5 Years NED – Uterine Carcinosarcoma (MMMT)
I saw my gynecological oncologist today and I’m happy to report that I’m still NED, five years after my treatment for Stage 3B, uterine carcinosarcoma (MMMT) ended.
When I was first diagnosed, reading reports of others with this type of cancer who had survived for several years gave me cause to hope that I might have the same result. So, I’m sharing this news for the same reason.
I did have a different chemo protocol than usual, followed by pelvic radiation. You can read about the specifics by clicking on my user profile.
I know that things can change in the future, especially since I have Lynch Syndrome. But regardless of what the future may bring, I’m grateful for the time I’ve had during these past few years. I hope that with expanded use of genomic/genetic testing and new therapies, others here will have the same positive results.
Comments
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Congrats, cmb!
What a milestone you have reached! You are entitled to some fancy celebrating. Woo hoo! Here is to the next 5 years!
xxoo
Denise
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I agree! Here's to the next five. I think it is really important for us to share the good news too. It does give hope to other women.
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What great news! Congratulations!
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Yay!
Congratulations! That is such great news! And so encouraging for the ladies walking the same MMMT path as well as those with different types of uterine cancer.
Wishing you another 5+ quality years!
You have been such a treasure to us between the knowledge you regularly share and all the work you have put into this board to make it an incredible resource for our members.
Kathy
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WONDERFUL NEWS!!! Congratulations, cmb!!!! I am so happy for you. May you have 5 times 5 many more NED years! Hugs my friend.
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cmb, BIG CONGRATULATIONS to you on reaching the 5-year post-treatment mark!! And thanks for sharing this spectacular news with us!
You have done so much for the members and those who have visited this board over the years that I would have sworn you have been here at least double that amount of time!!
Hope you're doing some serious celebrating of this very special anniversary!
MoeKay
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Thanks, everyone, for your good wishes! I’ve always regretted that I didn’t find this site until just after I finished treatment, although it has been very helpful to me as post-treatment issues have popped up. I’ve found it to be such a great resource for new and old members alike.
I haven’t scheduled anything in particular to celebrate this milestone, but plan to do so in the next few weeks. But as happy as my family and friends are for me at this time, none of them really understand how I feel right now. But I know you and many other members/guests here can relate in that deeper way.
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Dear Cmb, the rock of our board--
You have, more than anyone here, been the calm in the storm. The lighthouse. I want to thank you from the very bottom of my often-stressed heart for every single thing you do. You are a researcher. You notice obscure bits of information, which you generously share out. And you are simply a kind, thoughtful person.
Sending you great love and the most admiration I can ever muster!
Deb <3
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And ps, so damn glad for your health. What a gift your life is to so many.
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I think it is the one of the most difficult emotional thing that we experience, our family and friends have no idea what the toll this takes on us because we are always trying to spare them. Yes, 100% cmb, we understand in a way they can not. Your contributions to this board since I have been here (2018) have been invaluable. Thanks so much!
Denise
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Wonderful news! Congrats! A big hug and thank you for all you do for us!
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Congrats, CMB! You are our mountain.
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Dear cmb,
I’m sorry I’m late to this congratulatory party! I’ve been on vacation.
CONGRATULATIONS!! I’m soooo happy for you! And I want to thank you, too, for being the rock of this board!!
YOU ARE AWESOME!!
❤️❤️❤️❤️❤️, A
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