I love steroids

Since I last posted my health is pretty much the same.  The only exception being the wonder that is a reasonable dose of steroids.  My oncologist warned me that they could give me a false feeling of wellness.  But false is good enough for me.  It's better than lying poleaxed in my bed with zero energy.  I've yet to develop the puffy steroid face but my muscles have definitely been wasting (as warned) and all the skin on my arms and legs has turned wrinkly.  You win some you lose some.  You also buy expensive body lotion online and live in hope.

Although the steroids have helped massively with energy, my breathing problems remain the same.  So although I'm keen to do things, physically it's difficult.  The spirit is willing but the flesh is weak (and did I mention saggy).

Also, possibly steroid related, are my patience levels.  I have no time for what I consider to arsery of any sort.  So if you come round here be warned!   I make no apology for it, it's positively liberating. Light the fuse and stand back.

Meanwhile, of course, people have been lovely.  The mass ranks of the other-half's family did a 15 mile, very muddy, very hard sponsored walk to raise money for my local hospice.  What a bunch of good 'uns.  

The end of the walk and still standing (just)

My sisters have, as always, been troopers.  Baby sitting me, cooking, commode emptying and generally giving poor old Nev a break from me.

And as for the outpouring of messages, gifts and visits after my last blog post, well I was touched.  I'm afraid I didn't get around to taking photos of everything but thanks to everyone.  I luffs you all.  Here's a couple of pictures we received

Beautiful hand drawn artwork

 

Beautiful and very, very glittery artwork

And lest you worry that the three-legged monster cat got left out. Fear not.  Here is his  latest gift, a Bet Lynch style cat tunnel.
 

Tasteful

Despite the breathing problems I have been able to get out and about some days thanks to Nev, the wheelchair and portable oxygen. It can be a bit of a palaver but it's lovely to be outside, wheeling round the park in the sunshine.

 And even better is going down the pub in my posh new coat. 

Cheers!

In the wars

Remember the mystery (and huge) gnome that appeared in my garden last spring?  Well I'm afraid some recent windy weather has taken its toll.  And the gnome isn't the only one who's been through the wars lately.

I've been complaining about breathlessness for ages and it's got worse and worse.  I went to The Christie (the specialist hospital I've been attending in Manchester) a week ago for scan results.  The scan was good - no change, but the doc was not at all happy about my breathing and admitted me.

I spent a week in hospital with the poor other-half having to trek backwards and forwards to Manchester (a one hour forty minute drive each way on a good day) to visit me.  I have no complaints whatsoever about my care but, as I'm sure you know, hospital wards are not peaceful, restful places so it was all a bit of a strain.  Added to that I couldn't walk a step without becoming very breathless so commodes behind the bed curtains were the order of the day.  Necessary but not very dignified.

While all this was going on, the three-legged monster cat was safely at home.  Lounging on his special cushion, dignity intact.  Lucky blighter.

Lord Muck

During my stay the medical bods did a high resolution CT scan and still found no change in my lungs since May, so no obvious reason for the breathlessness.  

During some regular observations the nurse found that my heart was racing alarmingly. Within moments I was surrounded by medical staff and advised that it would be a good idea for Nev to return to the hospital even though he'd only just got back to the Midlands after visiting.  Two of his sisters kindly drove him back and he arrived in time to find that my heart rate had, thankfully, slowed.  

So the focus of attention moved to my heart. An echocardiogram revealed that there seemed to be some sort of pressure there so I was prescribed beta blockers and arrangements were made for me to have a cardio MRI in a hospital a few miles away from the Christie (cue a trip lying flat in an ambulance - but no nee-naws).  Before leaving the Christie I asked the medics to tell me straight what they thought the scan would reveal.  Their opinion was that it was likely that the cancer was pressing on my heart, in which case all treatment would cease.  I asked how long they thought I had but they were unable to say before seeing the scan results.  At this stage I had them draw the curtains around my bed and had a good blub.  

