This is a question I keep getting asked and what people want to know is the practicalities of what it is. It is a mysterious thing to most people (as it was to me a couple of months ago). The thing is there are literally hundreds of different chemotherapy regimes. Some are tablet form, some, like mine are intravenous, some are given daily, some weekly, some fortnightly, three weekly etc. I don't even know all the possible combinations and routines. Each type of cancer has drugs that have been designed specifically for it. Most people being treated for a primary Breast cancer will be on a very similar regime and set of drugs to me. Although, even within Breast Cancers it varies slightly and there are a whole different sent of drugs to treat secondary Breast Cancers (when it has spread outside of the breast to other parts of the body).
As you know I am currently on a combination of three drugs which are given intravenously over the space of about an hour and a half. These are at quite high doses and so three weeks is the minimum amount of time they can leave between the dose due to the effects of the drugs on non cancer cells, primarily the blood. Some people have lower doses but more frequently. Then next drug I am going to have for the next three cycles - Docetaxol is often given at smaller doses weekly, but as far as I know I am sticking to the three week routine. I think the variation depends partly on protocols at the particular hospital. The advantage of the weekly regime is that the side effects will be less due to lower dose but the disadvantage is you have to go in every week.
The actual getting of the 'stuff' is not a big deal. For me they put a cannula in my arm, connect a saline drip and then slowly syringe in the ridiculous amounts of the pink stuff then the clear stuff, then they change the saline drip for a drip of the other clear stuff. The whole thing takes about an hour and a half then I go home. It is not painful and other than a burning feeling in my nose and sinuses I feel no immediate effect from the drugs. But this is just the start...it's the weeks that follow when your body is desperately fighting to repair itself from the damage the poison has done, that's the tough part. A 'cycle' of Chemotherapy is the time from one dose to the next, so for me three weeks.
Each type of chemotherapy drug has its own, lovely, unique side effects. Some people have said to me - oh, I know such and such a person and 'they were fine on chemotherapy', or 'their hair didn't fall out', or 'they carried on just as normal', or 'it didn't affect them at all'.......well good for them......note for future - none of these statements are particularly helpful to someone on Chemotherapy! Not only do all drugs do different things and have different effect, each person reacts in their own unique way
The Truth?.....having chemotherapy is like having the life slowly sucked out of you. Dramatic statement but unfortunately that's where I'm at right now. Oh, don't worry, I am staying positive and still plodding on and I am very aware there is an end in sight. But so many people ask me what it's like and what they mean is the practical aspects and what if feels like physically. However, it is the emotional toll that is the real battle, a daily fight to keep living life and not curl up in a ball and shut down. Life sucking poison, that's what Chemotherapy is. Yet it is saving my life...killing the thing that is trying to kill me, how do you get your head around that?
A dichotomous marvel of medicine.
I didn't actually intend to come on here and rant, sorry. I am very tired at the moment and am once again writting this at stupid O'clock in the morning as another wonder of Chemotherapy is that I wake up at 3ish every night, no idea why, but I can rarely sleep after that! We have had a stupidly busy weekend with various activities, climaxing with Isla's Birthday Party on Sunday. We are all feeling wiped out now! It was a great party though and Isla had lots of fun even though she has a horrible cold and isn't sleeping well. Here are some pictures. Without my beautiful little people in my life it would be far, far too easy to just shut down and self destruct. As exhausting as they are, thank goodness for their needy little voices that rise above all else.


You sound tired and low, it's a hectic time of year that saps the energy of even the most fit and able. The grey days don't help either.
ReplyDeleteYou and your family are under enormous strain at the moment. Hopefully you can all have some peaceful family time over Christmas.
That destructive/lifesaving chemo will be gone one day when it's job is done.
Keep telling yourself positive things, it will make a difference, you will get there. Spring will come and you will start to feel like your old self again.
We will take the lake by storm and show those boys what menopausal women can do, whether they like it or not!
I'm sending positive vibes across the airwaves, have they got to you yet? No? They will soon
xx
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DeleteFeeling positive vibes from all around Heather, thank you :-) Gutted I missed your performance on Monday, I shall be wanting a personal session from you and Irene, perhaps whilst sailing at the same time! What would the boys on the lake make of that?!
They would be in awe of us.......obviously ......more vibes xx
DeleteJennifer you are absolutely going to get your down days... its ok to just let things happen as you have no control and feel powerless... the important thing is your only human and your being tested to the max...maybe it could help you by not looking back just look forward; start each day as the beginning, I can only imagine your day of the diagnosis and acceptance probably took a while.... your half way up that mountain and when you've reached the summit you will look down and see all your achievements and know you have come through it all.
ReplyDeleteTake all that strength and soldier on up that mountain....and you will just love that ride down ...see you soon Xxx
I'm getting there Jill, thank you. X
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ReplyDeleteHi Jen
You have two choices curl up in a ball or fight it. If you love your children and Adrian then it's a no-brainer, you need to start fighting the cancer psychologically as well as physically. Originally at 20, I was told I had a 40% survival rate. My Mum was so tough on me – there was no way she would let me feel sorry for myself, “come on get up, do something – we’re going to beat this”. Failure was not an option. We made goals about what I was going to do when I got better: education (I left school at 16 now have A’s and a couple of degrees + post grad) travel (I’ve done this extensively), run a marathon (London 6hrs and 6 minutes – a long time but at least I did it!). On days when I was very ill, Mum and I cut up squares of material and made a patchwork quilt out of my old clothes.
I will never forget the day, 36 years ago, I was told the radio and chemotherapy had worked and I had a 60% chance. I cried for the first time since my diagnosis, but these were tears of happiness. I remember every second of the next hour- I walked through Bournemouth Gardens, smelling every flower and shrub, feeling the breeze on my face, looking at the sun in the sky and knowing how lucky I was. Nothing had ever smelt or felt so beautiful. (Not sure what onlookers thought!).
The danger Jen is everyone may wrap you in cotton wool. I hope you have someone like my Mum: someone who loves you so much they are tough on you; her funeral was today and I owe my life to her. I hope by sharing this with you, my Mum may give you the same determination to beat cancer as she gave me.
One of the advantages of having cancer is that it makes you appreciate the little things that matter: a sunset, a sail on the lake, laughing so much when Jen puts full throttle on PB – again! So do you want those happy times again? Do you want to be a mother to your children – of course you do. Then determine to do something about it, you have the opportunity to beat this cancer, start fighting, start swearing at the cancer, and tell it to get out of your body. Do not consider for one second that the cancer will beat you; beat it. Make plans and dates for the future. Tell us what your goals are. List for us the things you are going to do with Adrian and the girls.
Now did you do that walk? How far? What exercise are you doing next week?
Irene, I am determined, please believe me, I am just having a bad week! I will not let this beat me down. Your Mum sounds like an amazing lady, I am so sorry for your loss, you obviously have some amazing memories to hold on to. My Mum is also a tough, no nonsense kind of lady so she would never let me get away without fighting.
DeleteMy exercise goals this week have not been met due to a horrendous cold and cough but I am putting my mini trampoline up again and plan to jog on that as my joints are no longer up to running outside. I'd love to get out on the lake sometime, lets book something in once Christmas is out the way. Lots of love and hugs to you, I imagine its been a very tough few weeks for you. Xxxxxx