Scott Walker Budget Deletes College Rape Reporting Requirements

Wisconsin Gov. Scott Walker’s (R) nearly $70 billion budget proposal deletes language requiring colleges to report their sexual assault statistics to new students and to the Department of Justice, Jezebel reported on Friday.

The budget, unveiled earlier this month, removes a requirement that directs “each institution and college campus to incorporate oral and written or electronic information on sexual assault in its orientation program for newly entering students and to supply all students enrolled in the institution or college campus with the same information in either printed or electronic form.”

It also deletes the requirement that any university employee who witnesses a sexual assault must report that assault to the dean of students, the requirement that each school report sexual assault statistics annually to the DOJ, and the requirement compelling the DOJ to include those statistics in crime reports.

Walker’s two-year spending plan does not appear to replace the rape reporting requirements with anything, and it’s out of step with federal law. Colleges are currently required to incorporate prevention programs and information about sexual assault reporting options in orientation per the Violence Against Women Act, and they are required to report their sexual assault statistics annually to the DOJ.

A spokesman for Walker said The University of Wisconsin system requested the deletion of provisions of “duplicative reporting requirements,” since the federal government already requires reporting.

“Throughout his time in office, Governor Walker has made protecting victims of domestic violence and sexual assault a top priority,” said Laurel Patrick, Walker’s press secretary. “In his last budget, he increased funding for sexual assault victim services while also providing significant funding to support partnerships and state initiatives to shelter and protect victims of domestic abuse. His recent budget proposal increases funding to continue protecting victims and their families.”

Walker’s move follows a year of unprecedented attention on the epidemic of campus assault by the Obama administration and Congress. Ninety-seven colleges and universities are currently under federal investigation for mishandling sexual assaults on their campuses, according to the Department of Education’s Office for Civil Rights.

The Best Low-Maintenance Indoor Plants

Plants are a great way to add dimension and color to a space. They freshen up the room and offer health benefits as well! Many plants feature air-cleaning qualities and studies have shown they have calming effects on the body. We’ve put together a list of the most beautiful low-maintenance plants that you can bring into your own space!

Fiddle leaf fig tree

Fiddle leaf This is definitely Laurel & Wolf’s favorite indoor plant. We have one in our office and we always suggest them to anyone looking for some greenery. It is also very low maintenance and only requires watering once it has completely dried.

Succulents

Succulents

Succulents have become quite popular in recent years, and it’s not hard to imagine why. They actually prefer dry soil and room temperature, so keeping them alive is pretty easy. They look beautiful in both clusters or singles.

Aloe

Aloe

Aloe not only looks great, but has health and healing benefits too. Plants comes in all sizes, from a few inches to a few feet wide, so you’ll definitely find one appropriate for your space.

Rubber Tree

Rubber tree

Rubber trees are great if you have tall ceilings because they can grow 8+ feet tall! If you’re looking for a smaller plant, you can simply trim it to shape. Rubber trees have shiny emerald leaves that reflect light beautifully.

Snake Plant

Snake Plant

The vertical sword-shaped leaves sport a unique pattern reminiscent of Ikat textiles. Snake plants sit well in corners and look appropriate both on the floor or elevated on a table.

Asparagus fern

Asparagus

A light and whimsical plant, asparagus ferns work well in hanging baskets. Just be careful nobody (including pets) eat the poisonous berries that occasionally grow!

Areca Palm

Areca Palm

This palm instantly makes any space feel more tropical. If you’re looking to warm up a cold or bare-looking room, this is the plant for the job!

Here’s to living green!

xo,

Laurel & Wolf

A Fight For Immunity

Every Thursday when I go on Instagram<, I am greeted with a myriad of baby photos captioned with a #tbt. Throwback Thursday, as it is abbreviated, is a time where a social network sharing the world in the present takes a trip to (in most cases) a nostalgic, happy moment in the past. Last Thursday, though, a very different type of #tbt came across my feed. My cousin, a successful, dedicated, radiant young woman and soon to be college graduate, had posted a photo of herself with a very swollen face. In the caption, she stated, "This is not an attractive #tbt. My face is swollen from being on a high dose of steroids for an extended amount of time. My body was extremely inflamed and my Crohn's disease and psoriatic arthritis were very active."

