There is no time more fitting to say thank you and Season’s Greetings from all of us at
The C Diff Foundation and to wish you a Happy Holiday Season.
Special wishes are being sent out to the many patients and families who have witnessed or have been diagnosed with a C. difficile infection; May you have a New Year of restored health, support, hope, and renewed happiness.
The C Diff Foundation Members
C Diff Foundation Board of Directors:
Nancy C Caralla, Scott Battles, Dr. Ahmed A. M. Al Mandalawi, MD,
Tiffani M. Eberflus, Rowaland R. Dory, Angelo Ortiz
Mental Health Advisory Committee
Lesa Bridges, LCSW, MSW, Chairperson
Research and Development Committee
Dr. Martha R. Clokie, MS, PhD
Dr. Simon Cutting, MS,PhD, Chairperson
Dr. David Cook, MS, PhD
Dr. Rahma Wehelie, PhD
Dr. Hudson Garrett, Jr., PhD, MSN, MPH, FNP, CSRN, VA-BC, CDONA,FACONA,DON-CLTC, C-NAC, PLNC
Medical Advisory Board:
Dr. Mark Wilcox, MD, Chairperson
Dr. Rosie Lyles, MD
Dr. Sadeq A. Quraishi, MD
C. diff. Nationwide Community Support Program:
Dr. Paul Feuerstadt, MD, Medical Advocate
Dr. Caterina Oneto, MD, Medical Advocate
Lisa Hurka-Covington – MD Support Leader
Scott Battles – MO Support Leader
Karen Factor, RD- FL Support Leader
Roy Poole, CO Support Leader
Pediatric Support, Research and Development Committee
Tiffani Eberflus, LPN, Chairperson
C Diff Volunteer Advocate Program
Angelo Ortiz, Chairperson
Marketing and Graphic Arts Committee
Anthony DelMonaco, Marketing VP
Joel Davis, BS, Chairperson
Biologic Research and Development Committee
Michael Kaleko, MD, PhD, Senior Vice President, Reseaerch & Development Synthetic Biologics
Joseph Sliman, MD, MPH, Senior Vice President, Clinical & Regulatory Affairs, Synthetic Biolgics
Andy Bristol, PhD, Vice President, Research & Development, Synthetic Biologics
The C Diff Foundation introduces the C. diff. Nationwide Community Support (CDNCS) program beginning in November for patients, families, survivors and for anyone seeking information and support.
C. difficile (C. diff.) infections caused almost half a million infections among patients in the United States in a single year, according to a 2015 study by the Centers for Disease Control and Prevention (CDC).
In addition, an estimated 15,000 deaths are directly attributable to C. difficile infections, making them a substantial cause of infectious disease death in the United States. [i].
As of 2015, there is an absence of professional C. diff. (CDI) support groups in America. The C Diff Foundation has pioneered a collaborative plan and developed support groups in a variety of availability and locations to meet the needs of individuals seeking C. diff. information and support.
“We found it to be of the utmost importance to implement this new pathway for support and healing after speaking with numerous patients, family members, and fellow-C. diff. survivors,”
We now speak for the thousands of patients within the United States who, each year, are diagnosed with a C. diff. infection. This growth, in part, reflects the value C. diff. support groups will provide, not only to patients, their spouses, and families who are living with and recovering from a C. diff. infection, but also to the countless number of individuals who will become more aware of a C. diff. infection, the importance of early detection, appropriate treatments, and environmental safety protocols. There will also be Bereavement support group sessions for C. diff. survivors mourning the loss of loved ones following their death from C. diff. infection involvement.
Beginning November 2015 the CDNCS groups will be available to all individuals via: Teleconferencing with some groups advancing and adding computer application programs in 2016. CDNCS groups will provide support and information to 15 participants in each session.
The CDNCS program sessions will be hosted via: Teleconferencing with leaders hosting from Maryland, Florida, Missouri, Colorado, Ohio, and Oregon.
The Colorado CDNCS group is offered at a public venue and will be hosted in Arvada, Colo. every third Tuesday of each month, beginning November 17th. The Meeting will start at 5:30 p.m. and end at 7 p.m lead by a C Diff Foundation Volunteer Advocate and C. diff. survivor Mr. Roy Poole.
To participate in any CDNCS group being offered during each month, all interested participants will be asked to register through the Nationwide Hot-Line (1-844-FOR-CDIF) or through the website http://cdifffoundation.org/ where registered individuals will receive a reply e-mail containing support group access information.
The Support Registration Page will be available on November 1st.
The C. diff. Nationwide Community Support group leaders will provide a menu of topics being shared each month on the C Diff Foundation’s website ranging from Financial Crisis Relief, Bereavement, Nutrition, Mental Health, to C. diff. infection updates and everyday life during and after being treated for a prolonged illness. Teleconference sessions will also host healthcare professional topic experts
There is evidence that people who attend support group meetings have a better understanding of the illness and their treatment choices. They also tend to experience less anxiety, develop a more positive outlook, and a better ability to cope and adapt to life during and after the treatment for C. diff.
There is a Purpose:
A diagnosis of a C. diff. infection is unexpected and almost always traumatic. As a result, it is not uncommon for newly diagnosed patients to experience a wide range of emotions including, confusion, bewilderment, anger, fear, panic, and denial. Many people find that just having an opportunity to talk with another person, who has experienced the same situation, to help alleviate some of the anxiety and distress they commonly experience.
Individuals also find that they benefit not only from the support they receive, but also from the sense of well-being they gain from helping others. It has been said “support is not something you do for others but rather something you do with others.”
“None of us can do this alone – all of us can do this together.”