The Scleroderma Foundation is a national nonprofit health organization dedicated to a three-fold mission of Support, Education, and Research to help fight this challenging autoimmune disease.
http://www.scleroderma.org/
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Scleroderma Foundation Home Page - Scleroderma Foundation | scleroderma.org Reviews
https://scleroderma.org
The Scleroderma Foundation is a national nonprofit health organization dedicated to a three-fold mission of Support, Education, and Research to help fight this challenging autoimmune disease.
scleroderma.org
What is scleroderma? - Scleroderma Foundation
http://www.scleroderma.org/site/PageNavigator/patients_whatis.html
Please leave this field empty. Patients and Newly Diagnosed. Learn More ›. Patients and Newly Diagnosed. Research and Treatment Centers. Find a Chapter/Support Group. Learn More ›. Find a Chapter/Support Group. Apply for a research grant. Learn More ›. Research and Treatment Centers. Find a Chapter/Support Group. Patients and Newly Diagnosed:. Please leave this field empty. Interactive Tool: Scleroderma and the Body. Gallery of Scleroderma Images. What scleroderma is not. How serious is scleroderma?
Scleroderma Foundation, Greater Chicago Chapter - Scleroderma Foundation
http://www.scleroderma.org/chicago
Patients and Newly Diagnosed. Cooking Up A Cure. Visit www.cookingupacurechicago.com. For more information and to purchase tickets. Walk Season is Here! Step out to cure scleroderma this summer! We cannot wait to walk with you! Patient Education October 15th. Join us at Northwestern on October 15th for the Patient Education Conference! You’re not alone - we’re here to help! Contact a support group leader to join. RSVP today! Follow us on the web! Please leave this field empty. Board Members and Staff.
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Omaha Heenans: November 2009
http://omahaheenans.blogspot.com/2009_11_01_archive.html
Saturday, November 14, 2009. The Goddaughters November visit. Our Goddaughters spent a week with us in November. It was quite a week that kept us running. They help cheer for the Hawkeyes between naps and playing! Barb is checking Facebook and email as Kate rest for a bit. We made several trips to the park and gave the swings a workout. Also a couple of trips to Skatedaze and the BIG playland inside. Always happy after a good nights sleep. Michael and Barbara Jo Heenan. Subscribe to: Posts (Atom).
Omaha Heenans: Spring Update
http://omahaheenans.blogspot.com/2010/05/spring-update.html
Sunday, May 16, 2010. Well hello to everyone. I just realized that not everyone is on facebook so I probably should send out an update on the Omaha Heenan's. I have limited pictures as I am away for training for the FAA in Oklahoma city. I brought Hagen with me this time and it seems to help. As you can see , he appears to be a bird dog although he is finding birds bigger than himself. Michael and Barbara Jo Heenan. Subscribe to: Post Comments (Atom). Omaha Scleroderma Support Group. Promote Your Page Too.
Helpful Links
http://www.ncacmd.com/index.php/helpful-links
Northern California Arthritis Center. American college of Rheumatology. Lupus Foundation of America. The Lupus Foundation of Northern California. Spondylitis Association of America. National Sjogren’s Syndrome Foundation. San Francisco Bay Area Scleroderma Support Group. Myositis Association of America. National Library of Medicine. National Institute of Arthritis and Musculoskeletal and Skin Diseases. National Institute on Aging. Centers for Disease Control and Prevention. National Library of Medicine.
Links | MARC - Mid-America Rheumatology Consultants, P.A.
http://www.marckc.com/helpful-links.htm
5701 West 119th Street, Building C, Suite 209. Overland Park, KS 66211. American College of Rheumatology. Http:/ www.rheumatology.org/. Kansas City Office: http:/ www.arthritis.org/kansas/. National Office: http:/ www.arthritis.org/. Lupus Foundation of America. Kansas: http:/ www.lupus.org/kansas/. National: http:/ www.lupus.org/. Http:/ www.myositis.org/. National Institute of Arthritis and Musculoskeletal. Http:/ www.niams.nih.gov/Health Info/. Psoriatic Arthritis - National Psoriasis Foundation.
