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Sarah Silverman got slammed for supporting a Palestinian teen — and she stayed strong.

Sarah Silverman has never exactly shied away from the outrageous, whether in her comedy or on Twitter. But when she stood up for a teen activist last week, the backlash was intense, even for her.

On Feb. 15, Silverman tweeted out a link to an Amnesty International petition to free 16-year-old Ahed Tamimi accompanied with the following message: "Jews have to stand up EVEN when — ESPECIALLY when — the wrongdoing is BY Jews/the Israeli government."

Pro-Israel advocates tweeted that Silverman should stick with comedy and "stay out of politics,” while others accused Silverman of being complicit in pro-Palestinian terrorism. You read that right: For some, supporting an outspoken young girl = terrorism.


If you’re asking yourself what the big deal is, buckle up: Silverman tiptoed onto the internet’s third rail.

The Israeli-Palestinian conflict has been deemed one of "the world’s most intractable conflicts" and continues to be a polarizing issue among many Americans. While the region is highly significant to three major Abrahamic faiths, to some, the conflict raises questions of who belongs in the Holy Land, as well as the legitimacy of Israel as a Jewish state in Palestine.

So what does Tamimi have to do with all this? She became the face of the global Palestinian solidarity movement when she was arrested in December 2017 for slapping an Israeli soldier.

Photo by Ahmad Gharabli/AFP/Getty Images.

The moment in question came just minutes after another Israeli soldier shot her 15-year-old cousin Mohammad in the face. He was unarmed and engaged in peaceful protest against President Donald Trump's declaration of Jerusalem as the capital of Israel.

After Mohammad was shot, two Israeli soldiers forcefully invaded their home with the intention to use their yard as a base to shoot at other activists protesting. The armed soldiers refused to leave, and when they attempted to force their way into their home, Tamimi slapped one of them. For her, this was an act of resistance.

In addition to her cousin being shot, Tamimi spent much of her childhood witnessing her relatives shot, tortured, imprisoned, and killed by Israeli soldiers and police. Her mother was shot in the leg and imprisoned four times, her father has been imprisoned three times, her 12-year-old brother was choked and beaten by an Israeli soldier, her uncle was fatally shot in the stomach, and one of her other cousins was shot in the head and killed.

Ahed Tamimi, A Teen in Search of Freedom

Tomorrow is Ahed Tamimi's 17th birthday and she will be spending it in an Israeli prison. Her trial is set for February 6th. There are currently more than 300 Palestinian children, as young as 13-years-old in Israeli prisons.

Posted by Institute for Middle East Understanding ( IMEU ) on Tuesday, January 30, 2018

Despite being a teenager, Tamimi has been denied bail and is currently undergoing trial for what some believe was merely defending her home.

Human Rights Watch and Amnesty International have called for her release. According to the Institute for Middle East Understanding, there are currently more than 300 Palestinian children detained in Israeli prisons. Furthermore, there are no basic fair trial protections and Palestinians face a 99.7% conviction rate in Israeli military courts. Tamimi is a part of that statistic.

No matter where you fall in the Zionist conversation, the fact is that this is daily life for the native inhabitants of Palestine. And it’s brutal.

Since the War of 1967, Israel gained control and occupied Palestinian land — the West Bank, East Jerusalem, Gaza Strip, as well as the Syrian Golan Heights and the Egyptian Sinai Peninsula.

Under the occupation, Israel has built more than 500,000 illegal settlements, eventually forcing many Palestinians to flee their homes. In fact, there are more than 7 million Palestinian refugees worldwide and about 5 million of them are eligible for humanitarian assistance from the United Nations.

In their June 2017 report, Human Rights Watch said that Israel has violated multiple international human rights laws. These include "forced displacement, abusive detention, the closure of the Gaza Strip and other unjustified restrictions on movement, and anti-Palestinian discrimination." It also referred to instances where a child was "imprisoned by a military court or shot unjustifiably," and checkpoints that bar Palestinians exclusively.

Silverman is not alone for standing behind Tamimi. More than 25 celebrities and civil rights icons have signed a letter supporting the imprisoned teen activist.

Dream Defenders, a civil rights group associated with the Movement for Black Lives, released a letter this month condemning Tamimi's detention and their public support for Palestinians "in their righteous struggle." "The Tamimi family stands up to Israel's brutality because they believe Palestinians, like ALL people, should be free," the letter read. "Dream Defenders stands with them and all Palestinians in their righteous struggle."

Some of the signees include entertainers Vic Mensa, Talib Kweli, Jesse Williams, Tom Morello, and Rosario Dawson; scholars Cornel West and Michelle Alexander; and civil rights icons Angela Davis, Alice Walker, Patrisse Cullors, and Alicia Garza.

[rebelmouse-image 19346276 dam="1" original_size="1024x1024" caption="Image via Dream Defenders." expand=1]Image via Dream Defenders.

The letter highlighted the parallels of the Palestinian community and the black community, both of who've notably been on the receiving systemic violence and social injustice:

"While our struggles may be unique, the parallels cannot be ignored. US police, ICE, border patrol and FBI train with Israeli soldiers, police, and border agents, utilizing similar repressive profiling tactics to target and harass our communities. Too many of our children quickly learn that they may be imprisoned or killed simply for who they are. From Trayvon Martin to Mohammed Abu Khdeir and Khalif Browder to Ahed Tamimi — racism, state violence and mass incarceration have robbed our people of their childhoods and their futures."

The letter also endorsed a revolutionary bill introduced by U.S. Congresswoman Betty McCollum that calls on the protection for Palestinian children from "widespread abuse by Israeli forces." The signees urged congressional members to join the other 22 cosponsors and sign the bill.

If you’re moved to support Tamimi too, there are other ways you can show your support.

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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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