In September 2009, CDC initiated the
National Hemophilia Foundation's (NHF) Hemophilia and AIDS/HIV
Network for the Dissemination of Information (HANDI) project. HANDI
is NHF's resource center that provides information, materials, and
support to people with bleeding and clotting disorders. Many
materials focus on parents and family members of newly diagnosed
children, but less attention is given to materials for children and
adolescents, especially about acceping the disorder, self-care,
school and career planning. Focus groups will be conducted to
ensure the health promotional materials are useful and on
target.
US Code:
42
USC 241 Name of Law: Public Health Service Act
US Code: 42
USC 247 Name of Law: Children's Health Act of 2000
On behalf of this Federal agency, I certify that
the collection of information encompassed by this request complies
with 5 CFR 1320.9 and the related provisions of 5 CFR
1320.8(b)(3).
The following is a summary of the topics, regarding
the proposed collection of information, that the certification
covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a
benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control
number;
If you are unable to certify compliance with any of
these provisions, identify the item by leaving the box unchecked
and explain the reason in the Supporting Statement.