Jump to content

David S. Kozin

Administrators
  • Posts

    587
  • Joined

  • Last visited

  • Days Won

    32

Everything posted by David S. Kozin

  1. SSPD domains are taken. ISSPD.org is not but ISSPD os the ISS of Personality Disorder in the .com.
  2. International Society for the Study of Perception Disorders (ISSPD.org) These will include, with their liking it or not, all disorders of perception. This is not the sensory problem (like needing glasses and a problem with the lens of the eye), but the part called processing: The moment the sensory trigger his the sense receptor or in many cases the perception exists without stimulus. So, the name is technical accurate and it is International.
  3. I had one and I have posted my results. In order for it to be done correctly, because it is based on a statistical database of prior results you would have to do it with Dr, Duffy (who essentially invented the q of the qEEG) and dr. abraham. It is not worth it if you don't have insurance and you know you have it.
  4. MORE PEOPLE NEED TO CONTRIBUTE A QUICK RESPONSE. I am leaning towards that direction with the name, I like it. It is similar to the International Society for the Study of Trauma and Dissociation. The longest association name ever, but a good group
  5. The Kozin Foundation is not happening, it is something i own so it is holding in place. However, I was thinking of a name that does not focus on the drug aspect and also covers the possibility for visual snow and persistent aura without migraine folk could be included. So, ideas: Council on Disorders of Altered Perception Council on Perception Disorders Society for the Study of Perception Disorders The Altered Perception Disorder Society Something?
  6. The forum is always free. A membership will always be free, but it isn't free for me. I should not have to pay for the web site and for the tools and the stress and see people decide they do not put value in the work and would not spend $5 dollars a month towards a research fund and basic operation. Everything would be transparent. We all work for free on here and I spent years working for free. I actually am broke, and have 180,000 dollars in medical bills at the moment. I can't get a job because people do not hire someone that when they search Google end up with 1000s of hits related to drugs, even if good info, it still shows that I am too complicated for the position. I know this because they tell me. So, a free membership will exist. A student priced, but equal to basic membersip will be available and have the same benefits. Why would someone who pays get more benefits than those who do not? Because if someone has a computer with internet access, and can buy a pack of cigarettes or a beer or buys 4 itunes songs then I am assuming if we offer even a payment plan for the membership where someone without a credit or debit card or bank account could send a few dollars in the mail when ever it was possible or willing to volunteer for a job on the site that is annoying (like you removing spam) then that would be cool. I see the statistics. It is not so much about us donating, as people willing to sign up and tell their stories and be part of movie so we create a narrative that is compelling. The gentleman who got beaten to near death in Detroit has received almost 200,000 in donations from people for his medical bills in just four days of it being announced. We need to create a compelling case, and I am sure we can raise the funds. I just need the membership basis and having doctors pay for listings or using Amazon.com affiliate links/etc can raise money with the amount of traffic we receive. We are just 2 hours of time (by each person) away from really having something extremely valuable. Also Jay, I will contact my friend Ali Toukan about some funding for film. He can independently fund projects and is Headquarted in Dubai. - dk
  7. Jay, sign up and I'll give you staff level permissions. You can run with it and people can volunteer for the documentary and it can be its own section of the web site. People can crowdfund it and also with their addresses you can find people to stay with. You can have your own blog/etc and also the design needs work (liquid or static) it is pretty open. I am also going to be sending messages to others to ask you to take a lead role if you would. I think for Jay he starts the documentary section that our collective funding (just 5 dollars a month from all of the regular readers that visit would be 300,000. Seriously. So, I am deciding that for the interest of the community it is time to wonder why we are asking others to come and help us when if