Special Edition · No. 2 · August 2026
What’s Pain Awareness Month? September. The American Chronic Pain Association established it in 2001, with a coalition of eighty organizations behind it. It has no federal charter, no budget, and nobody in charge of it. It runs on whoever decides to do something with it. This edition is a list of things you could decide to do — and of who is already doing them.
IN THIS EDITION Why This Edition · Where September Came From · What You Can Do · Ways In · What a Researcher Can Do · Credit Where It Is Due · The Program That Is Not There · The Calendar · One Question
Welcome
A Note from the Editor
One month, and then the other eleven.
Why this edition arrives before September does.
September is Pain Awareness Month. This edition comes out in August because a map is only useful before the trip.
PWLE Voices publishes a six-issue run through September. This edition is not part of that run and takes no number in it. It is the thing you read first — what the month is, what you can do with it, and who is already doing something.
For most of the year, we do the explaining. In September, for a few weeks, somebody else does some of it for us.
That is worth something. It is not worth everything.
One note about how to read what follows. Some of it is confirmed for 2026. Some of it is what an organization did last year and will very likely do again. I have labeled which is which, because a plan printed as a fact is how trust gets spent.
Awareness is not the goal. It is the doorway.
— Tom
Start Here
Foundations
Where September Came From
The month has an origin, and it is not a government one.
Pain Awareness Month is not an accident of the calendar.
The American Chronic Pain Association (ACPA) established it in 2001.
The ACPA did not do it alone. It convened a coalition called Partners for Understanding Pain — eighty organizations, health care professional groups and consumer groups side by side. The National Association for the Advancement of Colored People (NAACP) was among them, which tells you something about how the founders understood who was not being believed about pain.
The ACPA’s own account of the founding is short, and it is the only primary one. The rest of the early record comes from secondary write-ups, which agree on this much: a kickoff lunch at the 2002 conference of the International Association for the Study of Pain (IASP), and more than thirty partner organizations by 2003.
Those same accounts describe toolkits following — one for nurses in 2004, one for pharmacists in 2005, one for older adults — and a turn toward grassroots and media work in 2007, which is roughly where the month still lives. Treat that sequence as the received history rather than a documented one.
Notice the order of that founding.
It started with a group built around people with pain, and the institutions came after.
That order is still the one we are trying to hold.
A Tool You Can Use Today
For People With Pain
What You Can Do This Month
Seven things, none of which require travel, money, or a title. Pick one and stop there if you need to.
- Ask for a proclamation. Most governors, and many mayors and city councils, will issue a Pain Awareness Month proclamation if somebody asks. They do not renew on their own. Somebody has to ask, every year. Most governors’ offices post a request form, and the request usually takes one page.
- Tell one story, using a hashtag that already has an audience. #ThisIsPain (U.S. Pain Foundation). #RealPainStories, tagging @national_pain (National Pain Advocacy Center). #PainAwarenessMonth (IASP). #MyPainIsLike (iPain, the International Pain Foundation).
- Nominate someone for a Better Together Recognition. Nominations opened August 10 and close October 31, 2026. Recipients are announced November 30. Anyone may nominate, including yourself, and nominations are confidential unless the person is selected. The form is at chronicpainla.com/nominate/.
- Register for the IASP webinar on September 24. Free and open, and one of the few September events already fixed on a calendar.
- Work the ACPA’s own list. Tell friends and family. Tell your health care provider. Call local media and ask whether they are covering the month. Call local government and community leaders. And take care of yourself, which is on the list for a reason.
- Bring the month into a room you already sit in. If you belong to a support group, put one September item on the agenda. If you sit on an advisory board, ask what your group is doing for the month.
- Volunteer to review federal research. The Department of Defense Congressionally Directed Medical Research Programs (CDMRP) Consumer Reviewer Program seats people with lived experience as full voting members of peer review panels — usually two to four consumer reviewers alongside six to twenty scientists. More than two thousand consumers have served since 1995. You need a nomination from an advocacy or support organization, and there is an interview.
Where we sit: the editor has served as a CDMRP consumer reviewer since 2012, and co-chairs the recognition program named above.
Ways In
Programs, Panels, and Seats
Where the Rooms Actually Are
Ten doors into research and advocacy. Seven you can walk through this month. Three you watch for.
