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Showing posts with label USA NEDAW. Show all posts
Showing posts with label USA NEDAW. Show all posts

Wednesday, March 4, 2015

Sickness in the Brain: A Juxtaposition



Reflection During National Eating Disorder Week

by Chaya Jundef

It’s National Eating Disorder Week … A time which I usually celebrate.  Ironically, I spent much of the week in bed due to a serious brain infection.  All the resting hours have given me time to think…and think…

During the last week, I have been enveloped in love. From the moment my brain infection was diagnosed, family and friends came running: Can I help? Do you need supplies? Can I stay with you in the clinic?

The doctors treated me respectfully; reviewing the diagnosis and treatment options. The nurses were kind and happy to converse. My employers were understanding, and insisted I take off work. I was a PERSON, not an illness.

NO one said:
• What did you do wrong to get a brain infection?
• Why don’t you just get rid of it?
• If you try hard enough, the infection will go away on its own.
• It’s really selfish of you to develop a brain infection.
• This infection of yours is ruining your family.

And while I appreciate the kindness this week, my heart hurts. It hurts because I can’t help but contrast this reaction to my experience of 15 years battling a different type of brain infection….called an Eating Disorder.

During the years when my brain was “infected”, the reactions were not so kind. I experienced constant rejection:

• I was fired from my job of 8 years, where I had invested unlimited passion, after my boss discovered I had an eating disorder.

• The director of a National Youth Group (for which I volunteered 12 years) refused to allow me on the bus because, “You don’t belong with children” even though I had organized the entire trip.

• I vacationed with 4 girls in Miami who heard about my eating disorder while I was strolling outside. They placed my luggage on the porch, and locked me out of the house. I spent the rest of the vacation alone in a small motel.

• I was kicked out of the Israeli camp that I was directing after a friend told the owner about my eating disorder.  I wandered the streets in Israel for 3 days because I was too embarrassed to tell anyone….tired, dehydrated, lonely…. I finally boarded a plane to America and stayed in the airport because my parents wouldn’t allow me home. I had nowhere to go.


And then there were the comments….can I ever forget those hurtful comments?

Friend: “You need to try harder. Everyone can eat. So can you, if you try hard enough.”

Rabbi: “You know that you will go to Hell for destroying your body.” (Thanks, but I’m already experiencing Hell just living with an eating disorder.)

Neighbor: “I cannot allow you to enter my home because I have children, and you are contagious.”

Random Lady: “I never saw someone with so little hair. Did you just have chemo?” (Do you think I would tell a random stranger even if I did?)

Cousin: “You know, you were a pretty girl before you developed this illness.” (And now I’m just ugly?)

Aunt: “You destroyed all your chances of getting married.”

Principal: “You cannot have any communication with your students anymore, even outside of work. You are not a proper role model, and the students might catch your disease.”

Sister-in-Law: “Ummm….so I read about this THING that you have….and um….don’t worry, this THING doesn’t bother me.” (Thing = eating disorder…why can’t you just say it?)

Relative: “You know that your father’s hair turned white because of you.” (I loved my father, and his pain just increased mine.)

Rabbi: “You obviously are not a good Orthodox girl. You are trying to adopt secular culture, which idolizes fashion. You need to get this nonsense out of your head.”

Sister: “You are embarrassing me in front of all my friends.”

Sales Clerk: “What is wrong with girls nowadays? Are you trying to compete with the mannequin?”

Young Woman in Social Work Grad School: “It’s really interesting to speak to an anorexic. I mean, I learned about it, but you seem normal…… I recently read in a textbook that eating disorders are related to abuse. Were you sexually abused?” (Umm...does she honestly think I would discuss that with a stranger???)

Matchmaker: “You’re making it very difficult for your siblings. No one will want to marry someone whose sister has an eating disorder.”

Brother: “I have an idea. Let’s put you in a room with a tape recorder that says, ‘eat spaghetti’. And if you listen to it all day, you will start eating!” (Guess if that worked…??!!)

Friend:I wish you could teach me how to be anorexic for 2 weeks.  My sister is getting married, and I must lose weight before the wedding.”  (Should I also teach you how to have cancer? Or diabetes? Or lung disease? It’s so cool to know that illnesses can be TAUGHT.)

