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Pop Culture

Lost 'Sesame Street' episode once deemed too scary for kids resurfaces online and it's wild

This episode brought to you by the letters W-I-T-C-H.

sesame street found episode, sesame street wicked witch, wizard of oz

Hamilton was so good at her job.

Once upon a time, in the mid 1970s, "Sesame Street" traded its bright, sunny atmosphere for ominous gray skies. Most of us would have probably never known this had it not been for the power of the internet.

An entire episode of the beloved children’s show has resurfaced online after being initially pulled for allegedly being “too frightening” for kiddie viewers.

What on earth could be so scary in a place where the air is so sweet, you might wonder. As it turns out, even "Sesame Street" isn’t impervious to a wayward witch broom.

The video clip starts with upbeat, fast-talking David (played by Northern Calloway) exiting Hooper’s store, struggling to make his way through powerful gusts of wind.

“Look at that! Something’s falling right outta the sky!” he shouts gesturing up as the wind whirls. David drops to one knee and catches an incoming broom just in the nick of time. Suddenly the wind stops. Yay?

Unfortunately, our hero’s troubles are just beginning. Sinister music begins to play, and unbeknown to David, who should come lurking from around the corner but the original Wicked Witch of the West herself.


No, you’re not in Dorothy’s dream. That is Margaret Hamilton reprising her role as the one, the only, the Wicked Witch of the West. Guess that bucket of water didn’t quite do her in.

“I know I’m not in Oz anymore,” Hamilton says while looking around, concluding she “must be over the rainbow somewhere.” Determined to find her broom and fly away, she marches over to David, demanding he give it back.

Unfazed, David does not immediately give back the broom, insisting that she should be more careful and treat him with more respect (can’t have a “Sesame Street” episode without a life lesson, after all). The lecture only further agitates the witch, but David won’t budge. Finally she tries to snatch the broom away, only to be electrocuted.

“Oh I forgot!” the Wicked Witch exclaims. “I can’t so much as lay a finger on the broom as long as somebody else is holding onto it!" What an oddly specific and important detail to forget. Oh right, kid’s show.

The Wicked Witch disappears in smoke, promising that this is not the last we’ve seen of her. She proceeds to terrorize poor David throughout the entire episode, including creating an indoor thunderstorm and threatening to turn him into a basketball. Savage.

Finally the Wicked Witch concocts a plan to get her broom back by turning herself into a sweet, regular looking older woman, a scheme so fiendish she wins the heart of Oscar the Grouch in the process. The plan works, but the witch still has to ask for it nicely. So, you know … compromise.

Though Big Bird called the ordeal “interesting and exciting,” apparently audiences didn’t quite hold the same view. Mike Minnick, who posted the episode on YouTube, claimed that it only aired once in the mid ’70s before getting the pull for being “too scary for children.” According to an article published by AV Club, the show was on the receiving end of a deluge of complaints from the parents of freaked out kids.

Some reminiscing fans agreed that yes, as kids, the episode was terrifying. One wrote that it “scared me beyond belief when I was 5. I would anxiously watch the start of each episode after seeing this one, to make sure it wasn't the ‘witch one’ again.”

However, the main sentiment shared in the comments was gratitude that the footage found its way back into viewing.

“What a real joy to see ... I know she scared the bageezus out of me when I was a little one watching The Wizard of Oz every year on television. Now, it's just plain old nostalgic to see the original Wicked Witch,” wrote one person.

Another added, “People have no idea how huge this is. I honestly thought I'd never see the day. One of the holy grails of lost media has been found.”

Mostly, the whole thing became one giant Margaret Hamilton appreciation fest. Here are just a few of the heartfelt comments:

“From the bottom of my heart, Thank you SO SO much for making this available to watch and experience! This really was a great treat and seeing Margaret Hamilton as the Wicked Witch again just brought out the kid in me!”

“Lmao when she turns into a cute little grandma and does the evil laugh, I loved it! She is so cute, what a legend.”

“Margaret Hamilton…. I love her so much and miss her desperately. I love how 40 years later she was still able to play the wicked witch as incredible as she always was.”

