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24 Şubat 2017 Cuma

A moment that changed me: lashing out at a man who opened the door for the newly thin me | Stacie Huckeba

It was July 2014, Nashville Tennessee. I was walking into a gas station for a bottle of water when the man behind me stepped up to open the door for me. With that act of kindness, something inside me snapped and I flew into a blind rage. I began screaming at him at the top of my lungs.


“No, you can not open this door for me! You wouldn’t have opened it two years ago, so you damn sure can’t open it now!” I scowled and stormed away, completely enraged.


It was the third time that week that a man had done something polite for me. First a man had bought me a drink at a concert, and then there was the nice man who had helped me scoop up my groceries after I dropped my bag, and now this man with the door.


I know all this might leave you wondering if I had had a rough week, or a fight with my boyfriend or was in a terrible mood that had prompted me to lose my temper like that. The truth is more complicated.


Two years before this, in July 2012, I weighed 365lb, which roughly translates into 26 stone. I was enormous, and had been my entire life. I grew up an obese kid, was an obese teenager, an obese young adult, and by my mid-40s I had ballooned into a hugely obese adult.


But that summer I started a massive journey to lose 220lb, or almost 16 stone, over the course of four and a half years. As I sit here today, I’m literally a third of the body mass I used to be. I am an average-sized woman who wears a size medium pretty much across the board. And, I am happy to report, I am also a fairly happy, confident person.


But that day I had just begun experimenting with regular-sized clothes, and I was not confident. I was uncomfortable. I was uncomfortable with the attention my new body was receiving, I was uncomfortable about new social circles, and I was uncomfortable with the unexpected boost to my career.


I was uncomfortable but I didn’t know why. Everything seemed to be going so well. I should have been happy, but I wasn’t. And it wasn’t until I saw that man’s hand reach for the handle of that door that I knew why – and it pissed me off.




The idea that the size of my trousers had had anything to do with simple politeness was heartbreaking to me




I had been disregarded, overlooked and ignored because of my size for so long that I didn’t even realise it until people started being nice to me – until, in other words, I was “normal sized”. No one had ever done those things for me before.


He opened that door for me because I wasn’t physically offensive to him, and I knew. And it was in that moment that I realised how terrible we are as a society to people, based solely on their appearance. This realisation broke me. It broke me in a way that I’ve never been broken before. He certainly didn’t deserve my outburst, but in that moment I couldn’t help myself.


The idea that the size of my trousers had had anything to do with simple politeness was heartbreaking to me. Never mind men actually asking me on dates, career advances, better opportunities and much cheaper clothes (big girls get done over by the fashion world).


In every pair of trousers I have ever owned, I have been the exact same person; with the same thoughts, abilities, talents, intellect and heart. I didn’t just magically become smart, funny, talented and pretty when I could buy smaller jeans. I’ve been in here the whole time. But very few took the time to see me.


And when that realisation came, I grieved for the child, teenager and woman I had been and all she had been deprived of. I grieved for what experiencing that would do to my current self. And I grieved for all of the people who may have missed her along the way because they were too blind to see her. In that moment of grief, I lashed out at a perfectly polite stranger.


That moment changed every single thing about me. It has now become my life’s mission to help people realise their true beauty and strength; right now, in the body they occupy, this second. I’m a photographer and video producer, and it completely changed the way I shoot my clients, as well as prompting me to launch a second career, writing and speaking publicly, so that hopefully I can change the way we all perceive beauty.


I love my ass the size it is now. I love the way I look and feel, and the freedom it gives me. I can breathe. I actually love taking exercise. I love that my feet don’t ache and my back doesn’t crack. My boobs look like two baseballs in sacks but, whatever – they look great in lingerie and I can actually buy it now.


But the thing is, I was amazing before I lost the weight too. That girl had the strength to become this woman. That girl had the courage to leave home at 16 years old in search of a new life. She had the passion to pursue a career in the arts and actually succeed. And she had a big enough heart to not notice that people were mean to her along the way.


People are my business, and I’ve learned a lot about them over the years. I’ve learned that I’ve never met one that wasn’t stunning. No matter what they looked like or what they weighed. I’ve never seen a face or body that I couldn’t find beauty in or a person who didn’t possess compassion, humour and love.


