Showing posts with label demonstration. Show all posts
Showing posts with label demonstration. Show all posts

Wednesday, April 11, 2012

Rivka's "How To" Guide for ME/CFS Demonstrations

I'm posting the following on behalf of my friend and fellow advocate, Rivka Solomon.  Read on: Rivka covers everything you need to know to put on a successful demonstration!

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Feel free to distribute widely
Taking a Stand: 
A "How To" Guide and "To Do" Checklist for ME/CFS Demonstrations
By Rivka
Email: Rivka (at) ThatTakesOvaries (dot) org
April 12, 2012
So you want to take a stand and make a stink -- do something more visible to help your ME/CFS community? Good for you. Consider organizing a demonstration (demo) to advocate for people with ME/CFS. Consider going public, alone or with others, in your call for more respect, more attention and, most importantly, increased government funding for research and treatments. 
Organizing a demo is both easy and a bunch of work. Do keep in mind this reality check: After all the energy output, you could have a mild or significant relapse. Yet also keep in mind that you will have raised public and perhaps government awareness about a devastating disability, and thus you will have done something important for the world and for your community. In the end, you will feel good about having done it. And you will have the gratitude of those who are too disabled to take this type of public stand that we all know needs to happen in cities and counties all over the globe in order for things to change -- most especially in front of national and government health care institutions, such as, in the U.S., in front of the regional headquarters of the Department of Health and Human Services (HHS) and the Centers for Disease Control and Prevention (CDC). 
Below is a simplified, preliminary -- and certainly incomplete -- checklist to consider as you organize your demonstration. It does not go into great detail, but skims over the basics, including, deciding the location of your demo, deciding the tone, reaching out to others, permits and arrests, reaching out to media and more.
Remember, you can always do a mini-demo as a solo person with a single sign. In some cases, this may be a heck of a lot easier on your health, and it could still have an impact, especially if you get media attention or put it on YouTube and email the link to your national and government health care institutions.
I have included video links of my own past public and bedridden demos below this checklist. Some were solo and some were group demos.
== Checklist for ME/CFS Demos ==
Location 
a.  You will likely want to be somewhere public, where there are passers-by, and/or where media can get to or where they may already be present.
b.  Ideas: City or federal building, health care building, blood giving location, outside (or inside?) a health-oriented meeting, perhaps at a meeting or talk that includes a noted government official.
Tone
a.  Decide how animated, flamboyant, cartoony do you want to be. Do you want to be dressed in business suits, jeans or more attention-getting costumes with some type of theme? 
b.  Will you have signs or a banner? Will they be colorful, upbeat and playful, or serious? Home made or printed?
c.  Will do you something very attention-grabbing, such as a lie-in with sleeping bags, pillows, blankets?
Attendance
If you want others to attend, reach out to local ME/CFS groups.
a.  Ask: Will they join the demo? If yes, they will likely want to join the decision-making, too (i.e. location and tone).
b.  Ask: If not, will they at least help you get the word out for the demo in an email blast you write up that they distribute to their members?
c.  Have the email include all the important information, such as when and where and why you are demonstrating. Be prepared to have your name and email distributed around the web. So don't include your name or email or phone number if you don't want that. (Get a new email address just for this demo?)
Young people
Young people and young adults with ME/CFS, or the kids of parents with ME/CFS, who attend your demo may get more sympathy from the media, government officials and the public.
a.  Contact national ME/CFS groups (e.g. contact Denise at SpeakUpAboutME@gmail.com, or contact the young adult online group called kickHeal) to see if they know any youth in your area that you can invite.
b.  Contact local families with kids who have ME/CFS. 
c.  Ask local ME/CFS groups if they know young people with ME/CFS.
Permits
If you want everything to be legal, find out in advance what is needed in terms of permits.
a.  Ask city police what permits are needed to hold a demo with 1-25 people (or whatever you think it will be), at these locations: 
- on the sidewalk in front of the target location
- on the sidewalk across the street of the target location
- both in front of and across the street of the local federal building 
(note: at a federal site, like the Capitol Hill HHS headquarters, also call and ask Home Land Security and Capitol Hill police and any other federal police they suggest, to ask about permits. It may be that you have to contact the head of security for that particular department or building. In fact, that could be the quickest route to finding out what permit you may or may not need, and where you can protest legally.) (Note: across the street is likely not federal property.)
b.  Consider telling the police/security that it will be a demo of people who are disabled and who have been ignored by the government. This may win you some sympathy and extra flexibility. Or not. 
c.  Find out from the police/security folks of the building the rules of how close you can be to a federal building, and what is not allowed (e.g. I found out that sticks for holding signs are not allowed in front of the White House in Washington DC, and that you have to keep moving, and can't sit still).
d. Another idea is to *not* find out about permits and just do your demo without permits. It could cause a bigger splash if you surprise the security team, or not -- no one really knows. It is not likely they will arrest you, even if you need a permit but don't have one. It is more likely they'd just ask you to leave. And then you can just decide to leave. This could make for a short demo, though. Nothing is known for sure.
Arrest
First, you should know that I really know nothing about getting arrested as a result of demonstrating. With that in mind, here are some thoughts. I have been told that it is unlikely you will get arrested, period, no matter where you demonstration, because the police and security would first give you an opportunity to simply leave. After all, they don’t want the bad press of arresting disabled people. Thus, once warned, you can always leave. But if you don’t care about arrest, or if you think it will help with publicity if you are indeed arrested, then:
a.  Find out what could happen if you are arrested; really find out, as I have no idea. Will you go to jail, or simply get a ticket? Will you have to go to court later? Pay a big fine?
b.  Have a lawyer ready to help you if you are arrested.
c.  Have bail ready.
d.  Will you need your medications while in jail? How will you get them? 
e.  Find out ADA (Americans with Disabilities Act) regulations in terms of disabled folks on U.S. jails.
f.  Get educated: Read up online about getting arrested as a result of demonstrating. 
Government buildings
If you decide to hold your demo at a government building, there are special considerations:
a.  Find out who runs that office (i.e. in the USA, the local HHS or CDC regional office), and also who is in charge of public relations there.
- ask for a meeting with one or both, for the day of your demo