Principal of My High School (where I had been a star student, despite fainting numerous times) after I told her that I suspected a student had an eating disorder: “No student in this school has ever had an eating disorder. We are a respectable institution.” (Umm…So, I DIDN’T attend this respectable institution? That’s strange because my picture is hanging on the wall.)

Relative: “Do you realize how selfish you’re being?” (Do you have any idea how much I care for others, and how much I struggle to do anything for myself??)

Employer: “I suggest you teach boys instead of girls. Your illness won’t be contagious there.” (Because NO MALES develop eating disorders…???)

Friend: “Why are you trying so hard to look like a model?” (I had never even seen a model! I grew up without television or movies.)

Biology Teacher Who Saw Me in Hospital: “It would be interesting if you could come to my class. I could teach my students the entire human anatomy just by looking at you. You can see every bone protruding, even your ribs.” (Should I have agreed and charged for the lecture? Great idea for a future career…)

Social Worker Assigned to My Case: "So, you are an Orthodox young woman. I assume that your illness is your way of showing that you feel constrained within your religion." (No! No! NO! I only stayed alive because of my faith.)

Nutritionist Untrained in Eating Disorders: “So, have you been behaving good this week?” (Wow. Isn’t it great to know that my symptoms make me good or bad?)

Another Nutritionist Untrained in Eating Disorders: “So, you tell me that you’re not afraid of eating ketchup.  In that case, I want you to eat 4 cups of ketchup daily – 1 for each meal and 1 for snack. It makes no difference what you eat as long as you get calories.” (Honestly. And I followed instructions…until I got physically sick.)

 Nurse: “I can’t believe anything you say. I read that all anorexics are manipulative liars.” (Sure, because I'm just a textbook case. Do you know anything about my core values? How much I treasure honesty?)

Direct Care Worker: “I had plans for the weekend, but now I’m forced to work because a spoiled brat like you refuses to eat, and needs an adult to sit next to her by meals. It’s pathetic.”

Passerby: “Hey, Anorexic, get into hospital.”  (Yup. That’s me. I have no name or identity.  Just “anorexic”.)

Relative: If you really wanted to recover, you would go for treatment. You clearly don’t mind being sick.  (Do you know that I have been on a treatment waiting list for months? That I have to fight for insurance for any form of help?)

Friend: “You’ve done this long enough. Stop already.” (Oh. That's easy.)

Acquaintance: There are some people who are REALLY sick, like with cancer. They probably wish they could switch places with you. (Okay, let’s try it. I’m not sure they would agree once they experienced a day in the life of an eating disorder.)

Relative: “Don’t you think you already got enough attention? How much longer are you going to do this?” (I guess until I get MORE attention.....seriously, do you notice that I hide my symptoms? How embarrassed I am of my own behaviors?)

Aunt: “Your ED program sounds great. All you do is sit around all day, and meals are served to you. I wish I could have such a vacation. Stop complaining, and appreciate it.” (You’re right. I can’t believe I had the audacity to suggest treatment is hard.)

Matchmaker: “You have to be realistic about who will date you. I can suggest a paralyzed young man with cystic fibrosis, who can’t have children, and is missing one ear, but is WILLING to date a girl with your history.” (True story.)

Matchmaker # 2: “There is a man who is in his mid- 40s. He is currently unemployed and doesn’t look at women because he is really religious. I think he would be a good suggestion for you because he is obese, and you can teach him how to lose weight.” (Another true story.)

I would like to say Health Care Workers were better, but most were not educated:
• My pulse was below 40 one Friday…I went to the ER for help…after waiting for hours, the doctor said, “We don’t treat people like you. You need a psychiatric ward. Better yet, go home and eat some chicken soup with matzo balls.” Shabbos had already begun, so I explained that I couldn’t take a cab. He responded: “So walk”. Never mind that I was too weak to stand, and it was 10 degrees below zero.

• When the nurse tried to inject my first IV, I retreated in fear. She yanked my arm in frustration, pulling so hard that my shoulder was wrenched out of the socket, and left that way for nearly 24 hours. After all, I was just a crazy psychiatric patient who was overreacting. 

----------------------------------------------------------------------------------------------------------------

What can I say? My brain infection lasted 30 days. It was not terribly painful after the first few days of antibiotics. But, my eating disorder lasted 5, 475 days. Yes, five thousand, four hundred and seventy five days. Torturous days. Lonely days. Days where I prayed at night that I shouldn’t wake up in the morning b/c I couldn’t face another moment of this agony. Days where I sobbed and sobbed because I was so misunderstood, and the comments pierced my soul. And days where I didn’t cry at all because the pain was so great that I shut down completely.

