Thursday 30 April 2015

Your prayers please...


Andy again, sadly Julie is too ill in hospital to even look at the blogs currently..


Monday 27th April 2015, its been a long day, sod June 21st being the longest day, today is for me.


I've had less than an hours sleep since 08.00 Sunday morning, this isn't a time to sleep I've a very poorly wife and she needs me before I need my bed..


June and I headed in to the ward its Called the Short Stay Surgical Ward, Julie has her own side ward, in itself that's ominous. she's asleep, I was there for five hours, well I did my usual lets make the staff my friends in case I need to grab extra time with Julie, amazing what two dozen iced lollies or lollie ices as they call them here can do in terms of good will.

 
Sadly there were no Doctors about, Julie explained one had seen her earlier in the day and he said they would be doing ultrasound tests on her over the next couple of days and they intend to do an MRI scan on her brain. Julie said "He asked me what I want to do if we find anything on any of the ultrasounds or scans? She answered "I don't know right now, ask me when you find something." I knew instantly the relevance of what he was asking, Julie did too, she may be ill, she may have brain cancer but she hasn't lost her mental capacity. The next words I spoke were some of the hardest I've ever uttered. "Hunny, a few weeks ago you wanted to decline the Chemo and I begged you to fight it, a combination of June and myself willed you to carry on because you seemed fit enough to fight on, I also said at the time if I ever felt the time had come that your quality of life was falling away and that in my view you should probably reconsider all of your treatment options I would honestly tell you............., I truly feel after the last day that time has come" She looked at me and responded "I am not ready to give in yet, I want to fight it, IF Dr Haylock was to say to me that the tumour was growing and the chemo wasn't working on it then I'll call it a day". Its so hard being prepared to let the one you love, your soul mate know that you're prepared to let her go to stop her suffering, I feel guilty too in raising it, I am pro-life but I'm anti suffering, right now she has suffered more than most of us could ever handle....I told her that she had my full unconditional support and I felt she was being so brave, I held her hand briefly as she slipped in to another bout of sleep. Of the five hours I spent with her she was mainly asleep for four and a half of them. Part of me is questioning whether I did the right thing those few weeks ago in asking her to fight, I look at her today and feel I was being selfish, at the time I felt it was the right decision. I do not think Julie realises just how poorly she is right now, her breathing is shallow, she is constantly asleep and she is not eating food, it is a recipe for a situation that is far from wanting to fight this. Julie has made her decision though and I will continue to fight for the best for her no matter how little or long she has remaining.


During a short bout of awakeness her phone buzzed, "That's been buzzing all day" she had me check who it was, there were only three messages, she said "read them to me" basically she's lost interest in her phone, I asked her did she want her ipad bringing in? "No",


7pm came and I went to kiss her goodnight, visiting is over, "Please don't leave me, I don't want to be alone" she begged. I held her hand and sat back into my chair. she dozed off again soon her breathing was consistent with a heavy sleep, I left around 7.45 I'm exhausted i've been awake 36 hours all but and I have to update the family now. My bed, my empty bed was soon calling me.

 
I woke Tuesday morning, I headed into work, I called the ward to see what sort of night Julie had had. "Julie who?" came the response..... Err I'm not impressed. "Julie Shute, she's in room nine" the response was Julie had been moved to another ward. It turned out to be Ward 26 up one floor.. I considered getting off at the next junction and driving back to the hospital. Its a sign of Julie's illness that she is too tired, too ill to let me know. Again Hospital Staff... Moving a patient, surely a call informing the next of kin isn't too much trouble? Clearly it is....


I spoke to one of the staff nurses on 26, she said Julie had had an ok night but "She has pulled out her Vemplom line so she's missed two courses of her antibiotics" Doesn't sound like Julie to me. The staff nurse wanted to ask me some questions as "Julie is mainly asleep so we haven't been able to ask her". Two questions, 1) How does Julie cope with the stairs at home and 2) is she able to prepare her own food and feed herself? I gave her the answers, I need to get my head around what is happening here, so far as I know the MRI scan hasn't happened the Ultrasounds have found nothing conclusive.. The answers to the questions by the way are 1) She cannot walk stairs now hence I've had two stair lifts put in. The answer to 2) is She could (if she so wanted but she didn't want pre admission) have made her way to the kitchen to fetch a cold plated meal but hot foods, and cooking are too dangerous for her now AND besides that she has 24/7 someone with her, she cannot be left alone.

