Final #PatientsIncluded statement for
SPM’s first conference 10/25/2017
SPM = Society for Participatory Medicine, founded in 2009.
Statement written 10/23/17 by Dave deBronkart, co-founder and board member.
Here is our status on each of the criteria on the #PI conference charter page
1. Patients or caregivers with experience relevant to the conference’s central theme actively participate in the design and planning of the event
2. Patients or caregivers with experience of the issues addressed by the event participate [as a speaker, moderator, panelist, workshop leader, or in any other formal capacity] in its delivery, and appear in its physical audience.
3. Travel and accommodation expenses for patients or carers participating in the advertised program are paid in full, in advance.
We are self-certifying as honoring the intent of #PI to the fullest extent of our modest resources. See discussion in Appendix 1.
For full transparency, here is the full list of patient faculty, with status as (a) whether their employer or other paid for their travel, (b) whether they’re an SPM member (for scholarship eligibility), (c) whether they requested travel funds, (d) whether their request was granted (yes in all cases).
“Scholarships are provided by the conference organisers to allow patients or carers affected by the relevant issues to attend as delegates.”
[Footnote 3: “A minimum of two scholarships are disbursed, covering registration, travel, and accommodation expenses for two patient or carer delegates in full, in advance.”]
Free admission is is one option on the scholarship request form. Our registration system has been undependable so it’s hard to be precise (not all free registrations are showing up in the database) but at least six patients have been given free admission, as speakers or participants.
4. The disability requirements of participants are accommodated.
All applicable sessions, breakouts, ancillary meetings, and other programme elements are open to patient delegates.
Re disability requirements: we are of course happy to accommodate ordinary ADA needs, but we don’t currently have the resources (money) to go beyond, e.g. to provide captioning etc.
We would welcome sponsors who want to fund such additions. Write to email@example.com
All sessions are open to all.
5. Access for virtual participants is facilitated, with free streaming video provided online wherever possible.
The hashtag is #SPM2017 and is being promoted on Twitter.
Appendices with SPM travel fund details and #PI background information continue on next page.
The #PatientsIncluded movement (website) is the single most visible emblem of the participatory medicine movement around the world. The SPM blog has mentioned it often, and it’s often mentioned on Twitter, and important events are increasingly working to self-certify as Patients Included.
The goal is to nudge every aspect of healthcare to proactively involve patients and patient voices in every activity that touches or is about patients - to make a reality out of “nothing about us without us.” This is completely aligned with SPM’s purpose of transforming healthcare to incorporate patient-professional partnerships.
It’s natural that our Society, as one of the leading voices for patient participation, is expected by patient activists to acknowledge the subject, and self-assess. That’s what this document is for. In short, we need to evaluate ourselves and aspire to certify, when we can.
The most recent announcement, this Thursday (tweet), is the Cochrane Collaborative’s conference next year. Cochrane is blogging about its process; this document is in a similar spirit, for SPM’s conference.
Below is a list of the certification criteria, with comments in the margins, including from the #PatientsIncluded curator, Andrew Spong.