First, I would like to make a point (or state an opinion, really), that a bodily reaction to an illness, or a physical mark from such an experience does not make someone less attractive. It is, in a way, one’s own badge of courage. You have fought, you are fighting, or you have survived the fight. A physical change or a resulting handicap does not make you unattractive, it shows you are a warrior. That is exactly what my cousin is; that is exactly what anyone fighting any sort of illness is: a warrior.

A warrior displays courage, integrity, heart, and passion. Not many people I know would willingly share a photo of themselves at an incredibly difficult (and vulnerable) moment in their lives, but my cousin did, and she did it with courage, integrity, and heart. For it was a risk she took with a passion to make a change that could impact and educate our society on a topic that many know little about, but so many suffer from daily. Autoimmune diseases affect 50 million Americans. Researchers have identified almost one hundred different autoimmune diseases and there are at least 40 more diseases with an autoimmune basis. Autoimmune disease is one of the top 10 leading causes of death in women in all age groups, even female children. They are chronic, they are crippling, and they require a dramatic lifestyle shift that impacts every aspect of daily life.

I, too, was one of the millions of people that had no idea what these diseases were capable of. It wasn’t until the summer of 2011 when they would become a reality for someone whom I love, admire, and respect so dearly, my cousin Lilly.

That summer, Lilly woke up one morning with paralyzing joint pain. She was literally incapable of moving. She gained twenty pounds in one week from inflammation and was entirely dependent on her family for support in even the smallest of tasks.

After what seemed like one million visits to the doctor accompanied by the same number of medication trials, she was diagnosed with psoriatic arthritis. Soon after, she returned to school for the fall semester with a compromised immune system and a daily struggle with what should be effortless tasks.

One weekend during that following winter of 2012, Lilly was in and out of the ER three times. At that point, breathing and swallowing were even unfathomable due to the pain they caused. Every test was yielding negative results, though, and each day was ending with more frustration and pain. After admission to the hospital, a twenty five pound rapid weight loss, and a camera study, it was finally revealed that her stomach was infiltrated with bleeding ulcers, leading to the diagnosis of Crohn’s disease.

Lilly was an incredibly active young woman, and after that weekend she was bed-ridden for seven months. Even going down the stairs resulted in extreme exhaustion. I had no idea how incapacitating and debilitating this was going to be for her. No one did. No one could foresee how long this road to recovery would truly be. With the help of an incredibly supportive family, and one hell of a dedicated spirit, though, she was able to travel that road.

With the help of a mom who would never take no for an answer from a doctor, a mom who never stopped reading about ways to help and heal her daughter, a mom who cooked meals without sugar, meals without dairy, meals without gluten, a mom who read articles through the night to find a way that her daughter could be happy and healthy with a disease that would be with her for life, Lilly could walk the road to recovery. With the help of a father and siblings and family who supported her endlessly in every endeavor, every apartment move, every awareness campaign, she could walk the road to recovery.

The following year brought a return to school but not without weekly infusions, medication alterations, joint inflammation drainings and appointments. Her body was fighting every medication the doctors presented, but after years of trying and failing, one finally worked better than the rest.

And now we find ourselves in the present. Winter 2015. If you looked at Lilly today, you would never know the hell she has been through. If you look at any person with an autoimmune disease, you often would not. You would never have guessed that her diet needed to be refined sugar-, dairy- and gluten-free. You would never guess that just years ago she could barely walk, move or breathe. Today, Lilly shines brighter than she ever has. That is the thing about an autoimmune disease: it stays with you forever, but if you have the dedication and strength required to fight it, you will be a warrior, and you will win.

Lilly has dedicated and continues to dedicate her life to one mission: live in a way to ensure that someday no one will have to experience what she did. An autoimmune disorder does not disappear, but with the proper lifestyle and treatment you can successfully and happily live a life in remission from crippling pain.

