We get a lot of questions from consumers about health reform and what to expect in 2014. This new video, from the Kaiser Family Foundation, provides a great overview of the major changes in the ACA, including the way Americans will access health coverage and what it will cost.
"The YouToons Get Ready for Obamacare," The Henry J. Kaiser Family Foundation, accessed July 30, 2013, http://youtu.be/JZkk6ueZt-U.
If the video does not format properly, please follow the link above to watch on YouTube.
Tuesday, July 30, 2013
Tuesday, July 9, 2013
Traveling With Health Conditions
Check out this timely article from Lynda Schrager on how to travel with a health condition. She provides great tips to organize and prepare for your trip, as well as suggestions to enhance your vacation experience!
Lynda is a breast cancer survivor, mother of a child with Crohn's disease, and daughter of parents who have had every disease in the book. She is the author of Otherwise Healthy®: A Planner to Focus Your Thoughts on Organizing Life after Being Diagnosed with Breast Cancer. She writes a weekly health column for the Albany Times Union called The Health Organizer. It appears in newspapers throughout the country. Lynda is the only member of the National Association of Professional Organizers specializing exclusively in the area of organizing health information, presenting keynote addresses and workshops in the area of breast cancer treatment, survivor issues and health and wellness.
Monday, June 17, 2013
Trusting Instincts
Yesterday was a
Sunday like any other - I was working on my Masters thesis and transferring
various loads of laundry from washer to dryer and contemplating vacuuming my
house instead of watching The Golden
Girls marathon on tvland (The Golden
Girls won, by the way) when I remembered that my dog Beckett was out of his
favorite beef-flavored treats. Since there is very little Beckett can eat
thanks to a finicky digestive system that is probably the combined result of
his slow-to-develop “runt of the litter” organs and my reliance on the most
natural (read: most expensive) foods and treats on the market, I didn't want
him to go through the week without the little freeze dried chews he looks
forward to whenever he goes into his crate. So, even though I contemplated
staying inside where it was warm and quiet, my “mommy guilt” got the best of me
as I grabbed Beckett’s harness and leash. “Wanna go to Petco?” I asked. An
unnecessary question, since I could barely get him into the car he was so
excited.
The second we walked into the store,
Beckett, who has memorized the layout and is, like me, a creature of habit,
dragged me over to our regular first stop: the ferret cages. We always visit
them first, and he loves to stand on his hind legs and peer at them while they
slither around and play with each other and pretend to ignore him. He whines
and paws and seems to think they can’t see him, though I suspect they fancy
themselves better than him, as they turn their little noses up toward the
ceiling and go about the business of simply being ferrets. As usual, though,
his attention for the ferrets was short-lived yesterday, and within minutes he
was pulling me toward the bird cages. Once again, he was on his hind legs,
front paws in the air, head titling from side to side whenever the birds
tweeted at him. I can never tell whether he is happy or sad to be outside their
cages while they are locked inside, and I often wonder, when I look at him
wanting so desperately to play with his little friends, which side seems more
like captivity to him.
After Beckett sniffed a cute little
cocker spaniel and failed to amuse an older, lethargic looking golden
retriever, I finally coaxed him into the “cookie aisle” where he enjoyed his
usual sniffing expedition of all the rawhides and meat-scented chewy things
displayed at nose level. While I searched for the correct package and
contemplated a new brand of biscuits, Beckett smelled and groaned and did his
best to lick everything his little tongue could reach. Finally, I pulled the
regular cookies off the shelf and did my best to tug Beckett toward the cash
register. As usual, I had planned on a quick in-and-out, and, as usual, Beckett
had planned on tasting everything (and everyone) he could reach.
As we headed to the front of the
store, I stopped to price a package of squeaky toys hanging on the end of an
aisle. And that was when a woman who looked to be about my age approached
me.
“He’s
a sweet dog,” she smiled and nodded toward Beckett, who by then was frantically
pawing at the pork bones just beyond his paws.
I
thanked her, always worrying that I sound immodest when I admit that I actually
do, in fact, have the sweetest dog on the planet.
“Is
he good with children?” she went on. I wasn't expecting that question, so I
stuttered a bit before responding that, yes, he loves children, though he tends
to jump and lick any person short enough to serve as a potential playmate, so
perhaps not all children would agree.
“My
little boy … was wondering ...” she hesitated. “He asked if he could pet the
black doggie. So I just thought I’d see …”
“Oh
of course he can,” I replied, saving her from what seemed to be an awkwardness
I couldn't quite understand. After all, I was dressed in my Sunday sweat pants,
unimposing pony tail, feeling relaxed and approachable and open to conversation
(which isn't always the case, I admit with some regret), so I wasn't sure where
her discomfort was coming from.
