Wednesday, February 29, 2012
I went to the eye doctor yesterday, and again they did more tests. I hate when they probe into my eyes, especially with the bright lights. Their opinion is most likely it's residual damage from radiation treatments. At this time the effect on my vision does not warrant any treatment. I will be reassessed in 3 months.
Tomorrow, I will see my Oncologist. I will update you on that visit in the next couple of days.
Saturday, February 11, 2012
I can't believe it's already February. I've been feeling pretty good other than the stomach aches. They are usually a warning sign that I will be getting sick soon. I saw my oncologist and things look good. My headaches could be caused from the herniated disc at the top my spine.
I went to my optometrist to upgrade my glasses. She did a bunch of tests on my eyes and found my left eye to have some abnormal shadows. I have an appointment next week to see a specialist. There's a round circle behind the cornea and a bunch a little shadows scattered around near the nerves. I talked to my aunt and was told my uncle actually just had surgery on his eye for cancer. The surgery went well other than leaving his eyelid limp. He had to go back and have surgery on the eye lid. He's doing good. I think what they are looking for on me is either cancer or diabetes. I will keep you informed.
Jack and I are dealing with colds today. Jack is so funny, he hates his nose running and having to keep blowing it. He wadded up some tissue, put it up to his nose and taped it on his face. I wish I had a camera, he looks so silly. Unfortunately, I think I got my cold front him. He would sneakingly slide into bed next to me at night.
We are looking forward to next weekend where we will be up north visiting my parents. I have signed up for the relay of life. I will be walking for cancer in June. If anybody wants to sponsor me or join the team, you can go to relay for life.com caring for Cathy. I'm pretty sure this is what you need to do. If not, let me know.
Well I need to go check on my little man. I will keep you updated on my condition. Again, I would like to thank everyone for the prayers. I appreciate everything and take nothing for granted. Nikki Nolte thank you for calling me every day and checking up on me. You are a great friend and I cherish our friendship. Jen Klick, thank you for being such a good friend. I like getting together with you and doing crafts. I just wish we lived closer. All right again soon, thanks again everybody. Love, Cathy
Thursday, January 19, 2012
Wednesday, January 11, 2012
I was diagnosed with cancer in May 1st of 2008. The cancer was located in my left breast, 11 lymph nodes, my spine, and my brain. I was considered stage four with aggressive cancer. I had radiation for as long as the doctors would let me. Then I was put on chemo, which I am still on. The only difference is I am no longer on liquid chemo where I have to be in the office to receive it three times a week. I take a chemo pill three times in the morning and three times at night. It basically has the same side effects as the liquid.
The doctors removed my breast, and all my lymph nodes. They are unable to remove any lesions in the brain as there are too many. They are unable to remove the lesion in my spine, which is in my fourth or fifth vertebrae. If they attempted to remove the lesions in my spine I could very possibly become a paraplegic. Later on, I was diagnosed with cancer in my liver. Since then it has disappeared. So at this time, I have no cancer in my breast, lymph nodes, or my liver. The two cancers, brain and spine, will probably never go away completely. I have to keep taking x-rays to make sure the cancer is not spreading or getting bigger. I have been lucky as they seem to be not getting any worse. I was then diagnosed with a herniated disc near the lesion in my spine. This causes me to have headaches. Excedrin seems to help.
As far as the medications I am on, I do have different side effects. To me they are minor as they seem to be working. I will do whatever it takes to be with my family and friends. I will not give up. As far as the symptoms, I have lost a lot hearing, eyesight, balance, and I'm still a little bald. I do suffer from exhaustion and tend to get tired easily. If I get a burst of energy I use it to my fullest advantage. I do get stomach cramps and nausea. My husband, Mark, does do the cooking. He does however forget that my taste buds have changed. I cannot handle any hot spiced food, and have difficulty with just pepper.
As of right now I feel I'm at a standstill. I am on the same medication and see my doctor once a month, he checks all my levels and my reaction to the meds. Every six months, I either have a mammogram (half off, get it? ), MRIs, or pet scans. I totally trust my doctor and his PA. My doctors claim I'm a miracle. The mastistic cancer and stage I was diagnosed with made them feel I pretty much was a lost cause. My doctor confessed to me he didn't think I would have become a survivor this long. But, I'll never forgot he told me we had lots of options. He claims there had to be intervention. I know that intervention he is talking about is with the Lord Jesus Christ. I know I need to think my family, friends, and their friends, and even strangers, and their friends, for all the prayers they have sent my way. Thak you all!!!
Overall, I have to say this is not an easy journey, because I think about it every day. I try not to worry, as the load I carry is not so heavy with Jesus Christ by my side. I look on the brighter side everyday and tell myself it could've been worse. I will try to keep up my blog and keep you, my friends, updated.
As of right now, I still deal wth the symthoms everyday, never knowing which one will present itself. I do like surprises, lol. I take my meds, eat right, get rest, and try to live each day to the fullest.
I want to wish everyone a happy, healthy, wonderful New Year.
I love you all,
Thursday, August 26, 2010
I have been very busy this summer. I went to Ct. to visit my friend Alice. My cousin Carrie went with me. We had so much fun. I visited New York, it was wonderful, and surprising to many of my friends. the people were very friendly. In 3 weeks I will be joining my cousins, Vicki and Sue, for a trip to Hawaii. Vicki has time share she needs to use or loose. We can't let that happen now can we.
Jack started 1st grade. Its been difficult so far, he cries for mom. It just breaks my heart.
Ok, Friends and family, I need more prayers . 1st my son, Alex. I want him to change the facility he resides at. I am not happy with them. I cry when I see Alex, he looks so skinny. He shakes constantly. They don't return my calls. I want him out. Unfortunately, he is ready to leave but there are no facilities with openings. I would like him to be a resident of Clearbrook.
2nd, my friend and neighbor was surprised to be diagnosed with breast cancer 3 weeks ago. She is getting ready to begin treatment. Unfortunately, she was diagnosed yesterday with lung cancer. She is very scared. I want her to know her faith can carry her through the difficult days. Once she accepts the disease she will find it easier to cope. She needs to believe and be positive. She is only 30. Please pray for her to get the guidance she needs to believe she can beat this. I also pray that her family gives her the hope and care she will need during the coming months. I know all the prayers I've received from you all over the years has got me through some of the worse days and I thank you.
Enjoy the last month or so of summer and enjoy fall.
Love you all, Cathy
Monday, July 5, 2010
I am doing OK. I joined a new church and I am very excited about it. I am on the Chemo for the cancer in my Liver. It has alot more side effects than the IV. I am on it for 2 weeks and off 1 week. The week I am off the chemo I still feel the effects. To me, I feel, that means it has to be working or I wouldn't feel anything. I will have a cat scan on Thursday of this week to see if the meds are working or we need to switch to something else. Doctors say we have lots of options, so that's promising. I have been so busy this summer, I can't believe its July already. Jack and I haven't even been to the pool yet. He will begin school in one month, 1st grade. I will keep everyone posted.