First scan results are in

It's taken me a while to get this latest update written, the week of my scan results was pretty hectic and then I went away on holiday for a few days with my family.  So far it's good news, the chemo seems to be working, the timing is perfect because my side effects have been getting a bit worse recently. It's so nice to know that it's worth going through all the crap for a positive result.

I had my CT scan a couple of weeks ago now on 31st July and was due to get the results the following Tuesday.  Unfortunately the results weren't back in time for my appointment with oncology on the Tuesday so I had to wait a bit longer, a bit of an anticlimax! The registrar (Dr B) said that he would call me as soon as he got the results and let me know.  He called me the following afternoon to tell me that firstly the scan showed shrinkage in the cancer in my lymph nodes and secondly it showed that I had a blood clot near my liver which had restricted the flow of the iodine contrast dye injection during the scan and they couldn't get a good picture. Although he did stress that there was nothing on the scan to worry about at the moment, what they could see of my liver was fine.  Although Dr B wasn't worried about the blood clot posing a threat to my health, he still wanted me to come in to the hospital as soon as possible for some blood tests and to be given a course of blood thinning injections.

So the chemo is carrying on as normal, every week as long as my white blood count is high enough,. I've done 10 treatments so far, I think I could end up having 18 in total, so I'm more than half way through.  I do my injections at home for the blood thinning and am waiting to ask more questions about treatment plans and liver scans at my oncology clinic appointment next week.

Latitude - I almost didn't make it

Last weekend was quite a roller coaster but it had a happy ending with me having an brilliant time at Latitude Festival. The drama started at 5.30am on Thursday morning (the day before I was due to go) when I woke up feeling hot, I took my temperature and it was 38.4! Not good, so I took my duvet off, opened the window and tried to cool down, I took my temperature again after about 30 minutes, it was still above 38.  First rule of chemo club is high temperature = bad news, call the emergency number straight away, follow their instructions.  Shit, all I could think about was having to miss Latitude, it had been booked for months before I was re-diagnosed and I was determined to go. I waited until 7am and woke up my older sister who was staying in my spare room.  I felt fine, just hot, when I had a high temperature on chemo before I felt awful, I felt sick and couldn't stop shivering.  This was different, not nearly as bad, but as I had a temperature it could be a sign of an infection in my body, I have to be super vigilant about this.  The lovely nurse I spoke to on the phone said I should come into the assessment unit, get my blood tested and to pack an overnight bag just in case.... Eeeek!

I arrived at the LRI Osborne assessment unit at 8am, for what turned out to be a very long day.  The nurses were amazing, explained everything that was happening, they took a load of blood, pumped me full of antibiotics (the type I'm not allergic to, having chemo twice does have its upsides!) and I waited for the results to come back.  It took a few hours, but finally good news...no sign of infection, or anything wrong with my blood tests, I was free to have my chemo! I have never been so happy to be told this before, I nearly skipped round to the chemo unit.

My chemo didn't quite go to plan though, the chemo drug I'm having every week can cause my body to have an allergic reaction, this happened before on my third week, and on Thursday it happened again.  When it happens, I get a really tight chest, short of breath and my face goes bright red.  I have to push the emergency button for a nurse and they stop the chemo drugs going in for a bit, I get injected with some more drugs to counteract the reaction, and then the nurses start the chemo again at a slower rate. It's all hands on deck when someone gets an allergic reaction on the chemo suite, they bring over the oxygen tank and everything.  Luckily it only takes a few minutes to make me feel OK again and then I go back to reading Grazia, or fall asleep in the chair.  It can be bit scary when you are short of breath but I know what's happening now so it doesn't bother me too much, I'm just determined to get to all of the drugs in and not have my chemo delayed.

I had so many needles and drugs that day I was high as a kite, 1 blood test, 2 canulas, antibiotics, piriton, ranitidine, steroids, avastin, paclitaxel, hydrocortisone, more steroids and more piriton. Nine hours at the hospital in total, my sister waited patiently through all of it armed with snacks and didn't mind me nodding off for hours in the chair.  

When I woke up on Friday morning I felt fine, so I went to Latitude.  Yipppeeee.

My oncologist was right!

I have had 4 weekly treatments of chemo so far and I'm happy to report that my Oncologist was right, it's not been too bad! Phew.  I was scared about the level of fatigue, and how I would cope going back to work and achieving a balance where I'm still not too tired to see friends for dinner or do a trip to the supermarket.  I'm relieved I've not had any problems so far,  I'm more tired than normal but it's really manageable, oh and I get nosebleeds and a sore throat, but thats quite minor on the side effects scale.  Life goes on wonderfully normally at the moment, except for the weekly trips to the hospital.