March is autoimmune disease awareness month. Fifty million Americans are living with one of these diseases. Chances are, you know a few. Reach out, educate yourself, allow yourself to recognize the struggle that so many Americans face and help in any way you can. Celiac’s Disease, Rheumatoid Arthritis, Crohns, Psoriasis, Type I Diabetes, Grave’s Disease, Vitiligo: these are just a few of the over one hundred disorders out there. Sometimes in today’s society, it is hard to support a cause without a face. I hope after reading this, you see a face. You see a daughter, a friend, a mother, a brother, a husband — anyone.

If you are looking for a way to help, or just want to learn more, Lilly has kickstarted a Campaign entitled 50 Cents for 50 Million. If everyone simply donated 50 cents, we could be a whole lot closer to avoiding seven month bed rests and hundreds of failed hospital tests for the 50 million Americans living with these diseases. We could help to find a future where only one or two tests are needed to find one drug, so people do not have to suffer for years without ever receiving an answer or a cure.

To read more about Lilly’s story, submit your own story about a journey with an autoimmune disease, educate yourself on all of these diseases, or read more about supporting this cause, you can check out the campaign website here .

If you are suffering from an autoimmune disease and feel alone, or would like lifestyle and recipe suggestions, you can check out Lilly’s autoimmune blog that chronicles daily life with an autoimmune disease.

If you are discouraged by years of incapacitating pain, failed diets, failed medications, and failed treatments, do not forget this: you are a warrior. You live every day fighting for immunity. This March, let’s all fight, too. Let’s fight for immunity. For fifty million Americans, we will.

#TheDress Sparked A Huge Debate, But Science Is Here To Settle Things

What color is it?

That question had just about everyone with a social media account scratching their heads on Thursday, when 21-year-old Scottish folk singer Caitlin McNeill posted a photo of a dress on Tumblr.

“Me and my friends can’t agree and we are freaking the f*ck out,” McNeil wrote in the photo’s caption–and they weren’t the only ones who couldn’t. Some people saw the dress as white and gold, while others say it as blue and black.

The dress really is blue and black, so why do some perfectly sane people see it as white and gold? Here comes the science.

(Story continues below image.)
the dress blue and black
In the middle, the original photo of the dress. The photo on the left has been color-corrected as if the dress were white. The photo on the right has been color-corrected to blue-black.

“It’s a phenomenon known as color constancy,” Mitchell Moffitt, co-creator of the YouTube series ASAPScience, says in a new video (above). “People who picture the dress as white have brains who may be interpreting the dress in a blue-lit room for example… It makes perfect sense then that the white dress would be tinted blue and that the gold color wouldn’t really change.”

In other words, our brains automatically adjust our color perception depending on the context in which something is viewed.

Mystery solved.

Tulsi Gabbard's Choice For Chief Of Staff Perplexes Politicos

Bruce Coppa remembers well the first call he received as former Gov. Neil Abercrombie’s chief of staff. It was about a man who had just threatened to blow up a plane at the Honolulu International Airport. By the time Coppa picked up, the crisis had been averted. But he still needed to brief the governor about what had just happened. It was part of the job.

“They’re calling you because you’re the guy,” Coppa said. “You don’t get to test the water. Once you jump in — you’re in.”

It’s the hardest gig Coppa ever had, and that’s saying a lot. He’s now a partner at Capitol Consultants of Hawaii, the most powerful lobbying firm in the state. Prior to becoming Abercrombie’s right-hand man, he held top executive positions in both the business and labor sectors, including with the Pacific Resource Partnership and the large PR firm Communications Pacific.

That’s why he and other political observers find U.S. Rep. Tulsi Gabbard’s latest hire as the chief of staff so perplexing.

Kainoa Ramananda Penaroza, 30, who is the third person to hold the position in two years, doesn’t have the kind of political experiences found in the resume of a typical high-ranking congressional staffer.

