Archive for the 'Cancer Update' Category

August 12th 2008

Bone Pain…

Happy Tuesday,

I am so happy that I felt well all weekend and finally made it to church for the first time in a month.  What a blessing the service was with a focus on communion and what Christ did for us on the cross.  This world is not all there is, and my hope is in the Lord.

My hair?  Still mostly there!  Yay!  Today, though, I began having some bone pain from the white blood cell booster shots.  Last night was the first time it showed up, but I had it in my first round of chemo last year.  It’s pretty painful.  I couldn’t sit last night without pain.  I took some Extra Strength Tylenol and used a heating pad, and that seemed to help.  Today is a little worse.  I just took some Tylenol with Codine and am hoping that it kicks in soon.  The pain is mainly in my hips and lower back.  Please pray that it goes away or is controlled with drugs!  Tomorrow is the Angel’s Game, and that means a lot of sitting.

Thank you so much for your prayers and support.  I have been so blessed by so many of you!

Love,

Monica

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August 9th 2008

Hair starting to fall out…

The big news for today is that my hair is starting to fall out.  I am so bummed about it!  I was fine last time, but going through it again really makes it harder.  It has been growing now for 6 months and is finally at a point where I can style it.  Now it’s going away again.  At least I have a bazillion cute hats to cover my bald head. 

Today I felt well all day and even spent time in the pool with Kai at, his friend, Madison’s 2nd birthday party.  It was really fun to play with him in the water.  Sol asked him if he was swimming and his reply was, “No, I hitting people!”  with a huge smile on his face.  The other kids were so friendly with him and didn’t mind being swatted with a noodle!  🙂 

Noodle Fun 2 

Thanks for all of your prayers.  Kai is sleeping better and longer, and my side-effects are at bay for now!  🙂  It has been a good few days for me.

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August 8th 2008

Feeling Pretty Good

Well, today I was pleasantly surprised to wake up feeling pretty good.  I woke up at 5:30 and couldn’t fall asleep.  I took an anti-nausea pill to keep the “horse in the barn” so to speak and got up for a while.  I waited for the side-effects to hit, but they never came.  🙂  We ran some errands and drove by some houses we were interested in looking at.  It was fun.  Then I came home, took a nap and woke up to go get the first of 4 shots.  These shots sting!  They take about 30 seconds, and the whole time it’s stinging!  I can’t feel it now, but it’s not too fun when it’s happening! 

Right now I feel pretty good, but my stomach is starting to feel a little strange.  I hope that tomorrow will be just like today in terms of feeling ok. 

A couple of updates: My friend went through her surgery well.  They had to take more from her arm than they thought they would have to.  Now she is waiting for the results.  My other friend, who lost her husband, is having the services tomorrow. 

Thank you for all of your prayers!  I am so grateful for feeling so well.  Yippee!!!

Love,

Monica

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August 7th 2008

Chemo 2 – 3 treatments down

Hello Everyone,

Today was Chemo week 3.  It was two drugs Taxol and Avastin, which gave me VERY bad side-effects last time.  I got to the doctor’s office right on time and was told that I would have to wait until they heard back from Dr. Freimann.  My white blood cell count was too low, and they were going to see whether or not I would get chemo today.  Well, after waiting for a while, they said that I could get it but that the Taxol dose would be lowered and the Avastin would be the same.  Then they said that I am going to have to come in for four days for white blood cell booster shots.  So I’ll be having injections Friday, Monday, Tuesday and Wednesday.   🙁   Last time I only had chemo every three weeks, and they could give me a Neulasta shot (white blood cell booster) that worked for ten days.  Since I am having chemo every 7 days, they can’t give that to me ; I have to go in daily.   So, I guess I don’t get a week off…at least I get a break from chemo next week.   When I had the shot last time, that’s when I got bone pain.  So strange and so painful!  I am really praying that doesn’t happen with these daily doses.

On a strange note, one of the chemos that I saw someone else receiving was BLACK!  It was so strange seeing her tubing all black as it goes into her body!  I wonder what that was?  Martha, my mother-in-law, and Lark, a friend from work took turns hanging out with me today.  It was fun; we played Blokus (a really fun game) most of the time.

So right now, I feel tired and need to lay down, but I wanted to let you know that I am home and doing fairly well.  Friday is when the side-effects hit me last time, so please be praying against all the side-effects (nausea, diarrhea, gas, rash, shortness of breath, pain and now hot flashes to my hands and below my knees) and that the shots won’t give me bone pain!

Thank you so much!

Surviving another day!

Monica

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August 6th 2008

Wednesday before doom’s day!

Today is Wednesday.  This morning I had blood drawn.  They use the port, which is supposed to be easier, but today it didn’t want to cooperate.  I ended up having to lay back in the chair, and then they raised my arm above my head.  I was getting really nervous that it wasn’t going to work.  Finally, they were able to get it working and draw the blood.  I was so relieved!  Although since the blood was drawn, I feel a little dizzy and out of it.  I’m getting some food ready to eat, maybe that will help.