People ask how you get into these rooms. The honest answer is that most of the doors are unmarked, and almost none of them are as hard to open as they look.
Here is what we could confirm about each one, sorted by whether you can act on it now. Application windows move, so check the page before you spend an evening on a form.
Open now
Rolling or continuous — you can start any day this month.
Ambassador Program PCORI
The lowest doorstep on this page. You fill out an interest form and complete a short online training, and that is the barrier. Ambassadors carry research findings back to their communities, write guest posts and op-eds, and encourage others to get involved. It also functions as a feeder — ambassadors form a pool that PCORI draws on for merit review, peer review, and advisory panels. Questions go to ambassadors@pcori.org.
Merit Reviewer PCORI
You read and score actual funding applications. Merit review panels seat scientists, people with lived experience, and others from the health care community together, and every reviewer’s score is weighted equally. That last clause is the whole point — it is one of the few rooms where the vote is arithmetic rather than atmosphere. Applicants must live in North America. Write to reviewers@pcori.org. Veteran reviewers are later invited into a Merit Review Mentor Program that supports newer patient and stakeholder reviewers; that one comes by invitation, not application.
Volunteer Network U.S. Pain Foundation
Most of it can be done from a couch, which the foundation says plainly. Order and distribute materials, set up an information table, reshare posts, tell people in your support groups. Two specifics worth knowing: to facilitate an official peer support group you must first attend a Pain Connection training, and if you want to speak on the foundation’s behalf in public — a hearing, an interview, an op-ed — you need permission first.
California Advocacy Team U.S. Pain Foundation
Trained volunteer advocates who monitor legislation, educate policymakers, and support access to comprehensive pain care in California. The foundation states directly that no prior advocacy experience is required. It also runs an Introduction to Pain Advocacy and Policy training series — five two-hour sessions over Zoom, by acceptance.
Consumer Reviewer Program CDMRP
Described in the next article. Full voting membership on federal peer review panels, by nomination from an advocacy or support organization.
Global Alliance of Partners for Pain Advocacy IASP
GAPPA brings people with lived experience together with advocates, clinicians, and researchers across pain research, education, and advocacy. Membership runs through IASP. It also carries week three of the IASP Pain Awareness Month program.
PURPOSE Network NIH HEAL
Positively Uniting Researchers of Pain to Opine, Synthesize, and Engage — the NIH HEAL Initiative’s Coordinating Center for National Pain Scientists. It is an online network where pain researchers and people with lived experience sit in the same space, and it is free to join. Membership is by request at painresearchers.com; people with lived experience can also write directly to PURPOSE@painresearchers.com. What is behind the door: a career-development web series that has run more than a dozen episodes, including one on engaging people with lived experience in pain research; an events calendar carrying webinars and the annual meeting; a weekly digest; an opportunities board; and news and publications. It also carries a set of affiliate networks worth browsing once you are inside. PURPOSE has its own annual meeting, most recently co-located with the USASP meeting in Philadelphia.
Watch for the window
These open on a cycle. September is when you get ready, not when you apply.
Advisory Panels PCORI
Five panels advise PCORI’s Board, Methodology Committee, and staff — among them the Patient Engagement Advisory Panel. The application asks for a personal statement about why you are applying and what your experience would add, and you may name and rank up to two panels. Openings are posted periodically rather than continuously; watch the Advisory Panel Openings page. Panelists complete a conflict of interest disclosure.
National Consumer Scholars Camden Coalition
Running since 2016. It began as a scholarship so that people with lived experience could attend the annual Putting Care at the Center conference, and grew into peer-to-peer learning and leadership development. Scholars partner with Camden Coalition staff on projects and take an active role at the conference. The 2025–2026 cohort was fifteen people and was the first built around a single group — those dually eligible for Medicare and Medicaid, and family caregivers of people who are. Timing matters here: applications for that cohort ran in the spring, with an information session in May, and the cohort was announced in early September. So September is when you watch for the announcement, not when you apply. What you can act on this fall is the conference itself — Putting Care at the Center runs October 14–16, 2026 in Oakland, co-hosted by Kaiser Permanente, themed “Sustaining progress, building the future,” with reduced rates for people with complex health needs and family caregivers. Early bird pricing closed July 31. The Coalition also runs Amplify, a consumer voices bureau connecting organizations to leaders with lived expertise.
