[why food deserts abound] Surprise! Everyone hates broccoli

food deserts abound because people hate broccoli
Why food deserts abound. Surprise!

 Why food deserts abound. Surprise! Everyone hates broccoli!

 In inner cities and poor rural areas across the country, public health advocates have been working hard. Why?  to To turn around food deserts – neighborhoods where fresh produce is scarce, and greasy fast food abounds.

In many cases, they’re converting dingy, cramped corner markets into lighter, brighter stores.  that offer fresh fruits and vegetables.

In some cases, they’re building brand new stores.

To change inner city food habits they built stores that were attractive. 

“The presumption is, if you build a store, people are going to come,” says Stephen Matthews, professor in the departments of sociology, anthropology and demography at Penn State University.

To check that notion, he and colleagues from the London School of Hygiene and Tropical Medicine recently surveyed residents of one low-income community in Philadelphia before and after the opening of a glistening new supermarket brimming with fresh produce.

What people actually eat:

 What they’re finding, Matthews says, is a bit surprising: “We don’t find any difference at all. … We see no effect of the store on fruit and vegetable consumption.”

Surprise!  Everyone hates broccoli.

http://www.npr.org/blogs/thesalt/2014/02/10/273046077/takes-more-than-a-produce-aisle-to-refresh-a-food-desert

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Firenze Sage, Esq.  As usual,  the Obamas are wrong.

http://www.smashwords.com/books/search?query=four+more+obama+years

 

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http://www.dailyfinance.com/2012/04/04/food-deserts-where-have-all-the-inner-city-grocery-stores-gone/

Food Deserts: Where Have All the Inner-City Grocery Stores Gone?

by Jeremy Bowman  Apr 4th 2012 6:00AM

City grocery storesChicago entrepreneur Karriem Beyah grew up working in the grocery business, but when he courted some industry heavyweights to bring stores to the South Side, their response was disdainful: “Who wants to go over there, in that negative element?”

 

 

 

 

 

 

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parents manipulate process for autism services hoisted on their petard?

 

 

educator/parents manipulate process seeking services
parents manipulate process for autism services

Parents manipulate  process for  autism services hoisted  on their own petard?

Here’s a list of  what NOT to do when seeking services for a child with substantial delays such as autism or intellectual disability.

And if you do the following  – don’t expect the process to go smoothly!

That the parents are both teacher/ educators which is a profession prone to “know it all” types may have  played  a role in what happened and that these parents today  are still clueless.

The family  first went to  an  M.D.  who made recommendations that a handful of evaluations be done & then  to come back to discuss the results.  The parents  did not follow through on any of the MD’s  recommendations concerning assessment.

Instead, the parents went to a CA  agency that provides services to children with developmental disabilities.  There, the parents:

  • Told  the agency  exactly  what diagnosis to give their child.   And what diagnosis was not acceptable.
  • Spent most of the  first interview  saying NO when asked for additional info/ records.
  • Refused permission for the agency  to  observe the  child  with same age peers at school.
  • Created  a  pseudo history of  events via email trail.
  •  Provided false information  because their advocate told them to do so.

Overall, these parents/ educators  tried to manipulate the  process from start to finish.  What happened?

Hoist by they own petard!  One thing lead to another and the end result was that the parents did not get the diagnosis they expected.  So they they tried to change the diagnosis through a complaint process. And that did not work.

The parents feel “stuck” with a diagnosis they do not agree with. Shown the support for the diagnosis they still want to reject it. And the parents state that they feel that the process was a painful one.  Well, the actions they took (see above bullets) resulted in effects they did not expect.

It is hard for parents to accept that their child not only meets criteria for autism but also for intellectual disability.

What about the child?  The 13 year old substantially delayed child still does not have an Individual Education Plan (IEP). The parents, both educators, say that they don’t want their child  harmed through special education  categorization or certain medical  diagnosis which they don’t accept.

In my view, just as water seeks its own level, many children with disabilities are more comfortable educated with children who share similar  abilities.  I hope that this child does get an IEP and can have connections with children who share similar abilities and interests.