- have talking points and a letter ready to give them if you meet. Have this ready even if you don't get confirmation ahead of time about a face-to-face meeting (you still may ending up meeting them or just leaving the info for them at the front desk)
- include in the letter why you are there protesting and what you want (e.g. more government funding for research into the cause of ME/CFS and treatments and clinical trials now)
- ask them to relay this message to their higher ups, their bosses. Ask them to promise they will do this, all the way to the very top
b.  When you ask for a meeting, and/or once you secure a meeting, decide if you want to tell them about yr demo in advance or not. There might be pros and cons to letting them know you will be demonstrating that day, and pros and cons to not telling them until you are actually there with your sign. 
c.  In the USA, there are 10 HHS regional offices (http://www.hhs.gov/about/regionmap.html) in Boston, MA; New York; Philadelphia, PA; Atlanta, GA; Chicago, IL; Dallas, TX; Kansas City, KS; Denver, CO; San Francisco, CA; Seattle, WA. Plus, there are 10 CDC satellite offices in Anchorage, AK; Cincinnati, OH; Fort Collins, CO; Hyattsville, MD; Morgantown, WV; Pittsburgh, PA; Research Triangle Park, NC; Puerto Rico; Spokane, WA; Washington, DC. 
d.  Each of these above listed government sites is just calling for a small group of 1 to 5+ ME/CFS patients and their families to stand in front, on the sidewalk, demanding to be heard -- even for just 15 minutes. Each head of security of each site will be mandated to let their national headquarters know that there was a person there that day, holding a sign in front, protesting HHS/CDC's policies and lack of funding for ME/CFS. Eventually, with enough mini-protests, this will impact U.S. health care policy.
e.  There may be special considerations in terms of where you can demonstrate at a government building. See section above called "Permits" for more info. 
Media outreach
a.  Send out a short but appealing press release. Could send to print, radio and TV media. Send it via email, and also call all local newspapers and radio (you could ask me for a sample press release I used in the past). Pitch to a variety of press/media, such as health reporters, living reporters, city desks. Simply call the newspaper's main number and ask who covers those beats/sections, and who is the editor of each section. Pitch to both the individual reporter and their boss, the section editor. 
b.  Try to pitch to reporters and editors "live" (via phone), or leave your animated pitch on their voicemail. In other words, don't just rely on emailing your pitch, but do email it, too.
c.  Make sure you have a compelling story. For example, I wrote: "For much of the past 20 years, I have been bedridden or homebound with an illness that 1 million Americans have, but that gets almost no government funding for research." And, "We are a mother and daughter team protesting together in hopes to secure funding for the sick daughter who has spent much of the past 20 years bedridden or homebound, along with almost 1 million other Americans."
d.  Have a local angle: Tell them you are from the area.
e.  Include in the press release why you are there protesting and what you want (e.g. more government funding for research into the causes of ME/CFS, and treatments and clinical trials now!).
f.  If you don't reach reporters (phone or email), keep trying up to 3 times. They are busy and I have sometimes gotten a "Yes, I'd like to write an article about this," on the 3rd try. After 3 tries, you may want to give up or be considered a pest and a bother -- which is, we know, not the end of the world. The squeaky wheel gets the most attention.
g.  Consider a teleconference. It is when you have a press conference via phone; the press calls in to ask questions of a panel of patients, family members, expert doctors or whomever you decide to have present. This will take some organizing and work.
h.  Remember: Once you do a media interview, or have the media present at your demo, you will have no control over what, in the end, they say or write about you and no control over the spin they give the piece. It could be positive or negative. And please know this one thing now, before your interview (if you do have one), they will likely misquote you; they almost always do. 
Invite others
You can reach out to other groups to invite them to join your demo. This is a big task. Plus, be ready for rejection.
a.  ADA groups
b.  HIV/AIDS
c.  Autism groups
d.  Compassionate healthies, like the local Rotary Club, women's sewing circle, etc.
Prepare a one-pager 
a.  Have a one-pager to give the government official you meet with -- or don’t get to meet with, but you will then leave the letter/one-pager for them at the front desk.
b.  The same or similar one pager can be given to passers-by (for educating the public), the press, and for mailing to the government officials later. Or write up a smaller, colorful card for passers-by.
c.  This same or similar one-pager can be your prepared speech, if you want to give one to the public, the press or videotape for a video.
d.  Include in the one-pager why you are there protesting and what you want (e.g. more government funding for research into the causes of ME/CFS, and treatments and clinical trials now!).
Banners/signs with compelling messages
a.  Not much to say here except be creative!
b.  Below is a link to how I made a 25 foot banner (I bought paints, paint brushes and a large bolt of cloth all at once, at a local fabric store). I knew I would not have a lot of people at my demo, but I still wanted to take up a lot of space and get a lot of attention -- hence the 25 foot banner.
Accommodating people with disabilities
a.  Consider doing what the wise organizers of the 2010 London protest did: organize vans to pick up folks from their homes and bring them to your demo.
b.  Consider having folding chairs, wheelchairs and cots there for folks to sit and rest. Decide if these wheelchairs and cots will be a good or bad thing in terms of PR (public relations) and the media.
Media drawing tactics
This was discussed already above, but once again, consider all media drawing tactics, and if you want to do them or not.
a.  Using a huge banner you make or have made.
b.  Die-in or lie-in with pillows and pajamas? (If so, be ready for risking arrest).
c.  Blocking doors (again, be ready for risking arrest).
d.  Disrupting a meeting with a government official.
Videotape 
Videotape your demo so that you can get it on YouTube and the ME/CFS community can see it and be inspired.
a.  If possible, have at least two video cameras (Flip cameras are cheap and easy to use) and two camera people, in case one camera fails or one person does not show up. Have a still-camera or phone, too, for still photos. 
b.  Videotape the images and audio you want. You will likely want to include your homemade signs but also the official sign that includes the actual name of the building you are in front of (e.g. Red Cross, HHS, CDC, any government name). Also, include in the video the people who came who have agreed to be videotaped, and your own prepared or spontaneous speech. Videotape the speech and all images at least twice, since audio or lighting or something will likely fail in one of them. I speak from experience.
c.  Edit the video to be less than 5 minutes long, and put it on YouTube.
d.  Send a link to the video to government officials and press.
e.  Contact any ME/CFS blogs or forums and ask if they want to post a link to your video.
Write up
a.  Write up a short description of the demo, written in your own words, and distribute it to the ME/CFS community. This will inspire others to go out and lead demos of their own.
b.  Include in your write-up a link to your video and to any media attention you got.
That is it! Remember, your demonstration will make a difference, it will have an impact. 

