Advocates on Steps of Congress 2013
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Scleroderma Approved For DOD Funding for FY17
Staying Alive with Scleroderma
Our mission of support, education and research would not be possible without you
Winter - 2016 Angie and Al Crowl
Change
SCLERODERMA FOUNDATION EARNS COVETED 4-STAR RATING FROM CHARITY NAVIGATOR
Summer 2016 - Linda Baum
Persons with systemic sclerosis needed for research study to evaluate an internet self- management program
Meet Carly Bankovich
Still Blessed
From Scleroderma Patient to Published Author in Scleroderma
Lauren Beeson
Scleroderma Foundation Announces New National Board Members
Kate Hannon: Good Enough is the New Perfect
Ava and Ilene Nusblatt
Scleroderma Foundation CEO Appointed Co-Chair of Independent Coalition
National Staff Attends BBCON
Vancouver 12-year-old Battling Scleroderma
Q&A with Alexis Schwei
Joyce Roby-Washington Sees Beauty Come from Ashes with the Help of her Husband, Kim
A REASON TO FIGHT SCLERODERMA
Rapid Skin Improvement Seen after Treating Systemic Sclerosis Patients with Fresolimumab
Living with linear scleroderma en coupe de sabre
My sister has scleroderma
Mother's Day
Eric Goldstein: LEARN! LISTEN! LIVE OUT LOUD!
Q&A with KK Greer, Founder of Wristies
South Florida Laughs Out Loud to Support Scleroderma
McCoy Penland: A Source of Strength for Her Family
Pope Francis Visit with Third Systemic Sclerosis World Congress Participants
New Investigator Conference Nurtures Next Generation Scleroderma Researchers
Be Part of the #GivingTuesday Movement
Hard Word. Harder Disease.
Tune-in to "The Queen Latifah Show" Tomorrow
Tubey in Her Tummy
Scleroderma and Oral Healthcare
Sideline Spouses
Scleroderma Foundation of Southern California and Greater San Diego Chapter Merge to Enhance Support and Education
My Voice: Hannah Weber
JoAnna Harper
A Salute to Service and Dedication in the Scleroderma Community
Southern California to Host Life-Changing Educational Event for Individuals with Mysterious and Disabling Disease
Diagnosed at Age 67
The Face of Systemic Scleroderma
Scleroderma
Memory
Family, Friends and Foundation
My Mom, Margarita Herrada
I Was Certain That I'd Never Play Guitar Again
My Scleroderma Story
Then and Now
I've Lived with Scleroderma for 20 Years
My Music is My Therapy
I Have Learned to Be the Best I Can Be
Purple Feet
Resilience and Regularity
Surviving Scleroderma
Hi, my name is Diana Cortes and I have scleroderma
You Think it Won't be You
North American Agencies Partner During National Scleroderma Awareness Month to Grow "Know" Community
Diagnosed With Scleroderma a Year Ago
Help Share About Scleroderma
Cruise for a Cure 2012 (Video)
I Try to Not Let Scleroderma Be the Thing That Defines Me
What's this?
A life-changing journey
Put an End to "Sclero-What" During June's Scleroderma Awareness Month
The struggle is over..Heaven's New Angel-My Sister
I Suffer From Scleroderma - My Selfie
Scleroderma & Me
Scleroderma - My Journey
Diagnosed with Scleroderma Pulmonary Fibrosis
A JEWEL IS LOST... a Remembrance
Tej's Story
Dr. Kathryn Torok: Helping Kids Live Better Lives with Scleroderma
Study Could Lead to New Treatments for Tissue Scarring
Antonietta's Story
My Battle With Scleroderma
Pope Francis Prays for People with Scleroderma
Living With Scleroderma: Joy Bobo
My Voice - Q&A With Ashton Cooper
Taking Control: Joy Bobo
Scientific Peer Review of Department of Defense Medical Research Program
My father ... My angel
[Infographic] A Look Back at Scleroderma Online Communities in 2013
Scleroderma Foundation, ATS Award $80,000 to Dr. Cecilia Sanchez for Scleroderma Research
Elie's Story
Hope Raisers: Kim Brooks
Grace Meihaus
From the Heartland: Jackie Latka
FDA Approves Bayer's New Class of Drug to Treeat Adults with PAH
Consensus Guidelines Published on Screening for PAH in Systemic Sclerosis
Voices Ring through Halls of Congress on Historic Day
Calling All Kids!
The Foundation Maintains Its Leadership in Young Investigators' Research
New Study Published About PAH in Connective-Tissue Disease
Data is Promising for New PAH Therapy
Eric Priest: Evolving from High School to Dorm Room
Second Annual Sclerodoodle Contest Winner: Erin Thomas
Donna Stone Named 2013 Support Group Volunteer of the Year!