 I called the district nurses as they were meant to be visiting Julie today at home so I needed to cancel their visit (remember consider others even though you are focussed on your patient) . I used it as an opportunity to discuss options, if Julie is to be discharged with no treatment I need to plan for her comfort at home, I'm not sure I've got my head around this yet, am I jumping the gun on the strength of two questions?..... For sure now I'm going to need commodes upstairs and down stairs. The easy option would be to 'isolate Julie to our bedroom, its got all the comforts of downstairs and it would be easier to move her super dooper all dancing chair to the bedroom but I want to keep her life as normal as possible.

 
I worked until 1.30 and drove to the hospital Julie is in and out of sleep, she's not eating, she's blaming it on the bed, she can't sit upright. They've got her an air mattress to prevent bed sores there is a electrically adjustable bed outside her room ready to swap over for her, suddenly she is in panic, she doesn't want to get out of her bed because of her left leg, she's still of the view it wont work. Not long after and two physiotherapists come to visit Julie, what followed left me speechless. The lead physio introduced herself to Julie and explained they wanted to help her up and to see her with a walking frame. Julie just pointed at me and bellowed "Get him out of here now!" Wow, where the hell did that come from? I just backed out of the room and leant against the far corridor slightly up from her room, I wasn't watching or listening I was just checking my tweets etc when suddenly "Make him go away! Now!" I felt uncomfortable in my wife's presence for the first time in my life. One of the Nurses came over and rightly enquired as to my relationship to Julie, I explained "I'm her husband".. The Nurse wondered if Julie had been admitted with a stroke, I explained brain tumour and brain cancer. Julie's later justification for her outbursts was "You always speak for me, you always tell them how I am feeling" I explained I only (normally) get involved if she asks me to comment and I cannot possibly explain to anyone how she feels, only she knows that.


 
It turned out the physio was happy with Julie's left leg working ok-ish. As she left she said "you can go back in now" "If I dare", I stood at the door and asked "Well, can I come in?" she answered "of course"  whilst all this had been going on the Nurses had switched Julie's bed and she was straight back in it. She soon dozed off, I shot out to buy her  couple of night dresses. On returning a meal had been left for her and she was awake, despite the changing of the beds and being able to sit up, the meal remained untouched.. "I'm not hungry" .  I'm concerned by the lack of food intake.. I left not long after, I cant go straight home, our house is big, spacious and despite my size at times like this I feel tiny in it, I headed to the mouth of the Mersey to watch the Sun set over the Irish sea, I can just zone out here, I stay in my car for its still cold....Eventually I drove home straight to bed, On previous nights alone like this Julie's favourite 'non-stieff teddy 'Winston' has been a comfort for a 58 year softy however I took him in to Julie to watch over her for me...  



 
Wednesday and I'm in the lift and Julie messages me, apparently the Doctor was on the ward, he I wanted to see!

 
Again nothing could prepare me for what was to come when the Dr appeared. I asked him for an update on where we are... Ok; his boss was concerned at Julie's continuing low Oxygen levels, something is causing it so he sent Julie for X-rays and a CT scan. A Blood Clot has been located on Julie's lung close to one of the main arteries! Will this madness never end was my first thought?, then common sense kicked in.. "So the symptoms of a blood clot are low oxygen levels, breathing difficulties,  racing heart beat and low oxygen levels leads to tiredness?" yes they are all symptoms! It's probably the only time I can envisage saying finding a blood clot is a good thing, is this the break we've been hoping for? The team have already started to treat the clot, the Dr said "we'd hope to see an improvement from tomorrow!" I asked how long for the clot to dissipate? 7-10 days but no guarantees. It seems the power of prayer has found us some temporary respite... Its hard to describe the feeling, we still don't know if this is the sole reason for Julie's problems this week but we do know they were/are a significant contributor. Julie has said previously before the last tumour was confirmed that she knew it was back and that she knows her body, this makes it easier to accept her decision to want to fight on but why won't she eat??? I mentioned it to the Dr suggested food supplement/Nutritional  drinks like Ensure, he either hadn't been made aware of the lack of eating or he hadn't thought about it but he agreed with my suggestion, he's going to prescribe some for her.

