Saturday, 11 July 2020

Breaking Point

Sigh.

All of the shitty side effects have been for nothing. The nausea, rashes/blisters, migraines, UTIs, thrush, bone pain, stomach ache, fatigue, insomnia, abnormal heart rhythm, sore mouth, hair thinning the lot. All for nothing. The amount of time wasted in bed, all of the cancelled plans, the cancer has gotten worse, increased in size and stead further.

I now have tamoxifen for 3 months and if the next scans aren’t any better then it’s chemo.

I’m at an all time low. I’ve spent the last week in bed, can’t remember the last time I washed my hair, today I could barely open my eyes as I’ve had an allergic reaction to some bastard face wipes so I’ve spent all day in bed crying.

I’m done. 

I have nothing left in me, the fight has gone. I’ve spent 6 years with this crap and it’s taken everything from me. I already know it’s spreading, my left hip now hurts, everything I have been through has been for nothing. I’m so drained all i can do is cry. It’s so consuming, my heart is so heavy, I have nothing left.

Tuesday, 16 June 2020

6 years 10 steps back

6 whole years have passed since I was first diagnosed, 6 bloody years that’s a lonnnnng time and very little has changed. It still controls my life, I think about it when I’m trying to sleep and it’s the first thing I think about when I wake up. How sad. 

Bloody shit.

Treatment is fucking shit too, this new treatment plan has caused me nothing but crap. Every week headaches, migraines, water infections bla bla bla it can really get a girl down ...

Wouldn’t be so bad if it WASNT ALL FOR NOTHING

Yep, new in on Friday is that something “new” has appeared in my sacrum, brilliant.

It gets better, they aren’t sure what it is as the scan report is ambiguous. Excellent. Once again I one knows what’s going on and no one is capable of making a bloody decision.

It’s going for a second opinion on Thursday this week and I’ll get an asset on Friday. Apparently. Not going to hold my breath.  

I think I’m covering all outcomes when I say

1. they still can’t decide but 
a) I continue on current treatment
b) I start new treatment -tablet / injection 
c) I have more chemo
d) I have more radiotherapy
e) I have more bone biopsies 

2. It has got worse and is in fact more bone mets 
a) I continue on current treatment
b) I start new treatment -tablet / injection 
c) I have more chemo
d) I have more radiotherapy
e) I have more bone biopsies 

3. They decide it’s not bone mets
a) I continue on current treatment
b) I start new treatment -tablet / injection 
c) I have more chemo
d) I have more radiotherapy
e) I have more bone biopsies 

4. They still have no idea what it is
a) I have more bone biopsies and they Danny about some more and I don’t sleep

Answers on a post card

Sunday, 29 March 2020

Covid

23 days in (would have been 30 but before official shielding began I went to Helens for a night of red wine).

Like many, loads of shit has been cancelled, a family holiday to Spain (even Arron was excited about going), a trip to LA with Sammy -in fact we should be there now😩, the Edinburgh Fringe Festival, Ibiza, Crystal Maze, Gay Pride, 80’s-90’s Festival, the list goes on. What I do know is that the second we’re allowed were off to Jamaica followed by a much needed girls trip to Ibiza.

Wow I’m bored. It’s not like I haven’t done this before but this time it’s different, I have energy, I want to do stuff, well cleaning, I absolutely don’t want to do that, ever - lock down or not that’s not happening apart from the essentials - but well done to everyone else cleaning skirting boards and cupboards.. it’s just not for me....

I’ve mostly been filling my days with sleep (I now have to sleep alone as I’m “vulnerable”), watching TV - what the hell Carol Baskin....FaceTiming, meditating and good old fizz. Worst part is having to rely on Arron to do the shopping and therefor judging the bottles I’m getting through ...

It’s safe to say that the guys have loved having us (mainly Arron at home all day) But it does emphasise that I really need my girl dog Jackie Brown as I don’t get a look in






It has got me thinking though, Does anyone use the ribbon tie on a dressing gown?

Do the Kardashian’s use false lashes on the bottom lash- surely those aren’t natural?

I’ve carried out my own experiments on cheap fizz - skittles and the results are pretty surprising, red skittles were vile, and the top faves were green followed by purple - there you have it




And having witnessed Arrons work voice, WOW, he uses phrases like key elements, networking and going forward. He also has the strangest telephone voice when speaking to “clients” and solicitors.....

Many an hour of TV watching has been consumed, jumped on the Tiger King band wagon and wasn’t disappointed, it raised 2 questions, 1) they don’t get bit to death and more hauntingly where are their teeth 😳 ooh and also, now I really really want/need some cowboy boots.




But my saving grace has to be Schitt’s Creek, me amd Arron are both obsessed (special thanks to Sammy and Dave for the introduction)and there’s 5 lengthily series, it’s fantastic and should be watched by all.