 

http://http://www.autismsupportnetwork.com/news/category/parents-and-friendsaut.sagepub.com/content/3/3/273.abstract

Cameron Jackson, Ph.D.    DrCameronJackson@gmail.com

Dr Jackson is a psychologist with a private practice in Santa Cruz, CA   831 688 6002

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[voter ID required] Don’t do as I say, do as I tell you

voter ID required by NAACP for protesters opposing new voter ID law. Huh?
voter ID required by NAACP for protesters opposing new voter ID law. Huh?

Voter ID required for protesters of the new voter ID law in North Carolina. Huh? You heard right.

The North Carolina State Conference of the NAACP is holding a rally to protest that state’s new voter identification law.  

In a flier entitled “Important Dos and Don’ts for Marchers!!!,” the NAACP state at the top that all protesters conduct themselves “in accordance with the historic custom of the Civil Rights Movement.” They should also listen to their “marshals at all times” and follow the “Dos” and “Don’ts” underneath the opening paragraph.

In the middle of the NCCCP list, however, is :  “To go to the rally, you are asked to have “photo identification (driver’s license, passport or other valid photo id) with you and keep it on your person at all times.”

http://dailycaller.com/2014/02/08/naacp-requires-marchers-protesting-north-carolina-voter-id-law-to-show-photo-id/

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Koch brothers control NAACP printer?
Koch brothers control NAACP printer?

Firenze Sage, Esq:  Obviously the Koch brothers control the NAACP  printer.

Or is it the Marx brothers?

Marx brothers?
Marx brothers?

       jaj48@aol.com

 https://www.smashwords.com/books/view/238484

book: Four More Obama Years?
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[advise for Bieber’s mother] fantasy world of Michelle

Bieber
Advise for Bieber’s mother  from Michelle Obama

Advise for Bieber’s mother:

 Spend lots of time with him. First lady Michelle Obama’s advice to Justin Bieber’s mother is to spend lots of time with her son and get to know who he’s hanging out with, the self-proclaimed “mom-in-chief” said in an interview released Friday.

“I would pull him close,” Obama said of the 19-year-old pop singer in an interview with Univision, when asked how she’d guide the troubled pop star right now if she were his mom. “I don’t know if it would be advice as much as action.

I would be very present in his life right now. And I would be probably with him a good chunk of the time, just there to talk, to figure out what’s going on in his head, to figure out who’s in his life and who’s not, you know.”

She added that she’s seen that her kids “just want you near, you know, they want that advice from a parent. They want to see you on a daily basis” and because Bieber is “still a kid, he’s still growing up,” that lesson applies. The singer has faced multiple arrests, and reports of drug and alcohol use.

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WHAT BIEBER NEEDS
WHAT BIEBER NEEDS IS A BAILBONDSMAN

Firenze Sage, Esq:  Well Mrs O the kid is a gazillionaire in his private jet with booze, dope, and dames,and probably his father.

So finding out who he’s with is no problem. What he really needs is a bailbondsman.

 

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How to celebrate milestones of children with developmental delays?

 

How to celebrate milestones of children with developmental delays?

Children with developmental delays frequently do not graduate from high school.

One private school in Santa Cruz, CA which serves largely children with autism is the Bay School.  Per report by a parent, there is no graduation ceremony at the Bay School  when students finish their Senior year. 

So, what to do if a student with developmental delays wants to celebrate completion of high school but there is no ceremony or ritual?

Clearly, here’s an opportunity to innovate.  

innovate & make a ceremoney
innovate & make a meaningful ceremony for children with developmental delays

Make up a ceremony that will be meaningful for your child with delays. Each child is unique so the best person to decide are the parents and family and friends who support this young person leaving high school behind. 

Do you know a child with developmental delays? Find out their birthday and the date that they will formally  finish their Senior year.

Send a card and/or a small gift. Make a phone call. And you might include a fresh flower or two for the parent(s) who has taken this long journey with their child soon to be a grown up.  Below is a post by an MD on the same topic. 

licensed psychologist DrCameronJackson@gmail.com

http://blogs.einstein.yu.edu/celebrating-milestones-for-the-developmentally-disabled/

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What are probable causes of autism? Vaccines?

What are probable causes of autism in babies? Vaccines?

Defer vaccinations for some children ages 18 to 24 mo?
Defer vaccinations for some babies  ages 18 to 24 mo?