Until
her son walked around the corner. He was a beautiful little boy dressed in
overalls and a turtleneck. He had a sweet, diamond-shaped face that looked too
small for his large, square glasses. And he would not – could not – look at me,
even when I said hello. He did, however, fix his gaze on Beckett while he
pointed and repeated “pet the black doggie, pet the black doggie, pet the black
doggie” over and over and over again.
“Yes,”
his mother said. “You can pet the black doggie.”
Then
she looked at me, seeming to struggle for words, until she was finally able to
explain that her adorable son, who is seven, was diagnosed with autism several
years ago. She and her husband had been wanting to get him a therapy dog, but
he was so terrified of dogs that he become inconsolable and often aggressive
anytime a dog was nearby. On the advice of one of the child’s counselors, the
parents had been bringing him to Petco as a way of gradually exposing him to
leashed, well-behaved dogs in a controlled environment, and so far, the mother
told me, it had been working pretty well. The little boy could now walk through
the store, could see and hear and even be in the same aisle with another dog,
and not get upset. “Most of the time,” she added with a chuckle.
“But
your dog is the first one he has ever wanted to pet,” she almost
whispered. She was trying not to cry,
and, in all honesty, I was fighting back some tears myself.
“How wonderful,” was all I could manage,
before squatting a safe distance away from the little boy so I didn't crowd
him. “His name is Beckett,” I said. “And he would love for you to pet
him.”
Inside
I was panicking. At seventeen months of age, Beckett is just now coming to
terms with some of his training – probably because, after fifteen months as Beckett’s
mom, I have finally learned how to train him (which first involved training
myself). Even so, he still suffers occasional lapses, particularly in public
places where he is overstimulated and more than willing to suffer the
inevitable “Time Out” later for the sheer pleasure of misbehaving now. But this
moment was critical. A lapse for Beckett could become a lifelong fear of dogs
that this little boy would always trace back to today.
As
I thought about all the things that could go wrong in this scenario, imagining
every possible negative outcome, I suddenly realized that Beckett had stopped
sniffing and pulling and begging for the bones and toys spilling out of the
rack above him. Instead, while I had been talking to the boy’s mother, Beckett
had been sitting perfectly still, staring at the little boy, the little boy
staring back at him, both of them looking away from each other now and then, but
neither of them reacting to anything outside of whatever communication they
were having. Not even when other dogs walked by.
So
I did the only thing I could do. I knelt beside Beckett and said “It’s ok, buddy. Approach.” I was ready to pull his leash
tight if he started to jump, but I could see, without a doubt, that he knew. He
couldn't jump. Not this time. And he wouldn't. Instead, he approached the
little boy slowly, gently, pushing his nose toward the tiny, outstretched hand
until, eventually, child and dog touched. The little boy wiggled his fingers
and Beckett licked them. The little boy waved his arms and Beckett followed
them. The little boy crossed his legs and Beckett laid beside them. The little
boy put his hands in his lap, and Beckett rested his head on top of them.
And
we stayed like this, in silence, for twenty minutes. There was nothing else in
the world except a mother and me, watching a little boy stroke Beckett’s head,
his back, his tail.
“We've
been working on this for years,” was all she seemed able to say. Though she was
doing better than I was, as I stood there speechless, relieved, proud,
inspired.
Before
we parted, I gave the mom my phone number and told her that I would be happy to
arrange get-togethers between her son and Beckett, if she thought it would
help. She thanked me and assured me that she would call. And I hope she does.
But more than anything, I hope that this beautiful little boy will now be open
to the possibility of a therapy dog, and I like to think, if he is, that maybe
Beckett had something to do with that.
It's
funny how, even though instinct never fails me when I pay attention to it, I often
doubt myself and others, always letting my fears interrupt the natural flow of
things. Thankfully, Beckett knew what to do yesterday. And, despite my panic, I
knew it was time to let him try. Even the mother who approached me knew that,
scary as it was, she had to let her son pet a strange dog, and she had to have
faith that he would be alright. Still, it was the little boy who taught all of
us to put away our worries and our preconceived ideas and our fears about what
may have happened in the past. To simply experience that single moment, when his
instincts told him that Beckett was safe, when his instincts told me that all I
needed to do was believe in my dog and trust that he would do the right thing. I
am so glad I listened.