However, the cardio MRI revealed no problem with my heart.  This was good news obviously but it's pretty frustrating to be a medical mystery.  It felt like my life was turning into an episode of House.

So the next thing was to try steroids to ease the breathlessness.  This has worked to a small degree and finally, after a week in hospital, I was allowed to leave as long as I had oxygen at home.  I cannot bear to go into the frantic organising that went into ensuring that oxygen was installed on a Friday afternoon - but thankfully it was done.  Me stressed?  Never.  What a week!

Being back at home is wonderful.  I was absolutely exhausted so the peace, quiet and loveliness of my own bed, not to mention the total disdain of the cat, were blissful.

Yesterday I went back to Manchester again to see the docs. They have had conversations with the head honchos of the clinical trial I'm involved in and the consensus is that I have chemo-induced pneumonitis.  This means that I have to come off the trial.  On the one hand this is a bugger as it was working to control the cancer, but on the other that's not much use if I can't breathe.  The hope is that my breathing will improve as the chemo leaves my system and I've been prescribed a decreasing course of steroids to see me through.  

In a couple of weeks I will consult oncologists at both the Christie and my local hospital to see what, if anything can be done next.  There is at least one chemo I might be able to try but I have to be well enough to handle it.  Time will tell.  At the moment I'm just taking one day at a time and trying to put some weight back on.  At the risk of being totally shallow, as well as all the health palaver, I am not particularly enjoying rocking the scrawny-eyed wassock look.  Some fat, hair and eyelashes would be much appreciated.

At this point, at the risk of sounding like a tearful Oscar winner, I have to thank the other-half, his family, my wonderful (yes I did say that) sisters and friends for their concern, lovely messages and practical help during all this.  I even had fellow metastatic breast cancer pals from my online support group popping in to see me.  You're a lovely bunch you really are.  I appreciate everything even though I don't always show it.

Let's end on a brighter note and totally change the subject.  We have a new addition to the family.  Sis no 1 has adopted a second cat.  He's an elderly gent and doesn't do much other than enjoy being out of the shelter and in a warm, comfortable home.  But honestly, with looks like this, he really doesn't need to do anything.  Ladies and gentlemen I give you ..... Murphy.

No lack of fat, hair or eyelashes there.

AWOL

I haven't posted for an age.  I'd like to tell you something scintillating, saying my absence is due to me gadding about with the jet set or my ongoing commitment to the NASA training programme.  But the truth of the matter is I've spent much of the past few weeks feeling like the the other-half looks

And as if feeling grotty wasn't bad enough, the above photo was taken during my last visit to the Christie and shows just how attentive and alert Nev can be during my appointments.

A short break in the whinging though, to tell you the good news.  I had scan results last week and amazingly, after eight cycles of the trial chemo SYD985, there has been a slight shrinkage in the cancer in my lungs.  I was staggered and, obviously, very pleased.   

I hope you made the most of that bit of good news because I'm about to start moaning again.  I do want to try to be honest here and not be some sort of happy clappy falsely cheery cancer blog, so here goes.

Even though I had good results the breathlessness has got worse and worse.  I'm fine if I sit still but any sort of movement makes me completely out of breath.  As you can imagine this makes doing anything, let alone getting out, really difficult.  It's not like I have a wild social life but even so I've lost count of the things I haven't attended due to breathlessness and fatigue.  Thankfully I did manage to get to a recent appointment with the Palliative Care Consultant at my local hospice, who is worth her weight in gold.  She could hear a deterioration in my breathing but thinks the problem might not be a result of the cancer (although it might be chemo damage).  She has referred me to my local hospital's respiratory bods.  I'm currently waiting for an appointment and I really cannot wait.  If there's anything that can be done to ease my poor lungs I'd be extremely grateful.  

Also, if truth be told, I'm pissed off with looking dreadful.  I've got thin hair, no eye lashes, hardly any eye brows and watery eyes.  My appetite has gone west and so I've lost weight and am looking extra haggard.  Ah cancer, the gift that keeps on giving.