The Gay Best Friend Must Die

As my writing is wont to do, this will likely get me into trouble and incur the proverbial side-eye here and there, but it is time that the truth emerged. There are many wonderful things about being a modern American homosexual. The whole “having to fight for basic rights and constitutional protections” part notwithstanding, the gay community — and here, again, my experience pertains to the male portion of the community — is the beneficiary of a degree of affirmation unlike anything that’s occurred previously.

I’m not just speaking of marriage equality.

The nation’s attitude toward the gay community has undergone a paradigm shift at a breathtakingly fast clip. (And yes, this President saying what he said when he said it has a great deal to do with it. If you don’t understand the significance of his action, or question it — regardless of party — see me after class). We’re at a point of near coexistence. Though work remains — looking at you Georgia, North Carolina and Arkansas — by and large we’re in an astounding place. So, regrettably (not really) I’m going to have to break the hard news to you: The time has come for the gay best friend (or perhaps you prefer “GBF”) to, once and for all, experience a quick, clean and unequivocal death.

He’s become a staple of our collective zeitgeist. Who can forget the near ubiquitous web series that hastened us to “look at our lives and look at our choices?” I credit the onset of such lovable and decidedly pointed characters as Will Truman, the undeniably handsome Elijah, the ever whimsical Kurt and of course the inimitable Stanford Blatch with moving the needle on how mainstream Americans view the community. It’s a powerful testament to the sign of the times when most new primetime television shows either feature a prominent gay subplot, garner criticism for lack of one or some combination thereof. It means something when the chattering class questions the lack of diversity on the television. This has been the medium by which we as Americans see ourselves. When there’s a perception that the image we see is incomplete, without a piece of the LGBTQ community, that’s a potent assertion about who we are as a people.

That said, the GBF is a narrow interpretation of the beautiful array of personalities that comprise the LGBTQ community. It’s the unfair distilling of gay men to just one of the many things that makes him the guy who you want to be around because of his wit, sparkling personality or great taste in music. You limit his full agency when you do this. More succinctly: Don’t put baby in a corner.

Particularly odious is the act of referring to an out gay man or men as “my gay,” or “my gays.” It’s an understood rule of societal thumb that you don’t compare things to ownership. I will capitulate here. However, the triteness that is inherent in referring to ANYONE — sexual orientation aside — as “my” anything cannot be overstated. What’s next? My straights? My blacks? My GOD! For more on this, we turn to our field reporters Bette, Goldie and Diane.

The notion of the “gay best friend” works to calcify the idea of gay as other. It may seem to be a minor issue of nomenclature, but what you call something has meaning, in my most humble opinion. I don’t want to be limited by my sexual orientation. Nor do I wish to have undue expectations placed on me because of aforementioned orientation.

No dear, I don’t know why the guy you’re into won’t text you back. (I still haven’t figured that out for my own purposes.) Apologies, but I don’t have an opinion on everything you wear. (Unless, of course, it’s particularly heinous, at which point, all bets are off.) Nope, I don’t care to join you for pilates. (We banned torture… ish.) And, for the love of all that is good and HOLY: I am not — repeat, NOT — an honorary girl. I am proud to announce that after 24 years, my penis insists on staying around, and I’m ok with that.

We are entering a new era in this country’s discourse. The arc of the moral universe, long as it may be, is truly bending toward a more just, enlightened and connected collective conscious. Stale monikers, such as the GBF, function as constructs of a hetero-normative and insensitive past that have no place in where we’re going together. It may seem harmless, and I suspect that it did not originate from a place of malice — perhaps it even arose from a place of genuine respect and good intentions. I get that. The same thing can be said of the initial launch of healthcare.gov, Mondale for President and ARTPOP.

It does not mean that we’re in a rush to replicate any of those things anytime soon. I want my children to grow up in a country where they don’t have two gay dads, but just two fathers who love and care for them dearly. Once I’ve met that special guy and make the decision to commit my life to his, I won’t be gay married. I’ll be married. When we see the election of some qualified, stylish and proudly out individual as commander-in-chief in our lifetime, he won’t be the gay president. He’ll be the president. I don’t want to be your gay best friend. I just want to be your friend (we can iron out the “best” piece at a later date).