What are probable causes of autism in babies? Vaccines?   Research says mercury in vaccines does not cause autism because there’s no more mercury in the vaccines. That’s the beginning of the story …

But maybe the vaccines themselves overwhelm some babies who genetically are more likely to develop it than others.

What to do? Talk to your MD about a delayed schedule for vaccinations.  A particularly vulnerable window seems to be the 18 – 24 month period. Why not defer vaccinations if certain conditions exist.   drcameronjackson@gmail.com

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Research Reaffirms: No Vaccine-Autism Link

Jan. 7, 2008

By AUDREY GRAYSON

A new study may be the latest nail in the coffin of a theory that draws a link between the mercury-containing vaccine additive thimerosal and autism.

The research is the latest to contradict concerns over childhood vaccinations as a possible cause of autism — concerns that have gained publicity in the past decade as the number of children diagnosed with the disorder climbs steadily in the United States.

Because vaccinations are mandatory for all children at a certain age, some parents and doctors believe that the mercury once found in many childhood vaccines may contribute to the development of autism. However, so far a number of large scientific studies have shown no association between thimerosal and autism.

And the most recent research to nullify this association, published Monday in the journal Archives of General Psychiatry, reveals that the prevalence of autism for children ages 3 to 12 continued to increase in California even after 2001 — when all but trace levels of mercury had been removed from most childhood vaccines.

“If thimerosal exposure is a primary cause of autism, then the prevalence of autism would be predicted to decrease, as young children’s exposure to thimerosal has sharply decreased to its lowest levels in decades,” noted lead study investigator Robert Schechter in the commentary section of the research.

Much Ado About an Additive

Before 2001, thimerosal was used in many childhood vaccines to prevent microbial contamination. However, in July 1999, the U.S. Public Health Service implemented a precautionary measure removing thimerosal — which contains 49.6 percent ethylmercury — from all childhood vaccines.

To determine whether reduced exposure to thimerosal led to a decrease in autism cases, researchers at the California Department of Public Health analyzed data from the California Department of Developmental Services on the prevalence by age and birth cohort of children with autism between 1995 and 2007.

But instead of finding a decrease in autism following the elimination of thimerosal from most vaccines, researchers found that for each quarter from 1995 to the end of 2003, the prevalence of autism in children between the ages of 3 and 5 years increased from 0.6 to 2.9 per 1,000 births.

http://abcnews.go.com/Health/story?id=4099059&page=1

http://abcnews.go.com/Health/story?id=4099059&page=1

From 2004 to 2007, when exposure to thimerosal from childhood vaccinations vastly declined, the prevalence of autism in children between the ages of 3 and 5 years increased from 3.0 to 4.1 per 1,000 births.

The findings bolster the position that has been steadfastly held by the Institute of Medicine, and many doctors worldwide, that no link can be established between thimerosal and autism.

Some researchers say that the absence of a link has already been demonstrated in Denmark, where thimerosal was removed from all vaccines in 1992. Despite this move, autism rates in that country continued to rise until 2004.

“Conspiracy theorists will continue to engage this theory on the link between autism and vaccinations, but hopefully, they will take into account that this idea has been refuted on an international scale, not just by the CDC,” said Mark Slifka, associate professor in the Vaccine and Gene Therapy Institute at Oregon Health Sciences University.

“Studies out of Sweden and Denmark, independent studies on an international basis, have all come to this same conclusion.”

http://abcnews.go.com/Health/story?id=4099059&page=1

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Politics to making a diagnosis of Autism? Yes!

Politics to making a  diagnosis of Autism  and/or  Intellectual  Dsability? Yes!!

Comorbid conditions with Intellectual Disability include Autsm
Comorbid conditions with Intellectual Disability include Autsm spectrum disorders

Times have changed. In the last 5+ years,  a diagnosis of Autism is sought after as a diagnosis particularly if the other diagnosis  to rule in or out is Intellectual Disability formerly Mental Retardation. 

Intellectual Disability affects many more areas of functioning relative to Autistic Spectrum Disorders
Intellectual Disability affects many more areas of functioning relative to Autistic Spectrum Disorders

See the post below wherein the MD is haunted by a diagnosis of mild Autism which she made 20 years ago.  Perhaps if  that MD had suggested what treatments could be offered for mild Autism  and typical progress made through social skills training, then perhaps the parents might have returned on their own for follow up appointments.

