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CARCINOID CANCER

A rare form of "slow-growing" neuroendocrine cancer

Susan Anderson - An advocate for Carcinoid and Neuroendocrine Tumor Awareness

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-----Short Version
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WELCOME to my web site!  I was diagnosed with Carcinoid Cancer May 10, 1995. Go to my Carcinoid section (and other sections, see to your left) to learn more about Carcinoid Cancer and for links to additional medical and useful information sites for people (and their families) with Carcinoid. Be sure to check The Carcinoid Cancer Foundation, Inc. (CCF)
 
I was diagnosed with Infiltrative Ductal Carcinoma (IDC) Breast Cancer on June 18, 1999.  There is NO connection to Carcinoid, this is completely different!
 

PLEASE take time to read "My Complete Carcinoid Story" or if rushed read  the short version "My Short Carcinoid Story", and review the information through this web site and linked from here -- the result of over fifteen (15) years of  my research and work (since http://www.carcinoidinfo.info/mystoryshort.htm May 1995), which shall continue. 

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NEWS - My book that turned into two books! - NEWS - Coming Soon!

In January 2011 I started writing my book that I envisioned to be 1/3 memoir, 1/3 family history and 1/3 Carcinoid NETs.  I allowed two full years for this project.  The editor I am working with suggested that I split it into two book; one my biography, Carcinoid NETs journey and Carcinoid NETs information, and two a family history book.  As a result all that is involved in writing a book with professional editors and book designer it is taking longer than expected. 

The first book is Becoming Sunny Susan by Susan L. Anderson; I am honored that Dr. Richard R. P. Warner wrote the forward; and the second book is Pioneers Past to Present.  Both books have table of content, a multitude of picture and full indexes.   I have the ISBNs for both books.  When available on Amazon.com and through my web site, I will let you all know via: emails, ACOR mailing list, my web site and FaceBook:  my wall, Carcinoid Cancer Foundation, Carcinoid Cancer Café and other site on FaceBook.

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Mildred “Millie” Kowalski, of Novartis Oncology announced at the Carcinoid Conference, in New Orleans, 9/22/2012 that I, Susan Anderson, am the recipient of the 2012 Warner Advocacy Award. I was sorry that we were unable to attend.  I am honored and thrilled to receive this very meaningful award!  Dr. Richard R. W. Warner, at my request, accepted this award on my behalf.  http://warneradvocacyaward.com/patient/current-warner-award-winner-2012.jsp

THE WARNER ADVOCACY AWARD

A LASTING TRIBUTE TO MONICA WARNER

To commemorate the life and work of Monica Warner, who passed away in August 2009, Novartis Oncology, through Patient Advocacy and The NET Alliance, established the Warner Advocacy Award. This award is presented annually by Novartis Oncology to honor the patient, advocate, or caregiver who most embodies the passion, dedication, leadership, and spirit with which Monica Warner assisted patients, caregivers, and families affected by NETs.

The recipient will receive an individual nonmonetary award of recognition. Novartis Oncology will donate $10,000 to an approved 501(c)(3) charitable organization of the winner's choice. Institutions and non-501(c)(3) charitable organizations are not eligible to receive the award.

 

Photo: Congratulations to Susan Anderson on receiving the 2012 Warner Advocacy Award!! 

The award was announced at the National Carcinoid/NET Patient Conference in New Orleans this past Saturday by Mildred Kowalski, Director, Patient Advocacy, Oncology, at Novartis Pharmaceuticals Corporation.  To commemorate the life and work of Monica Warner, who passed away in August 2009, Novartis Oncology, through Patient Advocacy and The NET Alliance, established the Warner Advocacy Award. This award is presented annually by Novartis Oncology to honor the patient, advocate, or caregiver who most embodies the passion, dedication, leadership, and spirit with which Monica Warner assisted patients, caregivers, and families affected by NETs.  To read more about the award, click here: http://www.warneradvocacyaward.com/index.jsp

Created in 1997, Susan’s website is the first and oldest online personal website in the carcinoid/NET community. Susan is a carcinoid patient and awareness advocate. Her website has a wealth of information and should be one of the first personal websites you should visit. She is a longtime carcinoid and breast cancer survivor with an aggressive approach to maintaining an active and lifestyle.  Visit her site here:  http://www.carcinoidinfo.info/

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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On November 10, th the Carcinoid Cancer Foundation released the second video, "Faces of Hope," in its 2012 series. Meet NET cancer survivors Claire, Josh, Judy, Kathy, Kenneth, and "Sunny" Susan (and Howard as a “care giver”) as they share their journeys about being diagnosed and living with rare neuroendocrine tumors, including lung carcinoid, carcinoid of the ileum, and pancreatic neuroendocrine tumors".  http://www.youtube.com/watch?v=5IqspD6YDEo  If you don't suspect it, you can't detect it."