we buy one 5 dollar item that was not needed in a month and that could have gone to a gigantic fund that would pay for very high end research. I will force action if I need to, but I think people will want to do this. I have a women from Pew who is doing a book and this project is part of the story. It is about patients who take control of their research and we are a model group because of our unique challenges. Right now, the best thing you can do is just Text RECRUIT to +17474002617 to join. It will send follow up questions asking for your e-mail address, then you name and then address (maybe) but you will appear on the system and I will call you and ask you what your plans are. The site is not functional at the moment and still named the Kozin Foundation. As much as I love the name. LOL it is a holder until someone can have a better name and wants to pay for a domain name. Cheers, David
  8. NO MORE LONG POSTS. THE PATH I AM TAKING FOR GETTING ALL OF US TO MAKE CHANGE FOR OUR DISORDER AND CREATE THE FUNDING FOR RESEARCH & AWARENESS IS CORRECT. HERE IS THE SYSTEM IS AM USING AND SOON TO BE ONE OF A FEW OFFICIAL "EXPERTS" IN USING: Omidyar Network – the world’s most well-respected philanthropic investment firm – is joining their small board. They are leading an $8M investment, along with Andreessen Horowitz, to further their mission of making everyone a leader. eBay founder Pierre Omidyar and wife Pam established Omidyar Network based on their conviction that every person has the power to make a difference. Our work enables people to discover that power, improve their own lives, and make lasting contributions to their communities. I KNOW THIS IS THE WAY WE CAN DO IT HERE ARE OTHERS: --------------------------------------------- http://www.2020mom.org/ The 2020 Mom Project ("The Project") is an urgent national call to action that sets forth an aggressive new path for solving what some have called one of the biggest public health concerns of our time: the silent maternal mental health crisis which impacts up to 20% of expecting and new moms. --------------------------------------------- http://www.thebullyproject.com/ The BULLY Project is the social action campaign inspired by the award-winning film BULLY. We’ve sparked a national movement to stop bullying that is transforming kids’ lives and changing a culture of bullying into one of empathy and action. The power of our work lies in the participation of individuals like you and the remarkable list of partners we’ve gathered who collectively work to create safe, caring, and respectful schools and communities. Our goal is to reach 10 million kids or more, causing a tipping point that ends bullying in America. --------------------------------------------- http://www.notinvisible.org/ (DOCUMENTARY TRAILER TO OSCAR NOMINATED FILM ) Invisible No More is a non-partisan coalition working to end sexual assault within the U.S. military and to help survivors of Military Sexual Assault heal. Today, a woman serving in Iraq or Afghanistan is more likely to be raped by a fellow service member than to be killed in the line of fire. --------------------------------------------- http://www.hopeforpaws.org/ Hope For Paws And Fiona On Anderson Cooper With Co-Host Kristin Chenoweth. --------------------------------------------- PART OF THE PLAN IS THAT YOU WILL BE INVOLVED IN MAKING THE PLANS I WILL POST ADDITIONAL PLANS FOR THE PHASE 1 IN THIS EVENING. I HAVE CONTACTED AUTHORS AND OTHER INDIVIDUALS TO UNITE THE PROJECT WITH OTHER PROJECTS WITH SAME GOAL. Sending a text or e-mail to the recruitment page is a great first step and allows me to use as leverage when talking to others. You can choose to have your contact information private. Your first and last name is placed in two spots, and one is private. They use this system for political campaign contributions, so I trust the security on that level. Having your real address and name available to the system allows you to choose to be contacted when research occurs, receive printed materials, be alerted when a doctor takes the HPPD Pledge and is in your area, or elect to be visible to people in your area for meet-ups and help use plan a road-trip documentary. Also, this is how I can validate the research project I designed at Harvard and get it going. - David
  9. Yes, why I am trying to get the visual snow community and the other similar disorder groups on board. Why the site will not be called Hallucinogen anything.... because many drugs, not just hallucinogens, cause this problem. We can't ignore a reality, but part of that reality is good research may find no significant difference between all of our groups.
