Home

About Us - Slidell Support Group | About Us - Lafayette Group | About Us - North Louisiana Support Group | October News | History/Background | What is Scleroderma? | Prevalence of Scleroderma in Louisiana | Slidell Photo Album 1997-2000 | Year 4 Oct. 2000 - Sept. 2001 | Year 5 Oct 2001 - Sept 2002 | Year 6 Oct. 2002 - Sept. 2003 | Patricia W's Story | The Highway of Life | Newsletter Archive Page | Contact Us
Year 4 Oct. 2000 - Sept. 2001
Scleroderma Support Groups Slidell, Lafayette and Shreveport, LA

                    MEETING REPORTS

January 20 2001

Ellen C. Schneider, MD, opthamalogist, addressed the group to discuss the many problems scleroderma patients have with dry eyes and treatment for this symptom.

She gave out sample of over-the-counter drops that can be used to counteract dryness.

Her talk was very interesting and much appreciated by the members attending.

schneider.jpg
Pat Warr, Dr. Schneider, Maxine Konrick

 July 21 2001 Meeting

Dr. Francisco Candal, pulmonologist, gave an interesting talk addressing the types of scleroderma and the types of scleroderma lung disease.  He stated that 7 out of 10 persons with scleroderma develop pulmonary fibrosis and he stressed that everyone with scleroderma needs to be evaluated for chest disease.
 
The evaluation for chest disease should include a chest x-ray, a CT scan and a complete pulmonary function test (PFT).  One specific part of the PFT, the DCLO which is the gross measurement of transfer of oxyegen from and into the lungs, is key to diagnosing scleroderma fibrotic lung disease.  Echocardiograms and/or cardiac catheterization are the best tools to identify pulmonary hypertension.  Early diagnosis means early treatment and best results.
 
If there are no lung problems, persons with an established diagnosis of scleroderma should be checked every 1 to 2 years.  This checkup should include a chest x-ray and complete PFT.
 
Lung disease is the most serious comlication of scleroderma and recently has been shown to be the most common cause of death.  He reiterataed that the earlier the chest disease is identified, the more successful the treatment should be.  Patients treated with drugs such as cytoxan, flolan and immuran can get better.  The treatment course may run 2 to 3 years.
 
The important thing to remember is early evaluation and identification of lung disease and early treatment.
 
 
 

candal.jpg
Maxine Konrick, Dr. Candal, Shirley Walterhouse

 September 15 2001 Meeting

Twenty five people gathered to hear Dennis Peyroux, D. C. of Global Medical Center address the members on peak performance.  Dr. Peyroux used slides to demonstrate some techniques that can benefit everyone.  There was good audience participation.
 
He also waived the usual examination fee at his clinic for those persons present who wished to have a chiropractic evaluation done.
 
Some of the members present, interested in holistic health treatment, spoke to Dr. Peyroux about that aspect of Global's services.
 
And a first for the group -- we enjoyed delcious sandwiches from Subway provided by Dr. Peyroux and Global.
 
 

peyroux.jpg
Maxine Konrick, Dr. Peyroux, Shirley Walterhouse

Fundraiser Report

Third Annual Imaginary Tea Party

teatray.jpg

Five of the Support Group members participated in this annual fundraiser.
JOY CLIFF $ 75.00
BILL BURCH 300.00
SHIRLEY WALTERHOUSE 1125.00
PAT WARR 145.00
WENDY WILLIAMS 264.00
GRAND TOTAL $1909.00

Each donor received a note of thanks and acknowledgement.
Don Walterhouse donated the stamps for the 59 thank you cards mailed out.

Congratulations to each of you. Not only have you raised money for our cause but you have educated others and helped to raise awareness in our communities.

blu-lites.gif

Scleroderma in Morgan City March 2001

Karen Swensen of Channel 4 had a program about the high incidence of autoimmune disease in the Morgan City community and she was kind enough to show our support group phone number at the conclusion of the broadcast.
As a result we received about 40 phone calls and although many of them were from interested persons, we did make contact with 7 people in the area who have been diagnosed with scleroderma.  They were added to our mailing list.
 
There was a town meeting on 12 March in Morgan City which Don and Shirley Walterhouse attended.  It was interesting but not productive and efforts to start an ancillary group in the area were not successful.
 
We will keep in touch with Karen Swensen and update her on our group in the hope that she will find us newsworthy in the near future.
 

blu-lites.gif

       Our Group T-Shirt

tshirt.jpg

Our group logo, designed by Shirley Walterhouse and executed by her son Ken Walterhouse, is used to great advantage on our t-shirts.
Shirts must be ordered in bulk so if you are interested please let Shirley know the size and quantity so we can begin to place a new order.

blu-lites.gif

memcross.jpg

The Scleroderma Support Group continues to grow and evolve.  We are constantly expanding our membership and unfortunately we have also had to say "Goodbye" to some of our good friends and members this year.
 
In loving remembrance of:
 
Cathy Cole             1958 - 2001
Opal Gay Fontenot         -  2001
Eleanor Helminski   1945 - 2001
Johnny Terrell        1926 - 2001
Judith Truxilla        1958 - 2001
Kenneth Vincent     1944 - 2001
 

FOURTH ANNIVERSARY CELEBRATION
 
 

groupyr4.jpg
Joy Cliffs, Lucille Edwards, Barbara Lewis, Ron & Bobbie Quilling, Maxine Konrick

olsenburchyr4.jpg
Jean Olson, the Bill Burches