I received concern and access to top treatment for one illness. And rejection, scorn, and impatience for the other.

But they are both brain infections, aren’t they? An eating disorder is also an infected brain…

I thank God for the miracle of the brain to rejuvenate. To heal. To start again. But my brain remembers. It remembers the rejection, the comments, the pain. And my heart remembers too. The brain healed, but my heart didn't.

I do not write from bitterness. No, I write from a deep desire to educate. To teach. To change. Why is a brain infection different than an infected brain? Why is one illness more deserving of care than another? Why aren’t people with eating disorders treated with the love and compassion that they deserve?

Some days I want to climb the Empire State Building, the one that is currently lit in color in honor of NEDAW. I want to cry out to the world, “I had an infected brain. But I AM NOT infected! And neither are the thousands of men and woman struggling around the world.”

Brain infections are real. Even the ones you can’t see on an MRI.

Sunday, February 22, 2015

USA: #IHadNoIdea Weight loss and a "suddenly healthy" BMI could indicate illness and neither did the DOCTORS!


Eating Disorders are brain-based, biological illnesses with a strong genetic component and a psychosocial influence. They are not disorders of choice, vanity or family dysfunction. As with autism and schizophrenia, we don't know everything, but we do know we were wrong about a lot for a very long time. Help us challenge stigma and fight for resource parity for these deadly disorders!


Tara-Leigh Tarantola thought she knew what a person with anorexia looked like: "This really tiny, little, thin girl who won't eat." In other words, not her son, Zachary Haines, a happy-go-lucky teenager who once had a football player's bulky build.
But when Haines was hospitalized last spring after dropping more than 100 pounds, Tarantola for the first time heard the diagnosis applied to her child.
"I broke down because I couldn't believe that a doctor was telling me that he could have died at any moment, yet all of these other doctors wouldn't even take me seriously," says Tarantola. She had repeatedly pleaded with a primary-care physician, two endocrinologists, a liver specialist and nutrition experts to address Haines's exercise and eating patterns, which she knew were making him sick. "They kept telling me how wonderful it was that he had lost 100 pounds."
Like many people with eating disorders, Haines had restricted his caloric intake, exercised excessively and obsessed over his physique. He was irritable, constantly cold and doubled over with stomach pains after eating. At one point, his pulse dropped to 26 beats per minute (anything below 40 can send someone to the emergency room).
"All of the signs were there," Tarantola says.
But because Haines was once considered obese and never dropped to what the body mass index charts indicate as "underweight," his dramatic weight loss was overlooked, even applauded. For more than a year, the clinicians "didn't seem to think anything was wrong," says Haines, now a sophomore in recovery at Temple University in Philadelphia.
The above is taken from a timely and fascinating story on the American Psychological Association Website that reflects on how our focus on obesity is meaning missed diagnosis on eating disorders. In the co-ed online support group Eating Disorder Parent Support we consistently hear stories from parents who are worried about their children's new eating habits, but have concerns brushed aside because their child is "still on the chart." 
BMI charts don't take individual growth patterns into account and this is a dangerous practice that must be halted. If a child is always in the 50% for height and the 75% for weight, a drop to 50% and 50% is an enormous red flag that must be looked into. When weight drops from the 95% to the 5% the fact that 5% is "still on the chart" means nothing in terms of health.
One of the most important pieces of work we Eating Disorder Awareness Advocates and Activists have in front of us is to get an appropriate quantity and quality of education on eating disorders into medical schools. Eating disorders have the highest mortality rate of all mental illnesses, greater even than some cancers, and still it can took Tara-Lynn a year of searching for answers to get someone to recognize what should have been one of the first things looked for with her son's symptoms.
Eating disorders happen to males, they happen to people of color, they happen to people in non-Westernized countries and they have happened in all eras. When a zebra walks into a room, a doctor needs to recognize it as a zebra--this is, after all, why go to the doctor.



USA: #IHadNoIdea so many people had no idea males get eating disorders too!


Eating Disorders are brain-based, biological illnesses with a strong genetic component and a psychosocial influence. They are not disorders of choice, vanity or family dysfunction. As with autism and schizophrenia, we don't know everything, but we do know we were wrong about a lot for a very long time. Help us challenge stigma and fight for resource parity for these deadly disorders!