Twenty years ago we did not have internet. Now, it’s possible to get e-mails and immediately set up a connection with parents so as to address their concerns.

Recently, I diagnosed a 13 year old boy with Intellectual Disability, Unspecified. My guess is that he has Moderate ID, i.e., an I.Q around 40-50.    When the parents were interviewed they said that they  wanted  a diagnosis of Autism.  Later, at another meeting they  entirely rejected a  diagnosis of Intellectual Disability.  Because Intellectual Disability affects all areas of general functioning whereas Autism is more limited it will not take 20 years to see which diagnosis is more accurate.  The politics of this diagnosis still reverberates.  Parents want any mention of Intellectual Disability stricken from our records. Politics involved?  Yes!!

DrCameronJackson@gmail.com

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Haunted by an autism diagnosis: A sense of closure after 20 years

 | CONDITIONS | JULY 27, 2013

I believe most physicians have cases that haunt them, often patients whose treatment courses do not go ideally and who leave a mark on the physician, altering the way he or she practices ever after. When the physician is a surgeon, it might be a patient who died on the table. For a hematologist, it might be a patient with cancer who could not be cured. For a developmental pediatrician, it is likely a patient diagnosed with a developmental disability whose family vehemently disagreed with the diagnosis. Since the vast majority of developmental disabilities are lifelong in nature, when a child receives such a diagnosis, it is a life-altering event for the family. And such events do not always go well.Last week, I came to work and among the charts in my mailbox I found one from the medical records department. Such charts appear periodically and require my review and signature in order for records to be released. The records had been requested for social services documentation. A sticky note was attached, noting that it was a very old case. I recognized the name right away. I looked through my original notes and the case came back to me in detail, just as I had remembered it all these years.More than twenty years ago, when I was a brand-new fellow in neurodevelopment at the Children’s Evaluation and Rehabilitation Center, here at Albert Einstein College of Medicine, one of the first children I evaluated was a six-year-old boy. This boy was brought in by his parents—his father, a lawyer, and his mother, a social worker—for evaluation of his learning and behavior difficulties. To me he seemed bright, but I had to work hard to get his attention. His mind seemed to be elsewhere. He had poor eye contact and trouble having a conversation. No matter what we were talking about, he kept bringing the conversation back to the topic of dinosaurs, clearly his passion. And he was quite expert about that topic, with an impressive vocabulary.Fast forward to two decades later. I am now the director of autism services at the Children’s Evaluation and Rehabilitation Center, but even back then I was interested in autism. While I knew that this boy did not have frank autism, it was clear to me that he had the flavor of autism, with its hallmark social and communication impairments and restricted interests. In our subsequent multidisciplinary team meeting, I remember making the case to clinicians far more experienced than I (all of whom are now either retired or deceased) that this boy had mild autism, or pervasive developmental disorder not otherwise specified. The other evaluators were ready to diagnose the child with language impairment and attention deficit hyperactivity disorder, but needed convincing about the mild autism. I persisted. In the end, the team leader said that I could present my opinion to the child’s mother and make my case to her.

It was my first parent conference ever. I had watched an experienced social worker give a series of diagnoses to a family and now—following the “see one, do one” model—it would be my turn. Things started off well. When I reviewed the cognitive and language data, the parents were attentive and the mother’s nods indicated that the information was consistent with her own thoughts about her son. When I moved on to discuss the constellation of behaviors that included poor eye contact, conversational weaknesses and restricted interests and suggested that they might be manifestations of mild autism, the mother vehemently stated her disagreement. She said that she “had seen autism and this was not it.”

The family never returned for the scheduled follow-up appointments. I had no information about what had become of the boy. But I thought of him over the years; he haunted me. I went on to develop a clinical and research passion for autism and to head the RELATE program for early diagnosis and treatment of autism here at Einstein. The field of autism changed in the background, with the concept of the spectrum of autism becoming widely accepted. But I wondered through the years if, in my clinical debut, I had jumped the diagnostic gun. Had I given these parents an incorrect diagnosis for their son—one with lifelong implications? The case haunted me as I wondered whatever became of the boy and his family.