PATIENTS Professors Academy University of Maryland School of Pharmacy
The PATIENTS Program teaches its ten-step framework for continuous patient and community engagement — built as an answer to what the program calls helicopter research, where an institution drops into a community for data and is never seen again. Enrollment runs in cycles rather than continuously. The program page carries a flyer and video accounts from graduates.
One question to carry into any of these. Most of these seats are unpaid, some cover travel, and a few compensate. Ask which before you say yes, and ask it early enough that the answer can still change your decision.
An open door is not the same as a paid chair.
Where we sit: the editor has come through several of these doors — the PCORI Ambassador program, merit review, the Patient Engagement Advisory Panel, the Camden Coalition, the PATIENTS Professors Academy, and the California Advocacy Team. That is disclosure, not endorsement. Before you apply anywhere, ask someone already inside what it was actually like.
A Tool You Can Use Today
For Researchers
What a Researcher Can Do This Month
Eight things a team has already done. None of them invented for the occasion.
- Bring your PWLE partner to the microphone. In September 2024 the National Institutes of Health (NIH) Helping to End Addiction Long-term (HEAL) Initiative and the U.S. Pain Foundation co-hosted a Pain Awareness Month webinar where a HEAL researcher and her research partner with lived experience presented together. Not a thank-you slide. A shared microphone.
- Publish a plain-language version of something you already published. IASP did this for its 2026 Global Year on Neuropathic Pain, including a guide written for people with pain rather than for reviewers. One paper, one plain-language page.
- Name your partners in the acknowledgments, and ask them first. Permission to appear in a report is not permission to appear everywhere.
- Put a lived-experience mentor into the structure, not the margin. The HEAL National K12 Clinical Pain Career Development Award, administered by the University of Michigan, gives every scholar three mentors — one of whom is a mentor with lived pain experience. That is written into the award, not left to goodwill.
- Pay people, and say what you paid. Rates move and vary by program, so point to your own institution’s current policy rather than a number you remember.
- Send the result back to the people who enrolled. A trial closes and the participants often never hear what came of it. September is a reason to close that loop.
- Nominate a person with pain for a review panel. CDMRP consumer reviewers must be nominated by an organization. Researchers sit on those panels too. You can open that door from the inside.
- Report what the partnership changed. If a PWLE partner changed your protocol, your recruitment materials, or an outcome measure, that is a finding about your study. Write it down where someone can read it.
Featured This Edition
Credit Where It Is Due
Who Is Actually Doing the Work
Fourteen organizations, what each has planned, and how confident we are about it. Status as of August 28, 2026.
International Association for the Study of Pain (IASP) CONFIRMED FOR 2026
A four-week program under the theme “Understand. Advocate. Partner. Advance.” — one theme per week, built on the 2026 Global Year on Neuropathic Pain, with a free webinar on September 24 and the World Congress on Pain following in October. Week three belongs to partnership with people with lived experience, through the Global Alliance of Partners for Pain Advocacy (GAPPA). IASP also credits others on its own page, including the ACPA and the U.S. Pain Foundation. Hashtag: #PainAwarenessMonth.
World Patients Alliance (WPA) CONFIRMED FOR 2026
World Patient Safety Day on September 17, following the World Health Organization theme of safe care for noncommunicable diseases, with a nineteen-day campaign calendar, a global webinar, a social media toolkit, and grants for member organizations. Worth being precise: this is patient safety work, not a chronic pain campaign.
Patient-Centered Outcomes Research Institute (PCORI) CONFIRMED — NO SEPTEMBER CAMPAIGN
PCORI runs no Pain Awareness Month campaign, but its September belongs on your calendar anyway. The Broad Pragmatic Studies funding announcement closes September 1, and its stated pain interests include pain in sickle cell disease, urogynecological and pelvic pain, and pain management for people with intellectual and developmental disabilities or with Alzheimer’s disease and related dementias. Engagement Awards continue. The Patient Engagement Advisory Panel advises the Board.
Congressionally Directed Medical Research Programs (CDMRP) CONFIRMED — STATUS CHANGE
The Consumer Reviewer Program remains open, and remains one of the strongest votes a person with lived experience can hold in federal research. The dedicated chronic pain program is another story. See the next article.
