Tag Archives: C diff education

C Diff Foundation Members Volunteer Over 20k Hours Of Service To Raise Awareness and Educate Worldwide

The C Diff Foundation celebrated ‘National Volunteer Week,’  April 23 – 29 to recognize more than 150 volunteer members around the globe ~ dedicated in raising awareness of C.diff. infection prevention, treatments, environmental safety and support with the C Diff Foundation

 

 

 

and have collectively donated more than 20,000 hours of volunteer service to the Foundation over the past nine months.

Thank you!

We are truly grateful!

C Diff Foundation and C diff Survivors Alliance Network Share a Winter 2017 Bulletin

Greetings from the main office of the C Diff Foundation and the C diff Survivors Alliance Network located in New Port Richey, Florida.  As we close 2017 we mark the 5th anniversary of the two organizations. We want to share with you a summary and reflection on this year’s events and campaigns moving our mission forward and message delivered worldwide. The mission and promoting C.diff. Awareness has been shared this year with  listeners in over 25 Counties during Season III on C. diff. Spores and More Global Broadcasting Network (www.cdiffradio.com),  5,000+ visitors during global events, 9,600+ residents and business owners throughout villages and communities by our dedicated volunteer patient advocates, to over 1,000 clinicians who received up-to-date data expanding their knowledge during workshops and local symposiums offered worldwide, 3,000+ incoming calls received through the Nationwide Hot-Line 1-844-FOR-CDIF with the thousands of e-mails received seeking assistance.

After each event, workshop, meeting, introduction we thank the individuals for sharing  in five years of opportunity to provide life-saving data educating and advocating for C. difficile infection prevention, treatments, environmental safety and support worldwide.  The mission of the C Diff Foundation is the momentum of charity that has proven effective and grown over the past five years.  A single act of charity grows into more and greater charity worldwide.  The work each member of the C Diff Foundation, with hundreds of Volunteer Patient Advocates, promote the Foundation’s mission which never stops with a single act.  Instead, it builds, it grows, and it expands into an exponential impact of good in the world helping to save lives.  We thank you for your continued support and encourage you to continue your journey, proposing three verbs important to the C Diff Foundation and the C diff Survivors Alliance Network in general.

The first of these verbs is “to promote” C.diff. Awareness. It is the first step that opens doors in educating individuals, clinicians, communities in learning more about this life-threatening infection which causes a great amount of pain and suffering around the globe.  It is essential and it is the compass in reaching shared goals.

The second verb is “to heighten awareness” across the nation to continue proclaiming November Clostridium difficile infection awareness month. The Governors proclaimed November C. difficile (C.diff) infection awareness month in 2017 and we encourage them “to welcome” this proclamation in 2018 with more than a yearly executive order of greeting or inviting their residents to take notice.  We look forward to working with delegates, with your support, to make this proclamation statement nationwide and welcome the importance of the time, education, programs, and agenda in place addressing this life-threatening infection.  The C Diff Foundation advocates and supports the individuals and families suffering during and after being treated for a C. diff. infection.

Finally, the third verb that the C Diff Foundation and C diff Survivors Alliance Network propose is “to go.”  Here we are all challenged to do something big or small — with what we are able to do.  With the unity of members with volunteers with patients, families, and clinicians we can make a difference with enthusiasm and simplicity to get up and go.  We can do for others  today what we could not do for ourselves during our time of illnesses, during the long periods of isolation, during the losses, and during the pain and suffering.

As members of the C Diff Foundation we know that our enthusiasm  for our mission is the desire to bring awareness and promote C. difficile infection prevention, treatments, environmental safety and support worldwide.  We witness changes by the data and information being delivered within villages,  through major cities and in small communities — it is only by taking this path that we gain satisfaction knowing that the news delivered with enthusiasm “to promote, to heighten awareness and to go” with the members and volunteers in the C Diff Foundation and C diff Survivors Alliance Network creates positive results.

We are truly grateful for your continued dedication, efforts and support and thank you again for making this year’s November anniversary such a special occasion through the growth and advances made worldwide.   Let’s carry the mission into the New Year, carving new paths to witness the decline of newly diagnosed cases of Clostridium difficile (C.diff., C. difficile) infections and saving lives worldwide.

“None of us can do this alone ~ All of us can do this together.”

 

 

Have You Been Treated For a C. diff. Infection? Take a Brief Survey To Help Improve Education for C.diff. Patients and Caretakers

 
The C.diff Foundation is working with a partner to conduct a survey about your experience with a C.diff. infection to help inform educational initiatives for C.diff patients and caretakers.

If you or someone you know has had a personal experience with a C.diff, infection please go to our website, www.cdifffoundation.org, and take the short survey.

Thank you for making a difference and shaping the future of C. diff. infection prevention education.