The words that we choose and the way we identify one another mean things. They have to, lest all communication cease to be meaningful. So yes, comrades. The time has come. Take him off life support. Turn off the Cher. Put the rainbow paraphernalia away. The GBF needs a sunset. He’s served valiantly and has many other gifts to offer beyond his predilection for other men. It’ll be difficult at first, but I’m confident we can get through this transition together. If not, no sweat. Global warming will take us all out soon enough anyway.

Class dismissed.

'The Michelangelo Of Buttocks Injections' Testifies At Her Murder Trial

PHILADELPHIA (AP) — A Gothic hip-hop artist charged with killing a London break dancer she injected with low-grade silicone said Friday she never heard any complaints from the numerous transgender women who sought her services for a more plump buttocks.

Testifying at her murder trial in Philadelphia, Padge-Victoria Windslowe said she stopped performing the procedures for a time after the 20-year-old client died in 2011. Doctors have told jurors during the two-week trial that the syringe hit a vein and sent silicone to the woman’s lungs. Two other women testified they spent months in the hospital with similar injuries after visits with Windslowe, including one who received an injection on a dining room table at a “pumping party” later the same year.

Witnesses said they reached Windslowe through an intermediary and never saw her again after botched injections.

Defense lawyer David Rudenstein seemingly hopes to show jurors through Windslowe’s testimony that she prepped them with alcohol before and after the injections and took other safety measures.

However, prosecutors say she mostly used nonsterile, industrial silicone, not the medical-grade silicone that is encased in implants during standard cosmetic surgeries.

“I told (clients) I’ve been doing this for years, I’ve done it to myself and my friends, and I was trained by a nurse up in Washington Heights (in New York City) back in 1995,” Windslowe said Friday, explaining her credentials.

On the stand Thursday, Windslowe said she was trained by a doctor in Thailand and another in South America who performed her sex-change operation.

She said she started doing body sculpting two decades ago to help transgender friends. Transgender women often want to plump up an indent in the side of the buttocks they call “the boy pocket,” she said.

Windslowe charged about $1,000 to $2,000 depending on the amount of silicone requested. Some clients, including a pole dancer she discussed Friday, saw her a half-dozen times.

Windslowe told jurors Thursday that she has worked on thousands of people, earning the title “the Michelangelo of buttocks injections,” and uses the same products on herself.

Windslowe acknowledges she injected 20-year-old Claudia Aderotimi but says she thought the dancer became ill from alcohol. Aderotimi died in 2011 after injections at an airport hotel.

Prosecutors argue that she recklessly endangered her clients by practicing medicine without a license.

No, My Entire Party Hasn't Arrived Yet. Yes, I Still Think You Should Seat Me.

I don’t think of myself as a punctual person — I’m constantly pulling into movie theater parking garages just as they start to roll the trailers. So when I meet people at a restaurant for dinner, I’m rarely the first to arrive.

But a couple months ago, I was meeting my mom for dinner at a sushi bar called Hiko in LA’s Sawtelle neighborhood, and I happened to beat her there. When I walked in, I found it deserted. Although it was 7 p.m., there were literally no diners in any of the seats. The only other souls in the restaurant were a waitress and a sushi chef. I walked up to the waitress and asked for a table for two. Her expression darkened.

“Has your dining partner arrived yet?” she asked.

“No,” I responded warily, “But I was just texting with her and she’s only a few minutes away.”

“I’m sorry, but we only seat complete parties,” she said.

“Even though there’s literally no one else here?” I asked, confused.

“It’s the policy,” she said, clearly embarrassed. She gestured toward a row of stools in the hallway. “Would you mind sitting here while you wait for your companion?”

I did mind. The restaurant was empty! And I just wanted to relax, order a beer and peruse the menu while I waited. I didn’t want to perch on some uncomfortable stool in a drafty hallway for who knows how long. But I’d heard that the owner of Hiko was known for strictly enforcing a host of specific rules in his restaurant; he’s known for kicking diners out mid-meal. So instead of complaining, I sat down at a stool and waited five minutes, until my mom walked in and we were allowed to sit. Our food, for the record, ended up being superb — but when I’ve thought about the meal since that night, I’ve found myself focusing more on the restaurant’s lack of hospitality than its deft handling of blue crab.