VICTORIA'S MIRACLE: January 2011
http://victoriasmiracle.blogspot.com/2011_01_01_archive.html
DIARY OF A STEM CELL TRANSPLANT. Friday, January 28, 2011. I hope you're having a good day too. Saturday, January 22, 2011. Blip in the Road. Subscribe to: Posts (Atom). Bob and I (post-transplant). Victoria by the Pond, August 2008. Happy Mother's Day, Mom," by Gaby. Some of my angels. The Field Museum, Chicago. Walk Along Lake Michigan. How to Reach Victoria. National Foundation for Transplants. Dr Richard K. Burt. Not the ending, but happiness to report (follow-up article on Victoria Chavez). Please m...
Scleroderma Blog: June 2010
http://sclerodermablog.blogspot.com/2010_06_01_archive.html
Scleroderma is a chronic autoimmune disorder that can cause tightening and thickening of the skin, thickening of blood vessels, and damage to internal organs. Sunday, June 13, 2010. Off Cellcept for 6 Months. When the weather has been warm/hot, I can't get enough of the heat. We've had a few real hot days and while everyone else (my wife included) complains, I'm just loving it! I head back to see Dr Wigley in just over a month and will report back then. Enjoy the start of the summer. Subscribe in a reader.
Links of Interest - Scleroderma Association of Manitoba
http://www.sclerodermamanitoba.com/links-of-interest.html
SAM'S Blog and Announcements. News, Calendar and Photos. Presentations, Education and Research. First Annual Walk/Run - Wrap Up. Scleroderma Conference 2014 - Wrap Up. Scleroderma Conference 2014 - Wrap Up. 2014 Conference Program and Presentations. The Scleroderma Society of Canada. The Scleroderma Association of BC. The Scleroderma Association of Saskatchewan. The Scleroderma Society of Ontario. The Scleroderma Society of Quebec. The Scleroderma Patient-centered Intervention Network (SPIN). Presentatio...
VICTORIA'S MIRACLE: July 2010
http://victoriasmiracle.blogspot.com/2010_07_01_archive.html
DIARY OF A STEM CELL TRANSPLANT. Monday, July 26, 2010. Scleroderma Support Group Summer Party. It has helped me so much to volunteer, to get outside myself and focus my concern on the needs of others with this disease. I am a lucky one. To have had the opportunity to have a stem cell transplant which saved my life is how I was blessed. I am forever grateful to the Foundation for being there for me. National Scleroderma Foundation Conference. Again I would like to thank everyone for their support. Sacram...
VICTORIA'S MIRACLE: October 2009
http://victoriasmiracle.blogspot.com/2009_10_01_archive.html
DIARY OF A STEM CELL TRANSPLANT. Sunday, October 11, 2009. Yesterday Bob and I and Karin and Sheldon went to the Sacramento State Football Game.we won! It was a great fall day! Also, My daughter, Gaby, went to her boyfriend, Phil's, homecoming dance. As you can see I'm out and about so there may not be as many updates before. This is a good thing! Saturday, October 3, 2009. Hey, I'm back! Yesterday, I gave my best friend a ride to a very important interview and she got the job on the spot! I love life,.
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scleroderma.com.au - This domain may be for sale!
Find the best information and most relevant links on all topics related to scleroderma.com.au. This domain may be for sale!
The Scleroderma Blog
Is a group blog to which anyone can contribute. Write about your personal experiences, submit interesting links, or just vent! No need to register or give out personal information! To post an entry. Wednesday, Jan 24, 2007. Visit the submit page. Posted by staff writer Filed under:. Of all posts in this blog. Scleroderma: The Proven Therapy that Can Save Your Life. November 25, 2003. November 10, 2003. November 1, 2003. Is part of the. Child and Teen Health. A Journey Through Life. Eat Smart, Stay Fit.
scleroderma.net - This domain may be for sale!
