#NotAWitch

November 5, 2020 in Disability & Inclusion - No Comments

If you didn’t know it already, the children’s book The Witches by Roald Dahl, has been turned into a movie starring Anne Hathaway.  Hathaway plays the main character, you guessed it–a scary witch.

In the book her character, The Grand High Witch, has “claws” for hands to up her frightening factor.  There is no mention of missing fingers.  Growing up, it was one of my favorite books and Roald Dahl is a beautiful storyteller.

In the movie adaptation unfortunately, HBO Max and the producers decided to portray Hathaway’s terrifying character with missing fingers–which resembles limb differences like Ectrodactyly and Syndactyly or “split hand.”

 

We are better than this.

By portraying “villains” as having disabilities–we continue to perpetuate the narrative that people with disabilities are something to be feared and abnormal. The lack of awareness, empathy, and inclusion of Warner Brothers Studios is abysmal.

We continue to discount the experiences of others because we don’t SEE from their perspective.  We don’t invite them to the conversation.  They don’t have a seat at the table.

I can’t count the number of times people have openly STARED at Callie walking in her prosthetic.

Pointed and laughed even.

The amount of grown adults that have made an awful face and pulled back in disgust while she was swimming.

The amount of parents who have pulled their children AWAY from my daughter while in the pool as if she was not “good” enough to play with.

The amount of children who have called Callie a “weirdo” or said that her leg looks “gross” or “scary.”

The amount of people who “fight” for inclusion but leave out the disabled community.

The amount of times Callie has tearfully asked me to be “just like everyone else.”

Where do you think they learn that behavior?

Sure…..some of it’s sheer ignorance.  Absolutely.

But the rest of it?

It’s in the media and content we consume.

When we accept narratives that are portrayed in movies like The Witches, scatter dismembered limbs in our yards at Halloween, and call people with lower limb amputations “pirates”–we normalize using limb difference as something that’s frightening.

We normalize a negative stigma, a lack of awareness, and frankly uncreative ways to define characters.

You reinforce that disability is dreadful and scary.  You normalize that the disability is “bad” and needed to be “overcome” to be normal.  You normalize that a disability needs to be hidden away with gloves.

Differences should not be used to portray disgust.

Or to frighten people.

At all.

It literally works to undo what everyone who works so hard to change with children with limb differences.  I don’t ever want Callie to feel ashamed or hide her limb difference.  I don’t want her to get bullied or made fun of by other kids.  I don’t want her to question who she is or her value.  I don’t ever want her to feel like she is anything less or that her uniqueness is something to be frightened of–because it’s not.  I don’t ever want her to watch a movie and see someone like her portrayed as a monster.

Imagine if you saw someone “like you” portrayed like that?

We can do better.

 

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Jaime

Jaime is a writer, editor, and lifestyle storyteller focused on modern womanhood, slow living, and life after survival mode. As the founder of The Wildflower Edit, she creates thoughtful, beautifully honest content at the intersection of motherhood, disability, emotional healing, and intentional living. Her work invites women to edit their lives with care — keeping what feels true and releasing the rest — for anyone learning to bloom in their own way.

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For the women blooming in unexpected places…..

For the women blooming in unexpected places…..

Hi Y'all

Hi, I’m Jaime — writer, mother, storyteller, and the heart behind The Wildflower Edit. For nearly a decade, I wrote online as The Princess and the Prosthetic, sharing my daughter’s journey with disability and the lessons our family learned along the way. It was a beautiful season — full of advocacy, connection, and community — but as my daughter grew older, I felt a shift. She deserved more autonomy. More privacy. More room to decide how she shows up in the world. And I realized something else: My own story was expanding too. Motherhood was still here. Disability was still here. But so were grief, healing, womanhood, nervous system care, feminine energy, homemaking, identity, softness… the fuller, deeper pieces of life that were ready to be spoken aloud. Whether you come for the cozy routines, the motherhood reflections, the disability advocacy, or the soft life inspiration — thank you for choosing to share this space with me. Pour a warm drink. Settle in. Let’s grow a life that feels like you again.

Jaime

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