In other news my Eddie Redmayne look-a-like doctor at the Christie is moving on to other  film roles research so I'll be seeing someone new in future.  It was nice to wave him off as he gave me good news (the cancer shrinkage).  He was also able to give good news to a fellow SYD985 patient (and pal) who'd seen a significant shrinkage after just two cycles.  So to any Secondary Breast Cancer bods reading, who are HER2 positive,  I'd say the SYD985 trial is well worth considering.

Meanwhile, in spite of everything, life goes on.  And I do appreciate it, honest.  Christmas preparations are underway. The festive twig is decorated and on display (we don't run to the extravagance of a tree at Discombobulated Towers),  Hot Fuzz is on the telly and, hurrah, it's very nearly present time.

I leave you with evidence (as if any were needed) that a three-legged monster cat and a cream sofa are not a good combination.

Happy Christmas.

Snooze envy

Little sod

Look at the three-legged monster cat.  Fast asleep, which is how he spends about 18 hours a day.  I think the lucky blighter is taking the piss.  As, although I have been plagued with fatigue that has frequently had me housebound, sleep eludes me.  Last night was a particular bugger when I was wide awake from 1.30am onwards.  I think the pathetically low dosage steroids I'm on might be to blame.  I'm about to run out of them anyway as the onc wasn't particularly happy at prescribing them, but I begged as I was desperate to have some energy.  Hey ho.  While I'm in bleating mode I'm still struggling with constipation and the breathlessness on any form of exertion, like walking to the kettle, is incapacitating. 

So, that's the bad stuff but I do have some good stuff to report too.

Firstly I had CT scan results last week and again there was no change in the cancer.  Again I was astonished, and very pleased, as the breathlessness led me to believe that things were getting much, much worse.  I'm having more chemo in about 10 days time, so I will rugby tackle the onc to the ground then and stress the importance of trying to get the side effects (I assume) under control.  I say I assume that the breathlessness etc are side effects as I have no-one else to compare notes with.  However, I know a couple of people who are being assessed as to their suitability for the SYD985 trial I'm on, so perhaps I'll have someone to swap stories with soon (although I hope they're not blighted with breathlessness).  I just really hope all this yuckiness isn't my body waving the white flag.  I've now had about 60 cycles of various types of chemo since being diagnosed in early 2012 and I think that's a lot by anyone's standards.

As getting out and about is now very difficult I decided to bite the bullet and get a wheelchair.  This was, like the stair lift I got a few weeks back, a horrible idea in theory but in practice brilliant.  Also, I was extremely lucky in that I've got a rather whizzy wheelchair for free.  Some friends had a virtually unused chair that they no longer needed and they gave it to me for nowt.  Aren't people lovely!

Anyway last Thursday, out of nowhere, I had a good day.  So we quickly loaded up the wheelchair and headed for the hills.  The Stiperstones to be precise, where there's an all terrain track which enables people with disabilities to get out in the lovely Shropshire countryside (yeah, I know I'm biased).  Here's a picture of me pulling a very strange face and being rather windswept but, although appearances might suggest otherwise, enjoying myself.

Wagons roll

I'm hoping for some more good days soon so I can shout wheelchair steering instructions at the other-half and generally be a pain in the arse.  I'm also hoping to go wig shopping as my hair is thinning by the day (although more slowly than on some other chemos).  I usually just wear hats and scarves when bald but thought I might give a wig a try again, hopefully it won't be as sodding uncomfortable as the one I got a few years ago.

Also there was one good thing about last night's insomnia.  I found a hilarious twitter account (in fact I woke the other-half up by laughing so much).  Here's the link but don't click if you don't like swearing, rudeness, black humour and fluffy bunnies.  Don't say I didn't warn you.



 

No go

I have recently had a birthday.  Here are a couple of (poor quality) photos of presents from sis no 2 and my mate T.  Both were gift wrapped.