Also partaken in some House Party activity, where I’ve mainly been rinsed for my animal print clothes collection and lack of general knowledge... but it makes missing friends and family that little bit easier,




Easter was made even more fun for us as we were given a Lazy Spa by our friends Sarah and Wayne. I think I spent around 5 hours in it on Saturday -absolute game changer and just what I needed. Just need to get some cup holders and fairy lights and I’ll be well away and happy for the next 9 weeks.







But there to bring me back to Earth was the little reminder that I do have cancer in my bones (yawn), I’ve not been able to get up today due to bone pain in my back and hips, have a done some crying and feeling very sorry for myself. I try and remind myself that particularly at the moment I should be grateful for my health and there are a lot of people worse off... but it still sucks and is still extremely painful, I guess I’m starting to understand why I’m classed as vulnerable... not fun at all....





It’s also brought on the ever attractive eczema in and around my face, with my eyes swelling so much I could barely open them this morning. Rebecca sent me a load of Moo Goo products last time so fingers crossed they work again and I’ll stop looking as scary.



The gift that keeps on giving ey, but today it does give me a free pass to eat my dinner in bed so not all bad I guess, if only I could find where Arron has hidden my bell for attention.....


Sunday, 23 February 2020

Bed

Arh bed. Most people dream of laying around sleeping most of the day.

I’m bored shitless. This week it’s a migraine and chest infection, I don’t think I can watch anymore TV, I’ve got to the point where I’m willing it to be 7pm just so I can take my sleeping tablets and even those effects are wearing off now.

I’ve never been so bored in all of my life. There’s plenty I could be doing around the house but that’s all I seem to do. I spend most of my days alone, I can’t remember the last person that came to visit, how sad is that? Nobility has well and truly worn off...

Guess people have ordinary lives to get on with and aren’t completely ruled by hospital appointments, medications and side effects.

At this precise time I’m not loving my life, just existing.

Fuck you cancer.

Wednesday, 8 January 2020

Joyful Joyful

Christmas 2019

I bloody love Xmas, I’d keep my tree up all tear round if Arron would let me, I don’t buy into the whole bad luck thing, funnily enough.

22nd December I was at Burton A&E, exactly the same time as 2018, having the same x-Ray done on my left foot. Yep. The boot is back.

Christmas Day was actually lovely, I made Arron dress up as Santa, but Lolaah & George wouldn’t wake up so Arron stood outside from 6am-7am looking like a weirdo....

Dinner at my parents was lovely, the champagne flowed, there was barely any arguing, but then man flu hit me like a sledge hammer.

Fuck my actual life

I was looking forward to a Boxing Day night out, instead I spent the day alone ( it’s the one day of the year Arron actually likes going out so I wasn’t about to stop him ). I got up twice, to feed the guys. 

One person text me all day to see if I was ok.

I did not leave my bed for days, maybe a week?

Xmas ruined. I was so angry with myself, the flu and my bastard left foot, again.

2020 had better be better, 

Who am I kidding,

Fuck sake.

Who the fuck was I in a previous life 

OR

Shit, I deserve this ?

Friday, 25 October 2019

Realisation

I have Stage 4 cancer.

It will never be cured.

I am now classed as having palliative treatment.

Fuck

Yup, bone mets have been confirmed in my spine, neck and pelvis. They’ve increased in size, so I’ve started new treatment. Two hormonal injections, 3 loading doses every 2 weeks, today was my second lot.

I actually found out two weeks ago, not that many people know, to be honest I can’t keep going over it. I’ve been trying to ignore it all if I’m honest but I’ve been feeling pretty rubbish. Have spent most days in bed. It’s funny how social media allows you to portray your life, I don’t think anyone would have known.

It’s been horrible, actually, very lonely.

New treatment comes with new side effects. Today I went back to the clinic, I had my injections - numb bum now for the next 10-12 days, and was given some fairly “good” news. I’ve been given funding for a new drug to run alongside the 2 new injections, the bone injection and the menopause implant I have. I’m the first in the trust to get it, just have to make sure that My heart is healthy enough first. Well it’s pretty fucking smashed at the minute...

I will have to wait and see what that will bring, I’m told I could enjure a sore mouth, reduced white cell count, reduced liver and kidney function, hair loss, back pain.

More bloody scans.

More anxiety.

I didn’t really want much from life, I wasn’t particularly ambitious, I just wanted to be happy, I can’t imagine ever feeling happy again.

I wish I was anyone but me.













Thursday, 10 October 2019

I don’t even know what to call it

Friday 27th September, 2 days before my birthday I attended the oncology clinic for my CT results.

The CT scan I’d had 6 weeks prior, I assumed that no news was good news, if it was bad they’d have called, surely? Well that’s what the radiography team told me..

So I’m sat in the waiting room, where I’ve spent many an hour shitting myself, sleeping, bored, contemplating life... 

