Pronounced "I Am", as in "I am an advocate for those affected by primary joint diseases with an autoimmune component."

In the News!


IAAM WINS Best Ensemble Cast, WEGO Health Advocacy Awards
April 2013

This award nomination means the world to our organization, because we are 100% led by those affected by our diseases and we come together from all corners of the globe to make changes for our community.  From the newest volunteer to the CEO we are are equal.  Volunteers are officially trained for 3 month courses, and after graduation they are able to not only work on programs but help to CREATE those very same programs that will eventually benefit themselves and those they know affected by these diseases.  IAAM calls themselves a "team" and a "family" over volunteers because together they are moving mountains and changing the way the world views these diseases.

But IAAM has a Volunteer on board who is also up for two additional awards!  Niki Wyre, Founder of RA Chicks, was a finalist for both the Advocating for Another and Unsung Hero Award.  Niki, we are proud of you and your work and even more proud to call you part of our family!






New Zealand Volunteer Speaks Out on Rheumatoid Arthritis
February 2013


Sarah Clark, Founder of the Young Arthritics of New Zealand support group and active IAAM Volunteer, was featured in an article about her life with Rheumatoid Arthritis and dealing with a lack of understanding and awareness- especially diagnosed as a young adult.  Way to go, Sarah!  Keep on spreading the word! 

To read the full article, please view it here: http://www.niceties.co.nz/2013/02/magazine.html


IAAM Members Selected Clinical Trial Review Teams
February 2013


Founders Tiffany Westrich & Tami Brown were both chosen as potential 2013 Clinical Trial Reviewers for PCORI (Patient Centered Outcomes Research Institute), enabling them to work on assessing, rating, and critiquing clinical trial applications in the realm of arthritis and autoimmune diseases. 

In addition, Ms. Westrich was additionally asked to serve as an Ad Hoc Reviewer with NIAMS- the arthritis sector of the US National Institutes of Health. She is only one of two reviewers selected for this first year of incorporating patients into the review process.  "I am simply thrilled to have the opportunity to work hand in hand with NIAMS.  I was fortunate enough to meet two of the lead scientists back in 2012 and now to be able to go back and review cases that could potentially cross through that same lab where so much has already been done to help those with Autoimmune Arthritis diseases? Amazing."



IAAM Founders & Volunteers Head to D.C.
September 2012


Above: Dana Morningstar, Jenn Starzynski, Tiffany Westrich, Tami Brown, Wendy Koski, Therese Freeman Humphrey, Amanda John, Kelly Conway

While IAAM has visited Washington D.C. on several occasions, this trip was special, for many reasons.  To start, it was the first time this many IAAM'ers were together in person.  Our organization runs 95% virtually so spending face to face time with one another was an amazing bonding experience.  So why were so many IAAM'ers in D.C.? 
This trip was two-fold.  Dana, Jenn, Tami, Wendy, and Therese were traveling with the American College of Rheumatology (ACR) as patient advocates.  Tiffany, Amanda, and Kelly were heading to the capitol to join the others for an invited tour of the National Institute of Health and a personal tour of the NIAMS labs, led by lead US scientists Dr. O'Shea and Dr. Seigel.  IAAM'ers were honored to meet such industry change makers and to see first hand how their research directly affects those living with Autoimmune Arthritis diseases.  NIAMS and IAAM are currently discussing working together to create Medical Education materials for both patients and for practitioners, combining scientific language with a patient perspective.



Two New Members Selected for the NIAMS Coalition; IAAM accepted into AARDA's National Coalition of Patient Autoimmune Groups
August 2012

Two of IAAM's Founders, Tami Brown and Tiffany Westrich, have been accepted into the NIAMS Coalition, a group of professional and voluntary organizations concerned with the programs of the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS).  The group meets, typically virtually, to discuss issues and share ideas for advocacy and making a difference is the lives of those affected by arthritis diseases. 

In addition to the NIAMS Coalition, IAAM has also been inducted into the NCPAG through the American Autoimmune and Related Diseases Association, the leading 501c3 nonprofit in the US who advocates for all autoimmune diseases. 



IAAM's CEO Joins Clinical Trial Review Panel
August 2012

IAAM's CEO, Tiffany Westrich, was selected to be a part of the American Institute of Biological Sciences research panel, alongside doctors and researchers.  The panel convened in Virginia, USA, where they spent three days reviewing and analyzing clinical trial submissions.  The group assessed proposals then discussed the pros and cons of each application; the overall goal was to rate the potential effectiveness both medically and from a patient perspective.  "The experience of reviewing future scientific suggestions that may potentially benefit myself and other Autoimmune Arthritis diseases, then offer my professional opinions in regards to its' need within our community, was simply outstanding," states Ms. Westrich.  "I look forward to working more with AIBS and clinical trial review panels!"


