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  1. #1
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    CHD on Yahoo News!

    Press Release Source: National Psoriasis Foundation

    Multimedia News Release - National Psoriasis Foundation Urges Congress to Address the Needs of Millions of People Living With Psoriasis and Psoriatic Arthritis
    Monday February 27, 8:37 am ET
    Organization Recognizes Congressional Advocates who have Demonstrated Their Commitment to the Psoriatic Community


    PORTLAND, Ore., Feb. 27 /PRNewswire/ -- Members of the National Psoriasis Foundation are in Washington, D.C., today to educate legislators about the need for access to quality care for people living with psoriasis and psoriatic arthritis. In meetings with congressional representatives, the Foundation is urging members of the House and Senate to generate awareness about the serious physical and emotional impact of these diseases. With continued advocacy efforts, the National Psoriasis Foundation and patient advocates hope to secure much-needed funding to accelerate the discovery of additional safe and effective treatments and, ultimately, a cure.

    To view the Multimedia News Release, go to:
    http://www.prnewswire.com/mnr/chd/23636/

    According to Gail M. Zimmerman, president and CEO of the National Psoriasis Foundation, it's important to keep psoriatic disease at the forefront of governmental discussion. "Psoriasis and psoriatic arthritis are chronic, potentially disabling diseases that are often misunderstood. Capitol Hill Day offers the chance to educate members of Congress and to continue to advocate on behalf of those living with these diseases."

    Additionally, while in D.C. today, the National Psoriasis Foundation will officially recognize several congressional leaders for their commitment to enhancing federal level support of psoriatic disease education and legislation, including Senator Gordon H. Smith (R-OR), Senator Frank Lautenberg (D-NJ), Representative Tim Murphy (R-PA), Representative Stephen F. Lynch (D-MA) and Representative Jim Gerlach (R-PA). Last year, Senators Smith and Lautenberg spearheaded the Senate resolution that designated August 2005 as Psoriasis Awareness Month.

    More than 100 volunteers with psoriasis and/or psoriatic arthritis are participating in the National Psoriasis Foundation's third annual Capitol Hill Day. Capitol Hill Day is an annually organized advocacy effort that motivates people living with psoriasis and/or psoriatic arthritis to speak out about their conditions. Patient volunteers from the National Psoriasis Foundation will convene at the offices of congressional leaders to tell their personal stories of living with psoriatic disease and to shed light on the life- altering impact of these conditions.

    Building on momentum of past Capitol Hill Day events, today's program is specifically designed to allow members of the psoriatic community to lobby Congress to increase federal funding for psoriatic research, address the lack of access to effective treatments, and become personally involved in educating themselves and others about psoriasis and psoriatic arthritis as "champions" who directly impact the future of psoriatic disease.

    About Psoriatic Disease

    Psoriasis and psoriatic arthritis are chronic, inflammatory diseases that result from faulty signals in the immune system. The symptoms of psoriasis and psoriatic arthritis can significantly impact quality of life. People diagnosed with psoriatic disease may exhibit strong feelings of anger, helplessness, self-consciousness and embarrassment because of the appearance of their skin and the pain and discomfort they often endure. While there are treatment options available to help improve the symptoms of psoriasis and psoriatic arthritis, there is no cure, and many people still struggle to find a treatment that can lead to significant levels of skin clearance and decrease their pain.

    About the National Psoriasis Foundation

    The National Psoriasis Foundation is a patient-driven nonprofit organization working to improve the quality of life of as many as 7.5 million Americans with psoriasis and/or psoriatic arthritis and their families. We work to educate people about these diseases and their treatments, raise public awareness and support ongoing research toward a cure. The organization is headquartered in Portland, Ore. For more information, please call the Psoriasis Foundation at 800.723.9166 or visit http://www.psoriasis.org.

    The National Psoriasis Foundation gratefully acknowledges Centocor, Inc. for its support of awareness efforts in conjunction with Capitol Hill Day. Centocor is a leading biotechnology company dedicated to advancing dermatologic research and science through the development of novel therapies for the treatment of psoriatic disease.




    --------------------------------------------------------------------------------
    Source: National Psoriasis Foundation





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    The original 106

    I've got a fever, and the only prescription... is more cowbell!

  2. #2
    RichJ's Avatar
    RichJ is offline im gone fight my p till i can't fight now more
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    hi steve,
    thank you for putting a link on here and thank you and every one else that could go and try and help them from taking money away to find a cure. thank you all

    have a good night my friend and well done

    richard
    nascar lover and a poster on this can't be happening to me thread

  3. #3
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    Hi Steve,

    Thanks for posting this. Also thanks to all who were able to go and talk yesterday at Capitol Hill. We really appreciate it!!

    Sandy

  4. #4
    Photochick66's Avatar
    Photochick66 is offline Ambition is like love, impatient both of delays and arrivals
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    Steve,
    thanks for posting that. hope u got home well. nice "talk" at lunch too.
    x0x
    *Nemo*
    You told me I couldn't; so I am.
    Queeeeeeeen Beyoth is my hero
    Mr.yoo? are you there?

  5. #5
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    bump.......................

  6. #6
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    Angry NO REPLY!!!

    I have sent two emails to my congressional representative, Steve Chabot, about funding for p research & I did NOT get any response from him!!!

  7. #7
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    Quote Originally Posted by raydon14yp
    I have sent two emails to my congressional representative, Steve Chabot, about funding for p research & I did NOT get any response from him!!!
    Try not to be too discouraged by the lack of response. Not all reps will take the time to respond, or sometimes they respond after a long period of time. Just stay on them, and keep up the gentle pressure.
    Kim

    Back in the Humira saddle again....

  8. #8
    ouchyk's Avatar
    ouchyk is offline Keepin' the faith, just like big papi!!
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    Quote Originally Posted by raydon14yp
    I have sent two emails to my congressional representative, Steve Chabot, about funding for p research & I did NOT get any response from him!!!

    You could also call and ask to speak to a member of his staff. 202-225-2216 or at his district office 513-684-2723.

    and/or visit his website www.house.gov/chabot and see if that e-mail system works better. ( it might be the same one used by the NPF )

    if all else fails a fax might work 202-225-3012.

    Good luck, don't give up!

    Karen
    106 -Seize the moment. Remember all those women on the 'Titanic' who waved off the dessert cart.

  9. #9
    RichJ's Avatar
    RichJ is offline im gone fight my p till i can't fight now more
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    bump... thank you all
    nascar lover and a poster on this can't be happening to me thread

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