Honestly, people are amazing. You just have to really see them.



A moment that changed me: lashing out at a man who opened the door for the newly thin me | Stacie Huckeba

2 Temmuz 2014 Çarşamba

These newly diagnosed with dementia are "cut adrift" just when they require support most, charity warns


Shelagh had gone to the hospital alone when she obtained a diagnosis of dementia. With the medical doctor for less than five minutes, she compares the delivery of this news – which was lifestyle-altering in the excessive not only for her but her family members and pals – as ‘like getting advised I had tonsillitis.’ She refers to this day as the worst of her life but says it wasn’t the diagnosis itself, rather the lack of empathy and assistance that left her feeling so desperately alone.




Shelagh compares herself to a near buddy who was lately diagnosed with breast cancer. In that predicament, on obtaining the news she was immediately provided with a nurse who supplied comfort, assistance and, need to it be needed, a shoulder to cry on.




You would hope her experience was a one particular off, the exception rather than the norm, but sadly it isn’t. An Alzheimer’s Society survey published right now finds that a fifth of folks affected by dementia had been offered no details and assistance soon after a diagnosis – factors that are essential in assisting individuals come to terms with the problem, keep independence and strategy for a long term they hadn’t envisaged.




A single in 3 individuals above 65 will produce dementia – but dementia and despair do not have to go hand-in-hand. People with the situation inform us that with the correct data and assistance they can live properly, but it wants to be a lot far more forthcoming. It ought to by no means be the case that someone is left to trawl the world wide web (that is producing the large assumption that they have accessibility to it) to find out what their diagnosis implies how their problem is very likely to progress what adaptions can be created to their property and exactly where they can uncover help groups and providers in their regional neighborhood.




At present there is no national guidance on a minimal provision of support for folks impacted by dementia, nor is it clear regardless of whether the obligation for commissioning providers lies with wellness or social care. Just today the Association of Directors of Grownup Social Companies has launched a report warning that our social care system is dealing with monetary meltdown if budgetary pressures continue. The findings stage to a worrying imbalance between supply and demand – given that 2010 paying on social care has fallen by twelve per cent in genuine terms at a time when the variety of individuals seeking for support has improved by 14 per cent.




But to leave vulnerable folks adrift at the point of diagnosis is not only unacceptable but a false economy. The consequences of this is that individuals impacted by dementia miss out on simple support that can enable them to carry on residing the lives they want, which increases the chance of them reaching crisis stage and being admitted to hospital or into a care house.


Today Alzheimer’s Society is calling on government to ensure every single particular person with dementia has access to a Dementia Adviser, or equivalent, from diagnosis onwards. Dementia Advisers are a valued and trusted supply of expert information, advice and help. Their part is to be on hand to answer the myriad of concerns that will inevitably come following a diagnosis. They direct an personal to the most suitable supply of info, at the proper time and most importantly they can demonstrate folks that existence can and will go on after a dementia diagnosis.


Also many men and women like Shelagh are left to fend for themselves, relying on their close friends and loved ones to aid during some of the toughest moments of their lives. The health and social care method wants to be responsive to their demands, offering personalised care and support tailored to their situation. At Alzheimer’s Society we do our ideal to supply this kind of assistance and final 12 months published a dementia guide for anyone who has lately been informed they have dementia – but it is that personalized, encounter-to-encounter help that is so vitally important and we merely can’t attain every person. We need to have the government and the NHS to commit to and invest in help services which will make life less difficult for individuals residing with dementia.


This government has completed a good deal to increase awareness and commence to tackle the main difficulties that dementia presents. The recent G8 summit on dementia has offered a welcome concentrate on the search for a remedy. Nevertheless, measures like the ones we are proposing today will assist people impacted by the situation now. Everyone with dementia has a proper to information and assistance. The inescapable reality is that dementia will quickly touch every loved ones in the land – we require our health and social care providers to be prepared for it.




These newly diagnosed with dementia are "cut adrift" just when they require support most, charity warns

19 Şubat 2014 Çarşamba

Newly Elected President Of Institute of Medication Is On The Pepsico Board Of Directors

A group of Duke students protested the excessive compensation provided to some best Duke officials, including cardiologist Victor Dzau, who is the Chancellor for Well being Affairs at the University. In response to the protest, one mentioned advocate for overall health care reform says that Dzau has enriched himself even even more through support on four separate corporate boards, and that Dzau or Duke has been much less than forthcoming about completely disclosing Dzau’s board memberships.