IAAM Establishes World AUTOIMMUNE Arthritis Day (WAAD)- A Day to Differentiate Autoimmune Arthritis Diseases through Awareness & Educational Resources
May 2012

The first World Autoimmune Arthritis Day, running from May 19th 2012 at 6am ET/USA through May 21st at 5am ET/USA, exceeding it's reach of attendees around the globe, with over 4,000 Virtual Convention visitors from the United States, Canada, Guam, the UK, Ireland, Scotland, Italy, Spain, Japan, India, Pakistan, New Zealand, Switzerland and Australia.  This event included 12 On Demand Presentations and 3 Live Presentations, 3 Live Chat Sessions (all held by Patient Experts), a Chat Room (the "Lounge") where others could communicate in real time, Surveys, 7 Live "WAAM's!" (World Autoimmune Arthritis Messages, or scheduled Awareness Posters that can be shared around the world at the same time),  and a Resource Center filled with downloadable articles provided by nonprofits, doctors and patient bloggers. 
18 nonprofits around the world signed up to support the event, in addition to support from World Arthritis Day, an annual event hosted on October 12th of each year.  In addition, WAAD is listed on over two dozen health calendars internationally.
Moving forward World Autoimmune Arthritis Day (WAAD) and World Arthritis Day (WAD) will bridge forces and aim to collaborate in future years as a way to provide awareness for these diseases year around.  
Please visit the official WAAD website at  www.WorldAutoimmuneArthritisDay.org, join us on Facebook at www.facebook.com/WorldAutoimmuneArthritisDay and follow us on Twitter at www.twitter.com/WAutoimmuneAD !


You can visit World Arthritis Day at www.WorldArthritisDay.org .


IAAM's Media Awareness Hotline Helps Spur Retraction from 
Dr. Phil- Obesity is not a precursor to Autoimmune Arthritis
October 2011

On September 23rd's episode of "Overweight or Underfed", Dr. Phil McGraw made a statement suggesting that 'childhood obesity could lead to adult diseases like Rheumatoid Arthritis'.  Rheumatoid Arthritis is an autoimmune disease that affects the joints, connective and soft tissues, and sometimes organs.  It is caused by a faulty immune system, influenced by genetics and/or environmental influences.  Osteoarthritis, otherwise known as "arthritis", is degenerative and only affects the weight bearing joints.  It is caused by age, wear and tear or injury.  This is the type of arthritis that can be caused by weight putting excessive stress on the joints.

Immediately following this broadcast, IAAM put a Call to Action in motion, reaching out to the Autoimmune Arthritis world to reach a minimum of 500 letters requesting a retraction.  Volunteers worked diligently for 3 days, emailing, posting on social media sites and asking bloggers to get the word out to the community.  The following week, after learning of this grassroots campaign, MyRACentral contacted IAAM to feature in an article that was to be published about this subject on the morning of World Arthritis Day 2011.  That morning IAAM was contacted with information that the article would not be published due to a retraction agreement that would be posted later that day on Dr. Phil's official blog.  A combination of factors, including IAAM's mission to involve the public, brought a resolve to this matter.  Thank you, Dr. Phil...we applaud you!



IAAM Leaders Selected for the American College of Rheumatology's Capitol Hill Fly-in
September 2011
On September 20-21st, Tiffany Westrich, Founder and CEO, Tami Caskey Brown, Co-Founder, and Katie Emmerson, Volunteer, for the second year in a row, headed to Washington DC as selected Patient Advocates for the American College of Rheumatology.  Their participation will help to educate Congress on the value of the rheumatology subspecialty and the impact arthritis and rheumatic conditions have on ones' quality of life.  Each IAAM representative was partnered with a rheumatologist and other medical professionals, spending the day on Capitol Hill where they met with members of Congress from their individual states. 

IAAM will continue the contact with the representatives in their own jurisdictions, providing information that can be helpful in understanding the needs of Autoimmune Arthritis Patients.  In addition, Katie has started an initiative to feature patient story a month, complete with profile and interview, in order to assist in understanding the effect of these diseases.  IAAM will be sponsoring this program under our Awareness umbrella.




IAAM Becomes an Official 501c3 Nonprofit!
May 2011

What started as a sole declaration of awareness in the living room of a small apartment in Los Angeles, CA, has officially become a nonprofit!  In 2009 a "movement" began, with four major goals in mind- to create an organization that grouped together a very specific strand of diseases, all with similar symptoms, onset, and treatment options.  The idea was to create a bridge of like diseases, so that awareness may finally come to fruition.  Until IAAM, the "Autoimmune Arthritis diseases", as they were coined, were either represented in organizations that catered to the masses or were included under the umbrella of very specific conditions.  Now there is a bridge that focuses on those that are most similar, even though they may not necessarily come from the same disease family.  The mission is simple- bring this small group of like diseases together in order to promote stronger awareness, address wellness options for a primarily younger onset, become a hub to unite all different nonprofits under one umbrella, and create a platform where the volunteer can become the leader.  There is still work to do, but we are on our way!



  

 

 

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