Veronice “Raunnie” Edmond, Author, Health Coach, C.diff. And Breast Cancer Survivor Raises CDI Awareness

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Veronica “Raunnie” Edmond, Author, Health Coach,
C Diff Foundation Volunteer Patient Advocate, C. diff. and
Stage 3 Breast Cancer Survivor joined us on
September 20th, 2016, at the
4th Annual International Raising C. diff. Awareness Conference and Health Expo in Atlanta, Georgia.

Veronica bravely shared her tormenting, painful experience encountered with a C. difficile infection while simultaneously undergoing  treatment for Breast Cancer.

We are grateful for her full recovery from this life-threatening diagnosis and infection and for the positive attitude Veronica has in promoting breast health, wellness, and raising C.diff. awareness.

Thank you Veronica and to all fellow C.diff.  Survivors  www.cdiffsurvivors.org  sharing their inspirational journey

“No one can do this alone ~ All of us can do this together.”

C.diff. Survivor

C.diff. Survivor

 

 

 

 

 

Thanksgiving is a great time to reflect on the year’s blessings, reconnect with family, share a big meal and sometimes get indigestion. Often times, the overindulgence of a variety of foods may cause an upset stomach or stomach bug.

To be blunt, the rapid expansion of the stomach and foods rich in creams, sugar, and fat can cause gas, bloating and diarrhea. In most cases, the stomach discomfort is temporary and, with over-the-counter medicine, the symptoms are gone.

When should you be concerned, if the usual remedies are ineffective to control diarrhea?

One of the answers is when the pain from diarrhea, abdominal cramps and fever is so severe that it lands you in the emergency room. In Veronica “Raunnie” Edmond’s case, she was already hospitalized during her second round of chemotherapy for an aggressive form of stage 3 breast cancer.

Please click on the link below to be redirected to this most admirable story shared by Veronica with Marie Y. Lemelle, Contributing Columnist at Wave Newspapers

http://wavenewspapers.com/health-matters-a-case-of-diarrhea-that-almost-turned-deadly/

 

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Marie Y. Lemelle, MBA, a public relations consultant, is the owner of Platinum Star PR and can be reached on Twitter @PlatinumStar, or Instagram @PlatinumStarPR. Send “Health Matters” related questions to healthmatters@wavepublication.com and look for her column in The Wave.

“Support Is Only A Phone Call Away” C. diff. Global Community Tele-Support Program

CdiffTeleSupportNo matter where an individual is on the C. diff. Infection road a patient or family members and loved ones now have the opportunity to listen, participate, and discuss prevention, treatments, environmental safety products, and just about anything  with Healthcare Professionals, and fellow-C. diff. Survivors who know and understand the path and journey from the convenience and comfort of their home, office, anywhere their mobile phone signal will carry them.

 “You are NOT alone”

 

Register for a session today on-line  (click on the link below)

https://cdifffoundation.org/c-diff-nationwide-community-support-program-%E2%99%A5/

 

Call the U.S. Hot-line 1-844-FOR-CDIF

 

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The C. diff. Global Community Support Program is FREE to anyone seeking support from any illness, not just C. diff. and is available across the USA and accessible from 57 Countries .

“Support is only a phone call away”

Clostridium difficile (C. diff.) Infection; A Patient’s Spouse Perspective Living Through a “C. Difficult” Nightmare

HandsTouchingSun“Through better or worse, richer or poorer, through sickness and health — we survived not one but two separate C. diff. infections”  stated Angelo Ortiz, a C. diff. Survivor.

*the patient’s name has been purposely omitted for privacy.

C. difficult is an excellent term used to partially describe
the experience living through a Clostridium difficile infection with a partner,
a soul-mate, or a significant other.

A way of regarding this situation objectively ; a point of view shared with fellow C. diff. survivors also walking this path with their loved ones.

Interviewer:  Angelo, did you know what a Clostridium difficile infection was, also known as C. diff. ?

Angelo:  Yes, being in Nursing I have cared for patients diagnosed with C. diff. infections.  However; I did not surmise that my wife was suffering from this infection.  Usually patient’s bowel movements will have a significant obnoxious odor that can alert healthcare providers to surmise a C. diff. infection.  This is not always the case anymore.  Over the past decade healthcare professionals have noticed changes in symptoms, treatments, and the overall microbiology aspects of this infection.  The lack of odor in patients diagnosed with a C. diff. infection is one of them.