I bet you envy me having such caring friends and relations don't you?  

Yep it's fair to say I've been a bit bunged up of late.  Probably due to the liquid morphine I take to help suppress my cough.  In a vague and unsuccessful nod at being modern I bought some looser jeans a few months ago, a sort of cowardly 'boyfriend' fit.  I believe this was in vogue about five years ago, so pretty hip and happening by my standards.  Anyway these looser fit jeans have now become my constipation trousers.  I recommend them.  No fashionista would be without a pair.  Nice and roomy if you catch my drift.

So I don't bother blogging for ages and then I give you an opening paragraph on constipation.  Have you missed me?

I had results from a CT scan a few weeks ago.  I was very surprised and very pleased to learn that there was no change in the disease.  I really was staggered as the breathlessness on any form of exertion (eg brushing my teeth) had me convinced that the cancer in my lungs had been growing apace.  The medical bods then tried me on antibiotics as some inflammation in my lungs was evident but they don't appear to have done anything.  I'm now on a trial week of steroids to see if they help.  They don't seem to have done anything for my breathlessness but I do have a bit more energy thank goodness.  The fatigue has been pretty crushing at times.  To be honest the fatigue has been one of the main reasons I haven't blogged recently.  That and spending all my time in the loo (with scant reward for my efforts).

Oh I lie.  I did get a reward for all my lavatorial efforts.  A fractured rib.  I have pathetic bone density and the strain proved too much.  It's on the mend now but for a couple of days it was ouchy to say the least.

So there you have it, my past few weeks.  Very little gadding about to tell you about.  Although I did go to a vintage wedding.  Look we got dressed up

Somehow the other-half managed to get his (rented) hat coated in horse radish sauce.  There really is no end to his talents.  The hire company haven't said anything ... yet.

I have a whole blissful week ahead of me with no medical appointments.  Hallelujah.  But next week sees another CT scan and I'm afraid I'm not optimistic about the results I'll be getting the week after that.  But whatever I'll keep you informed, whether you like it or not. 

Oh and while I'm being a misog, I'm pretty sure I'm losing my hair again (for the third time) even though it isn't a listed side effect of my current trial chemo.  Arse biscuits!

Ta-ra for now.


 

More of the same

For the last umpteen posts I have been complaining about breathlessness.  This post is not going to be any different.  In fact the problem has become quite a lot worse.  I'm OK if I remain seated but as soon as I do anything, even take a few steps, I become breathless.  This has resulted in a new installation at Discombobulated Towers.

Going up in the world, or possibly down

At first I wasn't too impressed at having a big beige plastic monstrosity in my house, but to be honest I don't know where I'd be without it.  For anyone pondering about having a stair lift I'd say go ahead, don't delay, it's a godsend.  It also has its amusing side if, like me, you happen to have a sister (no 1) who has a vertigo attack while trying it out.

While the breathlessness is hateful/frightening/depressing/a sodding pain in the arse, the enforced inactivity has given me an opportunity to torment the other-half.  He has to do everything now.  I have no puff for housework, cooking, de-fleaing the cat etc.  I've never seen someone with ironing rage before.  Apparently the way I chuck my clothes into the washing machine is a disgrace; tights all bundled up in a knot, jeans with one leg inside out, tops buttoned up etc.  What a wuss.  You wait until he experiences the delight that is finding a handful of tissues have been left in a pocket when he empties the washing machine.   I think he will truly blow a gasket.

No, don't go feeling sorry for him.  Look, here I am angelically smiling through chemo

And what do you think Nev was doing while this was going on?  Soothing my not particularly fevered brow? Feeding me chocolate?  Regaling me with amusing anecdotes?  Nope.  He snored through the whole thing.  Here's the proof.

