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Parenting a Sanfilippo Child — Kelly Wallis

 

Houston-based Kelly is a music therapist working with special needs children every day. She’s also the organist for her church. She thoroughly enjoys having music weave into every part of her daily life and work. She’s been married to her husband, Jeff, for 25 years, and has two daughters, Abby and Emily. Kelly writes about life as a caregiver for Abby, who has Sanfilippo syndrome.

Featured Post
October 30, 2020 Columns by Kelly Wallis

The Roller Coaster of Parenting a Special Needs Child

Raising a special needs child is challenging. It is physically tiring and emotionally draining. But it is incredibly rewarding, too. Some days leave me feeling like I know nothing and can’t do anything right, while others are positive and uplifting. This is the roller coaster that parents of special needs…

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February 26, 2021 Columns by Kelly Wallis

Let’s Raise Awareness of Sanfilippo Syndrome for Rare Disease Day

My 25-year-old daughter Abby has a rare, terminal disease called Sanfilippo syndrome. The best way to describe the disease is to compare it to Alzheimer’s, but in children. It robs her of cognitive abilities, including speech, attention, and memory, and motor abilities, including walking, mobility, and motor planning. Sanfilippo syndrome…

January 15, 2021 Columns by Kelly Wallis

As Abby’s Illness Progresses, My Coping Mechanisms Change

Many parents will agree that our child’s diagnosis with a terminal illness was the worst news we could ever receive. I have been living this reality now for a little over two years. My daughter Abby has Sanfilippo syndrome, a rare, genetic, terminal disease that is similar to Alzheimer’s.

October 30, 2020 Columns by Kelly Wallis

The Roller Coaster of Parenting a Special Needs Child

Raising a special needs child is challenging. It is physically tiring and emotionally draining. But it is incredibly rewarding, too. Some days leave me feeling like I know nothing and can’t do anything right, while others are positive and uplifting. This is the roller coaster that parents of special needs…

September 11, 2020 Columns by Kelly Wallis

My Project to Remember and Honor Sanfilippo Angels

For a parent, the worst thought in the world is losing a child. The love a parent has for his or her child is unceasing. Bringing a human being into the world, then raising and loving them only to lose them is unfathomable. Yet, parents of children with terminal illnesses…

July 24, 2020 Columns by Kelly Wallis

Music Brings My Daughter Back to Me

My 24-year-old daughter, Abby, has a terminal disease called Sanfilippo syndrome. It is likened to childhood Alzheimer’s. Children with this disease gradually lose all speech, motor, and cognitive abilities until their bodies shut down completely. This not only strips away Abby’s independence, awareness, and ability to connect to others, but…

July 10, 2020 Columns by Kelly Wallis

Caregivers Should Take Time to Restore and Renew

The role of caregiver is a sacred responsibility. Caring for someone whose well-being rests solely upon you is an incredibly meaningful job. And it is a necessity, as there will always be a population that needs caregivers. Almost everyone at some stage in their lives requires someone to care for…

June 12, 2020 Columns by Kelly Wallis

When Pushing Forward Is the Only Direction to Go

Loss is a theme that persistently has occupied my thoughts lately, not only because of current events in the world, but also because of my personal life. At 24, my oldest daughter, Abby, has Sanfilippo syndrome, a terminal disease that slowly is taking her from me. I’m losing her,…

May 15, 2020 Columns by Kelly Wallis

Why I’m Feeling Numb

Do you ever feel like you are walking through life with no emotion? Getting up each day, going through your routine, but with little emotion attached to any part of the day? For some reason, that is my current situation. There are many reasons for me to be emotional each…

April 24, 2020 Columns by Kelly Wallis

Finding the Silver Linings in Heartbreaking Moments

My 74-year-old mom unexpectedly passed away two weeks ago. It is still surreal to even type that statement. She was such an important presence in my life and my family’s life. My daughter Abby, who has Sanfilippo syndrome, had a very special relationship with her. My mom kept Abby…

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February 26, 2021 Columns by Kelly Wallis

Let’s Raise Awareness of Sanfilippo Syndrome for Rare Disease Day

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January 15, 2021 Columns by Kelly Wallis

As Abby’s Illness Progresses, My Coping Mechanisms Change

December 2, 2020 Columns by Emily Wallis

Grief Is an Unwelcome Visitor During the Holidays

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