I looked back at the old chart and the release of records form and found that there was another sticky note affixed to the record. It said that the patient was currently being seen on the adult unit, and those recent records were also attached. I excitedly flipped through the pages to find the new report. The record began: “The client is a 29-year-old male who reports that he was diagnosed with mild autism as a child, that he completed high school, went on to college but could not manage it and dropped out and has been unable to hold a job since due to social difficulties. He comes seeking treatment.” The report goes on to describe his poor eye contact, trouble with topic maintenance and trouble understanding the examiner’s perspective. It was clear, based on the recent evaluation and current attitudes and criteria, that the patient has an autism spectrum disorder.

From a selfish perspective, this follow-up—more than 20 years later—gave me a sense of closure. The long-ago diagnosis had been accepted, at least by the young man himself, and he continues to show signs of this generally lifelong diagnosis. But I ached to know the course his family had taken in accepting the diagnosis and what help he had received along the way. Could he have done better and succeeded in his education and work activities if he had received more specialized help, such as social skills training—readily available these days but hard to find in the 90s? I don’t think the case will haunt me in the same way it had. Maybe in some new ways, though, it will.

Lisa Shulman is a neurodevelopmental pediatrician and director, infant and toddler services, Children’s Evaluation and Rehabilitation Center (CERC), Albert Einstein College of Medicine. She blogs at The Doctor’s Tablet.

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Autism: what parents can do early on

Keep a notebook and date when your baby does ...
Keep a notebook and date when your baby does …

Keep a notebook. For example,

Date the first social smile by baby and the following events.

Date  baby's first social smile. What age?
Date baby’s first social smile. What age?

When did the child first reach up his/her arms signaling non-verbally that the child wanted to be picked up.

Does the child turn her head when their name is called.

Will the child engage in joint play, looking at the object and also at the parent?

When you as parent point, will the child’s eyes follow what you are pointing at?

Will your child show interest in other children?  For example, if you go to a park with a couple pails and some spoons or shovels will  your child show interest in other children who also want to play “scoop” the sand into a pail?

Unlike many medical diagnosis which depend on blood and other tests, there are no  physical tests for autism. And because the worst aspects of autism are social deficits the child if at all possible be seen with other  same age children.

Cameron Jackson, Ph.D.   DrCameronJackson@gmail.com

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It’s time primary care doctors diagnose autism says pediatrician Somsak

 | CONDITIONS | AUGUST 1, 2013

I remember how my son’s autism diagnosis was delivered.  He was three years old.  It wasn’t a surprise really, merely a confirmation of something that I expected and feared.  He was already enrolled in speech and occupational therapy making very little progress.  He saw a developmental specialist at age two and two and half who initially believed that he was not autistic but merely delayed with sensory issues.  After we requested a more formal evaluation for autism, she referred us to the “autism specialist” in her division. 

The diagnosis was “officially” given after four appointments with various “specialists” at a Children’s Hospital.  Initially my husband and I met with a psychologist who took a detailed history.  A week later we returned with our son, so the psychologist could directly observe and assess him.  He mostly screamed.  At our third appointment a trained speech therapist administered the Autism Diagnostic Observation Schedule (ADOS), one of the few standardized tools that help physicians and psychologists diagnose autism.  Finally the fourth appointment we met with an “autism specialist” who summarized the results and confirmed his autism.  We were offered follow up in a year with either the autism specialist or her nurse practitioner.  We already had a firm plan for future therapy and education.  All we needed was a physician to sign off on the state autism scholarship form so that we could receive funding for him to attend a specialized school.  Fortunately, our health insurance paid for most of this diagnostic process, this bureaucratic, non-transparent, not especially helpful process.

By the time a child is three years old, he has had about 10 visits with his primary care doctor.  The doctor likely knows the family and the child very well.  If developmental screening revealed a delay or concern for autism (pediatricians generally screen for autism with the MCHAT at 18 and 24 months), the child has already been referred to early intervention and might be receiving additional private therapies.  The primary care provider has received the results of at least some of these evaluations and visits.  Depending on the state where the doctor practices, the early intervention team may have performed an ADOS and sent the result to the physician.

