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Scleroderma:     more books (100)

Scleroderma: The Proven Therapy that Can Save Your Life by Henry Scammell, 2003-11-25 The First Year: Scleroderma: An Essential Guide for the Newly Diagnosed (The First Year Series) by Karen Gottesman, 2004-01-05 The Scleroderma Book: A Guide for Patients and Families by Maureen D. Mayes M.D., 2005-05-01 Medifocus Guidebook on: Scleroderma by Medifocus.com Inc., 2010-04-21 Voices of Scleroderma (Volume 3) by International Scleroderma Network, 2006-01-17 The Scleroderma Book: A Guide for Patients and Families by Maureen D. Mayes, 1999-07-15 Voices of Scleroderma Volume 1 by International Scleroderma Network, 2003-05-13 A Journey Towards Health ... Reversing Scleroderma by Jane M. Parker, Victor Dyment, 2005-07-29 The Official Patient's Sourcebook on Scleroderma by James N. Parker, Icon Health Publications, 2002-08-26 Scleroderma: A New Role For Patients and Families by Michael Brown, 2002-03 The Scleroderma Book: A Guide for Patients and Families by Maureen D. Mayes M.D., 2005-05-01 Fiddler's Daughter: Living with Scleroderma (Volume 1) by Clauda (Martin) Lavertu, 2010-06-06 Scleroderma: Types, Diagnosis and Treatment by Jack Earl, 2009-06-09 Scleroderma - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-03-12

lists with details

1. The Scleroderma Research Foundation
   Information about the organization, research, mailing list and resources.  
   http://www.srfcure.org/

2. Raynauds & Scleroderma Association
   Information about the organization, contact information, publications and the latest research.  
   http://www.raynauds.demon.co.uk/

3. Scleroderma Foundation - Home Page
   National nonprofit health organization with 14000 members, dedicated to a three-fold mission of support, Category Health Conditions and Diseases sclerodermaThe scleroderma Foundation is a national nonprofit health organization dedicatedto a threefold mission of Support, Education, and Research to help fight this  
   http://www.scleroderma.org/
   
   Extractions: Email Your Questions Get a Free Info Packet Check Our Calendar Read About Our Magazine ... Click here to watch our "Living Well with Scleroderma" video We are grateful for your tax-deductible contribution to help fight scleroderma. Where your dollars go . Membership dues are $25/year. Details Our 2003 National Conference Chat Host: Carolyn Weller, R.N., National Director of Education and Research Our next Chat will be Wed., April 9, and will be an open chat (no speaker). The start time will be 9:30 p.m. Eastern Time. When it is time, click here to join the Chat or learn more about our twice-monthly online Chats. Read transcripts of earlier Chats.

4. Surviving Scleroderma - Scleroderma Support
   Click here to tell someone about this site! scleroderma. GOD WILL PROTECT ME  
   http://www.sclerodermasupport.com/
   
   Extractions: Read Site Go To Top Return Home Since 1996 our webmaster , site volunteers and caring participants of our interactive areas have remained dedicated to the mission of bringing scleroderma related medical information, current news and online support to the vast internet public. Scleroderma knows no boundaries, view a list of some of the countries our visitors are from. We hope you find what you need here. If we can be of assistance to you in any way please don't hesitate to contact us. Check It Out! New Discussions in our Message Board Community. New Entries in the Coffeehouse you can also Add Yours Read Stories From Others. Share Yours Scleroderma News Briefs For a complete listing of news articles visit our newsroom pages for: Scleroderma Medical Scleroderma in the Media Upcoming Events The Nonprofit Buzz ... SurvivingSD Website Event Alert: Updated Often Are you planning to attend the scleroderma foundation's conference in June of 2003? Visit our

5. I HAVE SCLERODERMA
   Collection of stories from people with this condition. Provides links, general information and contact numbers. Angela I am 24 both my parents (44 and 48) have scleroderma and raynauds syndrome.  
   http://www.ihavescleroderma.com/
   
   Extractions: Diffuse stories: Angela April I think I found the right cardiologist and a doctor that is VERY good in his field. Eileen So far it hasn't been too painful, but it is progressing fast. CREST/Limited story: Jenn My doctor diagnosed me with an overlapping connective tissue disorder of lupus and scleroderma. Linda I am still not back to work but hopefully one day that will happen. Morphea/linear stories Marie It started with what I thought was a new birthmark around the age of 14. Anonymous I am writing because I want to give parents hope. David It goes without saying that I was growing quite concerned. Tributes: Susan's Mom my mom never let you know how badly she was suffering...