Sally and Nate's Story

When my son, Nate, was 16 years old (fall of 2006), he started showing signs of an eating disorder. January of 2007, when he texted me from a high school trip to NYC and asked me how many calories black coffee had, that was my biggest wake-up call. He actually asked if I could get him an appointment with a dietitian because he knew something was wrong and he wanted to eat healthy. It took about a month to get into the dietitian and by the time he did, the dietitian told both my son and me that he had a serious eating disorder and needed help right away, probably residential treatment. That scared him, not only because he was physically dying, but because he was so ashamed and embarrassed. He thought eating disorders were just a female thing . . . and he is a straight male! 



He didn't want anyone to know, but, by the looks of him, EVERYONE knew he was very sick. After his nutritionist gave us a diagnosis, I immediately called his pediatrician who referred us to Laureate Eating Disorder Center in Tulsa, Oklahoma (where we live). He began outpatient treatment because Laureate only has an all-female residential program. 

He had an outpatient team of a psychiatrist, psychologist, and a dietitian, but after a few months Laureate advised us that he needed more intensive residential treatment. (He was hospitalized once for dehydration & another time for over-hydration, which gave him water toxicity which led to the start of some of his internal organs to shut down).

I was a mess inside of my head at this point, scared out of my mind! Laureate and I went searching for an all-male residential eating disorder program. The only one in the country in 2007 was Rogers Memorial Hospital's Ed Residential Program in Oconomowoc, Wisconsin (between Milwaukee and Madison). I called and they had a waiting list; when a bed finally opened, I flew him to Wisconsin. He was sooooo sick by then that he was ready to get this kind of intensive treatment. 

Leaving him there, so sick, and me living 763 miles away (11 - 12 hour drive), was not easy, but it was the only thing the doctors and I felt could be done to save his life. He ended up in Oconomowac, Wisconsin at Rogers Memorial residential ED program for males. And, thankfully, it was the right choice! Rogers ED center helped him tremendously and I will forever be grateful to them. 

To back up a little . . . before he went, he looked like a walking skeleton. He had been freezing all the time (even when it was hot indoors or outdoors)because he'd lost all his fat and some muscle. He was using laxatives, & later I found out that he was not only restricting & over-exercising, he was also purging. It all came clear when I noticed his strange eating & exercise habits. He'd go to the grocery store and be there for hours because he was reading the nutrition & fat labels on everything he considered buying! 

Anyway, the residential program told us it was mandatory that he stay at least one month and then they would re-evaluate. Well, he ended up staying there for ten weeks. Some of my family members and I went to every "Family & Friends" weekends that the program had. When my son finally returned to Tulsa, he move in with me and went to an IOP(Intensive Oupatient Program) at Laureate for eight months and he became fully weight restored. 

He still struggled mentally, but Rogers' ED program gave him the tools to stay healthy--one important one was that he must stay on a meal plan, which did. However, ED was always in his head. He begged to go away to college, which scared me and, honestly, it scared his treatment team in Tulsa, too. But he really wanted to do it (he'd gotten a academic scholarship), so he went to Oklahoma State University, which was only about 1 hour, 20 minutes away from Tulsa. That way, I could get to him easily and he could get to me if necessary. 

Anyway, he struggled with ED, but remained healthy, joined a fraternity, became Vice President of his fraternity and graduated with a 3.8 in Chemical Engineering. He is now living in Houston, working for Chevron-Phillips Chemical. He lives in a town-home with some other engineers and is doing very well. While in college, he started a Project Heal chapter, supported by NEDA & his college. It was a support group for students with ED or students who wanted more information on ED. He organized several NEDA walks in Stillwater, Oklahoma. 


He will be 25 years old in April 2015. Yes, ED still bugs him, but my son keeps fighting and WINNING!

I flew to Houston in 2014 to walk in the Houston NEDA walk that my son was involved in. He was asked by one of the organizers of the event to deliver his ED story in a speech to the other walkers before the walk. I am so thrilled because my son is my son again and instead of being in denial about Ed or trying to keep it a secret, he is now an advocate for helping people with ED. 

We both went to the annual NEDA conference in San Antonio in 2014 and plan to go to the NEDA conference in San Diego Oct 1 - 3, 2015. He is so busy at work, but he is still involved in a program in Houston called "Mentor Connect" & last I heard, he was mentoring (by email) a male in Australia who has ED. Both he and I want to be advocates that help others with ED. I know that ED is never really going to stop bothering my son, so there is always a chance for relapse, but I also know that my son knows that, as well so it helps him to stay healthy by helping others to get and stay healthy! I'm very proud of him!