Sleeping beauty

When it comes to chemo and blood tests and anything involving a needle my veins have finally waved the white flag.  So a couple of weeks ago I had a port implanted.  This has seen an end to the endless arm stabbing in a effort to try to find a co-operative vein but, to be honest, it's not as discreet as I'd hoped.  You can clearly see the port and some of the tube under my skin - it's a bit icky.  Hey ho.  Having it fitted was quite exciting.  It's done under local anaesthetic.  Imagine how thrilled I was when halfway through the procedure the fire alarm went off and the nurse announced "I don't think that's a test run".  We were on the ground floor and couldn't smell smoke so the nurse valiantly carried on and, thankfully, after a couple of minutes the alarm stopped.

I've been doing lots of traveling to the Christie (the hospital in Manchester where I'm currently on a trial chemo).  I've now had two cycles of the new swamp juice but, given the breathlessness, I really don't see how it can be working.  I'm having a CT scan on Monday so I will find out more shortly.  I suspect they will find more cancer in my lungs. Scary.  At least I don't seem to be having any other side-effects other than some fatigue.  So at the moment I am in limbo and feeling as cheesed off as Cyril (the three-legged monster cat) looks.

On the plus side I have been reading my head off.  My kindle is red hot.  And, although I can't really get out and about, as walking even short distances is difficult, I'm able to ride shotgun as Nev takes me out in the Shropshire countryside.  We drove over the Long Mynd the other day.  And I spotted something in keeping with the tone of this post - the Shropshire Sheep of Doom

And on that cheery note I'll say baa-baa for now.

I bloody knew it!

Picture from here

I got my latest scan results yesterday and, as I suspected, the little fuckers in my lungs are up to no good.  I suppose I had clutched a very faint hope to my moth-eaten and mutilated bosom that the endless bouts of coughing and attacks of breathlessness might be a side-effect from my current hormonal treatment, but nah of course not.  The grim reality is that the cancer in my lungs is growing.  

While the scan results were pretty predictable, the oncologist's suggested course of action came as a bit of a surprise.  I'm being referred to the Christie (a specialist hospital in Manchester) to see if they know of any clinical trials that might be helpful or even perhaps look at my suitability for immunotherapy.  I'm pleased about this, as it'll be good to be checked over by the experts, if only for my own peace of mind.  If the Christie can't help then I'll be going back to my local hospital to try another chemo, vinorelbine.  And that, I think, might really be my last chemo option. 

The news has affected me in a strange way.  Rather than taking to booze (any more than usual I mean), surrounding myself with doughnuts or lying sobbing in bed, I have an overwhelming desire to chuck out all my clothes and buy new ones.  This can only prove that I really am the most incredibly shallow person ever (yet more unsurprising news).   I'm not even sure what sort of clothes I want - just not the ones I've currently got.  How about I go for my 1983 look:

Robert Smith in a skirt

Yes, I am wearing leg warmers over woolly tights.  And yes, that was cool.

Anyway once I get a) a new wardrobe or b) an appointment at the Christie I'll be sure to give you all the news.  How you'll stand the excitement I just don't know.

Until then, simply because I haven't mentioned him for a while, I'll leave you with a picture of my beloved.

Cyril, the three-legged monster cat

 

Avoidance tactics

Here are some things I should be doing:

• Finding out about what will happen when the Cancer Drugs Fund (CDF) comes to an end next month.  I know it will be bad news and I haven't got the heart to read it.  (The CDF allowed patients in England to access some cancer drugs which were not otherwise available.)
• Starting an online course I registered for about immunotherapy.  But it looks like it might require thought.  Besides, the dog ate my homework.
• Looking at the scary form I've received questioning my right to receive Employment and Support Allowance (a state benefit) and asking lots of questions about my ability to work.  I don't have the mental stamina necessary to complete the form let alone hold down a job.
• Completing the skirt I started making last year.  But I'm at the stage where I have to do things with interfacing and attempt a button hole.  Cue an attack of the vapours.  The pattern says 'only one hours sewing time'.  Ha ha bloody ha

The material is now even more 'vintage' than it was last summer when I bought it

 Anyway, here's what I've been doing instead of all the boring stuff above.