Scleroderma.net has been informing visitors about topics such as Scleroderma, Symptoms of Scleroderma and Systemic Arthritis. Join thousands of satisfied visitors who discovered Treatment for Arthritis Pain, Treatment for Scleroderma and Rheumatoid Arthritis Treatment. This domain may be for sale!
Home : Scleroderma Program: Feinberg School of Medicine: Northwestern University
Northwestern University Feinberg School of Medicine. Northwestern University Feinberg School of Medicine. 675 N St Clair. Chicago, IL 60611. Research Faculty and Staff. Learn more about our mission and goals; connect with us. Learn more about our mission and goals; connect with us. Learn about Northwestern Scleroderma Program's innovations and successes. Learn about Northwestern Scleroderma Program's innovations and successes. 13th Annual Stepping Out to Cure Scleroderma Walk. 2015 Northwestern Scleroder...
Scleroderma Foundation Home Page - Scleroderma Foundation
Patients and Newly Diagnosed. Learn More ›. Patients and Newly Diagnosed. Research and Treatment Centers. Learn More ›. Apply for a research grant. Learn More ›. Research and Treatment Centers. Free online continuing education program "The Lung in Scleroderma" - just for health care professionals! Click here to learn more. PLEASE CONTACT YOUR SENATORS. Click here to send a letter. Meet the Faces of Scleroderma. Locate Local Chapters and Resources. Find a Support Group. Can’t download It? Get more news he...
Welcome to Scleroderma Queensland
Supporting sufferers of Raynaud's Phenomenon, Sjogrens Syndrome and other auto immune diseases. Understanding and Managing Scleroderma. Research Update June 2008. Dr Luke Garske's Presentation. Dr Judith Greer's Presentation. Carol's Story - Raynaud's. Brayden's Story - Morphea. Aust Rheumatology Assoc Meeting. AGM Scleroderma Australia 2008. Support Group Dates 2015. Chronic Conditions Self Management. Charity Golf Day 2010. New Office Opening Day. Welcome to Scleroderma Queensland Aust. IMPORTANT NOTIC...
Scleroderma | New Zealand Support Group
Scleroderma New Zealand Inc. See how others are coping Contact Us. The scleroderma support groups exists to help those suffering the disease and welcomes participation by anyone who has contracted it or who has a friend’s or family connection to it. Scleroderma US Ann Conf. We are based in Lower Hutt / Wellington, New Zealand but welcome participation regardless of geographical location. Wordpress development by Netco NZ Ltd.
Scleroderma
It is a chronic (long-standing) connective tissue, autoimmune condition in the rheumatic group of diseases. Scleroderma is from the Greek ‘sclero’ meaning hard and ‘derma’, skin. Hardening of the skin is a visible characteristic of scleroderma and its over-production of collagen though it can affect internal organs too. Diffuse Cutaneous Systemic Sclerosis;. Limited Cutaneous Systemic Sclerosis;. Localised or linear scleroderma and morphea (patches/plaques on the skin) are similar conditions, referred to...
scleroderma.researchstudyinfo.com
Bipolar I Depression Research Study
For more information,. Info on Clinical Research. Info on Clinical Research. Intedanib in Systemic SC. Clinical Research Study for. Scleroderma with Interstitial Lung. We all have reasons to keep fighting Scleroderma Lung Disease. If you have been diagnosed with Systemic Sclerosis with Interstitial Lung Disease (SSc-ILD), you could be eligible to participate in SENSCIS. A clinical research study of an investigational drug for SSc-ILD called nintedanib. To pre-qualify for this study, you must:. Have you b...
Сайт о склеродермии.
Загрузка. Пожалуйста, подождите. Check if on a shared computer. Спаси себя, и вокруг тебя спасутся тысячи. Поверить в себя может каждый. At 13-06-2013, 13:33. Никогда раньше мне не приходилось задумываться над тем, что у любого человека есть свой предел прочности. Преодолев который, он вдруг начинает болеть. Болезнь оказывается, как правило, трудно излечимой , или вообще не поддаётся никакому лечению. Начались походы по врачам…. Можно возразить : «Ну как же! Raquo; И что? У вас на это хватает энергии?
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