelsey had been featured on this site and I knew how thoroughly Alex (the founder of MACS) checks to make sure the child is legit and really sick. That is so sad, but these days you can never be too sure. I picked Katy, a child she had featured the month I began, February 1999. It was the only time I went to the Cross Stitch Pals for help, I posted all over their message board that I was looking for stitchers, it was the only way I knew to get stitchers. Well, stitchers I did get, more than I needed. So, I decided to do a second quilt with the extra stitchers, Emily's quilt and they kept coming and coming. By the end of 1999 we had made 8 quilts for the MACS kids! I was stunned and happy it was going so well, but a bit overwhelmed too.
In 1999 a really great stitcher, Vicki, approached me with help. She and I had been corresponding a lot and she knew I was very stressed with all that was going on, we were moving at the time too. She offered to help and continues to finish off many of the quilts for Love Quilts. She was receiving the finished tops (and in 2001 she even helped make every other quilt top too!) from me and she would put the batting and backing on, what a help that was! Love Quilts now has 10 finishers all over the US helping finish the quilts for our beautiful children!
The squares are first sent to Joan and she posts the scans on a site called Fotki. Joan then distributes the squares to where they need to go to be finished. Click on Fotki to see these squares!
Love Quilts has been published in two newspapers, one in Georgia and one in South Carolina and it was also listed in the Crafts 'N Things November 2001 issue and The Cross Stitcher February 2002 issue and in an article in the June 25, 2002 issue of Women's Day and in the cross stitch magazine Stoney Creek Collections in December 2005!

Love Quilts continues to grow. We have had stitchers from 33 different countries! (want to see the list? See the bottom of this page). We are now approaching 300 quilts made, amazing!! But I couldn't have done all of this without all of you out there and I will always be thankful for the wonderful stitchers who take their time to stitch for these children, you are all wonderful!

Well, on to other things about me, since this is an "about me" page :-) Thank you all for taking the time to read this long post about me and Love Quilts!

Cathy ~ Love Quilts Founder/Coordinator

Photobucket

Feb 13, 2012

There Can Be Miracles

In memory of Whitney Houston, I wanted to share this song that came to mean a lot to me in those first days of Chloe's diagnosis. My heart feels heavy, but also full this week. There is so much heartache for many I know and love, but there are also miracles and love and beauty.



Many nights we've prayed
With no proof anyone could hear
In our hearts a hopeful song
We barely understood

Now we are not afraid
Although we know there's much to fear
We were moving mountains long
Before we knew we could


There can be miracles, when you believe
Though hope is frail, it's hard to kill
Who knows what miracles you can achieve
When you believe, somehow you will
You will when you believe


In this time of fear
When prayers so often prove in vain
Hope seems like the summer birds
Too swiftly flown away

Yet now I'm standing here
My heart's so full I can't explain
Seeking faith and speaking words
I never thought I'd say

There can be miracles, when you believe
Though hope is frail, it's hard to kill
Who knows what miracles you can achieve
When you believe, somehow you will
You will when you believe


They don't always happen when you ask
And it's easy to give in to your fears
But when you're blinded by your pain
Can't see your way straight through the rain
A small but still resilient voice
Says hope is very near

There can be miracles
When you believe
Though hope is frail
It's hard to kill

Who knows what miracles,you can achieve
When you believe, somehow you will
somehow you will
You will when you believe

You will when you
You will when you believe
Just believe...in your heart
Just believe
You will when you believe

Photobucket

Feb 11, 2012

Heaven's Angel


Caleb Joseph Moody died on February 10th, 2012 at Primary Children’s Hospital due to complications from pneumonia. Caleb was born January 6th 2005 to Dallan Richard Moody, and April Baadsgaard Moody. He is dearly loved by his parents and his brothers Joshua Aaron, Matthew Dallan and Mitchell Ross, his grandparents Ross and Janene Baadsgaard of Spanish Fork, Utah and T. Dean and Patrice Moody of Kennewick, Washington, as well as 30 uncles/aunts and 38 cousins. Caleb’s spirit radiated pure love. He brought the love of God and light of Christ into the lives of all who knew him. Caleb’s life was a precious gift and a tender miracle. His winking eye was a daily reminder of Caleb’s deep love for all of us. Caleb could have quickly returned to heaven but instead he brought heaven to us for seven years.


April, Caleb's mom, is a member of the Kidz Krew and has shared many inspiring messages with us. Please include April and her family in your thoughts and prayers.

Feb 5, 2012

No Fight Left

Photobucket


It's hard to tell if my eyes are open
When all I see is dark
And it's easy, it's easy to lose my step
To lose my step

There is no fight left on the inside
But maybe that's where I should be
I've given up trying
I'm giving it all to you

And I used to dream of a life so lovely
There'd be no room for tears
Now letting go, yeah
Letting go is the hardest part
It's the hardest part
There is no fight left on the inside
But maybe that's where I should be
I've given up trying
I'm giving it all to you
Ohhh...

