Wednesday, February 24, 2010
Here comes the fun
Tired, achy, scalp hurts, neck sore, don't want to eat, have to eat...blech. Hopefully won't feel like this for too long.
Tuesday, February 23, 2010
Follow the Chemo Road
Overall it was a good day, even for having chemo. We dropped Sean off at daycare and drove into the city. We got there at 8:45am. I got my blood drawn, then it was upstairs for my appointment with the oncologist. The nurse practitioner gave me the run though of the day and possible side effects after. The oncologist examined me and it was off to chemo. They have 2 choices of rooms. You can either have a dentist like chair or a hospital bed. I chose the hospital bed because the room had a door instead of a curtain. Also I think it was more comfortable with my belly still stitched. My mom and Rob came with me. It was nice to have the company. They also have TV's in the room. The nurses were extremely nice and helpful.
My biggest fear of the day was get my IV in since I have such horrible veins and they can't use my good arm now because it is on the side of the mastectomy. The nurse looked at my veins and decided that she needed to get someone else to do it. I really appreciated that she didn't think she could get one on the first try, so she got someone else. The other nurse got it on the first try. Hooray. They first give you another rundown of the day and side effects after. They emphasize that I am not get to the point of throwing up and if I am nauseous, take my meds. They do not want me throwing up at all. The IV lasts about 3 hours. I first get saline, steroids and benedryl to help with any allergic reactions. I was given Cytoxan first and Taxotere second. Overall, it was not bad at all. I even got a foot massage by the roaming massage therapist. We are able to order in lunch, so Rob didn't even have to leave to get us anything. One of my friends was on her last treatment today, so we got to see her and she brought a chocolate cake to celebrate. Yummy. We are out by 2:30pm.
Here are some pics from the treatment:
My biggest fear of the day was get my IV in since I have such horrible veins and they can't use my good arm now because it is on the side of the mastectomy. The nurse looked at my veins and decided that she needed to get someone else to do it. I really appreciated that she didn't think she could get one on the first try, so she got someone else. The other nurse got it on the first try. Hooray. They first give you another rundown of the day and side effects after. They emphasize that I am not get to the point of throwing up and if I am nauseous, take my meds. They do not want me throwing up at all. The IV lasts about 3 hours. I first get saline, steroids and benedryl to help with any allergic reactions. I was given Cytoxan first and Taxotere second. Overall, it was not bad at all. I even got a foot massage by the roaming massage therapist. We are able to order in lunch, so Rob didn't even have to leave to get us anything. One of my friends was on her last treatment today, so we got to see her and she brought a chocolate cake to celebrate. Yummy. We are out by 2:30pm.
Here are some pics from the treatment:
After we left the Cancer Center, I had an appointment with the plastic surgeon. He is very happy with my belly. I did have 2 pinhole size opening on one side, so he took out 2 stitches, opened the area a bit and I have to put in this aquaseal stuff in everyday into the opening. Icky, but not too bad. I go back on Monday to hopefully get the other stitches out. He is liking how the rest is healing. We will see. Hopefully, the chemo won't interfere too much with the healing.
I slept very well last night considering I only got 3 hours of sleep the night before. I woke up this morning feeling good, until I took the steriods. Headache and feeling hot and yucky. But it is the only one I have to take today until my next treatment. My belly has been ok as long as I keep eating and drinking. Not too bad overall. They advised me to eats lots and lots of protein. It helps with the healing process. The nurse advised that it is very unlikely I will lose weight, but actually gain. Oh well, not the time to diet.
I went into the city at 12:30 to get my Neulasta shot at 2. It is a blood booster. The nurse showed me how to give it to myself in the thigh and the possible side effects of back pain and/or bone pain from the bone marrow growing. Next time, I can do it at home on my own. It is worth the $35 co-pay to do it at home. I was back on a bus home at 2:30. Very wet day to have to go into the city.
I think I am going to have something to drink and some green tea ice-cream and rest until the boys get home.
Thanks again for all the good thoughts and wishes yesterday. It was nice to see all the posts on Facebook.
Sunday, February 21, 2010
C-Day tomorrow
Tomorrow is chemo treatment 1of 4. I started my meds today and they made me feel nauseous, so I have been snacking all day. Rob is making a nice fish dinner for us tonight. I get my sleeping pill and I will be out.
Rob and my Mom will be going with me for my first treatment. I have my bag packed with snacks, blanket and things to keep me busy. I get my blood drawn first, then I see the doctor and after that the chemo. I also am seeing the plastic surgeon when I am done.