•  Getting out and about in the winter sunshine

•  Going on two, yes two, snowdrop walks.  Never let it be said I don't know how to live on the edge.  In case you're interested, or even if you aren't, one walk was the annual one in support of a local cancer charity, (many thanks to all the family members who turned out in support of this, once again you warmed my cockles) the other was at Rode Hall.

•  Going to Cambridge for the weekend.  It was very chilly and I walked my legs off

 

Trinity College (I think).  My brain had frozen by this point.

 

Punting?  In that temperature?  Silly sausages!

•  Stopping off at Ely Cathedral on the way home.  Truly my middle name is Culture (or possibly Louise, you guess).

•  Getting excited about finding a local shop (Whitchurch) bearing the family name

 

What can I tell you?  I'm easily pleased

•  Gazing soppily at a happy Cyril (the three legged monster cat).  Also taking him to the vet again after he got into yet another fight That's 53 quid on antibiotics thank you very much.

Bless his furry little chops

•  Purchasing (for reasons too complicated to explain) a Playmobil Elvis.  I'm pleased to say he was well received.

Now before you start tutting and shaking your heads about my avoiding all the things I should be doing, the reason is not, as you might have thought, cowardice, laziness or excruciating hangovers.  No, the truth is I have been traumatised and the shock has rendered me quite incapable of anything except the most frivolous activities.  One of my sisters discovered (I know not how) that our old family home is now used for this.  And to think I thought finding out I had incurable cancer was a shock.  What did I know!

Bugs

January.  Cor.  It went on a bit, didn't it?  I started and ended the month with the lurgy.  Not a serious lurgy, just the common or garden lurgy that everyone gets but even so.  What with that and the usual chemo stuff it seems like I spent most of January feeling moderately crap.  This is, of course, light weight crap compared to what lots of other people are going through but I'm not going to let something like that stop me from whinging.

And the weather.  The sodding, sodding weather.  Grey, miserable, windy, rainy.  Precious few of those sunny, chilly, crisp days that make winter bearable, even enjoyable.  In fact I think we've only had one frost this winter.  Which is probably why bugs, of all varieties, abound.  I'm full of germs, the garden is full of slugs and the cat is full of fleas.  Here he is, like me, feeling sulky.

I had my latest CT results toward the end of January.  Dear God I was scared.  I'm always frightened going for results but this was worse than usual.  I suppose it's because I know I'm running out of treatments.  There are a couple of chemos left for me to try but once all possibilities are exhausted there is nothing left but palliative care.  Of course, I knew this all along since day one of being diagnosed with metastatic breast cancer, but as the time comes nearer it all gets scarier and scarier.  My pal Kath has put it a million times better than I ever could.  Read what she has to say here. 

Anyway, this time I was lucky.  The CT showed stable disease.  Also, more good news, the medical bods are pretty sure that the stabbing pains I get in my chest and side are nerve related (from the surgery).  However, as I have now had 54 cycles of chemo the time has come, according to my onc, to give the chemo a rest and try a hormonal treatment, exemestane.   While I will be delighted to have a break from chemo, cannulas and all the associated palaver, I am a bit concerned about stopping a treatment that seems to be working.  I've checked this with the onc but she's definite that I need a rest and I assume she knows her onions.  I'll have another scan in three months time to see how things are going.

Although this has been a bit of a mega-moan January hasn't been all doom and gloom.  There's been the trip to see the other-half's nephew in panto (oh yes there has), my hair finally getting long enough to discard hats and scarves and, above all, sister no 2's latest foray into crochet.  A Death Star.  I kid you not.

