1 year ago!
In support of
Kinsley McLamore
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Kinsley McLamore
A year ago, our world changed forever when Kinsley was diagnosed with B-cell, Acute Lymphoblastic Leukemia. What followed was a battle no child should face – intense chemotherapy, powerful steroids, unthinkable side effects, and a future unknown.
Looking back, I remember taking videos of her lying down sleeping. I wanted to capture her breathing, as I feared that she may die and we would not be able to hold her in our arms again. Especially as we awaited the news about high or standard risk. Thankfully, she is standard risk, but we know we are never out of the clear.
Looking back, I remember taking videos of her lying down sleeping. I wanted to capture her breathing, as I feared that she may die and we would not be able to hold her in our arms again. Especially as we awaited the news about high or standard risk. Thankfully, she is standard risk, but we know we are never out of the clear.
Today, Kinsley is back in school, having fun in dance and gymnastics with ongoing maintenance treatments, spinal taps, nightly oral chemotherapy, weekly physical therapy, and countless appointments. Although the treatment regiment is less intensive than the first year, she still faces many hills to climb. Yet, she meets each day with remarkable strength and an unwavering will to push through.
Kinsley has accomplished so many things this past year. She still has 2+ years of active treatment, and we ask for your continued support in making her dreams of a life without cancer come true!
Please keep the prayers and positive vibes coming!
With lots of love,
Kinsley, Cooper, Rob & Keksi
Kinsley has accomplished so many things this past year. She still has 2+ years of active treatment, and we ask for your continued support in making her dreams of a life without cancer come true!
Please keep the prayers and positive vibes coming!
With lots of love,
Kinsley, Cooper, Rob & Keksi
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