The protesters took issue with Dzau’s total compensation for 2009 of more than $ two.2 million. The figure appears excessive, especially in the context of latest monetary difficulties at Duke, resulting in “frozen pay and eliminated jobs,” in accordance to newsobserver.com.


But Dzau’s compensation at Duke is far from uncommon, according to Roy Poses, creating  on Health Care Renewal. He notes that compensation for “leaders of not-for-profit organizations, which includes academic institutions, is now frequently in the millions per 12 months selection.”


But what is striking in this situation, in accordance to Poses, is the large sums of funds Dzau receives from sources outside of Duke. In particular, Dzau serves on many corporate boards, Alynlam Pharmaceuticals, Genzyme, Medtronic, and PepsiCo, even though his biography on the Duke website lists only his Genzyme affiliation.


Right here are the specifics of Dzau’s corporate compensation for 2009, as reported by Poses:



  • In accordance to the Alnylam Pharmaceuticals 2010 Proxy Statement, Dr Dzau’s compensation as a director in 2009 was $ 234,433.  In 2009, Dr Dzau owned the equivalent of 45,000 shares, well worth $ 424,800 at today’s $ 9.44 price per share.

  • According to the Genzyme 2010 Proxy Statement, Dr Dzau’s compensation as a director in 2009 was $ 412,942.  In 2009, Dr Dzau owned the equivalent of 75,137 shares, well worth $ five,312,937 at today’s $ 70.71 price tag per share.

  • According to the Medtronic 2010 Proxy Statement, Dr Dzau’s compensation as a director in 2009 was $ 173,698.  In 2009, Dr Dzau owned the equivalent of 14,552 shares, worth $ 493,895 at today’s $ 33.94 value.

  • In accordance to the PepsiCo 2010 Proxy Statement, Dr Dzau’s compensation as a director in 2009 was $ 260,000.  In 2009, Dr Dzau owned the equivalent of 25,065 shares, worth $ 1,622,458 at today’s $ 64.73 value per share.

  • So, in summary, in 2009, Dr Dzau received  $ 1,081,073 in compensation to be a director of these four companies.  In 2009, Dr Dzau owned stock or equivalent in these 4 firms valued at $ seven,854,090.  He has turn out to be what most individuals would take into account rich just from his work on these boards, in addition to the hundreds of thousands he has acquired from Duke.


Poses raises numerous critical queries about these problems, but focuses on the conflict of interest angle. He asks why Duke doesn’t totally disclose all of Dzau’s relationships and observes that all these firms signify “severe conflicts of interest” for Dzau:



Dr Dzau’s service on the board of each of these businesses implies he has fiduciary duties to every single business, and is supposed to show unyielding loyalty to the companies’ stockholders…. Even in the ideal case, showing unyielding loyalties to the stockholders of companies that make medication, medical units, and sugary drinks appears to be likely to influence a leader of an academic medical institution in ways that chance degrading the leader’s responsibilities to uphold the institution’s mission, i.e., to create significant conflicts of curiosity.



Poses then asks what is Dzau’s degree of responsibility for some of the troubling, properly publicized episodes that have plagued Genzyme and Medtronic in latest years. He points out, for instance:



Medtronic has been the source of several alleged conflicts of interest involving influential doctors. (see posts about Medtronic here).   Possibly someone could ask Dr Dzau what he imagined about such actions, and whether he would get any obligation for them.



Remarkably, Poses does not focus on Dzau’s involvement with PepsiCo, which strikes me as the most troubling of all. As a prominent and influential health care leader, how could Dzau treat a tax on soda, or a ban on vending machines in schools, or any of a multitude ofother well being policy problems relating to the weight problems and diabetes epidemic? In addition, might Dzau’s involvement with PepsiCo (and the other companies) make a chilling effect on the free speech and activities of Duke faculty and affiliated medical professionals?




Newly Elected President Of Institute of Medication Is On The Pepsico Board Of Directors