Remembering All C. diff. Survivors With Warm Thoughts and Gratitude In The New Year

2014 is coming to a close and 2015 is just a few hours away.CDIFF2015wordss

 

As the New Year approaches, our thoughts turn gratefully to those who have helped us in our progress and the progress of our communities.  It is in this spirit we say, simply and sincerely,  thank you.

 

 

Thank you for everything big and small you do to help make the C Diff Foundation a better resource in the lives of others, providing support, and for joining us in raising C. diff. awareness to the millions of families, healthcare providers, communities, and friends worldwide.

We are a giving Foundation and a lot of that giving is facilitated through each of you.  Giving makes a difference and there are so many different ways to give.  Whether it is through presentations at a conference,  sharing your journey with others, joining the Foundation’s volunteer program, or donating time in November for the “Raising C Diff Awareness” campaign in communities across the globe the partnered efforts and contributions are greatly appreciated. Through the many facets of giving and charitable support, the Foundation’s mission continues to move forward in educating, and advocating for C. diff. prevention, treatments, and environmental safety worldwide.

From all of us to all of you and your families,  we send our best wishes for a peaceful, happier, healthier, and successful 2015!

Thank you and Happy New Year.

C. diff. Survivor; Kristin Evans

Kristin’s C. diff. Survivor Story:
I contracted c.diff. when I had my gallbladder taken out in July of 2012. I was experiencing a lot of abdominal pain and diarrhea but attributed it to my body adjusting without the organ I went to the ER around 21 times over a year and a half before I was finally diagnosed with C.diff.
After that began the real journey, after loosing over 100 pounds in a year which took me from a size 10 to a size double 0 my doctor decided the repeated rounds of Vancomycin were not fighting the infection he suggested a fecal transplant. I was very confident in this procedure as I had only heard amazing and positive things about it.
I had the transplant done and waited a month to be checked again as I was told to by my doctor. I went in and of course the transplant failed. I was then put on more vanco and told to stay on it for another month then they would check me again.
Another 2 weeks went by and I was emergency admitted to the local hospital because my body had begun to shut down and my organs were beginning to fail. I was on full isolation for 2 weeks until the declared me c.diff. free. I was told sent home with a new problem caused by the c.diff. though.
I now had enlarged lymph nodes and they would not go down so I had an oncologist look at them and told me I had a possibility of Hodgkins Lymphoma and was scheduled for a lymphectomy a month later. After surgery I was cleared from cancer but I had contracted c.diff. back because of the surgery.
I was then diagnosed with chronic c.diff. and told we would try another transplant to try and kill the infection that was slowly killing me again.
The second *fecal transplant was again a failure and I was put on vanco for another year before I told my doctor I was going to die if he didn’t help me.
I had survived almost 3 years fighting this battle and my body was physically and mentally drained. I was tired of fighting, so he made the decision to hospitalize me again to try and cure this once and for all. I was in for almost a week before I was declared once again C.diff. free.
It has now been less than a month since my release and I am learning to deal with my new medical problems caused by c.diff. including gastroenteritis, ulcerative colitis, severe chronic IBS and permanent bowel damage.
I have been to the ER a total of 46 times throughout my journey with c.diff. and am still continuing to get my body back to way it needs to be with my weight and my eating which has become difficult due to the bowel damage.
But i will not give up and i will survive and fight this if it ever returns i will not let c.diff. take my life. Thanks for reading my story guys.

C. diff. Survivors Alliance Network Officially Launched

 

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The C. diff. Survivors Alliance Network, an affiliate of the C Diff Foundation,  is dedicated for providing healing support for individuals coping with both physical and mental pain, the complex treatments, psychosocial losses and alterations, and the excruciating grief with complex emotions that accompany the loss of a loved one.
 
We hope that you will find resources here to help you cope with, and eventually heal from, what may well be the worst pain experienced from an infection.