Interviewer  Had your wife been on Antibiotics or in a hospital being treated for an infection prior to being diagnosed?

Angelo:  No, she was not ill, had not been on antibiotics and not been a patient in a hospital.  Nevertheless; working in a hospital and being in close proximity with patients being treated for this infection may have played a big role in her acquiring it.

Interviewer:  Did the healthcare environmental operations utilize a EPA Registered product with a
C. diff. kill claim?

Angelo:  In 2009 Clorox Commercial Solutions Ultra Clorox Germicidal Bleach ® was named the first and only product to obtain Federal EPA registration for killing C. diff. spores on hard, non porous surfaces when used as directed.  Before then there weren’t any products available addressing
C. difficile spores and C. diff. spore elimination through disinfecting.  Since that time, we have come a long way and the available products EPA Registered addressing C. diff. and also UV Disinfecting systems available to healthcare facilities fighting major healthcare-associated infections.

Interviewer:  What were the symptoms your spouse was experiencing on a daily basis?

Angelo:   Where do I begin?  There was pain, so much pain that it made my heart break.  I cried when she cried and screamed.  Talk about feeling helpless.  Watching my beautiful wife lay curled up in a fetal position in a hospital bed that we had to rent and place in the living room because she was too weak to climb the stairs in our townhouse.  It wasn’t pain she would tell me, it was her intestines twisting and turning and we could hear the whooshing and active bowel sounds.  They were so loud and audible we didn’t need our stethoscopes to access them.  If a half of a sandwich was ingested, it was eliminated within 45 minutes.  Maintaining hydration was a challenge every single day.  The docs had my wife following a clear liquid diet and with each office visit she would tell each doctor assessing her, “I can’t eat, everything I eat just runs right through me.”  They would tell her to not worry about it, stay on the liquids, eat what you can.  There wasn’t a lot of nausea or vomiting, no fever, but there were times where she would shiver and complain of feeling cold.  Falling into malnutrition and also mal-absorbtion also  caused G.I. system complications later on, too.

Interviewer:   What healthcare providers were visited and rendered care?

Angelo:   It took six months of weekly visits complaining of the G.I. symptoms and pain, to receive a concrete diagnosis by the Primary Care Physician.   After three months, after being diagnosed with a CDI and after the algorithm of treatments were not making a difference, the referral to be assessed by a Gastroenterologist came about.   During the next six months my wife was seen by all fourteen Gastroenterologist’s in the one practice without any significant improvements noted under their care.  After the six month of weekly visits and continued changes in medications, the physicians recommended a referral to Hospice.

Interviewer:   Where did the next level of care take you?

Angelo:   A Physician studying Clostridium difficile, suggested getting a second opinion by a Gastroenterologist at Duke University Hospital in N.C..   I met with the benefits coordinator at work who assisted in the process to obtain the approval for the second opinion.   Just to let everyone know, always call the customer service phone number on the back of the ID card and speak to the Case Manager working on the care in progress to learn of “how to” obtain a second opinion or visit the benefits coordinator at work to learn more about this option.  It is good information to know and if it weren’t for the one Physician suggesting this option to us I wouldn’t have a wife to talk about today.

Interviewer:   What was done differently at the new Physician’s office at Duke?

Angelo:   This visit bought my wife her fourth Colonoscopy and Endoscopy, however; we didn’t fight it.  If it was going to help the physician diagnose and treat this infection, we’re all in.   The results were on the positive side, no noted new changes or new diagnosis and another negative Celiac/biopsy was done via: endoscopy.  The Physician made a decision to utilize a medication being clinical studied for C. difficile that was already FDA approved for a different gastrointestinal diagnosis.  The cost of the medication was, as they would show on a menu, $$$$$.  We were extremely happy that this physician had the medication samples available.   Ten days of taking the medication prescribed there were noticeable changes taking place.  There was less bloating, less cramping, a lot less pain, the explosive – watery stools that were >15 x’s in a day were decreasing.  We had not witnessed any positive changes in almost a year.
This was a down right miracle in our book.

Interviewer:   You mentioned the medication expense.  Did you encounter other financial expenses during this infection?

