Posted by: sarcomafoundation | August 20, 2012

Rita’s Story on “NY Med”

It is not too often that sarcoma patients and their families see stories of sarcoma in the media.  After all, sarcoma is a little known cancer that doesn’t get the attention that other cancers do.  Part of the mission of the Sarcoma Foundation of America (SFA) is to change this perception– to shine the light on sarcoma and raise awareness.

So, the SFA is thrilled that all of America is about to hear the story of one courageous woman who was willing to share the details of her fight against sarcoma.  Rita Saverino Romeo, an SFA Board Member and 2011 SFA Courage Award recipient, will be featured in the final episode of ABC’s “NY Med,” a documentary series that follows the doctors and patients at New York-Presbyterian Hospital in New York City.  The episode featuring Rita will air at 10:00 pm EDT on Wednesday, August 22.  During the finale of the series, viewers will have the chance to see part of the 18-hour surgery Rita underwent to remove her grapefruit-sized tumor.

Rita Saverino Romeo

Why did Rita decide to share her story on national television?  We’ll let her tell you in her own words.

“Cancer was something that happened to other people, until it happened to me.  There is no good cancer, but when you are told you have a rare cancer, not only is your life turned upside down, but it seems that doctors forget to tell you about hope. And hope is exactly what is needed at this most challenging time.

After my diagnosis – and by the grace of God – there were many serendipitous events.  First, I found many survivors that beat the statistics and were shining examples of courage in action.  Then I found the Sarcoma Foundation of America, whose mission it is to advocate for more research for sarcoma therapies.  Lastly, I found Dr. Tomoaki Kato, who after looking at my scans said, “It is difficult, but possible.” After seven surgeons said that I was inoperable, this was music to my ears.  I remember thinking, “If he can do possible, I will do difficult.” 

Once the reality sunk in about my diagnosis, I realized that in addition to being positive about how I would deal with the cancer, I could make a difference by helping to raise awareness of sarcoma and raise research dollars for more therapies leading to a cure. 

There was yet another serendipitous event.  ABC was filming “NY Med” at Columbia Presbyterian around the time of my surgery.   Together with my husband, we agreed it would make sense to share our story if only to raise awareness for the need for more research for this orphan cancer and give hope to another sarcoma patient.

Rare does not need to mean fatal.  Unfortunately because of the limited research for this orphan cancer it often does mean fatal.”

You can help Rita in her desire to share this story with others.  Please tune in to “NY Med” at 10:00 pm EDT this Wednesday night.  Ask your friends and family to tune in as well.  Let’s all take advantage of this rare opportunity to raise awareness for sarcoma.

 

Want to know more about Rita and her “NY Med” appearance?  Check out these links for more information:

Synopsis of Rita’s Episode of “NY Med”

Rita’s “NY Med” profile

SFA Press Release

Rita’s 2011 SFA Courage Award Video


Responses

  1. Thank you for putting yourself out there. There is lot to be learned yet about this cancer but keep up the positive thinking…you can and will beat it. Sometimes htey say the real battle is mental, if you think you can’t then you can’t but set your mind on it and FIGHT FIGHT!!!!

  2. Thank you for your touching story, my daughter is a 7 yr Sarcoma survivor also. Hers was a soft muscle sarcoma which required surgery and radiation, I read about your story on the SFA website and have been waiting for this episode. I’m happy you’re doing better,and wish you well. I woud like to be more involved in the fight for Sarcoma awareness for all of the people affected by this horrible disease. Thank you for helping to make people aware.

  3. Thank you for your courage and gift of sharing. I was glad sarcoma had a beautiful spokesperson this evening.

  4. My husband just passed away from LMS. There is a great need for more research into this orphan cancer and I’m happy to see it get some national attention.

  5. My brother , aged 52 , died three years ago today of sarcoma..he did three clinical trials and because of this one of the drugs that they tried is now a protocol drug..there needs to be so much more research and effort put into research for this cancer..so happy for Rita…one of the lucky ones..God Bless

  6. Finally some national exposure for this horrible and rare cancer! I am 3 yrs cancer free after removal of a “cantaloupe” sized tumor from my right thigh which left me permanently disabled (soft tissue sarcoma). The scariest thing for me was after diagnosis when I tried to get info on my sarcoma ~ there was almost none! I hope that collaboration between doctors and universities and all who do research will lead to something good soon. Thank you Rita for putting yourself out there and hope all your scans are clear!

  7. Rita,

    Thanks for sharing your story, it gives hope to me. I have been fighting Ewing’s Sarcoma for three years now. So little is known about this orphan disease. I was initially told resection would not be possible. Since then the tumor shrank with chemotherapy and was able to be partially resected. However, it appears the tumor has now spread to my lymph nodes and I am dealing with other secondary side effects. Thanks again for putting a face to.Sarcoma. -Jenn


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