Missouri Chapter President Honored with Lifetime Achievement Award
A Salute to Achievements in the Scleroderma Community
Scleroderma Community Gathers for Unique Conference Event in Atlanta
Scleroderma Spot to Air on 61,000 Airline Flights
My Mother's Story
Recognizing World Scleroderma Day, June 29
International Patient Advocacy Groups Mark "World Scleroderma Day," June 29
Scleroderma Awareness Month and World Scleroderma Day
Staying Strong
Tough Skin
Me & Scleroderma
A Daughter's Experience
Mysterious Symptoms
Message to the State for our service members
There is Hope
My Father, My Hero
American Thoracic Society Recognizes Scleroderma Foundation Collaboration
Digital Billboard to Appear in Seven States for Scleroderma Awareness Month
Scleroderma Awareness
Join the Fight to Spread Scleroderma Awareness in June
Living with Scleroderma
New Interactive Tool Illustrates How Autoimmune Disease Affects the Body
Betsy Craig: A Roaring Spirit
My Voice - Ani Lund
And the Winner of the Sclerodoodles Contest Is...Erin Thomas!
Rachelle's Story
SURVIVIOR
My name is Lenora
Retired teacher not stopping after double transplant
Struggling forward
My Mom Living with Scleroderma
The Journey
Enter the Second Annual Sclerodoodle Contest!
My Life with Scleroderma
A Twist on "Girlfriends Weekend"
The Journey of Rosa Johnson
New Scleroderma Awareness Video Focuses on a Patient's Perspective
Always Hopeful
How Can I Accurately Measure My Blood Pressure at Home
SF Partners with American Thoracic Society for Research Grant
U.S. Department of Defense Funds Two Scleroderma Research Projects
What's Up Doc? Flu and Oral Health
Golf Tournament to Raise Awareness of Autoimmune Disease
My life with Scleroderma
NeedyMeds
2013 Research Grant Recipients Announced by Foundation
Tips On Minimizing Holiday Stress
Foundation Attends 2012 American College of Rheumatology Conference
Scleroderma Tweet Chat Co-Hosted by Treatment Diaries
Maureen's Story
Children and Parents Needed For Study
2nd Annual U.S. Conference on Rare Diseases & Orphan Products
Scleroderma.org Wins Prestigious Award
Profile on John Keegan
Q&A: Jacqueline Valdez
Scleroderma
Save the Date: Wednesday, Nov. 14, 2012 is Congressional Call-In Day
My Mom
Scleroderma Foundation Announces New Heartland Chapter
I have Scleroderma
The National Conference In My Own Words
Q&A: Dr. Carol Feghali-Bostwick
Mom
My experience
Holly's Story
Writing Through Scleroderma
Heidy's Story
Amy's Story
Liz's Story: My Second Chance
Faces of Scleroderma: Erica and Emily
Faces of Scleroderma: Dr. Giuseppina Alessandra Farina
Faces of Scleroderma: Cynthia Maxwell
Ken Athans: Taking Control and Finding Answers
My Voice: Courtney Shatley
Caroline Clemens: A Scleroderma Story
My Voice: Ellie Brawdy
Ray Woolf: Trekking With Scleroderma
Hannah Tibtani: Hurdling Scleroderma
Amber Paris: Not Alone in the Lone Star State
My Voice: Caroline Dziel
My Voice: Brittney Berkey
The Five Rules: Abbye Gorin's Advice for Living with Scleroderma
Q&A: Bianca Podesta, Ph.D., author
Q&A: Billy Smith, Scholarship Recipient
Q&A: Ansley Lesley
Supreme Court Upholds Affordable Health Care Act
Scleroderma and the Modern C.I.C
Sclero and I
Scleroderma Patient Crafts Honor Veterans and Stress Outlet
MY DAY ON CAPITOL HILL
Scleroderma Blessings
Sclero-What??
Scleroderma's Not SO Bad
Promising New Research May Have Impact on Scleroderma Population
Scleroderma Summer
Scleroderma isn't my name
Scleroderma Sun and Storm
There is HOPE!
She flies with her own wings.
Strength through adversity
Scleroderma "Always Have Hope"
The Wolf
We have nothing to lose but all to gain for trying
Scleroderma- another challenge I WILL overcome.
Two Halves
The Lord is in control...living with Scleroderma
Solo Cyclist to Trek 4,700 Miles in Honor of Father Who Died of Rare Disease
Scleroderma Foundation Launches Unique Video Campaign Today
Scleroderma Advocates Take Innovative Approach to Awareness
Scleroderma Foundation Increases Research Awards in 2012
Scleroderma Foundation Names University of Michigan Physician and Researcher as "Doctor of the Year"
Tackling an Ironman: Racing to Raise Awareness for Rare Disease
Hundreds Expected for 13th Annual Scleroderma Patient Education Conference
June is Scleroderma Awareness Month
Scleroderma Foundation Announces New Chapter in State of Georgia
Scleroderma Foundation names Greg Marion to Board of Directors
Scleroderma Foundation awards six research grants for 2011