[Congressional Record Volume 163, Number 106 (Wednesday, June 21, 2017)]
[Extensions of Remarks]
[Page E865]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]




                  NATIONAL SCLERODERMA AWARNESS MONTH

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                           HON. PETER T. KING

                              of new york

                    in the house of representatives

                        Wednesday, June 21, 2017

  Mr. KING of New York. Mr. Speaker, I rise today in recognition of 
Scleroderma Awareness Month.
  Scleroderma is an autoimmune disease that not only affects thousands 
of individuals within my own constituency and the state of New York, 
but also thousands of individuals living in the United States.
  Due to the lack of research on the unpredictable progression of 
Scleroderma, many physicians find it difficult to diagnose their 
patients and find it even more difficult to provide adequate treatment 
since a cure has not been discovered. As we recognize the need for 
awareness of this troublesome disease, we must do more for the 
thousands of Americans who are diagnosed with this condition each year.
  In the past, I have championed legislation aimed toward galvanizing 
many federal agencies to fund research for Scleroderma with former 
Congresswoman Lois Capps of California. As a representative, I consider 
myself responsible for the health and safety of my constituents. This 
is why I urge my colleagues to join me in supporting federal investment 
for research as well as recognizing June as Scleroderma Awareness 
Month.

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