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Friday, November 26, 2010

After Thanksgiving......

My daughter and I made a great Thanksgiving lunch. She was such a great helper. We made a turkey, home made dressing, home made chocolate pies (2), devil eggs and potatoes salad. I enjoyed cooking. I spaced it out so I could sit and rest. I got hot and we opened up a window. I did get dizzy once. But over all it was great.
We had a great day. Jeff and our son cut and split wood while we cooked. 
I am so thankful for my husband, our daughter, our son, my friends, and my family. I am so thankful that I am getting my cancer treated and I am still moving forward with my treatments. I am thankful that I did well with chemo. I am so thankful for all the love and support everyone has given to me, cause I never knew so many people cared about me. 
I am so thankful for my husband who has done a great job of being here for me. It has been hard but we are making in through the hard times. Our love prevails through all things. 
Thanks!!!!!!!!!!!

Tuesday, November 23, 2010

LAST CHEMO!!!!!!!!!!!!!!!!!!!!!!!!!

Well that's it. I am done with chemo.I dose a little then once home I ate. I finally took a 1-2 hour nap. I went to bed around 9:30pm but couldn't sleep because belly was hurting. I finally did go to sleep about11. Then by 1am I was awake. Bladder was full. Then hot slashes, heart burn and belly hurting until about 5am. Then at 6am got up and got dressed. So not much sleep last night.

Today is shot day. Last one of those too.
Next step is Herceptin on Dec 16th then every three weeks. They said they would give me benydrel do to side effects.

Still have watery eyes, dry skin, hands peeling, finger tips sore, hands swell some, hot flashes and night sweats. Other than that things are good.


Just ready to go back to work cause I am bored and I broke my sewing machine. So now I can make nothing else. I had great plans for it too. I made a vest and purse. I was going to make other cool things but now that is on hold. I may try to sew by hand but finger tips may not let me do much.

I can do plastic canvas and maybe some knitting but have to do it in small intervals.


Well hope everyone has a great Thanksgiving.
I am going to try to cook a lunch then go to his sister in laws' for supper. I hope I am up for it.

Friday, November 19, 2010

Update November 19th

Well I feel great. My skin is peeling off my hands in places. I am using some great lotions and stuff. My fingers tips are tender or sore like. I have some swelling in my hands. Eyes keep getting watery. Doc said to used eye drops and some kind of other stuff. I used eye drops but not really helping much.
Stomach is back to normal.
Well, I go Monday for last Chemo. We figured I would feel better on Thursday if we moved it up one day. Cause I always feel bad after shot. My bones hurt more last time. I took claritin but didn't seem to help much.
I go to radiation doc on Dec 15th. Then we can start rad. I will go Mon-Friday for 6 wks. Holidays and weather may delay me but total I will have to go 30 times.
I hope to get this done and get ready for reconstruction surgery. I will have to wait 6 wks after Rad do have it done. Can't wait to be done with all this. I want to have fun this summer and be able to do things.

Have a Great Thanksgiving!!!!!!!!!!!!!!!!!!!!!!!!!!!!! 

Thursday, November 11, 2010

Day after shot

I am tired but feel good. Stomach messed up not from iron pills either. Same old stuff. I will survive. I added a photo. It was from my co-workers. They were wonderful. I miss them. The ribbon on the right is a cake.

Wednesday, November 10, 2010

Chemo #3 or 7 total

Well it went very well. Jeff made me laugh. I was telling the nurse about my feet trouble and she ask if I called them. I said no. She fussed so did Jeff. He picked at me about not calling them about stuff. I am not calling them every time I hurt somewhere. If it goes on too long or seems serous then I will call them.They have better things to do then to listen to my minor issues.
Doc said it was the chemo causes my ache and pains with nails and toes. As I already figured out.
Jeff told him how he disliked Metcalf. So he gave us a women GYN in knoxville. Susan something. I go to her next month.
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GREAT NEWS: On the way home I got the call we were waiting on. My Gene test came back NEGATIVE. I don't carry the gene which means there is a great chance our kids want get cancer. They are still higher risk than normal people but not any higher. That does help but we still have to make sure at the age of 23 they get screened and make sure they get yearly check ups and stay on top of it. If they don't have insurance then Jeff and I will do what ever it takes to make sure they get checked. I never want them to go through this. I pray that others don't have to go through this.


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I slept off on on during chemo today. It was sad to see a young guy with throat or thyroid cancer today. We over heard him say he had a real bad sore throat and that led to them finding it. Jeff said he saw them give him RED DEVIL. Poor guy. He had to be late 20's early 30's. I pray he gets well.

An older lady had a reaction to her 7th chemo. The nurses were great and Foust came in and he was great. It was scary for us to watch. But she was OK. They stopped chemo immediately and hooked her up to heart monitor and had oxygen on hand. I pray she is doing better.

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Well, I am talkative. I slept alot once home then Up once kids got home. It was midnight before I could sleep again. Oh yeah, I been getting hot flashes like crazy. It feels like a heater kicked on inside my body then I pour the sweet. It last about 1-3 min. Then I'm fine again. Doc said he could put me on pills to help it but I said it wasn't that bad yet. So he said let's keep a watch on it and if it gets worse he can get me on meds. OK.

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Stomache felt tight last night. I feel great this morning. Can't wait to be done. ONE MORE!!!! then herceptin for a year and pills for 5 yrs. Radiation for 6 wks. And then boob surgery after 6 wks rad wait 6 more weeks and get them fixed. YEAH!!!!!! I am glad it's getting closer to being done. It's been a trip which I hope never have to travel again.


My prayers go out to all of those going through this and their families. Don't forget the families. They have a lot of stress and worry on them. I'm thankful for my wonderful husband who I treasure more then he will ever know. He makes everyday better for me. My kids are just that kids. They do what they can for me. My friends well I have a few who are staying close in contact and they either leave comments here, email me, call me, or text me. They are great. I have few family members who call ever so often. Church friends check on regularly. I thank God for all of them.

Wednesday, November 3, 2010

Trouble with feet

My heals have been hurting for a few days now and my toes are sore. I am glad I don't have to stand on my feet because it would be worse. I soaked them in epsom salt which felt good but not sure it really helped. The tips of my fingers or fingernails are still sore too. I guess it's the chemo. My stomach is still messed up too. I stopped taking my iron pills Monday to see if I can get back to normal. I am trying to find foods high in iron to eat. I am going to look online for recipes with foods high in iron.

PS If you read my blog please leave a comment and let me know who's reading. Anyone can leave a comment. I really would love to hear from all of you. It would make my day to know that you are keeping up with how I am doing. Sometimes I think this is a waste of time. I hope that it can be helpful to someone some day. Thanks!!!!!!!

Thursday, October 28, 2010

How I feel today

I feel ok. I'm sore, finger nails sensitive, head ache, tired and stomach messed up. I am just laying around doing nothing. I would be really great if my head would stop hurting. I guess I need to eat lunch too. I can't type much today due to finger tips. I am doing well.