Ryan and Cristina had their baby yesterday!!! Sariah weighs 8lbs. 7 oz. I’m a very happy Auntie! There is nothing sweeter than getting to hold a brand new baby straight from heaven. Life is incredible! It is amazing to watch how life unfolds: some of us are taken from this earth as others are arriving. Such sorrow and joy can happen so quickly in our lives. I’m just thankful to be able to experience it all. This new life is all the more sweeter because I truly understand the sorrow of a loss. My heart was just overwhelmed with love and joy getting to see her today. My boys really wanted Ryan and Cristina to name the baby Sacajawea but have settled for a mix of Sariah and Sacajawea – they now call her Sacajariah. You have to love my boys and their imaginations. I also got a chance to take a few photos today. I have missed photography SO much! All my love to the newest member of the family! ~I love you Sariah!~
My Heart is Heavy September 27, 2007
This week I found out that someone I love who has been battling cancer for years has now been given days to live. Another man I knew back in San Diego who had a miracle of surviving cancer for 3 years when he had no hope has now relapsed. Today I found out the person I have been e-mailing with who has Hodgkin’s like I do found more tumors in her pet scan and now has to do a stem cell transplant. My heart is so heavy. This is such a hard battle to fight. It becomes so hard that there is a line that you come to that you just can’t do it anymore. This is a battle for life. Quality over quantity becomes your decision. My heart goes out to the families who are there by their loved ones sides. I know you are feeling helpless. The one thing that is comforting no matter what stage you are in is to know you are not alone and you are loved. All my love goes out to those who are battling this with their families.
My meaning of life September 26, 2007
I’m really trying to grow from this horrible day of nausea, bone pain and body aches. I feel like I’ve been hit by a bus and it feels better to just lay in a heap than to move. One more Chemo left you might cheer….. But on days like these one more chemo feels like a death sentence. To me it is like walking down the green mile into a torture chamber. All those who love you are walking you down for this horrible torture and there is no one to run to. You have given up hope for escape. I just have to obey and let it happen. It is twisted, but I have found everything involved with cancer is twisted.
Everyone will come to their own conclusions on what the meaning of life is for them. I think I have figured out a few for myself. One is to love. It is the most powerful tool we have each been given to use here on earth. Also experiences. We are here to experience things. We would never know the good if we didn’t have the bad. We couldn’t really cherish things unless we had felt loss. With everything we experience, our knowledge expands. We are able to find more depth to our souls through experiences. If we take time to really evaluate our own trials and triumphs in this, we will see how our lives have been molded by these experiences.
Just as bad as I remembered September 25, 2007
We began the morning driving to Sharp to pick up the copies of the PET scan b/c the radiology Oncologist didn’t have them. Then back up the Escondido (30 min drive each way) to deliver them to her for the apt, only to find out they didn’t copy both scans. So we don’t have a definative plan for my radiation treatment yet. You see, I’m once again a special case. I don’t fit all the perfect requirements to have radiation. But I do have bulky masses. Dr. Coleman, my radiology oncologist, is going to look at the other scans and talk to her associates, Dr. Shiftan and some doctors at Standford to see what they think. This is a very hard call. If I do get radiation there is a much higher chance I can get breast, lung, heart, skin and/or throat cancer b/c where they have to shoot the radiation. I also have a chance that I will loose the function of my thyroid and have to take meds the rest of my life. There will be permanent scarring in my lungs. If I don’t get the radiation, I may get lymphoma again. This is a VERY hard decision. The side effects of radiation are so scary. I don’t have a good track record of beating the odds. Now we are just going to wait and see what all the doctors think. If we do go ahead with radiation I will start the week of Nov 11th and will go 5 days a week for 4 weeks. That is one less week then I had mentally prepared for so that is good news already.
Chemo was AWFUL!!! I started throwing up in a bucket as soon as Judy pushed the A drug into my IV. I felt just horrible for the poople next to me watching this happen. I think one of the women there it was her 1st time. That must have been hard to see. Plus, when I see someone throw up I know it makes me do the same. But I couldn’t run to the bathroom b/c Judy had to finished pushing the drug. So I just sat there and kept throwing up in the bucket. It was hard to do that in front of everyone. I don’t like to throw up in front of anyone. After Judy was done pushing the drug and I was back to the bag of IV chemo I ran the bathroom. Then I just stayed right outside the door so I could go back in and throw up. It was a really rough round for me. I feel so sick and yucky. I hate it when your body is taken over by this horrible chemo force and you can’t seem to escape it. Even when I dream it seems to find me. I can’t wait for my last chemo. What a huge party we should throw. It is a party celebrating life and the blessing this truly is to have another shot at living it to the fullest. It is a great opportunity to learn and become better because of it. I pray with all my heart that I have learned what I need to from this and never have to repeat cancer. When people say, “Cancer sucks!” It doesn’t even begin to do it justice. Cancer rips the life out of you and breaks you down so that you wish you could die just to escape the pain. It also shows you humility, love and compassion for others in a way you would have never guessed. To be a Mother is such an honor. For all the times I’m stressed out by my little ones I do remember how truly lucky I am to be alive. I would not trade any hard stressed out crazy Mommy days to go through cancer. I will forever feel greatful and humbled by the fact that I will live and be able to watch, rear and love my boys. I can’t think of a greater gift I could have been given. Life is precious and so fragile. Life is not defined by our trials, but how we handle them. I hope tonight you take a moment and really appreciate your life and how wonderful it is to be here.