If not you, who? If not now, when?
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The below videos are related to my ME/CFS demos and activism in 2010-2011. I hope they may inspire others to demonstrate, too.
August 13-14, 2010
(5 min: Serious video of my one-women protest in front of Health and Human Services (HHS) and Red Cross Nat'l Headquarters. It was successful in that I was told this video inspired a bigger and more impressive patient demonstration in London:  http://www.youtube.com/watch?v=cdA4_feLkV4)
Description of HHS protest found here: 
September 6, 2010
(5 min: Comedic singing "Clinical trials now!" bedridden video with me and my family.)
October 3, 2010
(5 min: Comedic video pressuring the Nat'l Institutes of Health -- the resulting campaign was a success, but unfortunately it was stopped to early for significant results.)
November 29, 2010
(5 min: Comedic street theater video pressuring the Red Cross to ban ME/CFS blood donations -- the resulting campaign, which included a diverse group effort of a variety of tactics and approaches, not just mine, was a success.)
April/May 2011
(5 min: making the 25 foot banner for ME/CFS protests)
May 10, 2011
(5 min: I was told this was an historic, first-ever ME/CFS protest in front of the Dept of Health and Human Services in Washington DC, on Capitol Hill. ME/CFS patients from around USA)
Description of protest found here:
May 25, 2011
(6 min: Demo at Health and Human Services in San Fran, CA. ME/CFS patients from S.F.) 
Description of protest found here:

Wednesday, May 11, 2011

Protest!

It can be done!

My friend and fellow advocate Rivka organized a kick-ass mini-demonstration in front of the US Department of Health & Human Services on May 10, while the CFSAC met inside.  Watch her newest video, read her account, and consider doing your own mini-demonstration, especially during May Awareness Month!    

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ME/CFS Demo May 10, 2011 -- Dept of Health and Human Services, Washington DC
Contact: Rivka (at) ThatTakesOvaries (dot) org

On May 10, 2011, 6 individuals with ME/CFS, each sick and disabled from 9 to 21 years, demonstrated in front of the U.S. Department of Health and Human Services (HHS), 200 Independence Ave, S.W., Capitol Hill, Washington D.C. They carried with them just one sign, a 25 foot banner that read:

"Obama, Sebelius, HHS: Shame on you for abandoning 1 million sick and disabled Americans with ME/CFS and XMRV (Chronic Fatigue Syndrome and a newly discovered retrovirus). Clinical trials now!"

The representatives from the ME/CFS community were Kitty Lorenz, Karen Ravitz, Sharon Stapleton, Kat Stephens, a patient from New England, and the demo organizer, Rivka Solomon. They ranged from 21 to 70 years old and came from Connecticut, Massachusetts, North Carolina, Texas and Pennsylvania.

Around 2:15 pm, the demonstrators unfurled their banner in front of HHS's imposingly large building. They stood by the side of the street, thinking they were on what must constitute the public sidewalk, where, in most cases, people are allowed to partake in their civil rights to protest without arrest. However, it was hard to tell where the sidewalk was, given the design and layout of HHS's plaza. But it was a good guess, as the very traffic-y and thus noisy street, Independence Ave, was just a few steps behind the protesters. They choose not to position themselves across the street, on the opposite side of Independence Ave. By choosing to stay on the same side of the street as the HHS building itself, they knew they were taking more of a risk, since this would attract more police attention. The police that circulate around the vicinity of HHS include the Capitol Hill Police, the Washington DC Metropolitan Police, Homeland Security and of course the security for HHS itself. (Just before they started their protest, a cluster of 12+ cops were seen across the street. Later it was learned they were there for *another* nearby demonstration regarding abortion).

The ME/CFS demonstrators began filming themselves holding the banner and reading aloud a statement focusing on the plight of people living with ME/CFS. The statement included demands -- next steps they hoped the government would take. (Statement text found below.)