Guest Post, Heather Haskins
Tuesday, June 11, 2013
Estimating Your Healthcare Costs Using FAIR Health® Consumer Tools
For those who have
chronic conditions, managing your health usually involves ongoing care and
treatment. And although your health is the
main focus, it’s also important to manage and plan for costs related to your
care. This has always been true for
patients without health insurance. And now, more and more insured patients
including those with chronic conditions are assuming a larger portion of their
healthcare costs, whether they’re enrolled in high deductible health plans or
in other types of plans that require greater cost-sharing through co-pays and
co-insurance. Knowing how much you may
owe for care can help you make informed healthcare decisions. Use FAIR Health’s free website at www.fairhealthconsumer.org to research your out-of-pocket costs before getting
a service or procedure that’s either not covered by insurance or that is
out-of-network. The website offers cost
lookup tools that can be used to estimate out-of-pocket costs for medical and
dental services in every area of the United States. The estimates reflect common plan benefits and
can be adjusted to match specific plan provisions. The amounts estimated are based on the FAIR
Health database of billions of billed charges for medical and dental services.
The website also
offers educational features, such as the Reimbursement
101 curriculum, glossaries
and healthcare
resources to help consumers learn about, and better navigate, the healthcare
system. These tools and resources are also
available in Spanish at www.consumidor.fairhealth.org
and on a free mobile app, which you can download from iTunes
and Googleplay.
We invite
you to use the FAIR Health consumer tools to estimate and plan your healthcare
expenses, to inform discussions with your healthcare providers and insurers and
to learn about the health insurance system. We also encourage you to stay in touch with us
by subscribing to our free quarterly consumer e-newsletter
that offers tips on understanding and managing your healthcare costs and via Facebook and Twitter.
FAIR
Health is an independent, not-for-profit organization created in 2009 with a
mission to bring transparency to healthcare costs and health insurance
information. Learn more about FAIR
Health’s mission here.
Guest Post from FAIR Health, Inc.
Monday, June 10, 2013
Maintaining a Legacy
As you are aware,
Jennifer Jaff passed away in September of 2012. As the founder of Advocacy for Patients with Chronic Illness, Inc., she left behind not just an agency that she created and nurtured, but a set of
ideals and practices that have become the very foundation on which the agency rests. What I have learned about Jennifer is that
her life was truly dedicated to helping others in a way that generated not only
a fierce loyalty but an incredible network of individuals who helped support
the very work she spent her all too short life devoted to doing. The types of accolades I hear about her where
things like:
“She was a
super hero for my son, he truly felt like giving up in school until she came
into his life.”
“Jennifer was
always available and even if there was nothing she could do legally she
listened and that truly made a difference.”
“If it wasn't
for Jennifer helping me with my insurance appeal I would not have the dignity
and quality of life I have now, I can never forget her.”
“What can you
say about a total stranger who takes the time to listen, help and truly really
care about someone they never met? Is saint too strong? Is hero inappropriate? I don’t know but she was both to me!”
These and so
many more wonderful things were said about Jennifer by everyone I meet who knew
her or who were in some way touched by her zeal for advocating. What an incredible legacy to leave behind,
what a life truly well lived and how powerful a statement that you were someone's
hero!
It is unfortunate
that I never had the pleasure of meeting Jennifer Jaff. However, I am sure if I had, I would be
another of the multitude of individuals who were loyal and dedicated to her vision
and mission at Advocacy for Patients. Instead, I have been tasked with the Herculean mission of continuing her
legacy, and, in very real terms, of helping those who are truly vulnerable in
our society – the chronically ill who often suffer in silence and expect little
in terms of understanding from others.
By
now you must be asking yourself: Who is this person? So let me tell you a little about
myself. I, like Jennifer, have spent
most of my adult life advocating for those less fortunate or those who simply
have a harder time for one reason or another. I have come to Advocacy with 27 years of experience in social services
and management, dedicating many years to working with disadvantaged people as a
professional in social services and health care, as well as the law. In the late 1980’s, I left a successful
career working at a mutual fund company on Wall Street to begin my career in
social services, working for several New York City agencies dealing with concerns such as homelessness and literacy. I had decided that this was truly my life's work – helping those in
need. As a result, I decided to pursue a
Master’s Degree in Education and Rehabilitation Counseling and entered the
health care field, focusing on the mentally and physically disabled. As Administrator on Duty at Jacobi Medical
Center, as well as Director of Rehabilitation at North Central Bronx Hospital
Center, I gained extensive experience in hospital management and patient
advocacy. A growing desire to advocate
for disadvantaged people led me to attend law school, and I obtained my J.D.
degree from the City University of New York School of Law, whose motto spoke to
me completely: Law in the Service of Human Needs.