Count down…..2,1 September 24, 2007
I’m so happy I only have 2 left. I’m in a much better place this week then the last round. I think the vacation was a perfect break for me to feel like a normal person. Now I have enough in me to handle another chemo. We meet with the radiologists tomorrow morning to find out the plan for radiology. It is and hour and a half appointment. So I’m wondering if I get my tattoos tomorrow. Never would have pegged me for the tattoo kind of girl. But cancer certainly has brought me a few surprises. I had my acupuncture today and hope that will help lessen the side effects tomorrow. I hope you all have a wonderful day. Wish me luck with my poisons tomorrow….I mean wonderful cancer fighting drugs.
I’m Back September 23, 2007
We had such a wonderful time. There is nothing like a vacation to help you forget cancer. I was really amazed by the public transportation in San Francisco. I also watched how many people coughed in there hands then put their hands on the rails and seats. I was over sensitive to germs. I carried around hand sanitizer and was constantly washing my hands. It is amazing to watch how many people touch the same things. If there was ever an outbreak of some diseases it would spread like wild fire there. It was a relief to be back and in our car. That may seem funny but I really enjoyed the privacy.
My hair is growing back on my head. SO STRANGE! I’m still loosing my eyebrows and eyelashes, but for some strange reason my head hair decided it wanted to come back. I still have 2 more chemos left but my hair has decided it wants to grow again. I have to just sit back and laugh about how strange (I mean unique) my body is. My hair is coming in black. So to respond to all the speculation about chemo changing your hair color, it sure did for me. Tyler has informed me it looks funny and I should dye it. I have the G.I. Jane look going for me now. I think with my radiation tattoos I will be set for Halloween this year. Anyone have camo gear I can borrow.
San Fransisco September 21, 2007
I’m here in San Fransisco having a wonderful time! We have done so much in so little time. It is such a busy city with great people watching. We are going to go and do another double deck bus tour today and go see the parks and golden gate bridge. I saw Alcatraz yesterday and most of the city. We enjoyed some wonderful Chinese food in Chinatown. We had some Italian ice cream in North Shore. The first night we went to a dinner theater that was was really fun and entertaining. I”ll be home tonight after taking planes, trains and automobiles, along with trolleys, subways and a bus.
They have quite the public transportation around here. I hope you have a wonderful Friday. I feel so blessed and lucky to be here enjoying life. I really am in awe of life and how precious it is. Special thanks to MOM for watching our munchkins so we could be here. I love you!
So SLeepy! September 17, 2007
It was a long night with Luke and Adam awake. I had a hard time falling asleep because every bone on my body ached.. I can serious feel every little tiny bone in my body. It is quite annoying now and I just wish for this to pass quickly. It seems the more I can do to be distracted the better. My anniversary is tomorrow!!! Russ surprised me and is taking me to San Francisco Wed- Friday and my wonderful mother will watch the kids for us. I’m so excited I can hardly stand it. I just love being able to look forward to such fun things. It makes life so sweet! Life is too short to miss out on opportunities to celebrate. Too many people work too hard and never take the chance to just enjoy themselves. When we really have to evaluate our lives do we ever say, “Gee I wish I had worked a little more?” When it is all said and done the thing we will treasure the most is TIME. How we spend our most precious gift is up to us.
Calling all GERMS!!!! September 15, 2007
I would like to invite any other bug, germ or virus known to man to join my household. You would think I would be spared all these horrible bugs, but unfortunately they seem to be spreading. Adam came home from school Friday with a fever. I was up all night with him wheezing and 103 temp. He felt horrible. Adam was in the bathroom waiting for me to refill his drink when he said, “Mommy thank you for taking care of me.” That just melted my heart! No matter how sick I felt I seem to feel energized enough to do what is needed to help my child. It just broke my heart to hold this hot little body in my arms whispering to me b/c his throat hurt too much to talk. I called our good friend Dr. Mazur this afternoon to ask him if he thought I should take Adam to the ER. He was so kind and came down to check Adam out. We found out our poor little Adam has pneumonia. We got him some antibiotics but he is still so sick! I was so relived not to have to take AJ to the ER and deal with all of the horrible germs there. Dad woke up this morning with the flu. I’m praying we are done after this round. I want everyone to get this out of their systems and be immune for the rest of the season. TOO MANY SICKOS HERE!!!!!
One thing I realized through this is that I’m my parents child. It kills me to see Adam sick. I feel so paralyzed to do anything. I can just hold him and try to treat the symptoms. This must be how my parents feel. I forget I’m a daughter and their child. They must ache and cry because they can’t do anything for me. They have to watch their baby suffer. It really opened my eyes to see how hard this must be for them. I can’t stand seeing my kids sick. So I can now see and understand how much it pains their hearts to watch me go through chemo every other week. So Mommy and Daddy, “Thank you for taking care of me!”
Nose Hair September 13, 2007
I don’t think I have ever really thought about the hair in my nose before. I mean I know it has always been there but never really gave it much thought. Well now that I have no nose hair I have realized its purpose. #1 I can pinch my nose and my nostrils stick together with out me sucking them in. They just kind of stay there. Another thing is my nose is always running it seems. Now I have nothing to catch anything. It just all comes out. I know totally gross. But I thought I would share some new found knowledge with you on why you should appreciate your nose hairs. This is a picture of me with my new found trick of my nostrils sticking.
My brother Kevin and Dad joined me for Chemo this round. I have to tell you Kev took a picture of me getting the chemo as I downloaded the pictures I saw that picture & threw up looking at it. So I’m not posting that picture. My stomach can’t handle the memory quite yet. So maybe later after I’m not so queasy……