I would love any emails or you can call me on my cell phone tomorrow. If you don't have my number it is on Facebook or you can email me for it. Please send me all the good vibes and thoughts you have.
Rob and my Mom will be going with me for my first treatment. I have my bag packed with snacks, blanket and things to keep me busy. I get my blood drawn first, then I see the doctor and after that the chemo. I also am seeing the plastic surgeon when I am done.
I would love any emails or you can call me on my cell phone tomorrow. If you don't have my number it is on Facebook or you can email me for it. Please send me all the good vibes and thoughts you have.
Saturday, February 20, 2010
Relaxing Day/Countdown
So I treated myself to a manicure and pedicure in a nice green for St. Paddy's Day. I know it is still a few weeks away, but I probably won't get back before then. Beside I probably don't want to risk infection by going after the chemo.
Rob took me and Sean out to dinner with the money he won from his football pool at work from the Superbowl. We got hamburgers, fries and rings. I got this awesome beer from Brooklyn Brewery called Brooklyn Local 2. It was a yummy chocolate beer. It went great with the burgers. It actually came in a wine bottle with a cork. I thought the guy brought the wrong stuff at first. Since it was so large, Rob helped me finish it.
I also picked up my meds for my chemo on Monday. I got a steroid I have to start on Sunday, Ativan to help me relax and sleep Sunday night, and compazine for nausea, if needed. My appointment is at 9:30am on Monday. I also have to go back on Tuesday for a Neulasta shot. It is a red blood cell booster.
Belly is getting better. It is getting easier to move. I drove today to get my nails done. When the chemo starts, I know it will take even longer to heal. The stitches will probably be in for a few weeks.
Sean noticed Shirley, the wig, the other night and asked what it was. I explained to him why I had it and that I was going to lose my hair from my special medicine. He seemed ok with the explanation. He said something again today when he saw it. He said to Rob that it was for Mommy when she lost her hair. We are trying to explain things to him as they come in the simplest of terms for him to understand. He is handling it well.
Rob took me and Sean out to dinner with the money he won from his football pool at work from the Superbowl. We got hamburgers, fries and rings. I got this awesome beer from Brooklyn Brewery called Brooklyn Local 2. It was a yummy chocolate beer. It went great with the burgers. It actually came in a wine bottle with a cork. I thought the guy brought the wrong stuff at first. Since it was so large, Rob helped me finish it.
I also picked up my meds for my chemo on Monday. I got a steroid I have to start on Sunday, Ativan to help me relax and sleep Sunday night, and compazine for nausea, if needed. My appointment is at 9:30am on Monday. I also have to go back on Tuesday for a Neulasta shot. It is a red blood cell booster.
Belly is getting better. It is getting easier to move. I drove today to get my nails done. When the chemo starts, I know it will take even longer to heal. The stitches will probably be in for a few weeks.
Sean noticed Shirley, the wig, the other night and asked what it was. I explained to him why I had it and that I was going to lose my hair from my special medicine. He seemed ok with the explanation. He said something again today when he saw it. He said to Rob that it was for Mommy when she lost her hair. We are trying to explain things to him as they come in the simplest of terms for him to understand. He is handling it well.
Friday, February 19, 2010
Short Hair
Very weird with the short hair. When I went to wash it yesterday, I forgot how short it was and put the amount of shampoo I usually use on my long hair. It was way too much. The haircut is ok. I am not crazy about it. I think it is too long on the sides and it is hitting my ears, so I am putting in barrettes to pull it off my face. It's not worth going back to get it fixed, since I will only have it for 3-4 weeks.
The belly wound is looking ok. It doesn't seem to be opening this time. The plastic surgeon put in a lot of stitches. It is going to take a long time to heal, especially when I start the chemo on Monday.
The belly wound is looking ok. It doesn't seem to be opening this time. The plastic surgeon put in a lot of stitches. It is going to take a long time to heal, especially when I start the chemo on Monday.
Wednesday, February 17, 2010
New Haircut and New Wig
Big day today. My belly was still hurting from all the pulling and stitching, but nothing a little percocet couldn't fix. My mom and dad picked me up for my haircut. The hairdresser put my hair in a ponytail and snipped. She was only able to get 6 inches, so it is too short to donate to Locks of Love. I am a little disappointed at that. I got my haircut. I think I more like my sister now. The cut is a little longer than I was thinking of getting, but my hairdresser said to come back in a few weeks to get a shorter one before I shave/lose it. It feels very light and weird.