6. MEDLINEplus: Scleroderma
   scleroderma Handout on Health scleroderma (National Institute of Arthritis and Musculoskeletal and Skin Diseases)  
   http://www.nlm.nih.gov/medlineplus/scleroderma.html

7. Scleroderma
   Who to Contact scleroderma Research Foundation (SRF) PO Box 200 Columbus, New Jersey, USA 08022 Fax (609) 7236700 The scleroderma Research Foundation's mission is provide communication and support for persons and family members whose  
   http://www.familyvillage.wisc.edu/lib_scle.htm

8. Kids Get Scleroderma Too!!!!!
   Details about this organization who is working to provide educational programs about JSD, and to help Category Health Conditions and Diseases sclerodermaYou are visitor Bravenet.com since April 6, 2002!  
   http://www.jsdn.org/

9. Scleroderma Video
   A collection of 11 video presentations made by some of the foremost scleroderma experts in the US.  
   http://www.starlight-productions.com/scleroderma_video_series.htm
   
   Extractions: Home V i deo Titles ... About Scleroderma Scleroderma Video Series 11 Video Volumes available VHS Video Cassettes: $19.95 each The Scleroderma Video Series is a collection of presentations made by some of the foremost Scleroderma experts in the United States, including Rheumatologists, Cardiologists, Surgeons, Dieticians, Occupational Therapists, Dermatologists, Psychologists, Researchers and more. Topics have included: Overview and causes of Scleroderma Scleroderma Therapies Raynauds Phenomenon Genetics ... Drug Interactions much more Among the speakers that appear within the Scleroderma Video series are eminent experts in the field, including: Philip Clements, MD Daniel Furst, MD Sergio Jimenez, MD Maureen Mayes, MD James Seibold, MD Fredrick Wigley, MD For a complete listing of available titles, please click here Since 1994, Starlight Productions has produced over 30 videos directly related to Scleroderma. As we continue to videotape new presentations, we revise our offerings so that topic duplication is avoided, and outdated presentations are removed. Scleroderma Information - More than our business Our involvement with Scleroderma began as a commercial shoot in 1994. A previous client who had employed us for another type of service happened to be a Scleroderma patient, and a Chapter President within the former United Scleroderma Foundation. She requested our services for their annual chapter medical workshop, and, liking the results, recommended us the National Foundation for the 1995 USF National Conference.

10. Irish Raynaud's And Scleroderma Society
    Information about the organization and the promotion of a greater understanding of these diseases and related conditions. Events, news, mail order products and links.  
    http://www.mdimedia.com/irss/

11. The Scleroderma Society
    Offers support and information. Includes an introduction, news and a message board.Category Health Conditions and Diseases sclerodermaThe scleroderma Society.  
    http://www.sclerodermasociety.co.uk/

12. Scleroderma Clinical Trials Consortium
    Information about this international organization which is dedicated to finding a better treatment Category Health Conditions and Diseases sclerodermaAn international organization dedicated to finding better treatment for scleroderma. Areyou a scleroderma patient looking for support and information?  
    http://www.sctc-online.org/

13. Scleraderma Lung Study
    A research study into the treatment of pulmonary alveolitis with cyclophosphamide seeking patient volunteers. Brief details of this US study for patients and doctors. (May 2000)  
    http://sclerodermalungstudy.medsch.ucla.edu/

14. International Scleroderma Network (ISN)
    A major resource for medical and support information, with 200+ pages and 800+ links. Symptoms, treatments, clinical trials, and worldwide support group listings.  
    http://www.sclero.org/index.html
    
    Extractions: The International Scleroderma Network (ISN) Now Available in 18 Languages: Bahasa Malaysia Chinese Deutsche (German) English ... Worldwide Support Groups International Scleroderma Network We network and empower our worldwide scleroderma community. The ISN's dynamic team of volunteers empower our worldwide scleroderma community by providing medical, support and public awareness information via our Scleroderma from A to Z website and print publications in many languages. We offer free web pages website listings , and special events promotion for scleroderma organizations in all countries and languages.

15. Our Research Program
    The scleroderma Foundation 1999 Research Funding Program anticipates funding upto ten oneyear grants and ten two-year grants depending upon the quality of  
    http://www.scleroderma.org/research.html
    
    Extractions: Links Page Scleroderma Foundation Research Funding Program Guidelines for Submission, Review, and Awarding of Research Grants Types of Proposals Solicited Budgets Timetable Review Process ... Restrictions A. Types of Proposals Solicited The Scleroderma Foundation Research Funding Program is currently accepting proposals for research grants related to scleroderma. Each application should have the quality of an NIH proposal. Projects of investigators new to the field of scleroderma are preferred, although studies in new directions by established researchers will be considered. B. Budgets Budgets for up to, but not exceeding, $75,000 for a one-year award or $150,000 for a two-year award are acceptable. Principal or co-investigator salaries may be funded for no more than $10,000 upon evidence of the supporting institution's matching this amount. Salaries for support personnel or current research post-doctoral fellows engaged in the project may be requested. The Scleroderma Foundation Research Funding Program allows eight percent of proposal budgets to be allocated towards overhead.