You could say that Hamilton was born to play a witch. During her interview with Mister Rogers—yes, Hamilton frequented children’s shows in her heyday—she shared that as a little girl, she always dressed up as a witch for Halloween. So it’s no wonder that getting the chance to play perhaps the most iconic witch of all time made her “very, very happy.”

Hamilton felt her cackling, green-skinned, shoe-obsessed character wasn’t all that wicked, just misunderstood. She told Mister Rogers, “Sometimes the children think she’s a very mean witch, and I expect she does seem that way. ... She also is what we refer to as frustrated … because she never gets what she wants.”

Under that definition, there’s a bit of witch in all of us.

This uncovered relic, traumatizing as it might have been, has brought some major joy with its epic return. Perhaps even wicked witches can be a source for good.

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Three women, three MS journeys: How multiple sclerosis looks different for everyone

Gina, Nathalie and Helga share their reactions to being diagnosed with MS and how they stay informed and positive in the face of ever-changing symptoms.

Courtesy of Sanofi

Helga, Nathalie and Gina all have MS, and their experiences show how differently the disease can manifest.

True

It’s been 155 years since neurologist Jean-Martin Charcot gave the first lecture on a mysterious progressive illness he called “multiple sclerosis.” Since then, we’ve learned a lot. We know MS causes the immune system to attack healthy tissue, including damaging the brain and spinal cord. Resulting symptoms can be debilitating and include fatigue, blurred vision, memory problems and weakness. Huge advancements in our understanding of MS and its underlying causes, as well as treatment advances, have been made in the past few decades, but MS remains a complex and unpredictable reality for the 2.8 million+ people diagnosed around the world.

Ironically, the only real constant for people living with MS is change. There’s no set pattern or standard progression of the disease, so each person’s experience is unique. Some people with MS have mild symptoms that worsen slowly but sometimes improve, while others can have severe symptoms that drastically alter their daily lives.

All people with MS share some things in common, however, such as the need to stay informed on the ever-evolving research, find various lines of support and try to remain hopeful as they continue living with the disease.

To better understand what navigating life with MS really looks like, three women shared their MS stories with us. Their journeys demonstrate how MS can look different for different people and interestingly, how the language used to talk about the disease can greatly impact how people understand their realities.

woman with horse, woman riding horseGina loves riding her horse, Benita.Courtesy of Sanofi

Gina—Hamburg, Germany (diagnosed with relapsing multiple sclerosis in 2017)

When her youngest son was 4 months old, Gina started having problems with her eye. She’d soon learn she was experiencing optic neuritis—her first symptom of MS.

“Immediately after the diagnosis, I looked up facts on MS because I didn’t know anything about it,” Gina says. “And as soon as I knew what could really happen with this disease, I actually got scared.”

As her family’s primary income provider, she worried about how MS would impact her ability to work as a writer and editor. Her family was afraid she was going to end up in a wheelchair. However, for now, Gina’s MS is managed well enough that she still works full-time and is able to be active.

“When I tell somebody that I have MS, they often don't believe me the first time because I don't fulfill any stereotypes,” she says.

Overwhelmed by negative perspectives on living with MS, Gina sought support in the online MS community, which she found to be much more positive.

“I think it’s important to use as many positive words as you can when talking about MS.” It’s important to be realistic while also conveying hope, she says. “MS is an insidious disease that can cause many bad symptoms…that can be frightening, and you can't gloss over it, either.”

To give back to the online community that helped her so much, Gina started a blog to share her story and help others trying to learn about their diagnosis.

Though she deals with fatigue and cognitive dysfunction sometimes, Gina stays active swimming, biking, riding horses and playing with her sons, who are now 11 and 6.

Cognitive dysfunction is common in MS, with over half of people affected. It can impact memory, attention, planning, and word-finding. As with many aspects of MS, some people experience mild changes, while others face more challenges.

Gina says that while there’s still a lot of education about MS needed, she feels positive about the future of MS because there’s so much research being done.

woman in wheelchair holding medal, woman rowingNathalie is an award-winning rower with multiple international titles.Courtesy of Sanofi

Nathalie — Pennes Mirabeau, France (diagnosed with relapsing-remitting multiple sclerosis in 2002)

Nathalie was a teenager and a competitive athlete when she noticed her first symptoms of MS, but it would take four years of “limbo” before she was diagnosed.