Within seconds, HHS Security came out of the building. At their peak, there were 7 members of HHS Security standing around watching the protest -- but they never approached the demonstrators. Instead they stood back about 50 feet, allowed the proceedings to continue until the protesters deemed their work done (i.e. the shooting of the video), a total of about 15 minutes. The resulting video can be seen here: http://www.youtube.com/watch?v=_elj8mcd9Ak

After the shooting, the demo organizer, Rivka, walked up to the first tier of HHS Security, the men who had been closest, to thank them for allowing the protest and videotaping to go on uninterrupted. The one plain clothed security official present in that tier (apparently plain clothed equals higher up in authority) grumbled something, and then he and all the other (uniformed) men pointed behind them to two women standing further away. Assuming they were the bosses, Rivka approached the two women and thanked them, too. One was a security officer in uniform, the other was plain clothed, and it was she who was head of security for HHS. The conversation went something like this:

Rivka: Thank you for letting us to protest here.

Head of HHS Security: (grumbling, shaking head, angry)

Rivka: It was legal, right? We were on the sidewalk.

Head of HHS Security: No. No --

Rivka: (interrupting) But I spent last week calling the Capitol Hill Police, Washington DC Metropolitan Police and Homeland Security, trying to find out who has jurisdiction over the sidewalk in front of HHS --

Head of HHS Security: (talking at the same time) No. No. No. We have jurisdiction.

Rivka: (interrupting) And I talked to Commander xxxx from Homeland Security  -- did he call you and tell you about us?

Head of HHS Security: No, he did not call.

Rivka: He said he wouldÅ ? Or I thought he said he'd let everyone know. I mean, uuuh, are you head of HHS Security? He told me your name (drawing a blank) --

Head of HHS Security: Yes, I am xxxx xxxx.

Rivka: (nervous, but realizing that actions speak louder than words, and they *had* allowed the demo to take place) -- and Homeland Security Commander xxxx said the Washington DC Metropolitan Police had jurisdiction over the sidewalk, but that we'd --

Head of HHS Security: (angry, shaking head) No, if you had been on the other side of Independence Ave, that would have been legal.

Rivka: -- that we'd be fine protesting on the sidewalk as long as we did not do anything too outrageous.

Head of HHS Security: Not here. You need a permit here.

Rivka: Oh. Well, we really appreciate it. We came from very far away --

Head of HHS Security: (still shaking her head, but maybe, slightly, warming a bit?) I know.

Rivka: -- and we're very sick. Will pay a price for doing this demonstration. Could be bedridden a long time after thisÅ 

Head of HHS Security: I know, we had to put out cots for those at the meeting. [She meant CFSAC, happening inside HHS that day.]

Rivka: Right. Exactly. Well, uh, thank you again, we appreciate it.

It was clear she had cut us some slack by allowing us to demonstrate uninterrupted and without a permit. Rivka walked back to the protesters packing up, then did an about-face and returned to hand the Head of HHS Security the protesters' informational one-pager (same as what was spoken into the video), asking her to give a copy to Sebelius, and adding, "Could you please tell Secretary Sebelius that this happened, that we were here today?"

"Oh, she'll be hearing all about this, all right."

BINGO! SUCCESS.

Goal #1 Mission Accomplished: Put Sebelius on notice that she is being impatiently watched by patients and their families. After years of her ignoring the CFSAC recommendations, after her refusals to meet with representatives from the ME/CFS community, she will now most definitely hear (from the head of her own security team) that we exist, that we were on her home turf, unfurling a 25 foot banner, demanding attention, respect, action.

Goal #2 of this demo: Inspire ME/CFS patients to make their voices heard in mini protests everywhere; to not wait for that elusive big demo to be organized by someone else, but to instead (for those who are able) get out in public and just do their own mini-demos around the U.S. and globe. Goal #2 will be accomplished, hopefully, by folks viewing this video of the HHS May 10th demo: 
 http://www.youtube.com/watch?v=_elj8mcd9Ak
A hearty "Thank you, you were amazing," to the HHS protesters. They were brave, ready for action, fun and quite photogenic individuals who signed on just days before, or the day of, the demo. At least 3 of the 5 are MCWPA volunteers.