 

Unreliable

Oh dear.  I had hoped to go to Birmingham today to have a mooch around the shops before they get too relentlessly busy but instead I'm taking a leaf out of the cat's book and lounging around on the sofa doing a lot of this

I'm not sure if today's lethargy is chemo related or due to me having a flu jab yesterday.  All I know is I'm not firing on all cylinders.  In reality, compared to what some people suffer on chemo, I'm having a pretty easy time of it on Eribulin (so far).  But it does make me tired and also sends my temperature a bit haywire at times.  As a result I've had to bail out of a few recent social events, which makes me grumpy.  I hate being an unreliable friend but when I'm tired and grumpy it's probably best for everyone if I go into hermit mode.  The good news is that I've got a week off chemo at Christmas time (I wrote a begging email to my oncologist and laid it on with a trowel) so I'm hoping to be full of beans for the festivities, especially as a big family getaway is planned.  All I can say is watch out Hampshire.  You have been warned.  

The other-half and I have risked divorce and done some cooking together in preparation.  You wouldn't believe the blood, sweat and tears (and booze) that have gone into this cake.

We've yet to ice and decorate the cake - so the story continues

Anyway, unreliable as I am, constantly failing to turn up to planned shindigs, I cannot compare with my paternal grandfather.  Sis no 3 has been doing lots of work on the family tree but until recently my grandad was a bit of a mystery.  

The last known picture of my grandad (picture from here)

He walked out on his wife and four children (including my dad) in the early 1920s and was never heard of again.  I had tried to give him the benefit of the doubt over this behaviour (which caused a lot of hardship to his wife and kids) but my sister has finally managed to find out what happened and it's not particularly edifying.  Apparently he ran off to Coventry, Coventry I ask you, (apologies to any Coventry bods reading this).  Other highlights of his life include

• Entering into a bigamous marriage and having another family
• Somehow getting his name on a war memorial in Cardiff as having been killed in action in 1918
• Claiming (and receiving)  the old age pension two years earlier than he should have
• Being convicted of bypassing the electricity meter in his house and thereby defrauding the electricity company

What a total ratbag.  The other-half is dismayed at what sort of family he has married into.  

To finish on a brighter note, the other-half's six year old godson was chatting to us the other day and informed us that he was going to be an indicator in the school play.  Much confusion followed.  Turns out he's playing the innkeeper.

Green eyed monster

Yay, it's time for the Annual Shrewsbury Flower Show with it's usual brilliant display of kids' veggie art.  Here's just a few examples.  I've got heaps more of these to come but will save them for future posts, after all I don't want to spoil you.

There were other displays that made me green with jealousy

and hello to the lady in the pink coat

Not to mention the fluorescent loveliness of the park itself

Do not adjust your sets, the colours really are this bright

My sisters came away with plants galore, whereas I came home with, obviously, a two foot tall wooden bunny

Every home should have one

My jealousy of all things floral continued with a visit to some friends in nearby Staffordshire who live in a lovely old cottage.  To make matters worse they have the most gorgeous garden (these photos really don't do it justice) I was positively emerald with envy.

And now on to green eyed monsters of a different sort.  The other-half has been decorating (yes again) this time the bathroom and bedroom.  Cyril, the three legged monster cat, decided to help.  Here's some of his handiwork.

Freshly painted window sills, wooden floors and a delinquent cat definitely do not mix.

OK, on to the tedious medical update.  I had the first dose of my new chemo on Wednesday.  The following day I was back at hospital as my temperature went haywire.  It was much like the time a similar thing happened in Cornwall a few months ago.  Once again, thankfully, my white blood cell count was ok, so the temperature wasn't indicative of a rampant infection.  I had some IV antibiotics and some oral ones to take home just to be on the safe side but the doctors seemed to think it was the result of new chemo on top of old chemo and my body deciding it was all a bit too much to handle.  Anyway, I'm OK now.  We shall see what happens next week when I go back for a swamp juice top up.  Let's hope it doesn't result in this:

Although frankly that would be an improvement on this, a picture of me looking truly dreadful while recuperating, truly I have no pride when it comes to seeking sympathy.

Hello beautiful!