Alisa

Hey all. I just wanted to share my good news – I just had a combination PET/CT and the results are in and I’m still considered NED (no evidence of disease). Yeah!!!! I was really nervous because it’s the first time I waited 10 months for a test. I’ve been on a 6 month schedule for the last 5 years (I was on a 3 months schedule the first 2 years) and for the past few years my onc was trying to get me on a 1-year schedule and I finally agreed to wait 10 months. I was so stressed out waiting 10 months that I asked the doctor to put me back on a 6-month schedule next time and he said ok. So I will be getting a CT without contrast every 6 months as they are watching me for a new primary and not a recurrence at this point. I am so relieved and I can breathe for another 6 months now. I hope this gives others hope. I was Stage 3a and have been NED for 7 years since surgery and chemo. Blessings, Alisa

Hey guys. I've not been fortunate enough to attend any of our annual events, but I just had a thought - My sons and I will be in Orlando for Easter Week. We have a time share at the Marriott Vacation Club. It's not big enough to house guests overnight, but I'm sure I can arrange to use the facilities during the day for barbeques, miniature golf, picnic areas, boating, etc. If anyone thinks this is worth looking into, let me know. I believe you all would need to make your own rooming accomodations, cause the vacation club is booked in advance for Easter Week, but I may be able to get people special rates at any Orlando Marriott, because being a Marriott Time Share Owner and Elite Member gives certain perks. I look forward to responses and hope this is doable. Katie - what do you think?

Hi Joe! It's great to see you post and what a great milestone .... Best regards to you and your family, Alisa NYC

I was moved by your post. I have no words of comfort as it is so difficult. Before I was a lung cancer patient myself, I was caregiver to my mom towards the end of her lung cancer battle. It was so painful to watch her suffer. The only advice I can give to you and your mom is to say what you feel to your step dad whether you feel he is comprehending it or not. I was in denial, and refused to believe my mom was dying. Looking back I see it was obvious. But because I couldn't face it, I never said all the things I wanted to tell her and I wished I told her how much I loved her more than I did. I have issues with that to this day and am so sorry. So, keep telling him ....

I am so sorry to hear that John's mom passed away. That's hard news I know. Please tell Mr. Ry that you all are in my prayers. Love, Alisa

Tee Taa, my prayers are with you and your family. Love, Alisa

There's tons of posts on this subject. You should check out the section "Alternative/Complimentary Care". Take care, Alisa

I flew from NYC to Orlando to take my kids to Disney World in between my chemo treatments (I had 3 weeks in between each treatment). Not only did I fly, but I went on all the upside down roller coasters in the theme parks, and believe me, they seemed to go higher than the plane!

Nushka, you have my prayers. I look forward to hearing about a clean scan when you get the results.

I take the Acai Berry extract after reading many reports about the berry and anti-cancer. If anyone wants to know where I get mine, you can PM me.

Hi Jamie! Happy Milestones and Happy Anniversary. xoxo

Hey Debi! So you are relocating to NYC? Where? I live on the upper west side and work in midtown east. When will you be here and where?

I am a 7 year survivor. Had chemo, no radiation (see signature line). There are many success stories ...

Oh, that really s*cks. I'm so sorry. There's been a lot of new research news coming across the boards for sclc. Hopefully there is something good for your Dad.

Along these lines - a great book is "Many Lives Many Masters" by Dr. Brian Weiss. It helped me a lot. I highly recommend it.

Hi Cheryl. I'm glad you clarified your post for those that don't know you, although I knew just what you meant and support you! I'm glad to have you back posting as you've helped so many over the years. I pray for successful treatment for you also. xoxo

Great news, Heather!

Hi Jamie! I've been on Milk Thistle for at least 6 years. Not only is it good for liver support, but there's studies on milk thistle and lung support also.

Thanks Ernie. I am also into supplement/herbs/mushrooms and find your posts interesting. Lef.org also has some great reference articles on CoQ10 and cancer, among other articles.

That's wonderful! It's such a blessing to get a sign. When I was joking with an acquaintance once about my mother's spirit being in the house, the lamp next to us started flickering on and off. Take care, Alisa

Don, I think what you are doing with the ministry is wonderful and so meaningful. I wish you many blessings and peace. Fondly, Alisa

Yes, Katie's birthday is worth multiple postings. Happy Birthday!!!!!!!!!!!!

Mark, how can any of us ever forget Leslie! I loved her posts and her picture with the fish lips always brought a smile to my face. It's so nice of you to check in on us and I hope you are well. I can't imagine how much you must miss Leslie, as I was only a cyber buddy and I miss her. Best regards, Alisa

Great news, Cindy! Thanks for sharing.

Hi Cheryl! I was very happy to see you back on the boards when you returned. I'm sorry if I missed any posts because I would certainly reply. I never forgot you when you were away and I don't want you to think you are forgotten or not cared about!