  10. http://waggeneredstrom.com/downloads/DSCA-Summary.pdf More than half of survey respondents (55%) who engaged with causes via social media have been inspired to take further action. More than half of survey respondents (55%) who engaged with causes via social media have been inspired to take further action. The most common actions taken include donating money (68%), volunteering (53%), donating personal items or food (52%), or attending or participating in an event (43%). What motivates these further actions? Survey respondents indicated that stories are key; more than half (56%) agree they read a story on social media that made them want to do more. Other drivers include online videos (41%) and photos (40%), along with seeing family and friends also taking further action (39%). This is why you will be able to blog your story, include images and work on music and art for demonstrations. Independent film is important and our own footage and story telling. We will raise 100,000 before the end of this month. If we work and become motivated about learning what we are doing and how you are expected to be a part of the process that you can be proud of. - David
  11. I am creating a page for members that pay the details of how the money is spent. For members to review, the basic information will be published on the web site, but to access the accounting system requires additional work. Additionally, different specifications can be made for different types of donations. This is what we are all thinking about as a group. I have received 10 strong leads for individuals to participate and two donations from early adopters. - David
  12. A large new site that will be adjunt to this and does much more for the projects is under construction but also working. If anyone is interested in paying for a membership, which is not tax deductable but at this point nothing is, that would last for a year of full access as a "Founding Member" which would be carried as a status for the operation of our group company. We have pledge drives, fundraisers with tickets, donation by text message, online sales and other ways to get funds. I have layed out the basic purpose of the funds, but it will be held in an account at the moment (until this month runs out of hosting.) The best step is to join and provide your real information and this is going to be hidden and we will have usernames listed along with the others. However, with real address information the system can effectively help you with local events/etc. Text RECRUIT to +17474002617 to join or Text RECRUIT to+17349842496 to join Then goto http://www.kozinfoundation.org/membership for the basic membership plans that are far from being fleshed out, but it will be equitable at the end. Or goto: https://hppd.nationbuilder.com/donate to provide any amount. As far as where the money goes... I can say that the research I did under "NODID" for DP/DR os stated as 0.00 funding provided and a huge undertaking at no cost. The original diagnostic criteria for Depersonalization Disorder did not include options for Derealization and only had one symptom, we used an instrument to show that specific patterns exist that form the other symptom groups. Now it is a dimensional and multiple diagnostic questions to undergo. The system I am using we use with political candidates and the system is protected for obvious reasons. - David
  13. Recently, I had a very severe injury to my leg resulting in total absence from social media or work for a long time. Afterwards, I had to take what small positions I could to stay afloat. I have decided to make a commitment, for about as much time as it would take me to find some work, to make the new HPPD Initiative and Research plans my work. Dr. Abraham has conducted the majority, if not all, of his research regarding HPPD without any funding. They spawned off of other work where essentially the insurance companies are paying for the tests and he is reading the results. However, he does invest his own time and money and really deserves a lot of respect. Without him, I am sure HPPD would not exist in the DSM-5, and you would all be on the visual snow board where prejudice for your drug use would be a cause of fights and we may still be a myth. PROBLEM 1: The problem is that we do not have any EPIDEMIOLOGICAL DATA to present the groups that make decisions about grants. WHY?: Without data on how many people actually have HPPD, we can neither apply for special grants for very rare (orphan diseases) nor can we show that the problem is much bigger than they think. We need point prevalence data. I have designed the new system that involves a membership system serves as a good indicator for an individual to really belong in the HPPD population. If a $20 dollar a year membership was required to access all of the web site's features and money that pays for printed literature/etc (just hypothetical number) was paid by 10,000 people -- this is the number of people that I can guarantee by studying analytics from Google and server tracking -- many who do not register but visit regularly paid 20 dollars a year we would have 200,000 dollars for research, web site, expenses, etc. Wow, that is a lot. But it can be done. Now, each registered member is verified as a person with an address and name. I can have each complete my comprehensive survey about HPPD, which Dr. Abraham approved after some fixes. Now, I have maybe 7,000 people who took the survey from all around the world. Now, we have a major paper and would warrant larger research because misdiagnosis of false negatives can be shown to be common and a number of people with HPPD could be predicted from the error rate of diagnosis. Do you want to get research organized? Then we must organize as a unit, create the petitions and connect with the institutions and act as a lobbying group essentially for our disorder. This is a model that works, and the research I suggested Dr. Simeon and I work on ended up showing a population of 360+ people stating to have DP/DR took an important test and the results from the internet group were ALMOST exactly on the numbers of people who take it in person after a diagnosis. This was huge, as