A special thank you to Robert, a wonderful demo-collaborator who knows how to make a great banner (banner-making video:
http://www.youtube.com/watch?v=dcxtgyVuXYI )

The biggest thank you, however, is reserved for those who will take the next step, those who will hold their own mini-demos. It does make a difference, and it will have an impact. In the U.S., there are plenty of places to demonstrate:

- 10 HHS regional offices (http://www.hhs.gov/about/regionmap.html) in Boston, MA; New York; Philadelphia, PA; Atlanta, GA; Chicago, IL; Dallas, TX; Kansas City, KS; Denver, CO; San Francisco, CA; Seattle, WA.
- 10 CDC satellite offices in Anchorage, AK; Cincinnati, OH; Fort Collins, CO; Hyattsville, MD; Morgantown, WV; Pittsburgh, PA; Research Triangle Park, NC; Puerto Rico; Spokane, WA; Washington, DC

Each of these sites is calling for a small group of 1 to 5+ ME/CFS patients and their families to stand in front, on the sidewalk, demanding to be heard -- even for just 15 minutes. Each head of security of each site will be mandated to let their national headquarters know that there was a person there that day, holding a sign in front, protesting HHS/CDC's policies on ME/CFS. Eventually, with enough mini-protests, this will impact policy.

If not you, who? If not now, when?

If anyone wants to use our already made banner for their demo, we'll ship it to you.

==  Organizer's Costs Prepping for Demo (Money & Time) ==

1. Bolt of cloth (40 feet): $38.56
2. Red and black paint: $13.17
3. Paint brushes: $7.99
4. Popcorn for late night banner making: $3
5. Flight to Washington DC: $169.80
6. Taxi to Health and Human Services (HHS) demo: $31.10
7. Return trip Metro card: $3.40
8. Banner making: 2 wks.
9. Calls inquiring which police has jurisdiction over the sidewalk at HHS: 6 hrs.
10. Pitching to the media: 2 days. (Media that came: None).
11. Trying to get a 5 minute meeting with HHS's head of Public Affairs: 4 hours. (Minutes approved: None.)
12. Writing script/statement for the video; also served as the handout for the press (that did not come): Half a day.
13. Expected post-demo relapse (based on previous post-demo relapses): 6 wks in/near bed.
14. Influencing the U.S. government's ME/CFS policies and funding allocations: Priceless!


== Statement Read Aloud at Demo (and handed to HHS staff) ==

Why are we protesting at the Dept of Health and Human Services?
Advocating for people with ME/CFS -- Chronic Fatigue Syndrome
o  We are Americans who have spent much of the past 10-30 years bedridden and homebound with a severe disability that was given a belittling name by our government, Chronic Fatigue Syndrome (CFS).

o  Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is the full name of our illness.

o  It is an "invisible disability": We often look fine, but are severly disabled, many of us are unable to leave bed.
o  This belitting name, Chronic Fatigue Syndrome, sounds like we are "just tired" and thus it does not reflect the seriousness of our disease. But it certainly makes it easy for our government, medical community and media to dismiss and ignore those who suffer with it.
o  However, if you have ME/CFS it is not easy to ignore. It stops your life. We lose our ability to work, attend school or have a social life. Many of us are bedridden and using wheelchairs. Some of us have died early from leukemia, other cancers or health complications.

o  There are 1-4 million Americans with this illness --17 million people worldwide.

o  ME/CFS drains $18 billion to $23 billion annually from the US economy.

o  The US government, media and medical communities have delegitimized the illness and falsely psychologized patients.

o  This has resulted in very little federal money spent on research to discover the cause, treatments or cure of this illness.
o  Then, in 2009, there was a research breakthrough, and scientists found a retrovirus (called XMRV) linked to CFS. A retrovirus is a virus that never goes away (like HIV).

o  Still, the FDA has not banned people with ME/CFS from donating blood (the Red Cross has).
 Today, we are here protesting to demand that Obama and Sebelius (Dept of HHS):
- Protect the nation's blood supply: Ban peole with ME/CFS from donating blood.
- Fund research via Centers of Excellence just for this illness, including the Whittemore Peterson Institute (the lab that discovered XMRV's link to CFS).
- Fund fast-track clinical trials for treatments, medications.
- Act on the recommendations of CFSAC (the Chronic Fatigue Syndrome's Advisory Committee). They have ignored these recommendations for years, while patients and their families suffer with a devastating illness.