It takes both rain and sunshine to see the rainbow. This was created to have friends and family informed on my journey through this dark tunnel. I have entered the tunnel and now have taken the first steps on my way out.
Monday, September 19, 2011
Saturday, September 17, 2011
CHANGES
I have devided to try Take Them A Meal website and put a link on the side of the blog if you are interested. The password is 3013. Let me know what you think. My emaiil is kanglim@sbcglobal.net
Have a good weekend. The sun is looking nice out there. How about them Tigers! Cmon Lions!
Peace
Kelly
Have a good weekend. The sun is looking nice out there. How about them Tigers! Cmon Lions!
Peace
Kelly
Friday, September 16, 2011
New Drug
I started my new Chemo Drug called Havalen yesterday. Time will tell how it treats me. It's the newest drug on the market and suppose to be good on the body. By the time I got home I had a killer of a head ache. I can ask for something before I head home next time to help prevent that. Side effects are the usual. Hair loss, don't have to worry about that, fatigue...got it, neuropathy-got it, constipation would be new to me. Those are the most common. I'm still on herceptin too.
I go for my next treatment next Thursday and then have a week off. So I will be doing the opposite of what I was on.
My CT scan of my chest and abdomen results were in. Stable through-out. Only one slight growth of new tumor in liver. One slight decrease in one of the tumors in lung.
My CT scan of pelvis was done two days ago and I go to the radiologist Monday to get those results.
Rachel didn't make the volleyball team but joined the cheer team now.
James starts football games this Saturday. Emily waiting for swim stroke clinics still. Paul is in full swing of teaching and he is busy. Wow.
stay warm everyone...lets see how long we can keep the furnace off. I have my winter hat on my head already.
Prayers for peace to all
Love
Kelly
I go for my next treatment next Thursday and then have a week off. So I will be doing the opposite of what I was on.
My CT scan of my chest and abdomen results were in. Stable through-out. Only one slight growth of new tumor in liver. One slight decrease in one of the tumors in lung.
My CT scan of pelvis was done two days ago and I go to the radiologist Monday to get those results.
Rachel didn't make the volleyball team but joined the cheer team now.
James starts football games this Saturday. Emily waiting for swim stroke clinics still. Paul is in full swing of teaching and he is busy. Wow.
stay warm everyone...lets see how long we can keep the furnace off. I have my winter hat on my head already.
Prayers for peace to all
Love
Kelly
Monday, September 12, 2011
Craziness
Well I said I would update my blog after my chemo today but I really don't have anything to update you on. I have a few things so here they are.
I had a doctors appointment last Thursday. This appointment was a routine appointment that is usually done before my chemo treatment. I had my chemo appointment switched to Mondays for September because we have a wedding to go to at the end of September. IF I had my chemo on the Thursday before the wedding I knew I wouldn't feel good travelling out of town. So I asked for Monday afterwards. So back to the doctors appointment. I checked in what I thought to be 30 minutes early, they want you 15 minutes early. When she said I was early , I was 45 minutes early. AND the doctor is running an hour behind...UGGG. So I finally got called back 2 hours after my scheduled time. I complained that my toes were now completely numb..which is neuropothy...a common side effect from chemo. And I complained about right hip pain. This has been bothering me and slowly getting more prominent the last two -4 weeks.
Dr said well lets cancel your chemo on Monday, I want to put you on a new drug and I want to send you to the Radiologist to see what we can do about that hip pain. HUH? So I left being confused and went to see my chemo nurse and she explained to me that the radiologist will do any test to determine if I need radiation. All right that makes sense. Thank goodness I thought of talking to her . My brain just could not think fast enough to ask the Dr right then and there. And the Dr does give me a chance to ask questions. I just couldn't think of any.
And he scheduled me for a CAT scan. So Friday I received phone calls that both appointment would be Monday (today). But of course even though they were at the same building they were 4 hours apart.