Upon
graduating from law school, I served as a Prosecutor for the Bronx District
Attorney's Office for over three years. While
there, I worked in the Domestic Violence and Sex Crimes Unit, prosecuting cases
and advocating for the rights of victims. I continued my work with poor and indigent individuals as a legal services
professional with Legal Services of the Hudson Valley (LSHV), where I handled a
diverse caseload of domestic violence, custody, housing and disability matters. While at LSHV, I became the Deputy Director
and program-wide Domestic Violence Coordinator. In addition to my legal representation of clients, I was responsible for
developing a training and evaluation program for staff attorneys and other
stakeholders within the domestic violence prevention and legal field. In 2007, I went to work at the New York State
Office for the Prevention of Domestic Violence, an Executive level agency on
policy, among other functions. At OPDV, I
was the Director of Public Policy and Administration. While there, I was responsible for the
development and implementation of statewide training of law enforcement, the
judiciary, advocacy agencies and other stakeholders. With my team, I successfully wrote a million
dollar grant to develop a one of a kind, online, web-based training for police
officers in domestic violence case handling. In addition, I wrote policy for the State of New York in the areas of
officer-involved domestic violence, probation, parole and victim advocacy
agencies. In my role as the Director of
Administration, I was responsible for successfully steering the agency through
the recent fiscal crisis.
What does
this all say, other than I obviously wanted to help others? It means I hold in my heart the same passion and
dedication that Jennifer Jaff had for helping others and championing those in need. It says that, in hiring me, the Board of Directors at Advocacy thought
that I could and would keep the agency and Jennifer’s legacy alive and fully
operational. I am so honored to walk in
the footsteps of someone so well respected and so highly thought of. I will do everything within my means to keep
her memory, legacy, and mission alive and well, and I invite you all to please
help us do the same in any way you know how: refer clients, spread the word
that we are here to help, and, where possible, please donate, as we count on
your support to make this all happen.
Eileen F. Swan, Executive Director
Monday, September 24, 2012
NY Times Article on Jennifer
We want to thank everyone for the kind and loving messages. Jennifer's impact was far greater than she ever knew. There was a touching article in the NY Times today which we wanted to share here, for all of our followers.
We greatly appreciate everyone's understanding and patience during this difficult time. The daily blog posts will have to be postponed, but check back for updates about Jennifer's memorial service.
Thank you!
We greatly appreciate everyone's understanding and patience during this difficult time. The daily blog posts will have to be postponed, but check back for updates about Jennifer's memorial service.
Thank you!
Wednesday, September 19, 2012
Heavy Heart
It is with deep sorrow that we announce
the untimely passing of Jennifer Jaff, Esq, Founder and Executive Director of
Advocacy for Patients with Chronic Illness, Inc. Jennifer conceived of and
founded Advocacy for Patients because of her extraordinary passion and
commitment to ensuring equal rights for those living with chronic illness. She dedicated her life and career to
improving the quality of life for others based on her own experience with
Crohn’s disease.
Her advocacy on a personal level
with individuals, in chronic illness arenas for larger disease populations, and
in global forums for local and national health care reform was unparalleled in
its sophistication, conviction, judiciousness, and honor. Jennifer believed
fiercely that this cause was a civil rights issue, and her belief in the worth
and rights of every individual with a chronic illness set precedents and models
for equality nationwide. Her goal to
increase awareness of the need for and the power of advocacy for chronic
illness touched all of us who knew her as well as the population at large. She always
worked with amazing energy, grace, fortitude and resolve.
It was Jennifer’s aim to never refuse an opportunity to help someone in need and we know that there are many clients and companies with whom she was working at the time of her death. We appreciate the patience of our clients, friends and partners as the Advocacy for Patients staff works to contact those immediately affected by this tragic and unexpected loss and to develop plans for the future.
It was Jennifer’s aim to never refuse an opportunity to help someone in need and we know that there are many clients and companies with whom she was working at the time of her death. We appreciate the patience of our clients, friends and partners as the Advocacy for Patients staff works to contact those immediately affected by this tragic and unexpected loss and to develop plans for the future.
We know that Jennifer will always
be remembered for her dedication and the actions she took in the pursuit of
justice for those with chronic illness.
Be assured that the Board of Directors and the Staff of Advocacy for
Patients will do everything in our power to promote Jennifer’s great legacy.
We are informed by Jennifer’s
family that any funeral arrangements will be private, but we are planning a
memorial gathering for Jennifer in the next few months and we will announce the
date, time and place once those details are final. For those who want to donate gifts in her
memory, please send them through our website, or by mail to Advocacy for
Patients with Chronic Illness, Inc., 195 Farmington Avenue, Suite 306,
Farmington, CT 06032.
Thank you.
Carol Fain Walters
President
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