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The Anne Frank Center is going after Trump for his weak condemnation of anti-Semitism.

'Too little, too late.'

For months, the Anne Frank Center for Mutual Respect has issued statement after statement condemning the Trump administration.

Since entering the political fray, Donald Trump has gotten into his share of unexpected feuds. Whether he's battling the cast of "Hamilton," declaring the free press to be the "enemy" of the American people, hanging up on the prime minister of Australia, or reviewing the latest episode of "Saturday Night Live," there's no shortage of "Oh-my-God-I-cannot-believe-the-president-of-the-United-States-is-doing-this" drama to go around.

But while most of these feuds are blown-up distractions from larger issues, there's at least one that deserves more attention: Trump versus the Anne Frank Center for Mutual Respect.


Photo by Tim Sloan/AFP/Getty Images.

When Trump compared the CIA to Nazi Germany, AFC Executive Director Steven Goldstein called Trump's words "a despicable insult to Holocaust survivors around the world and to the nation he is about to lead." And as Trump unveiled plans for a southern border wall and large-scale travel ban, Goldstein accused the president of "driving our nation off a moral cliff."

THE STATUE OF LIBERTY WEEPSAS PRESIDENT TRUMP TARGETSMEXICANS AND MUSLIMSStatement of Steven Goldstein, Executive...

Posted by Anne Frank Center for Mutual Respect on Wednesday, January 25, 2017

The president has earned the organization's ire mostly for what he hasn't done — especially when it comes to threats against the Jewish community.

Over the past several months, Jewish Community Centers around the country have experienced a sharp uptick in bomb threats. In fact, just this year, JCC locations in 27 states and one Canadian province have received nearly 70 threats — all without a word from Trump.

Rabbi Hershey Novack walks through Chesed Shel Emeth Cemetery, where almost 200 gravestones were vandalized over the weekend. Photo by Robert Cohen/St. Louis Post-Dispatch via AP.

The closest Trump came to addressing the issue — which quite rightfully has members of the Jewish community feeling alarmed — came in a tense exchange during last week's wild press conference. Jake Turx of Ami Magazine, an Orthodox Jewish weekly, tried to ask Trump about how the administration planned to respond to bomb threats. Trump cut him off, saying it was "not a fair question," and responded: "So here's the story, folks. Number 1, I am the least anti-Semitic person that you've ever seen in your entire life. Number 2, racism. The least racist person. In fact, we did very well relative to other people running as a Republican."

The response was bizarre, in part because Turx had prefaced his question by saying he didn't believe Trump or his staff were anti-Semitic. Trump responded as if it were a personal attack, and he went on to accuse "the other side" of carrying out these threats.

"But let me just tell you something: I hate the charge," Trump added, responding as though he had been personally accused of anti-Semitism. "I find it repulsive. I hate even the question because people that know me — and you heard the prime minister, you heard Benjamin Netanyahu, did you hear him, Bibi? He said, 'I've known Donald Trump for a long time,' and then he said, 'Forget it.' So you should take that instead of having to get up and ask a very insulting question like that."

On Monday night, White House Deputy Press Secretary Lindsay Walters finally condemned the threats against JCCs using some especially vague language.

"Hatred and hate-motivated violence of any kind have no place in a country founded on the promise of individual freedom. The President has made it abundantly clear that these actions are unacceptable," said Walters.

Combined with the White House's decision to omit any mention of Jewish victims in its official Holocaust Remembrance Day statement, it comes off a bit like the administration is taking steps not to offend white nationalists, neo-Nazis, and members of the so-called "alt-right" who do possess anti-Semitic worldviews.

People protest the appointment of former Breitbart News head Steve Bannon to be chief strategist of the White House. Photo by David McNew/AFP/Getty Images.

The Trump administration may not be actively encouraging anti-Semitic violence, but it's not exactly going out of its way to discourage it, either — at least in strong terms.

In June of last year, the day after the Pulse nightclub shooting in Orlando, Florida, Trump called on President Obama to resign for refusing to acknowledge what Trump saw as the cause of it. "President Obama disgracefully refused to even say the words 'Radical Islam.' For that reason alone, he should step down," Trump said.

Using that same logic, why won't Trump denounce these attacks by name? Why won't he directly address the victims of this terrorism? Why can't Donald Trump denounce white supremacy and white nationalism?

On Tuesday, Trump traveled to the National Museum of African American History and Culture. There, he finally addressed the threats against the Jewish community.

"The anti-Semitic threats targeting our Jewish community and community centers are horrible and are painful and a very sad reminder of the work that still must be done to root out hate and prejudice and evil," Trump said.

GIF from the White House/YouTube.

The AFC, however, isn't letting Trump off the hook that easy, calling his statement "a Band-Aid on the cancer of Antisemitism that has infected his own Administration."

While Trump has now at least acknowledged the problem, he still hasn't said anything about how he plans to address it.

"Do not make us Jews settle for crumbs of condescension. What are you going to do about anti-Semitism in [the] White House?" the AFC tweeted.

MR. PRESIDENT, YOUR TOO LITTLE, TOO LATE ACKNOWLEGMENT OF #Antisemitism TODAY IS NOT ENOUGH. Statement of Steven...

Posted by Anne Frank Center for Mutual Respect on Tuesday, February 21, 2017

And they're right. Trump hasn't put forward a plan to address anti-Semitic violence. In fact, there's been talk that the administration may actually rebrand the government's Countering Violent Extremism program as the Countering Islamic Extremism program. Funds that would ordinarily go toward countering neo-Nazis and white supremacists may no longer be available. The singular focus on Muslim extremists could very well make the rise of white supremacist and anti-Semitic groups even worse.

While so much remains up in the air, we can count on the Anne Frank Center for Mutual Respect to keep it real and put pressure on the White House to do the right thing.

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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.

Joy

Sorry, Labradors. After 31 years, America has a new favorite dog.

The American Kennel Club has crowned a new favorite.

via Pixabay

A sad-looking Labrador Retriever

The sweet-faced, loveable Labrador Retriever is no longer America’s favorite dog breed. The breed best known for having a heart of gold has been replaced by the smaller, more urban-friendly French Bulldog.

According to the American Kennel Club, for the past 31 years, the Labrador Retriever was America’s favorite dog, but it was eclipsed in 2022 by the Frenchie. The rankings are based on nearly 716,500 dogs newly registered in 2022, of which about 1 in 7 were Frenchies. Around 108,000 French Bulldogs were recorded in the U.S. in 2022, surpassing Labrador Retrievers by over 21,000.

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America's Got Talent/Youtube

Mzansi Youth Choir received a Golden Buzzer for their cover of Nightbirde's "It's OK."

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Back in 2021, Nightbirde arrived on the stage with only a 2% chance of surviving a third round of cancer. But still, she kept to her philosophy of "You can't wait until life isn't hard anymore before you decide to be happy." She passed away in Feb 2022, but not before sharing her beautiful heart with the world.
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