Saturday, February 5, 2011

God is So Good!!!

I am so happy to say that I  am still officially in remission. I had a very stressful week. We cansirites call in Scanxiety. I swear I had a headache for a week before yesterday, I just knew that they were going to tell me that I had more brain tumors. But they didn't , WOOOOOOO HOOOOOOO!!!!! My oncology nurse also called me as soon as she received my PET scan report to let me know that everything is still stable. How many healthcare providers do you know that would go out of their way to give me the news asap ? The staff and doctors at Halifax Oncology ROCK!!!!!!! I am so lucky to have them in my corner. 
So to all of you, have a wonderful weekend,, I am going to get out and enjoy this amazing day that God has given us.

Wednesday, January 26, 2011

A story of Hope..

I just read an article from a woman named Katherine Russell Rich who is a 17 year survivor of metastatic breast cansir. Her story is one of hope. Some of what you are about to read comes from her book.  I am inspired and completely get what she is saying. So enjoy.
I deeply believe that there is no such thing as false hope: all hope is valid, even for people like me, even when hope would no longer appear to be sensible. Life itself isn't sensible. No one can say with ultimate authority what will happen with cansir ,a job that appears shaky or reversed fortunes .So you may as well seize all glimmers that appear.
Not to say that having stage 4 cansir is easy. It is tough, the waiting for scans, the pain, the drugs, the side effects, the not knowing what the future has in store for you. The dark days. Trying to plan for what might or might not happen. Some days I worry so much about what will happen to my family if this stuff decides to kill me. I try not to have too many days like that, but sometimes they just sneak up on me.
This past year I have had the joy of watching my sweet little boy, grow taller, get smarter ( he is so smart ) and learn how to talk . He is amazing. I also realized that my marriage is so strong and built on a foundation that only God has the strength to provide. I have a new appreciation for my family and friends. I am so excited about my work. I savor the opportunity to create someting beautiful for people that they will have for their lifetime.
I have new scans coming up on Feb 7, please say little prayer for me.
Wishing all of you blessed day. Do something today that makes you heart sing..

Friday, December 31, 2010

HAPPY NEW YEAR!!!!

As another year comes to a close, I find myself thinking about how blessed I have been . Things were pretty scary at the beginning of 2010. My future was so uncertain.
I now have 1 year as a cansir warrior under my belt. A lot of people use the word survivor, but I am still fighting so I think warrior is a better word. I have had the honor of meeting many more people just like me. They all have their own story to tell , some are very young and some are very old. Some of them talk to me, some won't, some think I am crazy. LOL!!! However, no matter what their circumstance I have learned so much from these brave people. I met a sweet lady during my radiation treatments who herself was diagnosed with breast cansir 3 years ago, the same year , her daughter was diagnosed with breast cansir and now her sweet husband is battling kidney cansir. I am lucky, she has been to hell and back. I have learned so much about myself this year. I have also learned that I have so many people that really love me. I am looking forward to 2011 with an anxious anticipation. I am so excited about the future . I am living my life 1 day at a time and hope to be the best person I can be for each one of them. So have the Happiest New Year that you can. I am going to.  Sending Love & Light your way.. xoxoxo..

Tuesday, December 21, 2010

Merry Christmas

I just want to wish everyone a Merry Christmas. It has been 1 year since my dx. It has not been an easy one, but I must say, it has not been as as bad as you would imagine. I am still here and able to work and take care of my family. Which is more than I can say about some of my friends with this disease. One of the women that I have had chemo with since the beginning died a couple of weeks ago.  She had the same kind of cancer as me. You know the statistics say that 1 out of 5 people with stage IV breast cansir will not make the 5 year mark. Wow!!!! 5 years does not seem long enough.( I know cansir is spelled wrong , but I read that spelling it wrong takes away some of it's power.) I am determined to be here at least 20 years from now. New treatments are being developed every day and I pray that in my lifetime there will be a cure. As of right now, I am still in remission, YAY!!!! I had a great report from my oncologist on Fri. We will know more about the brain mets in Feb, when I have a new scan. I hope those suckers are gone! That was the weirdest thing I have ever experienced. I felt like I was walking around on Mars. If any of you had a crazy conversation with me, I apologize. My head is feeling much better now.
HAVE A WONDERFUL HOLIDAY& ENJOY EVERY MINUTE!!!

Wednesday, November 24, 2010

HAPPY THANKSGIVING!!!!!

Oh my, where do I start. I cannot tell begin to tell you how thankful I am this year. For starters, I still here and starting to feel like my old self again. I finished  my radiation tx this morning and am so happy that is over. I  photographed 2 sessions today that were amazing. I just love my clients. My little boy looks up and just randomly says mommy , you are so cute!!! LOL!!!I know he was just trying to get his way, but I will remember that one forever. My husband still is and continues to be amazing throughout this. Did I mention how mean I have been .. Wow!!! he is really patient. So here it goes I am so thankful for.. God and all of the blessings in my life, my husband, my wonderful family, my friends, my sweet dog, my doctors, the sun, the moon, the rain, the trees, babies, children the bible, music, grass , flowers, chocolate, birthday cake, canon cameras, awesome lenses, all of my photographer friends, FPP, bright beginnings preschool., chemotherapy, radiation I could go on & on.
Here's wishing all you a wonderful and Blessed Thanksgiving... Love & Hugs,, Me

Monday, November 15, 2010

Feeling A Little Better

Wow, what a difference a couple of weeks make. I finally feel like I can do more than 1 thing at a time. That brain stuff is freaky.  I was and am still kind of shocked at how much it took out of me. I am finally getting some work done
For those of you that have known me for a while know how much of a workaholic I am. This little episode of my life has forced me to slow way down and realize that it is okay if I am not busy every single second of every day.  I am looking forward to a peaceful holiday season.
I just wanted to take a second to update, I am so hopeful that after my doctors appt. today, I  will be able to stop taking these steroids.  I can't wait to have my face back. LOL!!!!!
Have a love filled day. Find something that makes you the happiest and spend some time.  Sending Love & Light.

Wednesday, November 10, 2010

An Observation

Every day for the past 3 weeks I have attended some type of doctors appointment. Have you ever just sat and watched the people around you.  As I was waiting to have my therapy this morning I was watching all of the other people that have cancer too. There was a lovely couple sitting at the puzzle table, not saying a word to one another, but I could from across the room feel the love they had for each other. They were probably in their mid 60's. She was dressed in a hospital gown, so I am assuming that she was the sick one. I swear that I could feel his worry for her. They just sat there worked on the puzzle and enjoyed the moment. There is another man I also see every day. he cannot walk into therapy on his own and every day he has to wait for someone or a bus to pick him up when he is finished.  I am so lucky that i can still get there on my own.
Radiation therapy reminds me of a symphony. I lay on this table while the green and red lasers line themselves up with my body. There is always beautiful music playing. The lights from the green lasers do a little light show on the ceiling. Then quiet and you can hear the treatment. Only about 5 minutes and it is finished.  It is really kind of surreal.
I am always thinking about the other people that I have met since this all started. I hope and pray that many of them are still fighting and well, but I also worry when I don't see them . I wonder how their treatments are going or if they are going to make it.
Just an observation...