it validated our large sample for other reasons. It was the nail in the coffin for changing that diagnosis and to this day my proudest work. I am going to continue to work on the basic set-up of the new web site and accept people willing to craft it and how the entity works. So, this is what a membership could get a person at the "Regular [Full] Member" 1) User profile that can be public or hidden 2) A blog to tell their story as they chose 3) Access to all of the literature in a virtual library, access to online systems that the memberships could pay for. 4) Set-up text or e-mail message reminders if someone is setting up a meet-up within X kilometers from your home. 5) Receive text message if a doctor near your area has taken the pledge that HPPD is a disorder of the brain, has committed to reading the literature and as a result signs their virtual name to the web site and their office location is placed on the map. The system will look for people within a radius and alert them about the doctor. 6) Access to all of the authors stories, ability to comment, create your own meet-ups 7) Organize events, participate in seminars and receive discounts we use our size to procure. 8) Receive alerts to nearby research and contact information. Additionally, it would carry over and pay for this web site and then the work done for the printed material for all members and for the professional information web site. Is that worth the cost of a cheap American fast food combo meal once a month? If so, then it is worth $60 USD. If 5,000 members paid $60 we would have 300,000 dollars a year. We would have researchers drooling for that type of money if it was guaranteed. It is so simple for us to really take this and do it if everyone realizes how a small contribution, set up regularly and with many volunteers working and targeting the rights areas to request for grant providing money. Essentially, we all would be paying a premium on services to pay for grants to researchers and in that WE ALL OWN AND SHOULD TAKE VALUE IN THE RESEARCH. It is a co-op that hires a research team. If we have 100,000 dollars I am almost certain the donor group from the HPPD Foundation will feel this is a measure that it is worth it for them to make the financial contribution of an equal amount towards research and double the money. How close are we? As close as the desire of the people who decide what they value. Do you value that type of money that would allow us to have researchers begging for us or where we are begging to them because we all said we can not give up one hamburger and fries a month. Here are the site statistics, we have the ability to harness this power: Analytics www.hppdonline.com Acquisition Overview 20140101-20140410.pdf Analytics www.hppdonline.com Audience Overview 20140101-20140228 (1).pdf Analytics www.hppdonline.com Location 20140101-20140410 (1).pdf https___www.invisionpower.com_clients_index.pdf
  14. Funding. Dr. Abraham did his research without funding (in most if not entirely, or attached it along with a different project). I have two research ideas, but require funding and expensive at probably $150,000/yr for two years. I plan on a very simple and reasonable way to raise this money, and I hope the community takes advantage of it. Otherwise, money will never go to HPPD because money is limited and frankly they are close to eliminating it from the DSM and we have to push it down their throats. Dr. Abraham saved this entire disorder from elimination in the research area. Dr. Abraham and I worked on research ready to run, but need a little push with money. I can't eat, I need regular job. Instead, I am trying to push forward for a little bit with HPPD and see how it goes. Before I earned my bachelors degree I published four research studies with hard work and luck and changed the DP/DR diagnosis and my work has been cited over 80 times in a few years and it is growing. We can do this, but only if the community can put a value on research or if they are going to waste that same amount of money on a bottle of supplements that someone tells you will help but will not. I will actually write the post about this tonight. - David
  15. I'll provide an update on this unless someone else has one?
  16. http://hppdonline.com/index.php?/files/file/79-%7B?%7D/ http://hppdonline.com/index.php?/files/file/79-%7B?%7D/ http://nbuild.s3.amazonaws.com/pdfs/nationbuilder-feature-tour.pdf
  17. File Name: HPPD INITIATIVE MANAGEMENT SYSTEM File Submitter: David S. Kozin File Submitted: 09 Apr 2014 File Category: Publications http://nbuild.s3.amazonaws.com/pdfs/nationbuilder-feature-tour.pdf The HPPD System for Building this initiative. Click here to download this file
  18. For example, I would love an assistant to help fix spelling errors and grammar problems in the post above and also process incoming messages/etc for the project. I am reaching out to multiple connections in the industry about putting in support, and I have learned that even doing this full-time this is not something I can or would want to try alone. I want everyone to take the credit, but let me survive without going hungry. - dk
  19. RESEARCH & ADVOCACY AWARENESS INITIATIVE We are in an unprecedented moment in the timeline for Hallucinogen Persisting Perception Disorder, and the most important components to move us forward exist within our own ranks. The current active members of HPPDonline.com are by far the most vocal about their condition without concern for the backlash, are also part of medical research and some are open about their HPPD. We also possess funds to collectively have no trouble with $200,000/year research budget to HPPD and include artist and writers who can communicate the message to others. I read how many members on this web site want to take a next step, and today is the day it is going to happen. I am starting talks to the responsible parties of the HPPD Foundation. The Foundation's goal is to put $100,000 funding towards HPPD research a year, and I think this money would be served best to help the members of this community with their project ideas including: (These are ideas from the forum, chatting with peope and my own but collectively as "ours" no way suggest or want ownership, just putting them out there) 1) Creating an HPPD Documentary Movie / Raising the funds to do so / Organizing people around the world for film 2) Developing a non-forum web site for professionals about Hallucinogen Persisting Perception Disorder. Allow everyone to blog on a membership site. 3) Creation of high-quality documents -- informational hand-outs, public relations and awareness literature 4) Conducting research at school, uni or in their office or online. 