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Thank you for sharing my story i just hope it changes ONE person's life and make them understand that we are only here as long as god allows us to be. Your life can change with just one phone call, i know mine did.
I happened upon this site by accident and it seems as tho this is what I have been looking for. Thank you so much for taking the time to give folks a place to go
Hi there . LC survivor here from the UK . Treatment for LC continuosly April 1981 to August 1984. Side effects are many and varied after Chemotherrapy, Radiotherapy and operations. I'm not a person to hold back on what I tell people but much of the treatment I had will not now be used or will be greatly refined. My story is thatt there is a long future after treatment but its not all good news. Some of my side effects are quite severe at times. I'm just not sure that me writing my story truthfully would be of help despite me being 28 years clear of LC. Much love to you all xx
Welcome Debra and congratulations on your 2 years! Wishing you many, many more! xoxo Christine
Debra Burke says...I am into my 2 year anniversary of being diagnosed with stage 3b adenocarcinoma. I have lost alot of friends with this terrible disease. We all need to stand together and fight. Prayers to all, Debra
I am into my 2 year anniversary of being diagnosed with stage 3b adenocarcinoma. I have lost alot of friends with this terrible disease. We all need to stand together and fight. Prayers to all, Debra
You are absolutely AMAZING! What you are doing is so great! I feel so, so blessed to have you a part of my life and our teams! LOVE YOU!!
The new site and your words are wonderful Chris. In less you been in the shoes, you have no idea how it pulls at your gut and heart for a very long time. hugs to you , Sandy
Hmm I replied to the posts here but they don't seem to be showing up.. I want to be sure everyone knows how much I appreciate you coming by and signing the guestbook and also want you to feel free to share any and all comments and suggestions! Also please tell your friends to come by and say Hi and check out the content. The more people who come by, the more people we can educate about this horrid disease.
Love and Hugs
Haven't seen it ALL, but what I have, is awesome!! I'll be checking in on the blogs and maybe even putting my 2 cents worth in. You are incredible Christine and I am thankful to have you on my side! XXXXXXXXXX's Heidi