The American Academy of Pediatrics 2007 policy statement Identification and Evaluation of Children with Autism Spectrum Disorders states “pediatricians must be aware of local resources that can assist in making a definitive diagnosis of, and in managing, autism spectrum disorders,” but it stops short of saying that pediatricians are the doctors that can and should make that diagnosis.  The waiting list to see a specialist can be over year depending on where the child lives.

Furthermore, many specialists do not make a diagnosis at the initial visit forcing the family to wait even longer.  Even if a diagnosis is made, the specialist does not assume the care for the child the way an oncologist would for leukemia, a gastroenterologist would for Crohn’s disease, a psychiatrist would for bipolar disorder, a pulmonologist would for cystic fibrosis, an endocrinologist would for a new onset diabetes, you get the idea.  The situation differs from that of almost every other chronic disorder, yet we know that the care of autistic children is just as complex and crucial as the other disorders mentioned.  When no doctor steps up, mothers become frustrated warriors some advocating tirelessly for evidence based therapies, others work to green vaccines and cleanse diets while most do the daily mundane heroic acts of mothering a special needs child.

Primary care providers by default end up heading the autism team.  Shouldn’t they make the diagnosis?  Do they have the time?  If we can make time for depression and complicated ADHD, we can fit an autism diagnosis into our day.  Do primary care providers have the knowledge to make a diagnosis?  Autism centers have become the “experts” in diagnosis which creates a catch 22 because these centers cannot meet demand.  Despite this, they are not reaching out to empower primary care doctors to make the diagnosis nor do they accept the diagnosis given by a different ivory tower.

A recent study conducted by Vanderbilt University with the help of the Tennessee AAP Chapter demonstrated that after a two day training, local pediatricians felt comfortable making the diagnosis of autism and agreed with specialist diagnosis 90% of the time.  Similar trainings are underway in Ohio.  I completed this training and found it helpful.  Ohio has such a back log of children who need a doctor to evaluate children with possible autism, they are trying to recruit general pediatricians to see children outside their own patient practice.  This training should be online, standardized and offered by the national AAP as an Maintenance Of Certification activity and specialists should embrace it.

Denise A. Somsak is a pediatrician.

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Obama’s U.S. ambassadors: the state dept follies

 Obama’s U.S. ambassadors: 
  • Noah Mamet bundled at least $1 million in campaign donations to President Obama’s two presidential election campaigns, and now he’s in line to be the U.S. ambassador to Argentina, 
  • Last month the Obama nominee for a similar post in Norway demonstrated a lack of knowledge about that nation’s political structure and said he had never been there
  • Newly minted ambassador Max Baucus, now headed to Beijing, freely admitted in his own hearing that he’s ‘no real expert on China’
  • The new ambassador to Hungary is a soap opera producer and prolific Democratic fundraiser who couldn’t tell senators what America’s strategic interests are in that country.
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  • And they [our new U.S. ambassadors]  are now all led by the incomparable John Kerry who may [we hope] be smart enough to keep them alive [not like Bengazi where Stevens and 3 others died]. 
 t
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[USA athletes in Russia should get] gold medals for escape awarded

USA athletes  in Russia (a male)  break down bathroom door and another athlete (a female) does  not to to step into an open elevator  shaft.

USA athlete in Russia breaks down bathroom door to escape
USA athlete in Russia breaks down bathroom door to escape

After U.S. bobsledder Johnny Quinn realized he was trapped inside his hotel bathroom this weekend, the 30-year-old Olympian broke down the door. Quinn, who was phoneless post-shower, pummeled through the pseudo-wood to escape that small, steamy space — and tweeted the aftermath to the world.

http://bleacherreport.com/articles/1953210-american-bobsledder-johnny-quinn-breaks-out-of-bathroom-in-sochi

Elevator shaft escape:

 

British bobsledder Rebekah Wilson was greeted with an empty elevator shaft when she attempted to leave her room in the Olympic Village on Saturday morning.

She later said she hit the down button, the doors opened, and there was nothing there.

 

http://www.washingtonpost.com/news/olympics/wp/2014/02/08/bobsledder-has-scare-with-open-elevator-shaft/

________________________________________

Firenze Sage, Esq.
Not to worry. The whole country [Russia]  is a 3d world mess with Atomic bombs.

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