Angelo:   Financial Expenses?   We drained our savings first after my wife was forced to resign from her job.  You can’t work in Nursing when you are tied to the bathroom, they don’t go together really in any job.  You just can’t work and shouldn’t work if you are being treated for an active CDI because it is a contagious infection.  That is why in the hospitals and healthcare facilities isolation precautions are implemented to help stop the spread of the infection.  So we go from being a two income family to a one income family over night.  Is anyone really prepared for that kind of a financial change over night?  The 401K was utilized to cover healthcare costs, prescriptions, co-pays, emergency room fees, specialists, travel, outpatient diagnostics, and the monthly hospital bed rental.  The mortgage was based on our income — joint, the vehicles were purchased separately, there weren’t many monthly recurring bills — it was all of the new bills being created by this illness.   Now we’re faced with the medical bills, and how do we pay for the living expenses all on one salary coming in?  You do what you have to do, we drained all of the retirement funds and the golden nest egg was scrambled.

Interviewer:   How long did it take your wife to get back on her feet and back to work?

Angelo:   It took her almost two years to feel strong enough to re-enter the work force.  From being ill so long and bed ridden from exhaustion, there was physical therapy, there was working with two Registered Dietitians from the hospital to retrain the gut after being on a clear liquid diet for over a year.  There were weekly visits to specialists who were monitor all the systems that were affected by the negative impact of this infection.  Hematologist, Gastroenterologist, Cardiologist, Endocrinologist, and P.T., and so much more.

Interviewer:   Do you have any message that you would like to share with others who are the  spouse/partner/significant other with another diagnosed with a C. diff. Infection?

Angelo:   Sure.   Don’t give up!  There were so many days that were darker than nights and we didn’t think there would ever be a light at the end of the tunnel.  It’s through our faith, our hope, and support of friends who weren’t afraid to visit us, along with reaching out to dedicated professionals and the Foundation’s that work with these professionals that care and know how to maneuver through the thorn bushes that brought us forward and through this nightmare.  We’ll always be dedicated and supportive to the C. diff. community and the C Diff Foundation and their members for their continued help.

 

We thank Angelo for his time and for sharing this journey through a C. diff. infection with a spouse, partner, soul-mate, or significant other.

 

To hear more about C. difficile infection prevention, treatments, clinical studies, environmental safety products and home care —  access  the C. diff. Spores and More Global Broadcasting Network Podcast library and listen to topic experts share educational information focused around C. diff. and other healthcare-associated infections.
please  click on the logo below *

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4-11-16 C Diff Foundation

C. difficile Infection (CDI) It’s One Day, One Hour, And One Step At A Time

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Health, defined by the condition of being sound in body, mind, or spirit; especially :  freedom from physical disease or pain.

It can’t be bought, is usually taken for granted, and not easily restored.

 

Being diagnosed with a Clostridium difficile infection (CDI) or better known as C. diff., wasn’t too terrible.  The directions were received from the doctor, medication was ordered and picked up at the pharmacy and recovery was right around the corner.   So we thought.

It’s not an infection  I want to talk about at the bowling alley with my friends, the family doesn’t understand it, not too sure the doc fully understood the road I was about to travel either.

The countless hours began sitting behind the computer searching, reading, freaking out at the copious amounts of negative words describing this bug.

So now I have a pile of information, a sick – sick stomach, bottles of meds, a few bills attached, the jumbo pack of T.P., and an on-line order of products that kill the spores that live in the fecal matter that cause the nightmare.

How in the world did I get this?  Antibiotics?  Out in the community?  While visiting a friend in the healthcare building?  Maybe at the local gym?  Off a contaminated surface somewhere?

The possibilities are many.

It took over three months and three different meds to break the cycle.

Not what they call infected anymore but you tell my G.I. system that.  Still living with the now and then symptoms and upsets.  Never sure when the 100 yard dash is going to take place and always careful about eating out at social functions.  Only four weeks post-C. diff. but I wanted to share a few words with everyone going through this.

Don’t give up and speak up because as the old saying goes the squeaky wheel gets the oil.  Thanks to the C diff Foundation for the information and support.  They understood the pain and suffering when others shunned me and walked away.

Steve C.,   Survivor

 

C diff Infection; I Don’t Want To Feel This Way Anymore

No one understands the pain, the symptoms related to a C.difficile infection (CDI). The symptoms that cause isolation — either because others are afraid to visit or because you’re tied to the restroom or because the body is exhausted from depletion and the constant fluid shift. No, not many truly understand the pain that a body endures during the treatment for a C difficile infection and the healing process —- YOU are not alone and we do understand. For C.difficile infection information and support call the C Diff Foundation’s hot-line and speak with a information specialist today
1-844-FOR-CDIF (1-844-367-2343)

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Warm Holiday Greetings From the C diff Survivors Alliance Network

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The holiday season is upon us; A time to share warm holiday greetings while reflecting upon the many individuals combating a C. difficile infection.