 

C Diff Foundation Celebrates National Volunteer Week 2017

National Volunteer Week, April 23 – 29th

The C Diff Foundation celebrates National Volunteer Week, April 23 – 29 to recognize more than 150 members of the C Diff Foundation Volunteer Members, including Volunteer Patient Advocates, have collectively donated more than 20,000 hours of volunteer service to the Foundation last year. The theme for this year’s celebration is “Sharing Time, Touching Lives.”

“Through the years the C Diff Foundation Volunteer Members have served as ambassadors of goodwill, service and compassion,” said Angelo Ortiz, C Diff Foundation’s Treasurer and Chairperson of  the Volunteer Patient Advocate Program

The C Diff Foundation, a 501(c) (3)  non-profit organization, established in 2012, and comprised of 100% volunteering professionals dedicated at supporting public health through education and advocating for C. difficile infection (CDI) prevention, treatments, environmental safety, and support worldwide

Not only do the volunteer members provide financial support for the C Diff Foundation’s programs — it is through their dedication and passion that continuously expands the Foundation’s mission.  Some volunteer patient advocates have their own unique C. diff. Survivor Journey which is shared with compassion, dedication, and caring hearts touching patients, students, fellow healthcare professionals,  and residents in the community every day.

Volunteer members will be recognized on November 9th & 10th  during the C Diff Foundation’s
5th Annual International C. diff. Awareness Conference and Health EXPO being hosted
in Las Vegas, NV.  During the annual event the “Volunteer Shooting Star” awards will
be presented along with numerous Volunteer Patient Advocate certificates for service hours.

“We are fortunate to have such kind and giving volunteers,” said Nancy C. Caralla, Foundress and Executive Director of the C Diff Foundation, “It is an honor to recognize those who have selflessly given so much to help educate, and promote the Foundation’s mission worldwide.”

The C Diff Foundation Volunteer Program was organized in 2012 to provide volunteer services, promote community understanding of Clostridium difficile (C. diff.) CDI  Infection Prevention, Treatments, Environmental Safety and Support and to raise funds for special C Diff Foundation patient/family programs.

The C Diff Foundation Members, with  the Volunteer Patient Advocates, successfully promote
C. diff. Awareness”  nationwide and in fifty-six  (56) countries and host a
U.S. Nationwide information Hot-Line (1-844-FOR-CDIF) to support health care providers, patients, and families guiding them through the difficulties caused by a C. diff. infection.

Volunteers Members serve in 12 different committees;  Volunteers host monthly teleconference support sessions; Provide Education about C. diff. infection and other linked healthcare topics through workshops, community events, and literature with patients, their families, and residents from villages to cities around the globe; Triage Nurses assist patients, families, clinicians with answers to prevention, treatment, environmental safety and support questions Monday – Friday 9:00 a.m. – 5:00 p.m. EST;  Register support session participants,; Provide IT management; Give clerical and social media assistance to various departments;  Provide a “Global Broadcasting Network” with www.cdiffradio.com with their educational radio
program,C. diff. Spores and More which broadcasts live every Tuesday at 1:00 p.m. EST. We are grateful for our sponsor Clorox Healthcare for making this program possible.  Each episode becomes a podcast and is accessible from the C. diff. Spores and More living library located on the main cdiffradio.com program page. Each November the Volunteer Members gather at the annual conference to both present and provide assistance in making the attendees feel welcome and expand their knowledge base on a variety of health topics that are linked to the main topic ~ Clostridium difficile infections.

For more information about the C Diff Foundation Volunteer Program, please call 919-201-1512 (toll free in USA 1-844-367-2343 ) or e-mail:   info@cdifffoundation.org

 

C Diff Foundation Volunteers — Helping Us  Help Others and The Beacon Of Light On the Other Side Of Pain and Suffering.

 

 

 

Florida’s Tampa Bay Community; Raising C. diff. Awareness Event Planned For November 4, 2016

The Inaugural Tampa Bay Community Sunset Casual Dinner Dance

 “Raising  C. diff. Awareness”  Event

November 4, 2016   5:30pm – 9:30pm

2016CdiffNovFrontPC

 

 

 

 

 

 

 

Join us for the Inaugural 

Tampa Bay Community Sunset Casual Dinner Dance

“Raising C. diff. Awareness”  

on the evening of

November 4th  from 5:30 to 9:30 at the

Spartan Manor located in

New Port Richey, Florida

Community professionals, families, and friends will be gathered in a beautiful environment
while Raising C. diff. awareness.   There will be C. difficile Infection prevention, treatments, environmental safety information provided by clinicians and healthcare professionals and much more during this fun filled evening in New Port Richey, Florida.

Tickets are $25.00 each and are available through the C Diff Foundation

info@cdifffoundation.org   or Contact the main office toll-free:  1-844-367-2343

Enjoy a four course white glove plated dinner with entree choices of beef or chicken, with outstanding entertainment.