 
Today (Thurs) Julie has perked up just a little, is it the drug tackling the blood clot or was it her visitors who did put a smile on her face? Adele & her Mum who travelled from Doncaster and Rebecca who travelled over from Liverpool. she (Julie) is still not eating though, she is still sleeping heavily and a lot, I tried to lighten the mood with some of my daft humour but its not appreciated and one comment I made she just looked at me and said "I might just as well shut up".. I'm sensing she is beginning to 'push me away' I might be paranoid, but I've sadly seen this before. They're all the  classic symptoms of cancer I'm afraid and part of a downward spiral that needs to be broken is the refusal to eat if its not well the future looks short & bleak. I thought it might be the hospital food so I dashed to Sainsbury's and food shopped, half a spit roast chicken, salad, a mix of fruits that she loves, pears, grapes, raspberries, blueberries, sliced pineapple, despite all of this she either fears the acidity in them on her stomach and she still 'wasn't hungry'... Despite saying she wants to fight, currently Julie's actions are anything but the fight she said she wanted to continue, Its still very early days, so many factors so confusing.... I still feel I'm on a rollercoaster, I'm still convinced our time together is limited...I keep asking myself ... Where does this leave me or us?  So many questions, so few answers......... I'd ask for more of your prayers please...


Back in the land of Chemotherapy


On Friday  9th April I started my course of Lomustine (aka CCNU) it’s one capsule a day for four days and that’s it for the month.
I have to take it last thing at night with an anti-sickness drug, I never felt sick the first time around on my Temodal and I am fortunate that either the pills are doing what it says on the packet or I am naturally fine, I’m not taking the chance though.
Initially the only side effects were tiredness; I seem to sleep more on my (Soon to be gone) Chaise – more on this later down. By Tuesday I had developed a wheeze/rattle, I wasn’t sure if it was on my chest or not so I called Andy, he called our GP’s and fought through the beaurocratic nightmare of getting a booking, on hold for 13 minutes then cut off, answered after another 8 minutes then told “All of the day slots are taken you’ll have to call back in the morning” HA, must be a new receptionist or she would have known better, I’d love to be a fly on the wall in Andy’s office when he starts, he’s either sarcastically funny or he makes his point… Today it was “So, let me get this right, I have to hold on for 21 minutes including getting cut off once to then be told I cannot make an appointment now for my terminally ill wife who is undergoing chemotherapy and has a problem and needs to see a Dr?” Suffice to say within a minute he had an appointment for me at 11.00 the next day, Wednesday 15th April.
The phone went mad today! People calling me including the district nurses who our GP had asked to make contact with me and they want to come Thursday. Then late on the imaging team at Clatterbridge called “Julie, can you make it in at 08.45 for a scan? You can decline and we’ll find another later slot but we’ve got a slot then”, we’ll be there I tell them.  I also had the OH team ring me to see how I’m getting on think they’re sending someone out to see me too.
Andy walked in after work around 8pm he did a small shop on the way home, he’s worse than a kid! He comes home with stuff I never asked for and hahaha forgot the very two things I asked him to specifically get!  I soon forgive him for I got flowers too, bless him. Anyway I tell him about my day as we chat romantically me sat on the loo. “you have booked tomorrow off? I’ve got a scan at 08.45”.  Andy dropped in “that’s fine, I’ll have to cancel the appointment to get my leg wound dressed as that’s at 9”,  I’d forgotten and apologised, Andy has lower leg problems, in the summer mosquitos or gnats love his ankles and the clumsy sod caught the back of his leg with a suitcase last August and the resulting wound is taking forever to be recover/heal. He’s got poor lower limb circulation bless him, twice a week dressing changes, seven courses of antibiotics since December and it’s still not healed, he just plays it down but I do worry about him and I know sometimes it pains him, lol if we’d have been born horses we would have both been shot by now!
Wednesday and we are up at the usual daft o’clock I have my routine its very slow, from the time I get up until I sit down for my breakfast and we are both showered and dressed its around 90 minutes now, in days gone by maybe thirty. I am so slow nowadays; I want to scream at times.
We get to Clatterbridge as we parked up and as Andy was getting my wheelchair out of the car one of the charity office windows behind him opened and Karen was saying hi, me I was stuck in the car looking the other way, we’ll grab a coffee later hopefully.
