I enjoy speaking on college campuses.
No matter the main topic of my talk, I always mention post-exposure prophylaxis (PEP), the highly effective strategy for avoiding HIV transmission after one has been potentially exposed to HIV through sexual contact or a shared needle. The topic is invariably new to the students; only rarely are any of them familiar with PEP.
On World AIDS Day last year, I spoke at Simon's Rock at Bard College, in Great Barrington, Massachusetts. Several students stayed after the talk and we discussed PEP. One of them, James Krellenstein, expressed anger that he and his peers had not been educated about PEP.
He is correct in accusing HIV prevention efforts of negligence for failing to effectively promote better awareness of and access to PEP. I agree. It is atrocious that few AIDS service organizations promote PEP and there has not been an easily-accessible resource for finding PEP providers.
PEP has long been standard practice for healthcare workers after they get
accidentally stuck with a needle. If
an employee at an AIDS service organization, hospital or
clinic gets a needle stick, they are put on a 28 day
course of anti-retrovirals within minutes.
A quick response is important; the sooner to the point of exposure PEP is commenced, the more likely it is to prevent infection. After two or three days, it is vastly less effective.
But in a condom breaks or someone does something they quickly regret, it is difficult to access PEP even if one knows about its efficacy. Why are there not PEP hotlines or delivery services to provide information and treatment when it is needed, when it can still prevent an infection?
I know a student who, after a ridiculously long wait in an emergency room in New York, was told that the hospital would provide him PEP if he was sexually assaulted, but since his exposure resulted from a broken condom, it would cost $1600. He did not have the money; fortunately, he found another place that provided him PEP. But most people don't even know about PEP, let alone where to find it or get to the point of figuring out how to pay for it.
Many people diagnosed with HIV today know exactly when they were infected. Frequently they tell me that if they had known about PEP, they would have used it when they were exposed, thus in all likelihood avoiding infection.
Thousands and thousands of people have acquired HIV because they were not educated about or did not have access to PEP.
After my talk at Simon's
Rock, James and I began a correspondence that resulted in him developing a
proposal for a website to provide information about where one can access PEP. Dr. Joseph Sonnabend (the legendary HIV
clinician/researcher who first proposed the concept of "safer sex" as a means
to avoid HIV transmission) and I were advisors to James' effort.
I shared James proposal with Tom Viola at Broadway
Cares/Equity Fights AIDS. Tom
knows a great idea when he sees one and quickly made arrangements for a small
grant to realize James' idea. (Buying holiday gifts from their online store , like this cute
BC/EFA snowglobe, is a great way to say thanks to them). The North American regional affiliate of the Global Network of People Living With HIV/AIDS (GNP+), on whose board I sit, serves as the project's fiscal sponsor.
PEPnow.org went live a few days ago and it is doing what government, the healthcare system and AIDS advocacy has't yet
been able to do, which is provide timely information on where one can get
PEP.
Check out the site and add listings to the database on clinics, physicians and emergency rooms in your area that provide PEP or share your own PEP experience.
James recently started an internship at the Laboratory of Molecular Hermeneutics at Yale University School of Medicine. He is 19 years old.
While he is not yet a doctor, he is already saving lives.
Sean on:



















Comments on Sean Strub's blog entry "PEPnow.org Will Save Lives"
this not the right place i know,
but i have to ask why a lady i know who was first dianoised with HIV in 2005,she told me she was taking antivirals to keep her cd4 count up etc.i just seen her in hospital last month she never took any arv s ....why i will never know as she is thai and now she has lost her ability to speak english.and has a fungul infection in her brain and big sores all over her body.
the doctors sent her home to die 3 weeks ago and she is still here.her parents are taking care of her and have stopped all anitbiotics etc....they are waiting for her to die,her cd 4 count is 17.can any one tell me why she would not take her arvs........she has so much to live for.she was in her last year at uni and i bought her a new car she has a shoe shop in her city and a new house i did everything to make her want to live.because 3 years ago she told me she wanted to die and make it easy for every one (her family i think she means)now every one is very upset and she is getting so thin and weak,every one has given up on her thai style i suppose.