NIH HEAL Initiative — K12 and T90 CONFIRMED PROGRAMS — 2026 SEPTEMBER ACTIVITY NOT YET POSTED
The K12 requires a lived-experience mentor for every scholar. The T90 postdoctoral program runs across six sites, including Michigan, Utah, Mass General Brigham, Stanford, the University of Florida, and Washington University in St. Louis. HEAL has marked the month before, including the 2024 webinar with the U.S. Pain Foundation. Nothing specific to September 2026 was posted as of this writing.
PURPOSE Network CONFIRMED — YEAR-ROUND, NOT A SEPTEMBER CAMPAIGN
Positively Uniting Researchers of Pain to Opine, Synthesize, and Engage — the NIH HEAL Initiative’s Coordinating Center for National Pain Scientists, funded through the National Institute of Neurological Disorders and Stroke. It is the clearest example on this page of a researcher organization that built a shared room rather than a consultation. People with lived experience join free alongside researchers, at painresearchers.com. Its web series has devoted an episode to engaging people with lived experience in pain research. Its NIH funding is documented through August 2026; check the site for current status.
U.S. Pain Foundation PRIOR YEAR — 2026 THEME NOT YET POSTED
The 2025 campaign ran as #ThisIsPain, under “Unmasking Pain,” built on a national survey of more than two thousand adults living with pain and eighty-seven parents and guardians of children with pain. Weekly articles, daily statistics, and a volunteer push for state and city proclamations. The organization also publishes the INvisible Project. Check its page again before the first.
National Pain Advocacy Center (NPAC) PRIOR YEAR
#RealPainStories, collecting and sharing lived-experience stories during the month and past it, with its Community Leadership Council. NPAC is also the clearest voice in this group on equity and access — coverage denials, tapering harm, and the human rights framing.
Department of Veterans Affairs / Pain Management Collaboratory CONFIRMED RESOURCE
The NIH–DoD–VA Pain Management Collaboratory publishes “5 Ways You Can Support Pain Awareness Month,” written for veterans and service members, and runs sixteen large pragmatic trials of nonpharmacological pain care.
United States Association for the Study of Pain (USASP) CONFIRMED — SPRING, NOT SEPTEMBER
Its 2026 Annual Scientific Meeting runs March 23–26 in Philadelphia, with awards recognizing PWLE partners and teams, travel funding for PWLE attendance, and the PURPOSE annual meeting co-located just before it. September is a good month to start the nomination you will submit in the winter.
American Chronic Pain Association (ACPA) FOUNDING ORGANIZATION
The month exists because the ACPA built the coalition in 2001. Its action list is still the plainest set of instructions available to a person with pain in September, and its page is the only primary account of the founding we could find.
For Grace CONFIRMED ROLE
The Women In Pain initiative, on disparities in how women’s pain is assessed and treated, with a monthly lived-experience story.
iPain (International Pain Foundation) PRIOR YEAR
With Veteran Voices for Fibromyalgia and the Fibromyalgia National Health Organization, ran the 2025 theme “Our Pain” and reported forty-two state proclamations, aiming at all fifty. That figure is the organization’s own count.
American Academy of Pain Medicine (AAPM) PRIOR YEAR
The 2025 campaign, “From Awareness to Action,” paired clinical guidance with a resource hub crediting the U.S. Pain Foundation, the ACPA, and the World Patients Alliance.
Arthritis Foundation CONFIRMED RESOURCE
Runs a September Pain Awareness Month page and a chronic pain connect group. Several accounts place it among the original coalition organizations; we could not confirm that against a primary source, so we are crediting the current work rather than the founding.
Not found for 2026, and not for lack of looking: a Pain Awareness Month campaign from Patients Rising, The Pain Community, the Society for Participatory Medicine, or the National Fibromyalgia Association. If you know of one, write to us and it goes in the next edition.
Reported
Federal Research Funding
The Program That Is Not There
The Defense Department’s chronic pain research program has had no appropriation since 2023.
The Department of Defense funded a Chronic Pain Management Research Program beginning in fiscal year 2019.
The CDMRP funding history table lists it this way: seventy million dollars, fiscal years 2019 through 2023, four hundred nineteen applications received, sixty-five funded. The program’s own page says sixty-six awards over the same span. Both agree on the dollars and the years.
It has received no appropriation since fiscal year 2023. It now appears under “Previously Funded Research Programs.”
In February 2026, Congress provided $1.27 billion across thirty-four CDMRP programs. None of the thirty-four is a chronic pain program.