This was an extreme example. Few restaurants would refuse to seat an incomplete table if there were literally no one else in the dining room. But it speaks to a troubling trend in the restaurant world: Maitre d’s hatred of seating incomplete parties.

Intellectually, I understand why a restaurant wouldn’t want to seat someone before the rest of their party arrives. Since a party is unlikely to order food until everyone arrives, seating an incomplete table wastes space that could otherwise go to people who are ready to order. It’s an inefficient allocation of limited seating. That’s why I’m fine with a very popular restaurant refusing to seat incomplete parties during prime times — 8 o’clock on Friday night, say, or in the middle of the Sunday brunch rush.

But in my experience, this policy extends far beyond that. It’s ubiquitous. Restaurants everywhere insist on only seating complete parties, at all times of day and on all the days of the week. And it’s a major turnoff.

After all, the host is the first person you encounter when you walk through a restaurant’s doors. When they tell you that you can’t sit down, even though there are empty tables, it immediately signals that the restaurant’s owners are more interested in maximizing profits than in making their guests feel welcome and comfortable. It can be hard for a restaurant to recover from that foul first impression. Especially since someone who arrives before their dining companions might already feel vulnerable and awkward. Who hasn’t been the first one to show up for a date and worried that the other person will stand them up?

Plus, even if diners aren’t likely to order their main courses before their companions arrive, they’re very likely to start ordering little appetizers to share and, especially, drinks, which are the main profit centers for restaurants in any case. So it’s not a total waste. At restaurants with bars, hosts will often encourage early arrivers to wait for the rest of their table at the bar and order a drink in the meantime — and I’m generally A-OK with that.

But if the bar’s full, or the restaurant has no bar, and there are open tables, I really wish hosts would seat incomplete tables. Not if it’s just one person in a group of eight, I suppose, and not if the restaurant’s slammed. I wouldn’t want to replace one kind of rigidity with another. I’m just asking for hosts to be flexible and hospitable rather than blindly obeying ironclad policies.

I witnessed a stellar example of a smart attitude toward incomplete parties a few weeks after my meal at Hiko, when I was meeting a friend for dinner at Ludo Lefebvre’s hotspot Petit Trois. I walked in at 7 p.m. on a Tuesday and found it just as empty as Hiko had been. This was more surprising, as it’s a tiny restaurant that’s attracted a ton of buzz. Most of the time, it’s packed; it’s the rare LA restaurant that regularly has a wait for a table. So even though I was the only diner there, I felt sure that I would be asked to hover outside until my friend arrived.

But much to my delight, the waitress who greeted me at the door encouraged me to sit right down. She poured me a glass of water and asked if I wanted a cocktail while I waited. My friend soon texted to say that he’d mixed up his schedule, and wouldn’t get there for 20 minutes — but at no point did anyone in the restaurant flinch. Indeed, they were friendly and solicitous even as the restaurant started to fill up a bit and my companion still hadn’t arrived.

When he finally showed up, I had worked up an appetite while waiting and drinking, so we ordered a great deal of food and drink, racking up a larger bill than I had intended. But because the restaurant had welcomed me enthusiastically from the minute I walked in, I left eager to return. That’s what a good restaurant meal should always do.

EE kicks off 400 Mbps 4G trials at Wembley Stadium

EE was the first 4G network operator in the UK, and it’s now hell-bent on staying the fastest. After launching its LTE-A network (aka 4G+) in central London last October, it’s trialling new spectrum configurations that could boost speeds even further…

Aereo gets only $2 million from selling assets to TiVo and other companies

Aereo was expecting to sell its assets for at least $4 million (and up to $31 million) at a bankruptcy auction, following its loss in a protracted legal battle against broadcasters. Sadly, luck wasn’t on its side yet again: the company has managed to…