5) Create a database of doctors that have taken an "HPPD" Pledge, where they have read a minimal amount of HPPD and agreed to the legitimacy of the disorder and in turn get their office contact information in a searchable database 6) Have an organized system for meet-ups with HPPD people in different regions 7) Organizing effective grass-root awareness campaigns at targeted events. Other PR at target audiences. 8) Public Speaking about the Topic at conferences 9) Holding our own International Conference 10) Dealing with the media and responding to false information on the Internet 11) Creating art, publishing text and getting publicity for the work related to HPPD. This includes digital media as art and simulations. 12) Create a group that can find unique and non-traditional methods to ensure our goals and desires are met 13) Pay for media space in traditional outlets, while using SEO and clever methods to occupy more digital space. 14) Organize for placement on television shows with huge audiences (Dr. Oz, The Doctors) 15) Collect all relevant Research from the past to current and place it in a space for use by us, other researchers and clinical workers. 16) Conduct fundraising programs to further fund these operations 17) To leverage all of our own unique skill sets, positions in our lives and organize our talents to reduce cost and barriers to getting shit down. This includes translators for the main web site, documents that go to print and in-house graphic designers (we have some of the best) invest some time and with funding -- get paid vs. non-HPPD designers -- for work. 18) Help me with two research projects I have ready to begin and I have authored two Visual Neuroscience & Information Processing protocols that were discussed by Dr. Abraham and labs at Yale to UC:SF for finding a biomarker of HPPD and also enhancing our understanding of the neurochemical pathways that are involved with HPPD to further improve targets for pharmacological therapies. 19) Provide support to individuals as an organized group with one person always available via a hotline organized and operated with volunteers. 20 Become a model group for what can happen when the patients work collectively to change the way their disorder is understood, diagnosed, researched and treated. Become our own champions for the future, To do this, we need to work as a team and individuals with the ability to give more time & higher skill sets of different projects take leadership roles, but still work as a team. I AM DEDICATING FULL-TIME TO THIS. So, along with advice from others and now having the opportunity to do so, I am giving up hope for earning money to get me to the next step of my life and focus 8 hours of the day to the project and hopefully in 6 months we are moving forward at an excellent pace and I can afford to return to school for my advanced degree while working on this grand project. i have the first step for the organizing of all of the interested people on this site and more to become an effective autonomous and self-running organization that is essentially the computer system and design of Obama's political online campaign machine. I have used it for local political campaigns, and working with the company to get certified (to put me in a group of 10 people perhaps) as an Expert in their new system that just received massive funding and the founder of E-bay jumping on board. The system is being used for the large anti-bullying campaign to entire state's Party unified campaign software to non-profits and running local governments. I have the system set-up with the basics, but this is all that is needed to start. Two of our members donated the money to pay for the start-up of the system (very inexpensive and highly scalable) and to take all of these great ideas from the community and make them actionable we can start with the individuals who will become "early adopters" and work to discuss management issues and the best structure for the group as an entity (legally/etc) and generate the basics for the majority of the community to become a part of. I am clocking in all day this week and beyond for what yesterday was temporarily named the Kozin Foundation until the geniuses on here can come up with a succinct name that conveys the message and has a domain name we can get. However, I do have phone lines already set-up for the company. If you are interested to become a project leader or provide early work as a designer, programmer, researcher, attorney, funder or whatever you have thought of like a social media butterfly: You can contact me and we will organize communication if you do one of the following: 1) Text RECRUIT to +17474002617 to be part of the start-up. The system will record your cell number, and then ask you for your e-mail address and your name. This is recorded and will be viewable to core staff members. With this information, an account for you will be created but not public with this very basic information. I will be notified immediately to follow up and fill in the rest of the details and discuss what you would like to do. 2) Send an email (this will change when the domain name changes after input, but at this time is david@kozinfoundation.org). Include your contact information so I can follow up with you. I will also be alerted to take care of this. 3) Call and leave a voicemail at +17474002617 with your contact information. If I am not on the phone, I will pick up during normal hours. - David
  20. Do you want to work on organizing people who could be useful to this process as an early adopter and test of the new system. I will include my contact list and other individuals in the industry to put together a plan?
