I seriously tried to get here 2 weeks ago since it was my last week of radiation and I knew I was do for a recap. Well, 2 weeks ago I decided to go against doctor’s orders from 2 months ago and booked a last minute flight to Florida to attend the Breast Cancer Marathon! She told me not to do it because she didn’t know how badly I would respond to radiation and traveling may not be a good idea. Well, one week before it was done I knew I was doing well enough that I could make the trip and I did. That decision ranks up there with one of the best decisions I have ever made in my life! I had my final radiation at 8:00 a.m. then hopped on a plane at 10:30 a.m., the perfect way to wrap up the past few months of hell. Ok, things certainly could have been worse but it wasn’t the way I’d choose to get a vacation from work again!
Radiation went alright. I am tired and I ache like a 110 year old woman. At the end I did burn and am quite thankful that since I don’t have lymph nodes in my right arm that means I’m numb so I can’t feel the burn. However, I can see the blisters and they drain and ooze through my shirts so it’s not lovely but it could be worse. I’ve been done with radiation for over a week so I’m healing!
This week I have a follow-up appointment with my lymph-edema doctor this week but my swelling hasn’t really changed so I don’t think she’ll be concerned. I wish the swelling would go away but she said she has a few tricks up her sleeve and I have a feeling she’ll pull them out when I see her Wednesday.
The Herceptin, however, I can’t be so upbeat about. It is also contributing to my aching body, shortness of breath and has caused my left hand to go numb, basically my thumb, pointer and middle fingers. But, the wost thing is that it’s hurting my heart. I was warned that this was a real possible side effect and that is why I have an echo-cardiogram done every 3 months but I didn’t really think that it would happen to me. They did the echo 4 weeks ago and my heart has gone to operating at 75%, where it was when first diagnosed in June, to 52% now. I have another echo scheduled for the end of April and if my heart function has dropped to below 50% then they are going to take me off this drug. This drug is given to me every 3 weeks and I don’t want to wait until the end of April to find out how much damage it’s doing. Well, I actually won’t find out until May. I have scheduled an appointment with my oncologist for 2 weeks from now to discuss this with her. I think when I was told a week ago about it I was simply in too much shock to ask questions but now I have a bunch to ask. First off all, I want to ask for an echo asap to check it again. We can’t kill my heart, I only have one of those. I also want to know what I can do, if anything, to help strengthen it again. I imagine cardio is good but I also imagine that it’s only good to a certain degree. Should I change my diet? Will my heart recover once I’m off this drug?
Any other questions you might have or answers are welcome.
So, that’s where I sit. I’m done with everything except getting Herceptin every 3 weeks and that drug is hurting me so I don’t know how much longer I’ll be on it. Also, I return to work 2 weeks from tomorrow, my “vacation” is over. It’s hard to believe that this phase of it is “over”.

5 comments
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March 2, 2010 at 5:35 pm
Janeth
So glad you made it to Florida! I’m sure it was an awesome experience.
I am so sorry to hear about the complications. Hope you get some answers and can get this figured out and repaired!
March 9, 2010 at 12:43 pm
Steve and Suzanne Pietila
Vicky,
Ask the doctor about having a “Muga Scan” done.
I take Herceptin every Tuesday….. today I go in for my 55th trreatment!! (remember, I will be on chemo for the rest of my life….).
I never heard of a “muga scan” until I moved to Florida, and found a new doctor at “M.D. Anderson Cancer Care”. In fact, my new doctor down here looked ‘horrified’ when he found out I had 6 months of CMF and 3 months of Adrianmycin up in Traverse City, Michigan, WITHOUT ever having a Muga Scan. They did my first Muga Scan BEFORE attempting putting me on Herceptin!!!! They wanted to be sure my heart hadn’t been damaged. I was only given echo-cardiograms in Michigan……. So, I am not sure if your doctor/hospital gives this test……….
A muga scan is supposed to be a more thorough heart test. I get one every 3-4 months.
So far……….thank our Lord……… my heart is fine.
But this is always a worry for me too…….
As for the radiation, hopefully your doctor can soothe the discomfort. Mine lasted ‘too long’ ….. I just hated it. Hopefully I never need it again.
So, I know what you are going through!
Just hang in there!!
Stay positive!!
This too shall pass!!
You’ll do it! You are a very strong woman! And it is worth it! You have your wonderful children that love you soooooooooooo much! They need you! You’ll do it!
We love you!!! And I will continue praying for you……….never stop…….It is a very important part of healing too!!!!!!!!!!!
Love, Sue
March 26, 2010 at 4:21 am
Ana
Hello,
Just like Sue mentioned, hang in there be strong!! You can do this !! for you and your children!!!
Just make sure you keep monitoring your heart!!
I’m 35, married and have no children. I had a lumpectomy and my tumor was estrogen & progesterone receptive. Today, thank God I finished my 6th cycle of chemo with taxotere and cyclophosphamide. I’m very happy about that but now in 3 weeks I will start on herceptin and maybe radiation at the same time and further on start tamoxifen. I’m very worried because of the side effects and all the chemo I given already.
I would like to know if this is normal. To be given herceptin, raditation and tamoxifine at the same time ??? I would appreciate any ones feed back !! Should I request a muga scan because my doctor has not offered one???
Thank you and hang in there to you and all the women frighting this, always think of the possitive !!!
God Bless, Ana
March 26, 2010 at 4:48 pm
msscatter
I received Herceptin while getting radiation, if that’s normal, I don’t know but I trusted my doctors. I started the Herceptin when I started the Taxol but then I had a reaction to the Taxol and they changed me to Taxoltere. I have never had a muga scan, it’s never been offered and it’s sounding like most people get one. Radiation made me tired but not like chemo did. It’s none fun but radiation was the lesser of the 2 evils for me.
Stay strong. A positive attitude and my kids are what kept me going. As soon as a get a few minutes I’ll be doing another update here so keep checking my blog.
March 28, 2010 at 9:52 pm
Ana
Thank you for the support!!
Everyone tell me that the radiation is nothing compared to the chemo.
I guess I will see in 3 weeks. I will let you know what happens !!
Take care, Ana