USA: #IHadNoIdea not all #eatingdisorder treatment was #evidence-based

Eating Disorders are brain-based, biological illnesses with a strong genetic component and a psychosocial influence. They are not disorders of choice, vanity or family dysfunction. As with autism and schizophrenia, we don't know everything, but we do know we were wrong about a lot for a very long time. Help us challenge stigma and fight for resource parity for these deadly disorders!
Elena's Story 

My name is Elena and because we are still very much in the fight to bring my daughter J (15) from the depths of this hell called an eating disorder, this is an abbreviated version of our story...


Right now J is diagnosed OSFED (Other Specified Feeding or Eating Disorder) with co-morbids of anxiety and depression. Two years ago it started with bulimia and the co-morbids soon followed. We had no warning signs, just a journal found by her uncle.


I live in California's beautiful Central Coast and J's dad  lives in Las Vegas  where she attends school; we share custody. Both locations we were discover would let both us and J down in quality of care in treating eating disorders.


In the last two years it took J's first therapist 6 months to realize he was in over his head and say she needs someone who treats eating disorders (EDs) and knows medication; what we didn't know was that treating EDs and specializing in evidence-based treatment are not the same. 

It feels like we lost another year and a half seeing more therapists, teen psych unit stays for self-harm and two residential stays to try and beat this finally realizing at worst it strengthened ED at best it broke the cycle of behavior for maybe a few weeks, as ED is now entrenched and can manipulate most any therapist, dietician, or doctor. 

We finally found evidence-based care for J this year and hope it will turn things around, but that leads us to another problem, insurance.


It really hits you hard to hear your insurer (because we have coverage for J through both dad and stepdad) say things like " that's not covered, wrong diagnosis" or "maybe switch to PPO so more than urgent care covered out of state." With all the bills that have accumulated and us even splitting those copays, etc do they think we are choosing to struggle with HMO as it is or that J chose this illness? Do diabetics who are covered choose that?


The implied cycle of blame from health care providers and insurance is shocking. The lack of support in our communities for parents and those suffering like J (only 15 with no positive peer support) is heartbreaking.That those with the most power--the providers, insurance and lawmakers leave it to us the parents to try and change this system, all while we fight to save the life our child, is unimaginable.



USA: #IHadNoIdea One Did Not Need to WANT Help to BE Helped

Eating Disorders are brain-based, biological illnesses with a strong genetic component and a psychosocial influence. They are not disorders of choice, vanity or family dysfunction. As with autism and schizophrenia, we don't know everything, but we do know we were wrong about a lot for a very long time. Help us challenge stigma and fight for resource parity for these deadly disorders!
Our family in May 2013: It was a true celebration on many fronts--including the celebration of recovery for little sis and the joy of every one of us truly enjoying the cake. Because our family was never assumed to be the cause of Kinsey's anorexia, she was able to access the love and support of her parents and brothers and sister throughout her journey. 

In early 2012, my happy, healthy, bright and well-loved youngest-of-four 17-yr old daughter began to lose weight rapidly and experience a lot of stomach issues—the foods on her can’t-eat-this-it-hurts-my-stomach list quickly became longer than the list of what she could eat. Our pediatrician, a savvy and sensible woman, talked to my daughter about these issues over several visits and within a couple of months, after ruling out other possible causes, came to the conclusion the diagnosis was anorexia nervosa. Kinsey, the patient, disagreed and in fact never realized she was sick until she was well on her way to not being sick.

The doctor told us we would be going to the topnotch UCSD Eating Disorder Center for Treatment and Research. When I asked if Aetna would cover it she said she would fight for it. She explained UCSD was the only local facility utilizing a Family Based Treatment (Maudsley) model and research showed that to have the best chance for success. Thankfully, Aetna quickly agreed to write a single-case agreement and treatment started within a week.

Recovering from anorexia nervosa is never easy; eating disorders are brutal, persistent and misunderstood by most of society.  You didn’t know they are genetic, biological, brain-based disorders thought to be triggered by a period of malnutrition?  You are not alone. Fighting stigma is hard when you are also fighting for your own or your child’s life.