Here is the before and after:

We then went to find a wig. The place was very nice. Since they took insurance I didn't have to lay out anything for the wig, an added plus.
Meet Shirley:
It was hard to try on the wigs with all my hair, but we got a decent idea on the look. The lady said that they do not make many curly wigs because it is not the style right now. I have to go back for a fitting when I lose my hair and she will trim the wig to fit my face.
I was also able to get a prosthesis for my breast, since it is not fully formed yet and the plastic surgeon is not fixing my breasts until after my chemo is finished. I am happy with how it now looks.
The day wasn't as bad as I thought it was going to be. Thanks to everyone who posted thoughts and encouragement on Facebook. It was nice to see all the comments. Rob & Sean are not home yet. It will be interesting to hear what Sean will say about it. I know Rob was disappointed about me getting my haircut, but he would rather have me bald and healthy, then with a head full of hair. I think the wig might freak him out in the middle of the night, especially since it will be sitting on my makeup table in the bedroom. Hopefully the cats won't find it a new plaything.
I still have a way to go, but the finish line is getting closer.
Here is the before and after:
We then went to find a wig. The place was very nice. Since they took insurance I didn't have to lay out anything for the wig, an added plus.
Meet Shirley:
It was hard to try on the wigs with all my hair, but we got a decent idea on the look. The lady said that they do not make many curly wigs because it is not the style right now. I have to go back for a fitting when I lose my hair and she will trim the wig to fit my face.
I was also able to get a prosthesis for my breast, since it is not fully formed yet and the plastic surgeon is not fixing my breasts until after my chemo is finished. I am happy with how it now looks.
The day wasn't as bad as I thought it was going to be. Thanks to everyone who posted thoughts and encouragement on Facebook. It was nice to see all the comments. Rob & Sean are not home yet. It will be interesting to hear what Sean will say about it. I know Rob was disappointed about me getting my haircut, but he would rather have me bald and healthy, then with a head full of hair. I think the wig might freak him out in the middle of the night, especially since it will be sitting on my makeup table in the bedroom. Hopefully the cats won't find it a new plaything.
I still have a way to go, but the finish line is getting closer.
Tuesday, February 16, 2010
All Sewn Up Again
I went to the plastic surgeon again today. He decided to close up everything. He said he wasn't surprised that a few stitches had opened. He liked the progress of the areas that were closed. It took about an hour to reclose the wound and he did a nice job. I know, after the chemo is done, I might need some touch up work, but I still have to have my breasts finished also. His objective today was to get it closed, even if it did not look pretty. The belly is a little sore from today's work, but I am still having a problem with one of the nerves that runs from the incision up my belly. I don't know if I had mentioned it before, but is the source of most of my pain and lack of movement. The right side of my belly burns from the nerve being oversensitive. Hopefully now that the wound is closed, the nerve can heal. He is having me massage the areas 5 times a day to desensitize it.
I am also able to get rid of the visiting nurse. She was coming every day while the wound was open and 3 times a week when Fred was attached. I found out the other day that I was getting charged $40 co-pay on every visit. The total bill is probably going to be about $1000...blech. I am trying to work out a payment plan with them, since I am still unemployed. The doctor said that I can email him a picture of the wound everyday so he can keep an eye on it instead of the visiting nurse for infection. If any stitches open up or there are any problems, he will give me and Rob something easy to do so we don't have to get the nurse back.
The doctor gave the ok to start chemo on Monday. He said even though I am closed, it will still take a long time for the wound to fully heal and to expect that. Chemo delays healing. I am glad thought I can finally get that started. My chemo will be every 3 weeks and I will be having 4 treatments.
Tomorrow, I am getting my haircut finally. I will post pics tomorrow.
I am also able to get rid of the visiting nurse. She was coming every day while the wound was open and 3 times a week when Fred was attached. I found out the other day that I was getting charged $40 co-pay on every visit. The total bill is probably going to be about $1000...blech. I am trying to work out a payment plan with them, since I am still unemployed. The doctor said that I can email him a picture of the wound everyday so he can keep an eye on it instead of the visiting nurse for infection. If any stitches open up or there are any problems, he will give me and Rob something easy to do so we don't have to get the nurse back.
The doctor gave the ok to start chemo on Monday. He said even though I am closed, it will still take a long time for the wound to fully heal and to expect that. Chemo delays healing. I am glad thought I can finally get that started. My chemo will be every 3 weeks and I will be having 4 treatments.
Tomorrow, I am getting my haircut finally. I will post pics tomorrow.
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