I’m taken down to the MRI suite for my scan, all the usual but essential questions about health and whether I’ve got any metal in or on me. All essential the M in MRI is for Magnetic (powerful magnet!), they don’t even allow wheelchairs that are made of magnetic materials so I have to swap to one of them, it’s no hardship. Ladies, even your bra has to come off only because of the bones and hooks & eyes. This scan takes around forty minutes and midway through  they inject a colour contrasting dye in to my veins, it doesn’t hurt but afterwards you have to drink extra fluids to flush this out. 
Once out we pop into the WRVS coffee shop for a drink and some toast, Andy ordered then  he shot across to the adjacent charity office to see if Karen wants a coffee but they’re all in a meeting, I’ll catch up with them all soon I am certain. Coffee done and we’re off to our GP’s. Seems I have a wheeze in my bronchial tract as opposed to on my lungs so its not a chest infection, phew. The Dr prescribes me a new inhaler, think this will take me to nine drugs a day to take now… I rattle as I walk hehe. I got a bit upset in the Drs, Andy did the very thing he’s often accused older consultants of doing and whilst at times in my best interests I’d love him to give me the chance to explain my symptoms, circumstances etc. I feel like I’m invisible at times now, it is hard I know for sometimes I need his help other times I just want to do it all myself.  He’s apologetic as was the Dr, I know it’s a hard call for I could miss something crucial out, I don’t know, I think he will now just let me talk and get on with it. Why oh why am I so ill and why is life full of dilemmas for me???? !
On the way out Andy checked if they’d managed to rebook his leg dressing change with our lovely practice Nurse Bernie, she’s lovely an amazing patient approach I feel so at ease with her. Anyway, Andy’s appt had been swapped and he was in next. We went in together, I am very clingy nowadays, I don’t want to be on my own for what if a seizure started or worse? Earlier in the day I mentioned to Andy I felt I still had a piece of a stitch in my head, so he mentioned it to Bernie and lo and behold I did so she quickly had that out with not too much whinging from me. I saw Andy’s leg wound bless him, it’s not deep but it looks yucky to me.  Anyway now its home! Well for me anyway, Andy still has to go into the office though, no peace for the wicked Mr Shute uh? Hehe. Letty arrived to see me with her grandson, we haven’t had a catch up for a few weeks, I love this woman to bits.  I slept afterwards, on my trusty chaise. Sadly it’s got to go, part of me being a burden is I need my legs up for my ankles swell these days, but as my left leg is so weak now I cannot lift it up, Andy moves me into position but he’s a strapping guy, its nigh on impossible for woon. So I’ve made a decision, I am buying myself a chair that can recline raise my legs almost catapult me out of it and so it will be going where the chaise goes. (Anyone wanna free chaise lol) So I’m eagerly awaiting delivery of my new chair.
Andy comes home with the two items he’d stupidly not got me the night before and he’s armed with two new videos! He’s not safe to be let out on his own!  I’m not feeling too good; I’ve been sleepy & I feel like I have a cold coming on, sneezing, I’m nasally… Is the chemotherapy weakening my immune system as it can? I’m checking my temperature daily at the moment and I’m not running a fever, seems it’s ‘just a cold’, yes guys a cold not man flu hehe.
Thursday arrives and I am ‘snotty’ but my temperature is fine and I feel ok despite seeming to be full of a cold.
Well Andy ordered my chair on Thursday and its now Tuesday and he’s heard nothing, we are meant to get a call saying when it will be delivered. Now here is stupid for you…. We could have had free next day delivery but that means a courier delivering the box(es) to the door, Andy isn’t about during the day and this chair will be heavy, the company, part of one of one of the top two chemist chains in the country… offered delivery via their own team but it carried a cost of £50, that included setting it up in the house for me, Andy haggled them down to £40 (Always ask if there is a discount or deal at worst they can say no) . Anyway he assumed as he hadn’t been told different that it might take a couple of days. So Tuesday he calls, this is his account of events. Ok… I called explained politely to a young lady about ordering the chair, no phone call etc only to be told “Well its 7-10 working days for delivery” Ha, really?? I explained there was no way on earth I would have placed the order on knowledge of that..the response was “You would have been told when you ordered it all of our call handlers follow a script and that’s part