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Check the "Monitoring Carcinoid" section to read about tests and test frequencies recommended by several experienced Carcinoid physicians, and the "Local Support Groups" to learn if there is a group in your area.  
 
I was diagnosed with Type 2 Diabetes December 6, 2004.  

You shall find useful books on cancer, healing, wellness in my Medical Library

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My husband, Howard, and I reside in beautiful Tempe, Arizona, USA, where the sun shines more than 300 days each year, the flowers are always in bloom, the birds are always singing, we usually have bright clear blue skies, and it is a great place to live, count our blessings, and enjoy life! 

April 27, 2012 was the 15th anniversary of this page.  As of 4/29/2012 there had been 376,401 "hits" or "visits" to the page. 

The guest book was added Nov. 16, 1998, but had to be taken down April 20, 2004 due to infiltration by spammers!

PLEASE continue to scroll down this page, thank you!


My Mission

I believe many of us may lead a full and active life while LIVING with Cancer, and other chronic conditions.  I have provided information and links for medical / drug databases, local support groups, humor, books, Bluegrass music, prayer lists, travel, political issues, AZ information, cowboy poetry, and much more that may assist you in living a full and almost normal life!  (Click the buttons on the left side of this page, or use the "Search" button to find a specific item of interest.) I have provided information and links to information I wish had been on the internet when I started my research in May 1995.

MY MISSION:  Answer the emails from around the world, generated by my web site, and provide solid medical information and/or links to such information.
Encourage people to:
           1) learn all they can about their kind of Carcinoid/Cancer,  
           2) consult with a doctor experienced in Carcinoid,
           3) do aggressive treatment, if appropriate for their case,
           4) do not obsess over the disease, and
           5) get on with life, give thanks for each and every day and live life to the best of their ability.


I consider myself an "advocate for carcinoid cancer and neuroendocrine tumor awareness".  I am a survivor of Carcinoid Cancer and Breast Cancer.

DISCLAIMER:  I am a patient and NOT a medical doctor or health care professional.  I share information and links to information that has been helpful to me and that I believe to be correct and good, but I cannot guarantee the accuracy of this information, except for MY stories.  I urge you not to rely only on this information but I believe you should discuss your situation and information with your medical doctors and/or other medical professionals.  "Sunny" Susan Anderson


 

Click on any picture above to see an enlarged image, thank you.

From left to right:   Howard and me in San Diego, CA, August 1995, within three months of my Carcinoid Cancer diagnosis and surgery; Kauai, HI, September 1997; Susan and Levi "The Birman" cat, October 1997;  at the first Carcinoid Seminar, Sarasota, FL, March 3, 1999; at my computer Oct. 1999; after the Carcinoid Symposium, Sarasota, FL, May 13, 2000; Susan giving presentation at the first Patient Support Advisory Board meeting in New York City, Nov. 2001; Susan member of Red Hat Society, Dec. 2003.
 

Contact Information

To email me:  SunnySusan@Cox.Net (Please see below)

Since 1996 --- when I first located others with Carcinoid --- I have answered every email sent to me, although some replies were delayed longer than I liked. I am NO longer able to reply to all e-mails due to the volume and other things going on in my life (all good).  I do love hearing from others, but an unable to reply to all individually.  This web was 15 years old on April 27, 2012, and my plan is to keep it updated for many many years to come.

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Since my husband "retired" I am away from my computer for days, and sometimes, weeks at a time.  Yes, there is wireless internet and we have tried that a number of places.  But, if I deal with email when we are away from home then it is not a "restful vacation" for me.

PLEASE use the SEARCH capability at the top my pages.  You may search for a word, a phrase, a drug, a treatment, a book title or anything you can think of. You may search this site only, or search the complete World Wide Web.

To speak with a person please know you may call the “telephone information and support line” of the Carcinoid Cancer Foundation, Inc. (CCF), Tuesday through Thursday  10 a.m. to 4 p.m. Eastern Time at  1-888-722-3132 (free) or 1-914-683-1001.   “The information and support line” is staffed by medical professionals.   Mondays and Fridays are research days, if you call then and do not reach a person do leave a clear message.  The Carcinoid Cancer Foundation’s (CCF) superb web site is at http://www.carcinoid.org

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CCF -  Serving the carcinoid/NETs  patient and medical community for 
more than forty years (chartered in 1968)
   “Meets Extensive Standards of America’s Most Experienced Charity Evaluator”
Better Business Bureau

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DISCLAIMER:  I am a patient and NOT a medical doctor or health care professional.  I share information and links to information that has been helpful to me and that I believe to be correct and good, but I cannot guarantee the accuracy of this information, except for MY stories.  I urge you not to rely only on this information but I believe you should discuss your situation and information with your medical doctors and/or other medical professionals.  "Sunny" Susan Anderson

Since 27 April 1997, you are visitor number:

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Last modified: 04/16/13