Two months after hearing she has cancer, Lynn tells us about starting on chemo and going for her first dose of radiation therapy. (Click here for her previous message.)
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Hi there,
Well, we’re into week 1 of treatments and so far so good!
After much humming and ho-ing about whether to start my chemo tabs on Sunday night or Monday morning, we finally decided to start last week Sunday.
I say “we” as, of course, Andre had to be part of the decision considering that he was the one that may have been thrown up on if I had a bad reaction to the tabs. We were weighing up the pros and cons of taking the tabs at night and sleeping through any horrible side effects (or potentially not sleeping and having the side effects), or rather waiting to take the tabs in the morning.
The oncology nurse told me that if I had a bad reaction I wouldn’t have to stay on the night schedule for the whole week – I could switch to a morning routine immediately, if necessary, so we decided to do the night routine.
I got everything ready - I read the instructions, I took the anti-nausea tab half an hour after I’d eaten, waited another half an hour, took my two (very expensive) chemo tabs and then… fell fast asleep on the couch while watching the Sunday night movie! Nothing unusual there. And then went to bed when the movie was finished… and still nothing. A real non-event actually. YAY! Same thing the whole week.
Starting radiation
On Tuesday I went for my first radiation on the three ugly sisters.
We had an appointment with Doc Wilson beforehand who showed us the CT scan of my chest and the plot and plan for the radiation.
The area where the three ugly sisters are (and where they’re radiating) is just where my gorgeous (now more ample than normal) cleavage is and a little bit up – about 5 cm x 3 cm, but they’ve extended the radiation area a bit to allow for a margin of error (and my growing size!) when radiating.
They put me on this table contraption with lots of comfy spongy things for my feet and my legs, and they marked me up, using these teeny tiny little tattoo markers they made when they did the CT scan week before - as reference points.
So, I finally have a tattoo (three in fact), but they really are like tiny pin pricks so don’t have a heart attack, mom! Then they rolled me and twisted me until I was “just right” and did the radiation thing.
I’m not entirely sure what happens as I had my eyes closed the whole time, not because I was scared, just really comfy and thought I could catch a quick napster! Apparently there are cameras in the room so they can see that you’re okay - not sure if there are speakers in there to hear if you snore!
Anyway, just heard some whirring sounds and then it was over.
The strangest part was them telling me that I was not allowed to wash my lovely blue chest marks off, and not to put any lotions or potions over the radiated area, front or back, as it might interfere with the radiation.
The only thing I am allowed to use, nay, encouraged to use, is Maizena. “Maizena” I said, “as in cornflower? The stuff you cook with?” and yes, this is apparently true. Not exactly sure what it is about Maizena that makes this the talcum powder de jour for radiation, but there you have it. So, between my sunflower oil face mask and my Maizena chest sprinkle I’ve decided that I’m going to be one saucy bird by the end of this experience!
Like being punched in the chest
I must admit to feeling like I’d been punched in the chest after the first radiation, but the radiologists thought it unlikely that I’d feel such a physical effect – particularly not on the first treatment – and I felt really whacked about an hour or so later and was very grateful to be home and be able to have a sleep.
Again the radiologists think it is more likely the effects of the chemo rather than the radiation that is making me feel so tired, but perhaps it’s a combination of both.
I’ve now completed my first (of six) courses of chemo (well the 5 days on part and now I have three weeks off) and I’ve finished 4 of 10 radiation treatments.
I’m definitely feeling a little whacked and don’t have as much energy as normal so I’m trying to pace my days a little better.
I’ve been warned that these next three “off” weeks I might experience some of the other chemo side effects like the drop in my immune system (picking up everything going – which is maybe why I’m feeling so tired as my cells are racing around trying to fight all sorts of other little buggers they don’t normally have a problem with) and also a dryness of the mucous membranes (one of the places where cells rapidly divide so they are affected by the chemo) which I’ve experienced and it’s really weird. Feels like I’ve been sucking on a lemon and my cheeks should have contracted in - if only this was true! I still look like Moonface in the Faraway Tree!