Thank you for all the prayers for little Kai.  The past two nights have been better.  He has been falling asleep faster and staying asleep longer.  Tuesday morning he woke up at 5:30 and only cried for less than a minutes and fell back asleep until 7:30.  It was a beautiful thing.  Today he was up at 6:45.

Tomorrow is already making me nervous.  I am getting the two drugs (Taxol and Avastin).  Last time I experienced many side-effects and ended up in the ER with shortness of breath, pain in my chest and swelling in my arm.  Please pray for a smooth treatment and for no side-effects.  My mother-in-law, Martha, is coming on the train today to be with me.  My friend, Lark, is going to be with me tomorrow for treatment.  I feel so blessed to have people who will take time off of work and out of their busy schedules to sit with me and care for my son while I’m down and out.  I’m feeling loved!

Thank you for all of your prayers and support!  I couldn’t do this without you all!  Please add a friend of mine to your prayers.  She is having surgery in a few hours on something on her skin.  They think it might be some really rare (1 in 10 million) sarcoma but aren’t sure.  They will know more in a week after looking at whatever they take out today.  Pray for peace and rest, and pray that it’s not DFSP (short for some LONG complicated name)!!!  She has three young boys and a wonderful husband.  My heart breaks for her!

Thanks for reading my blog.

Love,

Monica

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August 1st 2008

Praise, Felt Good All Day…

Thank you for all of your prayers.  I was blessed with absolutely no side-effects today.  Sol, my wonderful husband, let me stay in bed while he got up with Kai and got him ready and off to school.  It was just what the doctor ordered.  I woke up around 11:30, and felt great!

So I believe that Avastin is the culprit for all of the side-effects last week.  I’ll be having Avastin every other week, so that is something to really pray about for next week.  I don’t want to end up in the ER again, so I’d covet any prayers sent up for me!

Love,

Monica

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July 31st 2008

Chemo 2 – 2 treatments down…

Well today was the second chemo for me in this new series.  Thank you, Sunshine, for going with me today!  I only had one drug today (Taxol) and am hoping that tomorrow morning won’t be too bad. I feel pretty good right now. They were able to use the port, and it was so much nicer than having to find another vein. It was only supposed to take about an hour to an hour and a half, but I was there for a little over three hours. They started late because I had to talk to the billing staff at the office.

I had received bills from them, but knew my coverage (I’d read it inside-out and upside-down, you know!), and that my insurance should be covering it all, so I didn’t worry about it. The bills were very minimal (under $100), so I just left it alone. I got a call last night from them and was told to talk to them this morning. I told them that my insurance covers everything except a $15 doctor visit co-pay. She checked it out again and ended up confirming that for herself. In the end, they are going to resubmit it to my insurance and told me not to worry about it. It’s never just one thing, is it? Good thing I know what my coverage is and that I checked it all out! Sometimes it just gets so ridiculous.

So here I am at home resting. I was pretty tired from the benadryl, and have been resting for a few hours. Usually I feel ok on the first day, it’s the 2nd, 3rd and 4th days that are the worst. Tomorrow morning I’ll probably wake up and freeze to assess how I’m feeling. Then, maybe, I’ll roll out of bed very carefully not to upset anything! 🙂 It’s always a guessing game. I sleep with anti-nausea medicine next to the bed. I am hoping that since I only had Taxol this time, it’s the other one (Avastin) that took me for a ride last time…here’s to hoping! I guess we’ll see.

I was encouraged today, multiple times, as I sat there getting chemo. There were three ladies, all named Barbara (felt like a sit-com), and one of them, Barbara #3, is going through chemo and surgery for the third time. She was so positive and funny. She told me about her husband who had some rare type of cancer and was hospitalized for 6 months, developed blood clots in his legs, was put on blood thinners, developed something in his brain, had brain surgery and is doing just fine right now. She said it’s all about the positive attitude. “If your mind starts to go someplace else, don’t let it!” she said. She is 64, but looks maybe 50. She said that chemo is her trick to staying young. Her own little slogan – so funny!

Then there was a guy there who has been having chemo for 9 years. Nine Years! He’s the happiest man and was joking that he was going to have to change his name to Barbara just to fit in around here!

Then I read an article in a magazine talking about Sarcoma and how more people are hearing about it and raising awareness about it. I learned that there are over 600 sub-types of sarcoma and that they all have such varying identifiers that it’s difficult to find what works for each one. The article stated that a family doctor on average will only see 2 sarcomas in his whole career! It said in the article that they are trying to find what works for specific ones, and for angiosarcoma, the newest thing is Avastin. That made me feel good about the treatment I am getting. The specialist that I saw at Cedar’s Sinai was quoted in the article as well as someone I’ve met on a sarcoma chat. It felt great to see that there is more being done to bring awareness to everyone about sarcomas.