When I had chemo before for my primary diagnosis, the dose was so strong that I used to leave hospital with big bags of drugs to combat all the side effecta, I had 3 types of anti sickness tablets, antibiotics to combat any possible infection, injections to boost my white blood cell count, laxatives to counteract the anti sickness medication that bungs you up.  This time is very different, I only have my indigestion tablets to take in the morning and the rest of the week no drugs.  It really helps to keep my brain clear and I feel like less of a cancer patient because of it.

There is one big side effect that's starting to happen...my hair is falling out, not as fast as last time but it's getting more and more each day.  It's held onto my head with a combination of hairspray and hope at the moment.  I'm going away with my boyfriend this weekend and I'm desperately hoping that it stays put for another couple of days.  Most of my morning routine is spent collecting up the hair....off my pillow, from the plug hole, out of the brush, from the bedroom floor.  I am prepared with a lovely new wig for when the time comes to say goodbye to my real hair.  I've gone all out this time and got an expensive one, this is when it seems perverse to appreciate having cancer for a second time, I know all the tricks, the best wig shops to go to and I don't feel like a rabbit in the headlights this time. So very soon I'll be sporting my super wig, she's called 'Cody' (not my choice, this is what it says on the tag).

As far as success of the treatment goes, I should be getting a CT scan around week 12 (mid to end August) this will monitor the effect the chemo and Avastin have had on my lymph nodes and liver.  In the interim my Oncologist has said that the weekly blood tests I have could also show an indication of the success of the treatment, they monitor my liver function and calcium levels in the blood so will see if anything major is going wrong with my liver and bone mets.

The photo below is of the hanging basket my Dad bought me, he's jet washed my patio, bought me new flowers and donated a table and chairs.  It's the practical things he can do because he can't control what's happening to me health wise, and it's so lovely to sit out in the summer evenings and have my dinner Al fresco.  It's the little things that count when you're going through crap like this, we both love fuschias and I sent this photo yesterday to prove that I had kept them alive.

Then some more of me having a lovely time with my best friends and family (hair still clinging on).

Diagnosis #2 cancer comes back

I've wanted to write another update for days now but I've not been able to find the right words. So I've decided there are no right words because all the words to describe my latest diagnosis are wrong and scary but most of all just bloody depressing.  This is my problem, I want people that care about me to know what's happening but I don't want anyone to be sad for me, I'm not upset, I don't cry and I don't want anyone else to either.

I now have secondary breast cancer, otherwise called metastatic breast cancer or stage IV cancer.  It's when cancer cells from the original breast tumour spread around the body to other areas, I have cancer cells in the lymph nodes of my chest and neck and also in my liver.  This type of cancer is incurable.  The terminology in the cancer world is very specific, I'm not 'terminally ill', the way it is viewed at this point is similar to having a chronic illness where my condition can be stabilised or controlled for some time through medical treatment. Nobody can predict right now the amount of time I'll have, it depends on how well I respond to the wonderful drugs the NHS have on offer.

Since my last post I have now met with my lovely new oncologist and have a treatment plan.  First step is more chemo, I'll be having weekly doses of Paclitaxel via IV infusion, starting on Tuesday.  It's a lower dose than the chemo I had before and it's given on a weekly basis, I've been told that the side effects should be minimal and my immunity to infection won't be as low as when I had chemo before.  I'm hoping to be able to continue working, just on reduced hours and more importantly keep seeing all my friends and family as much as I possibly can.  I'm keeping my fingers crossed that I'll be well enough to make it to Latitude Festival in July.

I'm taking part in a clinical trial for this next round of treatment, it's to test a new targeted therapy drug along with the chemo. There's still a 50/50 chance I will get the placebo instead of the real drug but it means my response to treatment is going to be closely monitored over the next few months, more so than if I wasn't on the trial.  My Oncologist is also sending me for more gene testing, as I'm young with triple negative breast cancer it's likely to be a genetic fault that has caused me to be susceptible but not one of the main BRCA genes I've already been tested for.

So that's the sciencey bit over with.  Coming to terms with my new situation has been surreal, I always thought I would lose control if this ever happened and have to live out the rest of my days high on Valium.  It's all felt weirdly calm and after a week spent with my family I went back to work. I have just been carrying on as normal, pretending like nothing happened.  At the moment there are two things I'm very grateful for: going to the doctors as soon as I found the lump above my collarbone and then delaying getting my results until after my trip to Paris.  I had an amazing time, even cancer couldn't ruin it.

I'm sorry for the downbeat nature of this blog, I had an overwhelming desire to spell out the facts first  and then I'll follow up with the most sickeningly, life affirming blogs you've ever read.  I promise! 

Me and my wonderful friends in Paris, nearly 20 years of good times and lots more to come !