“Ultimately, the diagnosis was more of a relief, than a shock,” she says. “Because when you have signs and you don’t know why, it’s worse than knowing, in the end, what you have.”

However, learning more about the disease—and the realities of disease progression—scared her.

“That glimpse of the future was direct and traumatic,” she says. Her neurologist explained that the disease evolves differently for everyone, and her situation might end up being serious or very mild. So, she decided to stop comparing herself to others with MS.

She said to herself, “We’ll see what happens, and you’ll manage it bit by bit.”

By 2005, Nathalie’s MS had progressed to the point of needing a wheelchair. However, that has not dampened her competitive spirit.

Nathalie began her international rowing career in 2009 and has won multiple world titles, including two Paralympic medals—silver in London and bronze in Tokyo. Now, at 42, she still trains 11 times a week. Fatigue can be a problem, and sometimes hard workouts leave her with muscle stiffness and shaking, but she credits her ongoing sports career for helping her feel in tune with her body’s signals.

“Over the years, I’ve learned to listen to my body, letting my body guide when I need to stop and take breaks,” she says.

Nathalie explains that she used to only look backwards because of the initial shock of her diagnosis. In time, she stopped thinking about what she couldn’t do anymore and focused on her future. She now lives in the following mindset: “Even when doors close, don’t miss out on those that open.” Instead of focusing on what she can’t do, she focuses on the opportunities she still has. Right now, this includes her training for the 2024 Paralympic Games in Paris, where she will compete for another rowing medal.

“I only go forward,” she says. “Well, I try, anyway…It’s easy to say, it’s not always easy to do. But that’s what I try to do.”

woman exiting water after swimming, woman with great daneHelga's Great Dane has become a helpful and beloved companion.Courtesy of Sanofi

Helga—Johannesburg, South Africa (diagnosed with relapsing multiple sclerosis in 2010)

When Helga first started having balance issues and numbness in her feet, she chalked it up to her training as a runner. But when the numbness moved to her face, she knew something was wrong. She never guessed it was MS.

“When I was diagnosed, I felt completely overwhelmed and clueless,” Helga says. “I felt that I had nowhere near enough information. I did not know anything about the disease…I had no idea that it was going to be a process of continually monitoring and adjusting your lifestyle.”

In the beginning, Helga’s symptoms developed slowly, and she didn’t appear ill to others. She was even able to run for a few years after her diagnosis, but she couldn’t do marathons anymore, and she began to fall frequently due to balance issues and right-foot dragging. Then her cognition issues became more problematic, especially in her job as a trainer in a printing company.

“My executive function, decision-making and short-term memory were affected to the point that I was eventually medically unfit for work,” she says. She stopped working in 2017.

However, she didn’t stop living life. Even though she could no longer run, she continued to swim competitively. She got a Great Dane puppy and trained him as a service dog to help her walk. She also serves as vice chair of the patient support organization Multiple Sclerosis South Africa, and she advises others who have been diagnosed to join a patient advocacy group as soon as possible to get reliable information and meet others with MS.

Helga says she is “hopeful” about the future of MS. “I must say that I am so grateful that we have all the new medications available, because my life would not be the same if it wasn't for that,” she adds.

Part of how she manages her MS is by looking at the positives.

“If I could tell the world one thing about MS, it would be that MS is an incurable disease of the nervous system, but it's also the greatest teacher of valuing your health, family, friends, and managing change in your life,” she says. “My life is diversified in a way that I never, ever thought it would, and MS has been honestly the greatest teacher.”

Each MS journey is unique – with each person impacted experiencing different struggles, successes, and feelings as they manage this unpredictable disease. But the common thread is clear – there is a critical need for information, support, and hope. We are proud to participate in World MS Day and share these incredible stories of living life while living with MS. To learn more about MS, go to https://www.sanofi.com/why-words-really-matter-when-it-comes-to-multiple-sclerosis.

MAT-GLB-2301642-v1.0-05/2023

This article was sponsored by Sanofi. Participants were compensated when applicable.

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