Vulval cancer and waiting on mri result for possible cancer in mons pubis

Hi Rosena,

I have been speaking with you on another post and have been unable to help you with your question. I wanted to comment here to say I hope someone that can help comes along soon.

Vulval cancer warrior xx

Rosena, I am so truly sorry for all your cancer and surgeries. I feel so bad for you and what you are going through. I am in the USA so I know things here may be different from treatment you are getting, it really all depends on our oncologists and their way of treating recurrency. I'm 52 and have had many many recurrences and surgeries as well. Please stay on top of any and all changes, tumors, lumps, itching you find because only you know your body the best. As you continue to have surgeries though you may find you have lost nerve feeling, have a lot more scar tissue and so on, along with lymphadema and other issues that may arise from cancer treatments. Although I have had cancer too many times to mention and too many surgeries to tell you, I will give you some hope that I am now 3 years cancer free since 2007, I saw my daughter get married this summer and looking forward to more living. xoxo

Hi Lisa, thank you for your lovely reply and I will keep on top or one step I front if I can, your advice I have noted so thank you for that, I'm so glad your cancer free thats amazing, well done, Im so glad you attended daughters wedding which is very special in one's life, I too went to my daughters wedding,

I wish you the very best and send my good wishes across the pond

Thank you once again reply appreciated xxxxx

I haven't posted my story but was diagnosed with VIN II and III earlier this year and had a WLE in early June. I am outside Chicago and just wanted to say to you Lisa that your posts are a big part of what helped me get through this (from you advice to you story) and continue to inspire me now as the waiting game starts for what will happen next. Can't tell you what it meant to me to see your post now. Thank you. Jill