My daughter had an early diagnosis*, top-notch treatment and she still lost a semester of high school and one of college to her disease; she continues to be followed today to ensure her recovery stays solid. She fought hard to be where she is today (18-months of independent recovery away at University and studying abroad currently) and she and we are the lucky ones—we’ve had access to treatment that is evidence-based and that we could afford.

Our story is atypical; I’ve spoken to few people whose path has been this direct. Most struggle with uninformed physicians which delays diagnosis. Most have to search, often fruitlessly, for a treatment program that is both evidence-based and accessible. Most have to battle their insurance company endlessly. Most have to follow paths far more rugged than ours (which was decidedly no walk in the park).

Today I fight because parent pioneers like Laura Collins deserve to know there are those committed to carrying on their work. I fight for the opportunity to recover my daughter had not to be an anomaly. I fight for the access to treatment every person affected by an eating disorder deserves. I fight because I know too many mothers who have lost their children and too many who face that prospect. I fight because the researchers who have taught us much in recent years need and deserve funding on par with what other diseases get. I fight so people will understand this disease has nothing to do with vanity or choice and everything to do with brain wiring. I fight because eating disorders are serious and there is hope and together we will raise our voice to ensure there is progress.
.

* For more information on the importance of early diagnosis and treatment, please check out this article, "Anorexia Nervosa: New research underlines importance of getting help before chronicity sets in.

Tuesday, February 17, 2015

Canada: Recovery Cannot Be Halfway

Eating Disorders are brain-based, biological illnesses with a strong genetic component and a psychosocial influence. They are not disorders of choice, vanity or family dysfunction. As with autism and schizophrenia, we don't know everything, but we do know we were wrong about a lot for a very long time. Help us challenge stigma and fight for resource parity for these deadly disorders!
Recovery Cannot Be Halfway 

Having struggled with both severe anxiety and an eating disorder for over half my life; I don't know how I found the courage to embark on such a journey to seek treatment - but when I did, it was even more of a challenge to find the right help to recover.

After waiting six months to hear from the hospital about my referral , I was directed to attend a weekly group meeting to prepare for the intensive three stage eating disorder program. This meant I needed to  either  commute 4 hours by public transit or have my father drive me part way.  It was recommended that I relocate to the city so I could take part in the outpatient portion of the program which was to be completed after two months of inpatient treatment.

A month before my admission I packed up my apartment, left my 15 year old cat with a friend, and with a mixture of great anticipation and anxiety, left the home I had lived in for seven years. I was leaving the security of the comfortable turmoil I was accustomed to – to living with the possibility of a new positive and productive life.

Being ill for so many years I have never really been able to live a “normal life”, finish school or hold down a full time job, having to be supported by disability payments. 

The financial burden associated with the treatment program was high. I had to pay for housing and storage of my possessions during the inpatient portion of the program so I would have a place to live during the intensive day treatment portion. This was in addition to the costs of transportation and the additional food costs that were mandatory for the program.

The inpatient program was located inside the psychiatric unit and had only 4 beds.  In total the group of approximately 14 patients and two staff were literally squished around two big tables at meal times. It was difficult to eat without bumping elbows. Group rooms were located outside of the unit so we would be paraded out into the mental health outpatient waiting room and down the hall several times a day.

I am very grateful to have had the opportunity; however, due to the narrow scope of the treatment modality, other comorbid health concerns which could impact the success of treatment were not adequately managed. Like me, many people with eating disorders struggle  with other mental health conditions, (e.g.: anxiety, depression, OCD, etc…). If programs focus solely on eating disorder treatment and fail to properly support the person as a whole, this leads to greater chance of relapse. Unfortunately, this is exactly what happened to me.  I started to slip even before I left the program.

Three years later I am again looking for treatment and am extremely frustrated with the very limited options there are in Ontario.  It would be beneficial to have residential treatment in Ontario that is publicly funded - a place conducive to repairing the holistic health of each individual person. Just because we are diagnosed with the same disorder does not mean we are carbon copies of each other.
There is not enough help within our communities. Currently, people are forced to put their lives on hold in order to receive treatment, waiting until they are deemed sick enough, or not getting any help at all. We need to stop ignoring eating disorders in Canada.  This is a growing problem that must cost the government a fortune with the revolving door of emergency visits, disability payments and no end in sight!  


There are so many Canadians who have so much to give the world but are being held captive by the most powerful of forces, their own brains.