Leonore Gordon, LCSW
130 8th Avenue #3A
Brooklyn, NY 11215
(718) 783 1986
(347) 489 9123
3/14/2016
Re: a personal plea to
Valeant Pharmaceutical
Dear CEO Pearson and members of Valeant’s Board of
Directors;
First, I hope you are feeling better after your long bout
with pneumonia, Mr. Pearson.
I am a 60-year woman with 16 years of Parkinson’s, receiving
Social Security Disability, who cannot afford to pay for one of your products, Tasmar, which I very much need, as it really
helps my other Parkinson’s meds to kick in. Because of Tasmar, I can walk, be independent, exercise, dance, lead my
Parkinson’s support group, and participate in the other activities that help me
get through the day. A few weeks ago, my Rite Aid pharmacist called me in
consternation to ask if I knew the 2016 price for Tasmar? She went on to inform
me that it would cost me $2,259.00 for a
one-month supply of 45 pills. I was flabbergasted!!!!!
What kind of human being
puts a price like that on any medicine? And with what justification?? Is it
made on Mars? Who on earth can afford that?
Last year Tasmar cost
an equally unaffordable $1800.00, (quite a price hike!) but I got lucky when a friend gave me
a bottle of her Tasmar because she no longer could take it.
Nor can I afford
Tasmar’s generic, Tolcapone, costing me $1800.00 for the same number of pills. Tolcapone is a product made by Oceanside Pharmaceutical, owned by
Valeant. The price is the same for Par
Pharmaceutical’s version of Tolcapone.
Furthermore, Valeant’s
purported Patient Assistance program for Tasmar excludes those of us who
receive Medicare Part D, which I grimly read as I got to the bottom of page 2 of your
application form. Do you really believe we
in those excluded categories can afford 2259.00 for a bottle of pills?
Like so many in the US
and Canada, I can’t take this medication I need because I can’t afford it. No one in my world has either
$1800.00 or $1500.00 set aside for a needed vial of pills for one month. Perhaps
that price feels reasonable to you and members of your board, but not in my
world. When I researched Valeant on the Internet, seeking a Patient Assistance
program, I stumbled on innumerable news reports that Valeant is actively under
fire for its unethical, inhumane arbitrary price hikes from multiple arenas,
including by the
Congressional committee on Accountability and Government
Reform. I watched the Feb.4th hearings online the other day, as the bi-partisan
committee interviewed your temporary replacement, Mr. Schiller. I was intrigued
to see him promise to make a quick phone call to the NIH after being told they
couldn’t afford to include one of your heart medications, promising to correct
that problem.
If Public Relations and “image” was important enough
to your company that you dropped the prices of two of your heart drugs after
being scolded by a Congressional Committee, why not do a huge turn-around and
announce a Public Relations campaign to drop the prices on all of your pharmaceutical products so that people like me,
my friends, and millions of others can afford the medicines we need? And I don’t mean a PR campaign like your
already existing “Patient Assistance Program” which, as I referred to earlier,
excludes people receiving Medicare Part D, veterans receiving Veterans’
Assistance, and others on HMO’s. In a news article, I read the memo written by Valeant
marketing executive Jeff Strauss, referring to this
Patient Assistance initiative, justifying your inhumane drug costs, by saying "These
patients are not profitable for Valeant, therefore the price increases offset
the costs associated with supporting this initiative... Kind of hard to paint
us as greedy if we have removed financial barriers for patients." This
does not look good to your investors, Congress, or the public.
Last week, someone sent me a link to Hillary Clinton’s new tv ad
targeting Valeant’s price-hiking as “predatory.” I know your stock value
dropped dramatically since being investigated, and since Clinton’s commercial
aired, but before you drop the Neurology unit of your company, or your
pharmaceutical component, why not seriously go public with repentant new
policies dropping all of your drug prices to humane ones your child’s teacher
can afford, and apologizing for your “depraved indifference” to us regular
people out there, and thus distinguish yourselves from the arrogance of
Turing’s Shkreli, who truly is a villain? Mr. Pearson, perhaps you could say
you had an epiphany while lying ill, especially after seeing your drug costs?
Please do something soon, as I really need my medication, and
I’m not alone. I will be cc’ing this letter to the NY Times, the Wall Street
Journal, and several other news outlets. Thank you.
Sincerely,
Leonore Gordon, LCSW
My husband was diagnosed with early onset Parkinson's disease at 68. His symptoms were shuffling of feet, slurred speech, low volume speech, degradation of hand writing, horrible driving skills, right arm held at 45 degree angle. Things were tough for me, I too was diagnosed of COPD but now we both finally free from these diseases with the help of total cure herbal foundation, He now walks properly and all symptoms has reversed. He had trouble with balance especially at night, getting into the shower and exiting it is difficult. Getting into bed is also another thing he finds impossible. We had to find a better solution for his condition which has really helped him a lot,The biggest helped we had was totalcureherbsfoundation .c om They walked us through the proper steps, im highly recommending this herbal formula to anyone who needs help.
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