Julie and son Xander
Mark your calendars for Saturday, May 11th! As we start planning for the 2019 #Millions Missing rally, here’s a recap of last year’s event.
May 12th 2018 saw our first #MillionsMissing event. We held the rally at the state Capitol in Denver late morning to avoid a hot afternoon. So, of course, the morning started gray and drizzly. We had plastic sheets to cover our display boards and flyers on the tables.
The weather improved by the time our scheduled activities started. Several members told their stories about living with ME. Two people who were unable to attend sent their stories to be read by volunteers. Continue reading
We are thrilled to share this Letter to the HHS that Sen. Bennet, and Reps. DeGette, Perlmutter, Neguse and Crow sent to the HHS regarding the CFSAC (CFS Advisory Committee). The letter demands answers after the committee was disbanded. Please see below for how to thank them on social media.
Last year, over 40 members of Congress including 2 from Colorado, signed a letter to the HHS. Not content to just do that, the staff of Sen. Bennet worked with us to craft a Colorado-specific letter which was signed by 11 of us from MEAction CO plus Diane Bean from the Solve ME/CFS Initiative Board of Directors. Sen. Bennet’s office added a cover letter and contacted all Colorado Members of Congress to come up with support from 5 of them.
This comes as a direct result of your support for our advocacy. All your emails and calls truly made a difference in catching Congressional attention in a big way. Continue reading
Update as/of 1:25 pm Thursday March 1:
Unrest is still on for tomorrow but stay tuned for any last minute weather updates.
MEAction of Colorado is proud to present a screening of Unrest, a Sundance award-winning film by Jennifer Brea, with a panel discussion. Invite your friends, family, and doctors to join us!
The event will be held at 1:30 pm on March 2,2019 at the Co-Op at 1st at 5045 W 1st Ave, Denver, CO 80219-1005. Doors open at 1:00. Refreshments will be served after. Come early to check out the indoor farmer’s market! Continue reading
Kristen Aguirre from 9News Denver did a very nice segment on MEAction Colorado’s planned participation in the Womxn’s March providing some visibility that is greatly appreciated by those whose lives are so badly impacted by this ‘invisible disability’.
Group photo courtesy Tom Strobel
Our small but mighty team grew a little bigger with the addition of some last minute volunteers who braved the below freezing weather and helped represent those fighting ME who can’t physically make it through the march. Continue reading
Got some visibility for MEAction Colorado ahead of the March.
Pictures and story to follow.
UPDATE: Jan 15,2019 – Here is the updated map for the Womxn’s March showing our meeting place and the shorter, alternate ADA route that we will be following.
Raise ME awareness in a big way at the 3rd annual Women’s (Womxn’s) March!
We invite anyone with ME who is willing and able, to meet and walk the shorter ADA route, along with our healthy allies, friends and families who can push wheelchairs to represent the #pwME that we love who are too ill to participate.
In February 2018, MEActionCO started as a FaceBook group with a handful of members. With guidance from MEAction’s national team, we managed to organize and plan for the first Millions Missing event in Denver. As the group grew slowly to about 35 members we pulled together to organize the event.
May 12th – We pulled it off. It was a drizzly cool day at the state Capitol when we got together for the first time for a morning of speakers and live music and mutual support. We scored a little media coverage with stories about Pam and Nora. Continue reading
Biff Gore sings at IDA Gala
We would like to thank Lee-Anne Du Plooy of Highlands Ranch, CO for attending the 2018 Invisible Disabilities Association’s Award Gala. IDA was a proud supporter of us at the 2018 MillionsMissing. Their mission resonates with many PWME – not being believed about their disease simply because it’s not as visible as many other diseases. The organization promotes believing patients, disease awareness, education and connection for people with invisible disabilities. Two of their key missions are having invisible disabilities recognized by a new symbol that does not represent visible challenges only; as well as their “Cleaner Indoor Air Campaign” which strives to help so many of us with environmental sensitivities.
In addition to being a great fundraiser, the Gala featured live music, headlined by Biff Gore from Season 6 of The Voice, and many awards for activists of invisible diseases. The event was live streamed and I believe that videos of it will be made available at some point. Lee-Anne said she had a great seat up front and that the event was festive, uplifting and inspiring, with lots of good food, and that it was incredible to hear Biff up close like that. You can check out a recap of much of the night’s events at https://www.facebook.com/InvisibleDisabilities/videos/331493710731521/ .
Julie and John at office of US Rep Ken Buck
Recently we had meetings in the Colorado offices for Democratic Rep. DeGette and Republican Rep. Buck to discuss the situation with the disbanded CFSAC (Chronic Fatigue Syndrome Advisory Committee) and to start educating our Representatives’ offices about ME so that they will more readily ally with us on current and future requests.
We were there for these reasons:
- To educate them on ME and why it is important to support our cause
- To ask them to join forces with other Reps. who are in discussions with the HHS (Health & Human Services) on our behalf to find out why they got rid of the CFSAC
- To ask them to send this letter to a health committee asking for investigation into the ME/CFS health epidemic
- To be willing to support us with future ME legislation when it is introduced.
- Since DeGette is on that health committee, we asked her to use her role there to make sure that ME gets proper consideration and floor time.
As always, the people we talk to were friendly, willing to learn. Neither had heard of ME before, which highlights how critical the education and awareness component of these visits are. The people we met with were (as always) non-committal and agreed to discuss things with their colleagues in DC. I am cautiously optimistic that we’ll have support to one degree or another. We will be following up with them and see what if anything we need to do to push it forward with them.
Dan and John at office of US Rep Diana DeGette
We’ve taken care of visiting Reps. DeGette and Buck and have people in charge of Joe Neguse (running to replace Rep. Polis) and Rep. Perlmutter. We need someone to help with the other three districts. It is much easier than it seems and the volunteers from the other districts who have been through it can help you every step of the way. Please email firstname.lastname@example.org if you want to help, or contact me on FB or by PM. Everyone who has visited a Congress office has felt heard, validated and seen in a powerful way.
You can enter your zip code here to find your congressional representative. People with ME, loved ones, friends and allies are all welcome to help. The only qualification is that you should be in the district of the Representative you are helping to contact.
Note–I know that the name “CFS” is a hot button for many people and that some prefer names other than ME, but in talking with congress offices, we match the names that the members of Congress would be familiar with, thus the names CFSAC and ME/CFS.
Colorado #PWME Alison Sale was accepted into an ME study at the NIH, the “NIH Intramural Study on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.” Alison writes that “the criteria is very specific and I feel so lucky that I qualified and will have more answers soon.” The NIH will be covering all expenses including travel to Bethesda and a stipend and conducting many necessary tests and providing consultations with specialists.
The study took a lot of work to get into–for Alison it involved “submitting LOTS of records and sending them a list of every provider I have seen since several years before I got sick even including pediatricians,” and will no doubt take a lot of mental and physical energy during the study, but will absolutely be worth it to get some well-deserved answers for herself and to contribute to ME research.
As far as we know, the NIH is still accepting participants who qualify for their very specific criteria which are listed at the above link. There seem to be a few criteria groups, including healthy control group and Lyme Disease group, and some outpatient groups. The NIH website says, “The objective of this research study is to begin to understand the clinical and biological characteristics of ME/CFS.” The study seems to be very extensive and to be done by solid ME researchers.
Alison, we all thrilled for you and hope you get answers about how to improve your situation and we all appreciate the large effort you went through, and will be going through, in order to advance ME research! And perhaps there are others in our CO community who might check this out and see if they qualify as well.