 Music and entertainment will be provided by ML Productions

SpartonManorBanquets-and-Special-Event-Venue

We look forward to sharing an enjoyable evening with  you on November 4th

 

(click on the above logo to be redirected to our sponsor’s website)

A World of Thanks To the C Diff Foundation Volunteer Patient Advocates Around the Globe

National Volunteers Week     #NVW2016

 

Did you know that it is  NATIONAL VOLUNTEER WEEK
April 10-16, 2016

President Richard Nixon established National Volunteer Week with an executive order in 1974, as a way to recognize and celebrate the efforts of volunteers. Every sitting U.S. president since Nixon has issued a proclamation during National Volunteer Week (as have many U.S. mayors and governors).  Since then, the original emphasis on celebration has widened; the week has become a nationwide effort to urge people to get out and volunteer in their communities.

To each C Diff Foundation Volunteer Patient Advocate, , on behalf of all the staff and the thousands of members around the globe we want to say THANK YOU!

Your continued support and efforts contribute in a significant way to our mission of educating, and advocating for C. diff. infection prevention, treatments, and environmental safety awareness worldwide.

November marked our third  year in “Raising C. diff. infection Awareness” campaign and we thank the many organizations who supported and contributed by sharing information with others.  We are all working toward a shared goal in witnessing a reduction of newly diagnosed C. diff. cases and “None of us can do this alone…..all of us can do this TOGETHER!”

We celebrate our volunteers and this week stands as a reminder that our daily work sharing information, educating, and advocating for C. diff. infections, remains not only critical but it is urgent.

We do not know when new interventions to prevent, to treat, and protect our environments with products that will  eradicate C. diff. spores will become available to the public.  The good news is that we do know that there are many positive interventions presently in clinical trials, which give us all HOPE.

Visit the website for updates and feel free to inquire if you or a loved one would be considered a candidate to participate in an ongoing clinical trial:

 https://cdifffoundation.org/clinical-trials-2/

This is why acts of sharing the C Diff Foundation literature during every opportunity quickly opens doors of knowledge helping others learn how to prevent acquiring this painful and life-threatening infection, treatments available, and disinfecting products with EPA Registered C. diff. kill for environmental safety–  to  help save lives.

Reminder that there is always information and support  available and  only a phone call away 1-844-FOR-CDIF

The C Diff Foundation Volunteer Patient Advocates build awareness, help build support and provide education of C. difficile infection prevention, treatments, and environmental safety measures  to patients, survivors  their families and community healthcare professional centers/offices.  They also  guide individuals in giving a voice to patients, survivors and their families on healthcare-related infections, informing the public,  health-care providers (hospitals, healthcare professionals, etc.), organizations of health-care professionals, the educational world, with the medical, Governmental agencies, and pharmaceutical research communities.

We provide our Volunteer Patient Advocates with the necessary tools, and updates to generate positive results.

Do you have a few extra minutes to share vital information with others to raise C diff. infection awareness in your community?

By becoming a C Diff Foundation Volunteer Patient Advocate you will make a BIG difference and help spare others the pain, suffering, and tragedy of loosing a loved one that is caused by a C. diff. infection.

Contact our office for additional information and register today by e-mailing the C Diff Foundation your name and a valid mailing address to receive an official  C Diff Foundation Volunteer Patient Advocate Packet

info@cdifffoundation.org

On this day, and throughout the year ahead, we want you to be confident that your Volunteer Membership in the Foundation is bringing important information out into the communities and throughout the world through the educational brochures, cards, letters, and from sharing your own personal experiences with others.  Please be sure to share your journey with others in need of “HOPE” on the C. diff. Survivors Alliance Network website  http://www.cdiffsurvivors.org

Your continued donations received during the year are always appreciated. Your gifts assist the Foundation in promoting C. diff. infection prevention, treatments, and environmental safety education, and advocacy to healthcare professionals, families, patients, and communities world-wide.  We are grateful for your assistance, dedication, and support and we hope the Foundation has also been helpful to you.  If you have any suggestions about how we can serve others better or share the information more effectively, please let us know.  You are welcome to email, telephone, or write to the Foundation at any time.

We certainly look forward to your continued Volunteer Membership in the Foundation.  There is so much more that needs to be accomplished and we continue to move forward together promoting our mission, which is entirely dedicated for the good of others.

May you and your families experience continued HOPE for good health, happiness, and peace throughout the year.

Thank You for helping prevent further pain and suffering worldwide by sharing in the

C Diff Foundation’s mission today.

 

C. difficile Infection (CDI) C Diff Foundation Opens a New Avenue – C. diff. Nationwide Community Support Program

CdiffForRelease-1

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 https://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.”

 

Follow the C Diff Foundation on Twitter @cdiffFoundation #cdiff2015 and                                        Facebook https://www.facebook.com/CdiffFoundationRadio.

Note/citation: [i] http://www.cdc.gov/drugresistance/biggest_threats.html