There is no place I can go
Where you don't already know
How to reach right down and pull me out
I need you, I need you, I need you

There is no fight left on the inside
But maybe that's where I should be
I've given up trying
I'm giving it all...

There is no fight left on the inside
But maybe that's where I should be
I've given up trying
I'm giving it all, yeah
I've given up trying
I'm giving it all, yeah
I've given up trying
I'm giving it all to you

Feb 2, 2012

Safeguarding the Siblings of Children With Special Needs

Photobucket


By M. Sue Bergin of BYU Magazine.

Families should know the potential risks, get support, and expand their faith.


As Brandon M. Ogden and Jenny Watson Ogden raise four young children in Gilbert, Ariz., their third child’s special needs have the potential to eclipse the needs of the other three, which could contribute to resentment and alienation. Instead, 8-year-old Austin’s limitations and peculiarities—and also his loving disposition—are mostly a blessing to his siblings.

“We have taught our kids from day one that Austin’s syndrome does not define who he is. He is first a child of God, an individual, and their brother. We often discuss why God made him this way, and why He sent him to our family. Our kids comment that even though Austin has issues that are difficult to deal with, Austin brings a lot of love and happiness into our family,” says Jenny.

All families who have a child or children with special needs struggle for balance. Whether their child has autism, cerebral palsy, or diabetes, most parents can quote the incidence rates per 100 children, list symptoms, talk about causes, and explain treatments. Some, however, are not versed in the potential risks to siblings of a child with special needs and the protective factors that can help all their children thrive in the face of tremendous challenges.

For several decades, professors Susanne Olsen Roper and Tina Taylor Dyches, and their colleagues Barbara L. Mandleco and Elaine Marshall, have been studying families that include a child or children with special needs. While their studies show that these families generally do quite well, and, in fact, may benefit in some ways from having a child with special needs, they say parents can minimize the downsides by understanding the risks, getting support, and drawing on their faith.




Know the Risks

One of the first things parents can do to support their typically developing children is to get a handle on the potential risks to the siblings and their relationships within the family. One risk is resentment. “Research shows that children take on extra responsibilities, especially the older sister,” says Roper, associate professor of family life. “She might feel like she can’t go out and be with friends because she needs to take care of her sibling with special needs, or because Mom is too worn out and Dad is working a second job. These children can become resentful, even if no one’s asked them to take on the extra duties.”

The Ogdens work at preventing resentment by expecting Austin to at least try to do what’s expected of his siblings, such as chores, schoolwork, and practicing good manners. These are not easy tasks for an 8-year-old with Williams syndrome, a genetic condition characterized by a wide range of physical and intellectual difficulties. “When our kids see that Austin also has to make his bed, treat others kindly, not yell, and follow the rules in the house, they don’t have those negative feelings towards him,” says Brandon. As the children observe Austin struggling to do his best, it’s easier for them to accept his limitations.

Siblings may also be at higher risk for being bullied, perhaps as they try to protect their brother or sister from tormenters. While they might become physical guardians, they also can feel pressure to overachieve academically. “If you have a child who is not functioning normally intellectually, the sibling often feels like he or she has to overcompensate—‘I’ve got to get straight As and be the top violinist so I even things out,’” says Dyches, an associate professor of special education. Parents should be alert to these behaviors and reassure their children that they accept them as they are, she says.

One of the most powerful protective factors in all these risks is ongoing conversation. If parents explain a child’s special needs to the family when a diagnosis is first made but then don’t bring it up again, their children can be at greater risk. Rather, parents should cultivate an open relationship where their typically developing children feel comfortable disclosing thoughts and feelings, no matter how distressing. The Ogdens nurture this gestalt daily.

“Our kids say, ‘When will he ever learn?’ a lot in frustration, and we accept their feelings,” says Jenny. “We talk all the time about what’s going on with him and with them, and they know we’ll listen even if we’re not thrilled about what they’re saying.”

Get Support

As every parent of a child with special needs knows, finding help can be daunting. The more significant the disability, the harder it can be for families. A typical 13-year-old babysitter would not be able to handle, for example, a nonverbal 4-year-old with autism who has self-destructive behaviors. “So parents say, ‘I can’t trust anyone with my child or children to do the job that I can do, so I’ll just do it all myself,’” says Dyches. Giving up on the search means that parents don’t get a break, which in turn means they may be less available both physically and emotionally to each other and to their other children.

Dyches and Roper urge parents to persist in looking for support until they find it. While state programs for respite care can have long waiting lists, parents should get on the lists. They also can enlist adult sitters, hire two sitters at a time, trade time off with other parents of children with special needs, and take advantage of special programs. In Utah County, for example, parents who do not get state assistance or are on a waiting list can bring their child with special needs to Friday’s Kids Respite, www.fridayskids.org, where competent adults, often BYU student volunteers accompanied by a nurse and other professionals, provide free childcare for an evening.

