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Still Finding Sunshine

Sharing the story of our family and our daughter who was diagnosed with Spinal Muscular Atrophy, type 1

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Category: Blake

Forget
Blake · Family · Kenley

Forget

August 1, 2016 BlakesMama3 Comments

The other day Jeff and I were packing the kids up to run an errand. Jeff put Blake in her car seat while I helped Kenley get her shoes on. He suddenly remembered that he left the dogs in the backyard, so he ran outside. I picked up Blake, held Kenley’s hand and started toward… Continue reading Forget

All about Blake
Blake

All about Blake

June 10, 2016July 16, 2016 BlakesMama6 Comments

I’ve realized a lot of time in this blog has been spent talking about SMA. In the beginning, we were really focused on bringing awareness so another family wouldn’t have to go through what we’re going through. In the midst of that we’ve been getting many, many questions about SMA (which is good, because we… Continue reading All about Blake

A picture
Blake · Family

A picture

May 19, 2016May 19, 2016 BlakesMama4 Comments

The featured image is one of my favorites. Brand new baby Blake in Daddy’s arms. I’ve been taking even more pictures than I used to. The other night I started going through them. I had just ordered hundreds more to add to the stacks of pictures I still have to sort through. I was really good… Continue reading A picture

Being a mom
Blake · Kenley

Being a mom

May 9, 2016May 9, 2016 BlakesMama8 Comments

My mom always says I’ve been a mother my whole life, even when I was a little kid. I loved dolls; I was borderline obsessed with them. My family called me “little mommy”. I begged my big sister to walk me to the hospital, three blocks away from our house, so I could go and… Continue reading Being a mom

Blake · Family · Life

Genetics

May 2, 2016May 2, 2016 BlakesMama4 Comments

I’ve learned a lot about SMA, but I’m still no genetics expert. Jeff and I have an appointment in the future with our hospital genetics department for just the two of us. We want to understand a lot more and I know we’ll keep learning. With that being said, I want to talk about my experiences during both… Continue reading Genetics

Hard
Blake · Family · Life

Hard

April 26, 2016April 26, 2016 BlakesMama12 Comments

I’ve had a lot of people say some really nice things. They say I’m strong or doing so well under the circumstances. Those words really do mean a lot to me. I appreciate them more than I can express.  However, I want to make sure not to give anyone a false sense of reality. I’m… Continue reading Hard

Dreams
Blake

Dreams

April 24, 2016April 24, 2016 BlakesMama4 Comments

From where I sit, dreams are a blessing and a curse. They often feel too much like reality. I’ve had the same dream over and over since Blake was about 2 1/2 months old. In this dream I’m holding Blake, she smiles at me, babbling. I smile back and make funny faces. Then, I stand… Continue reading Dreams

What she needs
Blake · Family

What she needs

April 20, 2016 BlakesMama7 Comments

I’ve had an amazing relationship with Blake since the day we met. I have a great relationship with Kenley, too, but things were different when she was tiny. I was a first time mom; nervous and trying to do everything perfectly. With Blake, I relaxed a lot more and just kind of went ‘with the… Continue reading What she needs

Pissed
Blake · Family

Pissed

April 12, 2016April 19, 2016 BlakesMama8 Comments

I’m sure it’s obvious from previous posts (and since I’m a human being) that anger is something I feel on the regular. I never thought anything could happen to my child. Bet that sounds naive. It is.  I always figured, once your baby is born and examined, you’re good. I knew raising children would include… Continue reading Pissed

The days after diagnosis
Blake · Family

The days after diagnosis

April 10, 2016April 10, 2016 BlakesMama11 Comments

After you’ve been told your baby has a fatal illness, nothing in the world makes sense. Everything is wrong, so very wrong. I think back on the first couple of days after we found out, which wasn’t that long ago, and I don’t remember a lot. Obviously, a ton of crying happened… a ton.  I… Continue reading The days after diagnosis

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