  21. AlexWhiteSTV, this is where crowdfunding and the tools of the management web site will allow us to contact people in the industry and organize for a documentary (even sending out blast emails to members in a region for meetings en masse for film). A friend of mine, who is waiting for a clear and organized project is Ali Toukan, Director of Development at Phoenix Pictures. He also funds films independently. If you are not familiar with Phoenix Picturtes: Phoenix Pictures is one of the premiere entertainment labels in the film business, bringing quality films to audiences around the world. Led by Mike Medavoy and Arnie Messer, two of the industry’s most respected senior executives, Phoenix has established a reputation for consistently developing first-rate projects with some of Hollywood’s top creative talent. With over 25 feature films to its credit, the company has collaborated with sought after director talents such as Martin Scorsese, David Fincher, Darren Aronofsky, Oliver Stone, Milos Forman, Andy Davis, Bryan Singer and Terrence Malick, as well as some of the industry’s biggest stars, including Leonardo DiCaprio, Robert Downey Jr., Sean Penn, Arnold Schwarzenegger, John Travolta, Ben Kingsley, Kate Winslet, John Cusack, Jude Law, Renee Zellwegger, Kirsten Dunst, Michelle Williams, Edward Norton, Samuel L. Jackson, Robin Williams, Shia LaBeouf, Jake Gyllenhaal, Ewan McGregor, Mark Ruffalo, Sigourney Weaver, Jennifer Lopez, Anthony Hopkins, Jamie Foxx, Eva Mendes, Adrien Brody, Woody Harrelson, Nick Nolte, Ian McKellen, Barbra Streisand and Jeff Bridges. The company was formed in 1995 by Mike Medavoy and Arnie Messer, with partners including Sony Pictures Entertainment, Onex, Fremantle Media and Showtime. Phoenix ’s first three films were The Mirror Has Two Faces, directed by Barbra Streisand, two-time Oscar® winner Milos Forman’s widely acclaimed The People vs. Larry Flynt and Oliver Stone’s U-Turn. In 1997 legendary filmmaker Terrence Malick returned to filmmaking after 19 years with The Thin Red Linefor Phoenix Pictures, which went on to receive seven Oscar® nominations: Best Picture, Director, Screenplay based on material previously published, Cinematography, Editing, Score and Sound. That same year, Phoenix produced Urban Legend, which was the fifth top-grossing film released by Columbia/TriStar in 1998. Phoenix has also produced Dick, Lake Placid, directed by Steve Miner, Whatever It Takes, directed by David Raynr, Mad About Mambo, the sequel Urban Legends: Final Cut, directed by John Ottman, Roger Spottiswoode’s The 6th Day starring Arnold Schwarzenegger, Basic, directed by John McTiernan; Holes, based on the award-winning New York Times best selling children’s novel, directed by Andy Davis; In My Country, Stealth, directed by Rob Cohen, and All the King’s Men, directed by Steve Zaillian. In 2007 came the independently financed Miss Potter, directed by Chris Noonan, Pathfinder, directed by Marcus Nispel, Resurrecting the Champ, directed by Rod Lurie, License to Wed, directed by Ken Kwapis and the critically acclaimed Zodiac, by David Fincher. Shutter Island, directed by Martin Scorsese and starring Leonardo DiCaprio, Mark Ruffalo, Ben Kingsley and Michelle Williams, will be in theaters in February 2010. Phoenix is currently completing Shanghai for The Weinstein Company, directed by Mikael Hafstrom, starring John Cusack and Gong Li, and will soon be starting on Darren Aronofsky’s Black Swan, starring Natalie Portman, Winona Ryder and Mila Kunis. Other feature films in development include a remake ofRoboCop for MGM, and an adaptation of John Grisham’s best-selling novel Playing for Pizza.
  22. I spent days house sitting for Rick Doblin of MAPS. I know their opinion, and they have their opportunity. The best news coming from that area is from Dr. Charlie Grob announcing, for the first time, that HPPD is real and they better deal with it. Grob is very influential, but I spent a year with MAPS folk and they are raising money for other areas. Your logic is correct, and people in MAPS I know state, "It should be a priority to study HPPD to reduce risk and understand possible harms to reduce them." However, despite being there... it is not the place I want to have you put your HPPD money in. However, you can join and work to put together a group for identifying and communicating with the HPPD Foundation and restart their interest. I'm here all day. - David
  23. http://hppd.nationbuilder.com/volunteer_phase1 Text RECRUIT to +17349842496 to join
×
×
  • Create New...

Important Information

By using this site, you agree to our Terms of Use.