So I was encouraged by all of those things and am trying my best to stay positive!

Thanks for praying and please continue to pray for those specific side-effects. Tomorrow will tell!

Love to you all,

Monica

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July 30th 2008

The Port, a Lovely Visitor…

Thank you so much!  They used the port to draw the blood and there wasn’t pain!  Apparently they use a numbing spray to numb the skin before poking the needle into the port.   That would’ve been good to know last night, so that I wasn’t so scared about it.  I couldn’t look while they drew the blood, but what I saw before it started was what looked like a tack!  I know that sounds strange.  I thought so, too!  It connects straight into the port and sort of locks on.  Kind of a strange feeling.  It was so awesome!  I really liked not having them search for a vein.  I think this port thing is going to be so worth the pain of the past week in the long run!

Sol’s aunt, Robin, called me this morning to see if she could come visit.  It was such a blessing to have her here to cry with, talk with, and shop with.  She shared many inspiring stories with me including the miracle of her husband who has beat this cancer beast!  I really enjoyed my day with her and know that God brought it together to bless us both!  Thanks, Robin!

Tomorrow is Chemo.  I am already having a bit of anxiety about it.  I will only have one drug tomorrow, so I hope to have fewer side effects on Friday.  Thank you for all your prayers and support…I’ll keep you posted.

Love,

Monica

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July 29th 2008

Port might be ready…

Thank you so much for all of the prayers that went up today as I went in to have the port checked out. They took off all the tape and steri-strips, with some skin, and removed the sutures. It was actually very painful. Any and all adhesives take my skin with it, so I have red marks in the shape of squares where the bandages were and lines where the steri-strips were removed. I guess I heal well and quickly. The sutures were somewhat embedded into my skin making the removal of them more difficult and involved. They had to pull them out from the skin before they could cut them. I thought today would be easy, but I guessed wrong. Two nurses removed them apologizing the whole time for the pain.

In the end I had to wait for a doctor to come and look at the wound and tell me that it was a bit red, but that was probably from all the tugging and tape removal and it should go away. He said that I can shower – Yay! It’s been a week, so I know that Sol is excited about that (as am I…feeling pretty gross!). 😉

When I asked about using the port tomorrow for the blood draw, the nurse said that it was probably ok, but that there would be some pain. They have to feel for the port and then actually pinch it a bit before putting the special needle right into it. I don’t know which would be worse. Using the port tomorrow or having them search for a vein to draw blood through. I have to choose the lesser of the two evils. She told me to take a pain pill before going in…it might help. I’m scared and can’t wait for this part to be over and the port to be fully functional with NO pain!

I’m going to try to get some much needed sleep tonight. Thanks for all the emails and reminders that you’re praying for me. I need to hear it and enjoy reading your encouraging words!

By the way, Kai was fine at school. When we finally got through to the school, they said everyone was ok. He was a little scared talking about it later when we picked him up – so cute.

Love,

Monica

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July 27th 2008

Visit to the ER last night…

Well, I started having shortness of breath on Friday and it only got worse yesterday.  It got to the point where every breath I took was painful.  The pain started near my right shoulder blade and moved around under my right arm and around to my chest.  My right arm became swollen.  I couldn’t take a deep breath or a short quick one.

We called my oncologist and he said that the shortness of breath could be a side-effect, but the pain was concerning.  He was concerned about blood clots and wanted us to go get checked out.  We were at the Lang’s for dinner and ended up leaving Kai there.  Sunshine took him back to our apartment after he ate to be with Sol’s mom for the night.

We got to the ER about 7:45pm and were taken in right away!  That was such a praise because it was so busy!  They still can’t use the port, so another IV line was put in…on the back of my hand!!!  Ouch!  They did multiple tests including a Chest x-ray, a Chest CT, Blood Work, and an Arterial Blood Gas Levels (another prick).  They gave me Morphine and Benadryll which made me pretty woozie.  Sol’s aunt, Nena, came and stayed with us for hours!

In the end, we were released about 3:30 am with “Shortness of Breath with No Apparent Cause”.   They said that the oxygen levels were normal and that even though I feel a shortness of breath, not to worry because there is enough oxygen.  I guess it’s just something I am going to have to deal with.  Hopefully, when the port is situated and “mature” my chest won’t be so tight and my muscles will be more relaxed.  Maybe that will ease the pain I feel.

Thank you for your prayers.  It was a pretty scary night.  I woke up this morning feeling much better, but am worried that this will be something I will have to deal with each and every time.  I have a bit of a rash on my neck.  I’ve taken Benadryll, and am waiting for that to get better.

I’ll keep you updated with any new news.

Love,

Monica

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