On the head front
On the head front, the proton thing is definitely not going to be happening. This Friday I’m going for another MRI and head CT so that they can get an update on the remaining brain tumour, T1 (it’s been two months since we first got acquainted, can you believe?). I’ll have a new mask made for the different type of photon radiation therapy - stereotactic radiosurgery is the official name.
They will then plot and plan the head radiation. Prof Vinemann says I’ll probably need 6 to 8 radiation treatments, but more about that next time.
Doing well
Overall we’re all doing well. The heat in Cape Town on Saturday was a bit of a killer because I’m sure I balloon even more, but at least we’ve had a cooler, overcast and rainy day today.
Andre and the girls are doing great and the girls have been understanding, particularly when I’ve needed to rest. We’ve had great support from the school moms who are cooking us dinner on a couple of the “busy” nights each week which is proving to be a huge help - not to mention giving me the opportunity to meet some of the mom’s I didn’t really know that well.
My mom has been amazing, keeping everything together, but please keep her in your prayers as she has been our rock and support for so long and needs support and prayer to keep going too.
Thanks for all your support, prayers and news… and of course keep them coming!
Hi Lynn - I'm so glad u can treat this with a sense of humour. U don't mention anything about nutrition. I was diagnosed with cancer a yr ago and found that a strong immune system, keeping yourself 80%alkaline [20%acid] and well oxygenated can beat cancer as it cannot survive in thoe conditions. The trouble is the oncologists don't tell you any of this. Good luck and if you ever want to talk you can get in touch. I live in Somerset West. - yoey
Good luck, read this
3/8/2008 4:10:14 PM
Hi Lynn - Keep the attitude positive, believe me it gets more difficult as time goes by and learn to appreciate all support especially from your husband and spoil him once in a while as he is suffering with you. My wife was diagnosed with breast cancer 4 years ago, she was pregnant at the time in her second tri-mester, we now have a beautiful young 3 1/2 year old healthy son. She has been on anti-cancer (chemo) since then. You are welcome to mail me for a chat. Good luck you will get through. - Ivor Ballack
Hang in there
3/9/2008 8:49:59 AM
Hi Lynn,
Just wanted to say that I will keep you in my prayers and thoughts as you go through this. We are also walking the cancer journey with my daughter's leukemia.
Hang in there! Lea White whitesinnz.blogspot.com and bravefighters.blogspot.com - Lea White
Yeah well no fine!
3/9/2008 11:23:24 PM
Hi Lynn
Been there done it and still going 12 years later. As long as you and nobody believes you can do it. You have won
Bless you - Susan vz
RE: You don't have to do chemo
3/14/2008 10:10:27 AM
Hello Lynn, This may come as a strange comment but I think it necessary. After reading through above I had to write to u. I know everybody has a solution for cancer & everybody wants to provide with a solution but chemo therapy kills all your good cells in your body as well as the cancer. Have you heard of ozone therapy?Oxygen therapy. Cancer cannot live in oxygen. I am currently treating a girl with breast cancer and in 7 days it has shrunk - no side effects. Pls call me 0117021411 to direct u - Beverleigh
RE: Alkaline/Acid
3/14/2008 10:14:14 AM
Second comment - as per the top comment, you need to change your diet - the alkaline/acid thing is true. I would love to direct you to the right people and you don't have to do the chemo thing...The people who run this ozone centre have not lost one single cancer patient in 2 1/2 years plus - since it has been running. It is a complete change of lifestyle to prevent recurrence so drop me a line when you can. God can work a miracle in you..
Much love and I hope to hear from you. - Beverleigh
Alternative treatment
3/14/2008 10:18:32 AM
For all those reading this, it is my hearts desire to reach you. If you know of anyone with cancer and would like to follow an alternate treatment - ozone therapy, please drop me a mail - bev@back-to-eden.co.za . this is my other e-mail for my health business. It is a very cost effective treatment with high success rate..Also for treatment of diabetes, AIDS, addictions, all forms of arthritis etc..I promise this not to be a lie..and when you contact me, I will prove it to you. - Beverleigh
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