16. Scleroderma
    Read the posts or post a message for those who have or who are interested in this disorder.Category Health Conditions and Diseases sclerodermaA message board where people living with scleroderma can cometo discuss issue that we deal with on a daily basis.  
    http://pub59.ezboard.com/fsclerodermadiscussionboardfrm1

17. International Scleroderma Network (ISN)
    A major resource for medical and support information, with 200+ pages and 800+ links. Symptoms, treatmen Category Health Conditions and Diseases sclerodermaA major worldwide resource for scleroderma medical and support information,with 800+ pages in 18 languages. International scleroderma Network.  
    http://www.sclero.org/
    
    Extractions: The International Scleroderma Network (ISN) Now Available in 18 Languages: Bahasa Malaysia Chinese Deutsche (German) English ... Worldwide Support Groups International Scleroderma Network We network and empower our worldwide scleroderma community. The ISN's dynamic team of volunteers empower our worldwide scleroderma community by providing medical, support and public awareness information via our Scleroderma from A to Z website and print publications in many languages. We offer free web pages website listings , and special events promotion for scleroderma organizations in all countries and languages.

18. Scleroderma Webmaster's Association Directory
    The scleroderma Webmaster's Association makes it easy for people to find sclerodermainformation on the Internet! International scleroderma Network.  
    http://www.sclero.org/support/swa/a-to-z.html
    
    Extractions: This Site The Web Scleroderma Webmaster's Association: Sites to Surf! Special Thanks to Judy Tarro of SD World for SWA site design assistance and to Judy, Lynn and Syl for moderating SWAlist for webmasters. EMAIL We're dedicated to helping you find the comfort and/or information you need for dealing with scleroderma or related illnesses. Please feel free to email me at any time. Shelley Ensz, Webmaster Now Available in 18 Languages: Bahasa Malaysia Chinese Deutsche (German) English ... Worldwide Support Groups Scleroderma Sites to Surf! We make it easy to find scleroderma information worldwide. All our services are free, to members and visitors alike. Worldwide Support Free Web Page for Groups - Arabia (United Arab Emirates) - Africa - Australia - Belgium (Belgique) - Canada (Main Page) - China (Chinese) - Denmark - Deutsch (German) - Francais) (French) - Germany (Deutsch) - Greece (Greek) - Hungary (Magyarul) - India - Ireland - Israel (Hebrew) - Italy (Italiano) - Japan (Japanese) - Kannada (India) - Kenya (Africa) - Kiswahili (Kenya, Africa)

19. Pediatric Rheumatology Home Page
    A resource for families and physicians caring for children with arthritis, lupus, scleroderma, Kawasaki disease and other rheumatic diseases.  
    http://www.goldscout.com/
    
    Extractions: All information is provided as a public service and no warranty is expressed or implied. KEY WORDS: arthritis scleroderma childhood arthritis dermatomyositis JRA juvenile rheumatoid arthritis Kawasaki Disease pediatric rheumatology polyarteritis nodosa SLE systemic lupus erythematosus vasculitis CLICK for Patient and Family Information CLICK for Books on Childhood Arthritis CLICK for Physicians' Information CLICK for Information on the Hospital for Special Surgery ... PLEASE NOTE: It is not possible for Dr. Lehman to provide individual medical advice over the Internet. Every patient and family must find a physician they are comfortable with. If you are uncomfortable with your present physician you may get help in finding a new one from your local office of the Arthritis Foundation or other community organizations. This site provided by Thomas J. A. Lehman MD

20. RI Scleroderma Support Group
    Mutual support in Rhode Island and New England for scleroderma patients.Information, meetings, events. RI scleroderma Support Group.  
    http://www.angelfire.com/ri/scleroderma/
    
    Extractions: Inherited, as a general rule. NEW! February 24, 2003 Carole's Hope Garden for a Cure for Scleroderma (photos, graphics intensive, but worth it!) The Rhode Island Scleroderma Support Group (RISSG) meets on the fourth Wednesday of most months at 7:00 p.m. at the Day Treatment Room (first floor, handicapped accessible from side entrance), Roger Williams Medical Center, 825 Chalkstone Avenue, Providence, RI 02908, United States of America. The support group is not a medical clinic of any kind, but is simply for peer to peer information and assistance. For further information, please phone

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