I arrived early enough before my CAT scan to have the chemo nurse access my port because they are just better at it then anyone else. I then headed to the floor where I had to have my CAT scan and registered and filled out paperwork and drink my lovely juice. And then there was a nurse in front of me before I even started on my juice. I said:you're ready for me already....30 minutes early...she said not exactly. I looked at her confused and she said...you have to go back upstairs they didn't use the right needle for a CAT scan....NOWAY you got to be kidding. Sure enough back upstairs I went. The nurse that did it was so apologetic. I hugged her and said I forgave her. The rest of the scan went with out a hitch. We went to lunch and then headed to the dr appointment with the radiologist. He couldn't tell us anything because we hadn't had any test on my hip. He thought my oncologist scheduled something and my oncologist thought he would let the radiologist decide what test he wanted to do. So now I 'm having another CAT scan on my hip. The other scan just covered my chest and abdomen. My chemo is scheduled for Thursday and this drug I need to have on Thursdays once a week for two weeks in a row then off a week then another treatment. Off a week and then back to the beginning I think. I'll find out Thursday for sure. This will not mess up the traveling for the wedding as my old schedule would have.
Wow that was more than I thought.
Paul's teaching m w nights and all day on Fridays. James has football t and Thursdays and games on Saturdays. Rachel is doing gymnastics to get ready for winter competitive cheer and Emily will be doing swim stroke clinics on Saturday starting in October. Mom will just try to keep up with everyone.
If I can ask a favor please pray for good results from the CAT scan today and for the one I will have whenever they schedule it. And Two pray that this new drug I will be having for Chemo is as good as they say it is.
Thanks again for all the support through everything you have done.
Love and Peace to you
Kelly
I had a doctors appointment last Thursday. This appointment was a routine appointment that is usually done before my chemo treatment. I had my chemo appointment switched to Mondays for September because we have a wedding to go to at the end of September. IF I had my chemo on the Thursday before the wedding I knew I wouldn't feel good travelling out of town. So I asked for Monday afterwards. So back to the doctors appointment. I checked in what I thought to be 30 minutes early, they want you 15 minutes early. When she said I was early , I was 45 minutes early. AND the doctor is running an hour behind...UGGG. So I finally got called back 2 hours after my scheduled time. I complained that my toes were now completely numb..which is neuropothy...a common side effect from chemo. And I complained about right hip pain. This has been bothering me and slowly getting more prominent the last two -4 weeks.
Dr said well lets cancel your chemo on Monday, I want to put you on a new drug and I want to send you to the Radiologist to see what we can do about that hip pain. HUH? So I left being confused and went to see my chemo nurse and she explained to me that the radiologist will do any test to determine if I need radiation. All right that makes sense. Thank goodness I thought of talking to her . My brain just could not think fast enough to ask the Dr right then and there. And the Dr does give me a chance to ask questions. I just couldn't think of any.
And he scheduled me for a CAT scan. So Friday I received phone calls that both appointment would be Monday (today). But of course even though they were at the same building they were 4 hours apart.
I arrived early enough before my CAT scan to have the chemo nurse access my port because they are just better at it then anyone else. I then headed to the floor where I had to have my CAT scan and registered and filled out paperwork and drink my lovely juice. And then there was a nurse in front of me before I even started on my juice. I said:you're ready for me already....30 minutes early...she said not exactly. I looked at her confused and she said...you have to go back upstairs they didn't use the right needle for a CAT scan....NOWAY you got to be kidding. Sure enough back upstairs I went. The nurse that did it was so apologetic. I hugged her and said I forgave her. The rest of the scan went with out a hitch. We went to lunch and then headed to the dr appointment with the radiologist. He couldn't tell us anything because we hadn't had any test on my hip. He thought my oncologist scheduled something and my oncologist thought he would let the radiologist decide what test he wanted to do. So now I 'm having another CAT scan on my hip. The other scan just covered my chest and abdomen. My chemo is scheduled for Thursday and this drug I need to have on Thursdays once a week for two weeks in a row then off a week then another treatment. Off a week and then back to the beginning I think. I'll find out Thursday for sure. This will not mess up the traveling for the wedding as my old schedule would have.
Wow that was more than I thought.
Paul's teaching m w nights and all day on Fridays. James has football t and Thursdays and games on Saturdays. Rachel is doing gymnastics to get ready for winter competitive cheer and Emily will be doing swim stroke clinics on Saturday starting in October. Mom will just try to keep up with everyone.
If I can ask a favor please pray for good results from the CAT scan today and for the one I will have whenever they schedule it. And Two pray that this new drug I will be having for Chemo is as good as they say it is.
Thanks again for all the support through everything you have done.
Love and Peace to you
Kelly
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