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Lesly Wiltshire

<div>Hello, my name is Lesly and <strong>Mini (Mirna) is my mom</strong>. She lives with a disease called Scleromyositis. The disease entered our lives about 10 years ago—three undiagnosed, seven diagnosed. Myself and my three brothers have given her 24-hour care every single day since then. I’d be lying if I said things were easy, especially for her. Such a beautiful and extremely motivated individual to be limited to such extreme measures what seems to be like overnight.

</div>

<div><br />

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<div>My brothers and I do the very best we can with doing and also getting her everything she needs since this all started. Unfortunately, she has reached a point where she needs special neck, arm, and back braces to complete her physical therapy, a wheelchair, shower chair, handicap bathroom adjustments, and a special bed to sleep because of her progressed condition. The list goes on. <strong>These things aren’t cheap or easy to get. So we are willing to take whatever we can get to make my sweet mother’s life a little bit easier!</strong> Blessings to all and Happy Holidays ❤️

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Support Mirna’s Journey with Scleromyositis

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Lesly Wiltshire

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Support Mirna’s Journey with Scleromyositis

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