That day I’d forgotten my I Pad, I’d planned to catch up on Power, but instead I’m clock watching. My appointment time comes and goes, one of the nurses comes out from the clinic and amends the board, Oncology Clinic delayed by 60 minutes..... brilliant, so now I’m here waiting with a load of people past retirement age, all looking at me wondering if I’m in the right place. Then my bottom lip goes





I’m called in.

Fuck.

I sit in the room with the registrar, she asks the general questions, how have I been, am I in pain, any new side effects, how am I coping with my current treatment? I reply all is well, (I can’t really moan that I fucking hate the menopause, I feel like an old lady, the hot sweats are awful, I spend most of my days feeling disgusting and an absolute mess, I have a baggy hormonal stomach, my hair and nails are shit, my mood swings are insane and I wish for just one night I could fall to sleep  relatively early or just like a normal person, without the use of sleeping pills, alcohol or CBD.

The she ever so casually tells me that there has been some changes to my most recent scan.

What the fuck.

Ok. Wasn’t 100% prepared for that.

No one has called me, the only reason I have an appointment today is because Arron made one for me. 
she then tells me that she’s unsure of the next stage as it hasn’t even gone to MDT and says that she will go and find out, leaving me alone.

With the report on the screen.

Fucking shitty fuck sticks. 





Well.

She returns and tells me that it needs to go to MDT the following Thursday, and they will have me back in clinic the next day, and the hands me a tissue.

I hand in my appointment card to reception and burst into tears, she’s lovely and tells me that They’ll write to me so I don’t have to stand in oncology reception crying. I then proceed to the toilet and throw up. And cry. And when someone else comes into the toilet I put my hand over my mouth so I don’t make a noise and when they leave I cry some more. 

Time passes and I become angry, I decide to go back into the clinic and demand to see my Consultant. I do a bit more crying and before long I’m sat in the quiet room with a cup of tea - even had sugar in it. 

My consultant calls me through after another hour or so. 

Christ this is such a long winded story.. bare with me.

She tells me yes there have been some changes to my spine and pelvis. She reminded me that they were never 100% sure if it was bone mets, she also said that it might not be, but also that we might never know for 100%. More tears.
Then she told me that she wanted to discuss it at MDT but was away the following week, so she would delay it until she was back (which is actually today - 2 weeks later). If after MDT they’d decided my treatment should change, she would personally phone me, if nothing would change, she would see me at my next scheduled appointment in November. Knowing that I was due my bone injection the following Thursday so asked me to get cancer markers done via a blood test. She then asked how I was, how Arron was, what I was doing for my birthday, told me that if she could prescribe champagne, she would. I did some more crying, and she very kindly prescribed me a short court of sleeping pills.

I cried all the way home. Met Arron at home and drove to London for my birthday weekend.

After lots of fizz and Karaoke we were back home and impending doom set in.  Thursday I went for my bone injection.

Bloody waiting room again




An hour and a half passed, I see a friendly face, one of the chemo nurses, she calls my name. In I go,

Niceties over, I’m told that I’m all good to go a head with my bone injection. This means that my Vitamin D and calcium are all good. I nervously ask about the cancer markers.....
The nurse takes a moment to look at the computer and says that she can’t interpret the results. 

Part of me is relieved because I get more time in a non terminal world. The nurse inside me (yep it’s there somewhere) tells me that the computer system would flag up shit results and she’s not telling me. She’s lovely and says that she will get a specialist nurse to phone. She said that she would hand deliver my name and number to her. Probably because at this point I’m crying hysterically and causing a bit of a scene. On the up I’m told that my kidney function is now back in the 90’s !! (Post Ibiza it went down to 60ish...)

I have the injection, say bye to everyone, Do a little cry and head home. And wait for the phone call.

The phone call never comes.

Today my scans were seen at MDT. My oncologist didn’t call. That’s good right? Or is it bad news but she’s seen that they’ve accidentally booked me an appointment the following day (tomorrow).  Or does it genuinely mean that there’s no changes after all to my scans which means no changes to my current treatment?

I waited all day for a phone call. Never came,

This is good right? Or is it?

I’m absolutely our of my mind. My mom asked me to call her last night, my first thought was that she’d somehow found out something and wanted to speak to me. Then I was messaging one of my friends and I convinced myself that because she works for the trust, she 100% knows something but can’t tell me.

I’m actually insane.
I’ve lost it.
I’m fully aware of this, and yet I can’t stop.

It’s now 1am, and there’s so sign of me getting any sleep tonight. I want to hide. No actually I want to jump on a plane, see everything, go everywhere. Sit in the sea in 7 mile beach and watch the birds catch the fish, the. Meditate and watch the sun set.

Tonight might actually be the last night before the chaos starts once again.

I’m stuck on a merry go ride, I want get get off, but I can’t.