The Peer Reviewed Medical Research Program received $370 million for fiscal year 2026, spread across fifty-two eligible topic areas. Chronic pain is not one of them. Neither is pain management. Neither is fibromyalgia, and neither is neuropathic pain.
Painful conditions did survive on that list, and it would be dishonest not to say so. Endometriosis. Interstitial cystitis. Peripheral neuropathy. Musculoskeletal health. Myalgic encephalomyelitis and chronic fatigue syndrome. Ehlers-Danlos syndrome. Pancreatitis. A person with pain can reach a study through one of those doors.
What is closed is the door marked chronic pain itself — the one that funded work across conditions rather than one condition at a time.
One more thing, because leaving it out would make the story easier than it is. The CDMRP total went up this year, not down. The chronic pain program was left out of a budget that grew.
I am not going to tell you what that means.
I will tell you that the line item is gone, and that nobody asked us.
Appropriations move, and a number printed today can be wrong by the next cycle. Check the current status at cdmrp.health.mil before you repeat any of this in a letter or a meeting. Then repeat it.
The Month at a Glance
Dates
The Calendar
Confirmed as of August 28, 2026. Verify anything you plan to forward.
| DATE | WHAT IS HAPPENING |
|---|---|
| September 1 | PCORI Broad Pragmatic Studies, Cycle 2 2026 — application deadline, 5:00 p.m. Eastern |
| September 17 | World Patient Safety Day — World Health Organization and World Patients Alliance |
| September 24 | IASP free webinar: “Human-Centered Approaches to Neuropathic Pain: From Mechanisms to Translation” |
| October 14–16 | Putting Care at the Center — Camden Coalition annual conference, Oakland, CA |
| October 19–20 | PCORI Annual Meeting — Marriott Marquis, Washington, D.C. No charge to attend; the hotel room block is full |
| October 26–30 | IASP World Congress on Pain — Bangkok |
| October 31 | Better Together Recognitions — nominations close |
| November 30 | Better Together Recognitions — recipients announced |
One Question
After September
What is your seat allowed to decide?
The month ends on a Wednesday. What is left is whatever got built while people were paying attention.
On the first of October the hashtags go quiet.
The proclamations get framed or filed. The webinars become recordings that nobody opens. The survey results become a citation in somebody else’s introduction.
So use the month for the other thing. Ask for the proclamation, and then ask the office that signed it what it funds. Tell your story, and then ask the researcher who shared it what your story changed. Take the seat you are offered in September, and ask what the seat is allowed to decide.
Patient engagement is an invitation to advise. Patient empowerment is holding a real vote.
September is a good month to find out which one you have been handed. Tell us what you find: editorpwlevoices@gmail.com.
— Tom
SOURCES
American Chronic Pain Association. “Pain Awareness.” acpanow.com/pain-awareness.html
International Association for the Study of Pain. “Pain Awareness Month.” iasp-pain.org/advocacy/pain-awareness-month/
International Association for the Study of Pain. “Global Year on Neuropathic Pain 2026.” iasp-pain.org/advocacy/global-year/neuropathic-pain-2026/
World Patients Alliance. “World Patient Safety Day 2026.” worldpatientsalliance.org/world-patient-safety-day-2026/
Patient-Centered Outcomes Research Institute. Broad Pragmatic Studies funding announcements. pcori.org/funding-opportunities
Patient-Centered Outcomes Research Institute. “2026 PCORI Annual Meeting” and meeting agenda. pcori.org/annual-meeting
Patient-Centered Outcomes Research Institute. Ambassador Program, Merit Review, and Advisory Panel Openings pages. pcori.org
Congressionally Directed Medical Research Programs. “Funding History.” cdmrp.health.mil/about/fundinghistory
Congressionally Directed Medical Research Programs. “Peer Reviewed Medical Research Program, FY26 Topic Areas.” cdmrp.health.mil/prmrp/topicareas/topicareas26
Congressionally Directed Medical Research Programs. “Consumer Involvement.” cdmrp.health.mil/cwg/default
Congressional Research Service. “Congressionally Directed Medical Research Programs Funding for FY2026.” IF10349. congress.gov/crs-product/IF10349
National Institute of Neurological Disorders and Stroke. Director’s messages on Pain Awareness Month and on learning from people with lived experience of pain. ninds.nih.gov
NIH HEAL Initiative. National K12 Clinical Pain Career Development Award. heal-k12.med.umich.edu
NIH HEAL PURPOSE Network. painresearchers.com; PURPOSE@painresearchers.com