We especially call to mind those who have passed away from a Clostridium difficile infection and/or
C. difficile involvement while fighting other diagnoses simultaneously.

 

 

The all-encompassing nature of chronic illness and its disruption of life and plans can elicit a wide range of emotions. These responses include: stress, grief, anger,fear,depression, and anxiety.  Be kind to yourself.  Take time for you during the holiday season.

Try experimenting with different ways of managing stress and painful emotions. When you find a technique that works, try to incorporate it into your daily or weekly routine. Some ideas include exercising, walking, yoga, listening to music, deep breathing exercise, meditation, cooking, reading, writing in a journal, and spending quality time with family and friends.

We would like to take this opportunity to say that during the year it has been truly appreciated to stand along-side the many patient focused and educational organizations, healthcare professionals, and scientists researching and developing new preventative measures, and treatments to combat C. diff. infections along with the long list of  “superbugs.”

Through continued education and advocating for C. diff. infections and Healthcare-Associated Infections (HAI’s) positive effects are taking place in raising awareness  in prevention, treatments, and environmental safety worldwide.

In 2016 we look forward to releasing newly developed tools for patients, “C. diff. Survivors,” families, healthcare professionals. and residents in every community while  working toward a shared goal in witnessing a reduction of newly diagnosed  C. diff. and Healthcare-Associated Infection (HAI’s) infections.

None of us can do this alone…..all of us can do this together.

Thank you for your continued support and from all of us at the C Diff Foundation, and we wish you and your family warm holiday greetings.

It’s Not All About Twinkle Lights and Bows During the Holidays

After battling a year’s worth of illness and nine rounds of Vancomycin antibiotics to rid the body of recurring C. difficile infections — the holiday season was more of a struggle than a joyous time of the year.

 

 

Without working and knowing what a paycheck looked like after a year how was I supposed to celebrate the holidays with family and friends?  The jewels of diamonds and rubies had been sold to pay for the extreme cost of antibiotics to treat this never ending infection, the IRA’s used to keep a roof over our heads, the 401K used to keep the car in the driveway, and the savings accounts emptied to cover co-pays and medical bills.

Life was not as it used to be with twinkle lights and big red bows.  It was looking more like “brown paper packages tied up with string,” (My favorite things Lyrics by Rodgers and Hammerstein).That too became a positive vs a negative as the value of life became elevated and not the values in life that we collect.  Realizing that family and friends also valued the little things like fresh baked cookies over gold trinkets purchased at the local jewelers, and the boxes of home-made ornaments I created hung elegantly on their walls and holiday traditions instead of the boxes of store bought items that I never really noticed them enjoying or using over time.   We put too much emphasis on the gifts during the holiday season instead of cherishing the times together.  Share time, create lasting memories, give love, cherish moments, embrace smiles, enjoy the hugs, and never miss the chance of taking a photo to freeze frame it all.

After being referred to Hospice and introduced to their organization it was an absolute wake up call.  It was a call to LIVE ~ a time to kick up the sand and give it all I could give because there was way too much more to do than lay down.  Don’t ever give up ~ don’t accept every deck you are dealt ~ seek other avenues and keep reaching for the stars.  Our thoughts are stronger than we think they are and our beliefs are the strong hold in life.  As the saying goes, “Begin each day with a grateful heart.”

The holiday season is right around the corner and so are you with your talents and strengths.  Keep the anxiety down to a dull roar and try not to fall into the depression of dwelling on the “have-nots” when you have SO much ~ so much to give of you ~ so much to share with others ~ so much to embrace.  YOU are special to SO many and focus on the true meaning of the holidays ~ it is not about the packages, twinkle lights and bows ~ it is about YOU and about what you are in the world ~  You are a gift to others.

Try to have an enjoyable holiday season — through the losses, through the struggles, through the treatments ~ we understand and walk beside you each day ❤  You are not alone  ❤

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

 

December’s  support sessions are open for registration. Don’t delay

and register for a group today.  Registration is through the C Diff Foundation’s website

http://www.cdifffoundation.org

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C Diff Foundation Opens a New Avenue – C. diff. Nationwide Community Support Program

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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. (See note below [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,”

The C Diff Foundation 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 and fellow C. diff. survivors  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 Thursday of each month, beginning November 19th. 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. Both Community based sessions and Teleconference sessions will host healthcare profession 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