Parents can also enroll their children in the Sibling Support Project, a workshop that helps normalize the experience of having a sibling with a special need (siblingsupport.org). The monthly “Sibshops” are held in 340 locations throughout the world. “It’s a fun, engaging two or three hours where these kids can feel like they’re not alone. They can talk to other kids who are likely to relate to their experiences when they say, ‘Yeah, my brother has seizures, too’ or ‘Once my brother was life-flighted to the hospital.’ They can talk about these experiences that have really affected their lives in a friendly, easy-to-communicate environment,” says Dyches, co-founder of Sibshops of Utah County.

The Ogdens are very selective about whom they entrust with Austin, and that means their chances to get away wax and wane with what help is available. They don’t live near extended family, so they don’t get as many breaks as they would like, but they do try to go on a date each week. “But,” says Brandon, “if Austin’s behavior is more difficult at times, we won’t put the burden of babysitting on our other kids.”

At different times, the Ogdens’ support system for Austin has included a behavior coach, physical therapist, occupational therapist, speech therapist, music therapist, and respite providers. The support team also includes his schoolteacher and aides. Of great help has been joining the Williams Syndrome Association in their area. “We share ideas that help us solve some of our problems and we laugh about the funny things our children have in common. We support each other. It also helps to know that someone else knows what you are going through and how you feel when things get rough,” says Brandon.

Expand Your Faith

While having a child with special needs poses risks to other children in a family, much of Dyches and Roper’s research shows that this situation can be positive emotionally and spiritually. “Children in these families can develop high levels of empathy and higher self-control,” says Roper. “It may be a natural consequence of seeing siblings in difficult situations.”

In the Ogdens’ case, Austin’s syndrome includes high social abilities, making him easier to enjoy and be around. For families whose child with special needs means decreased social abilities, staying attached and bonded—and sympathetic—can be much more challenging.

Whatever the idiosyncrasies of a child with special needs, his or her parents and siblings are likely to wonder, “If we just had enough faith, could this child be healed?” Or perhaps they’ve had someone else present them with that disconcerting question. The response, says Dyches, is in becoming secure enough in their faith to know that this is a calling. “Christ’s disciples asked who had sinned that caused a man to be blind from birth, the man or his parents. Christ answered that no one had sinned but that the man was blind so ‘that the works of God should be made manifest in him’ (John 9:3).”

While Christ healed the blind man physically, Dyches believes that families with special needs children can be healed in multiple ways. “When we accept God’s will and we accept the circumstances he’s given to us—if we do that with an open heart and with faith—then we are healed, and our children are healed, emotionally and spiritually.”

Photobucket

Feb 1, 2012

4 Tips for Photographing Special Needs Children

Last year, I realized something extremely disturbing. You see, at the end of each year I go through all our photos and compile the "best of..." Yes, there are generally still hundreds, but at least I clear out the obvious bad pictures. I usually choose my 12 favorite pictures of both of the girls and create a calendar for my parents. Well, Samantha has always not been super easy to photograph, but as she has gotten older, it has seemed even harder to get a good picture of her. And last year, as I went through our pictures, I couldn't even find 12 pictures of Samantha that were "good." I was heartbroken. Devestated. Her future, like many of our kids, is so uncertain. What if all I have left one day are these pictures? And I can't find even 12 to sum up an entire year? I immediately save up money from my tutoring jobs and went out and bought a much better camera!

Yes with a camera that takes 7 shots a second, I have gotten a lot more pictures of Sammy that I adore. But she's still not all that easy to photograph.

Today on Pinterest (let's all give a prayer of thanksgiving for that wonderful little location on the web), I came across a fantastic article: 4 Tips for a Successful Session with Special Needs Children. The article is written more for professional photographers, but I these 4 simple tips can be useful to all of us...especially to those who have a DSLR or something similar to it. It's worth reading.



Again, it's hard to get pictures of our kids -- any kids really. But when you have a child who won't/can't smile on demand or won't sit still in a posed position, doing the whole picutre thing can be sad. (After leaving a JCPenney photo session one time, I felt so discouraged believing that I would never get a picture with Samantha and Callie together. Not one turned out. The only picture I bought was one when Sammy was crying as Callie hugged her. Not what I'd call a "successful" picture, but memorable nonetheless.) But when I do get a picture of Sammy that is good -- so good that it's like seeing her real self -- her eyes shine and her smile is so full of joy...my heart swells up. And those are the pictures I want to hold if a time ever comes that I can't hold her.

So, read the short article, get some tips, and if you don't take the pictures yourself, ask your photographer to use some of the tips. It'll be worth it.

Photobucket

LinkWithin

Related Posts with Thumbnails