Camden Coalition. National Consumer Scholars and community engagement pages. camdenhealth.org
University of Maryland School of Pharmacy. “The PATIENTS Professors Academy.” pharmacy.umaryland.edu
U.S. Pain Foundation. Pain Awareness Month, Volunteer Network, and Advocacy pages. uspainfoundation.org
National Pain Advocacy Center. nationalpain.org
Pain Management Collaboratory. “5 Ways You Can Support Pain Awareness Month.” painmanagementcollaboratory.org
United States Association for the Study of Pain. 2026 Annual Scientific Meeting. usasp.org
American Academy of Pain Medicine. “Pain Awareness Month 2025: From Awareness to Action.” painmed.org
For Grace. “Women In Pain.” forgrace.org/women-pain/
iPain Foundation. “Pain Awareness Month 2025.” internationalpain.org
Arthritis Foundation. “September Is Pain Awareness Month.” arthritis.org
Help Us Make This Reachable for Everyone
We want PWLE Voices to work for every member of our community — however you read, listen, or take in information. If the current format is hard for you, or a different one would help — larger text, an audio version, plain-language summaries, anything — we want to know.
Tell us what would make this easier to use: editorpwlevoices@gmail.com
— Tom
A Note on How This Edition Was Made
This edition did not go to the Editorial Advisory Board. It was built quickly, against a September 1 start date, and there was not time to put it in front of the board the way the numbered issues are. That is a departure from how PWLE Voices normally works, and you should know it rather than assume it. The framing, the emphasis, and every judgment call in these pages are mine alone.
Nobody is profiled in this edition, so no contributor review was required. Every organization named here is credited from its own public materials, not from private correspondence.
If you find a mistake — a name, a date, a figure, or something that simply reads wrong — tell me and I will correct it and say so: editorpwlevoices@gmail.com. Corrections are published, not quietly patched.
— Tom
How This Newsletter Is Made
PWLE Voices is written and edited by people in our community. For this edition we also used an AI assistant — Claude (Anthropic) — in a limited, supporting role, so that a small, all-volunteer team could make this material clear, accurate, and easy for everyone to read. For this edition specifically, that meant: searching public sources for what each organization has announced or done for Pain Awareness Month; checking dates, figures, and program status against those sources; copy editing and formatting; and organizing the material into the order you are reading it in.
The editorial judgment about what to include, what to leave out, and what any of it means is the editor’s. AI did not decide what matters here.
Because AI tools can state things confidently and still be wrong, a person checked the facts these tools surfaced against the original sources, which are listed above. Where a claim could not be confirmed for 2026, it is labeled as a prior year rather than printed as current. The responsibility for accuracy is ours, not the software’s.
We also want to be honest about the trade-offs. Running these tools uses real electricity and water, and there are social concerns too — the labor behind building them, data privacy, and uneven access. We try to use AI sparingly, only where it genuinely helps. To learn more, see the U.S. Government Accountability Office overview Artificial Intelligence: Generative AI’s Environmental and Human Effects (gao.gov, GAO-25-107172).
Correction, September 28, 2026: This box originally called our team “mostly volunteer.” PWLE Voices is all-volunteer.
The views, positions, and recommendations expressed in this edition are based on my personal experiences. They are solely my own and do not necessarily reflect the views, policies, or positions of the American Chronic Pain Association (ACPA), the Patient-Centered Outcomes Research Institute (PCORI), or any federal program or committee on which I serve. AI was used for research, editing, and organizing; final text is my own.
PWLE Voices is a community publication. Nothing in it is medical, legal, or financial advice. Descriptions of programs, funding opportunities, and deadlines are accurate to the best of our knowledge at the time of publication and can change without notice — verify anything you intend to act on with the organization running it.
Better Together Recognitions are non-monetary. Recognition is not a substitute for fair compensation, and this publication does not accept payment for coverage or for recognition of any kind.
PWLE VOICES NEWSLETTER
Your voice. Your community. Better together.
chronicpainla.com • editorpwlevoices@gmail.com
Los Angeles Chronic Pain Support Group