of it, we do record our calls you know”… Really? Well the one thing I am is a good listener and no way was I told. My response was “I certainly was not told and so be my guest replay your recording” this kind of threw her and the conversation started to get negative, she said “I’ll email the logistics manager and ask them to chase the date up” I added and add “Please call the customer before 5pm with the delivery date” her response was, well, disappointing but I say to you all as part of the advice we are trying to pass on, dig in and although always be politely don’t back down… She responded “I can add that but I can’t guarantee it will happen”… Me really quick response  “Well tell you what add this instead…Please contact the customer by 5pm tonight with a delivery date or he will cancel his £500 order with us”… Again poor response, “That’s up to you Sir”… At this point I politely asked her if she had a supervisor and of course she did so I asked to speak to her.  Bad start by the Supervisor "Mr Shuter, How can I help?" Me - "Well start by removing the non-existent R in my surname.....I started the conversation by asking the Supervisor if she was up to speed on my call or did I have to explain it again, she confirmed she was so I asked her to give me her understanding of the situation (Use a phrase like Ok give me your understanding of where we are at) . In fairness it was pretty spot on.. Always do this, they might think they have the full story but they could be well off the mark  it will save your breath and probably help your blood pressure too.
I did add at this point the reason for needing the chair and justified why I would not have placed the order on a 7-10 (working day basis), I also in case like this always add “Do you feel this is the excellent customer service you say you offer” when you do this if they waffle at you lol I just add "the question warranted a yes or no answer, is this good customer service that I’ve experienced?…." (The answer is clearly no)  this lady assured me she would speak to the warehouse team and come back with a date for me before 5pm… There, wasn’t too difficult was it? Within ten minutes I was called back and she broke the news the chair would be delivered Thursday quite proud this was just five working days from my ordering it…
Julie here again. Well the chair arrives and it’s all singing and dancing, I’m very happy with it, the only thing is at the moment I have it facing the wrong way for the power leads are too short, Andy the smart ass said the night before he’d leave an extension cable out, I told him It wouldn’t need it, I knew there would be a smart ass comment when he gets home (grr why is he right so often?) I called him “Told you” was the reply but he said he’d pick me up one to match the dark wooden floor..
I met a lovely lady last December called Nicki Spindler, she and Andy keep in touch via twitter and she wanted to come visit me so we arranged it for today, she’s beautiful and blooming at 7 months pregnant and she’s brought me tulips, I love flowers but.. that’s no hint if you are visiting, I like the odd discrete vase of flowers but I’m not living in a funeral parlour yet and lol Chocolates or sweets are banned, I wont eat refined sugars now and the fat frog doesn't need any encouragement hehe!! We had a great chat and we had the best Cath Kidston mugs out. I love visitors though I apologise now for being so tired all the time and I’m drained so my sense of humour isn’t quite what it once was and I drift in and out of sleep.
Well Friday comes and Andy is off to give Vince moral support on his Son Andrew’s (Another Andrew!) Stag do, I’ve got Emma, Chloe & Abbie coming over, also Letty & Blue Eagle, it’s a mini agents meeting with three of the four of us undercover hehe.. They’re here until Andy gets home Sunday, I’ll miss him but I know he needs a break from me, I keep apologising to him for being such hard work he won’t hear it but I know I am, I am so dependent on him now. Letty is going to be sharing my bed in his place. DOWN BOYS! hehe
 
We had great fun, the girls are lovely, Emma has obviously explained how they need to be quietish and in the main it worked though occasionally I’d stress and yell at them, I feel so bad but I can’t help myself or cope, I don’t want to be remembered as the grandma that always shouted at us… My brother Phil turned up too bless him, so I've seen all four brothers in the last month now.
Saturday night my left leg would not work, bless poor Letty, my trip to the loo took us an hour to make, its not twenty feet from my bed.. I’m breathless, I’m not feeling steady, I’m shaky, something isn’t right I know it.
I dozed in and out of sleep on Sunday, bless her Emma has come all this way and I’m sleeping, I feel bad.
Andy arrived home about 4pm, Ollypop was on him like a rash, she has him curled around her little finger, her big eyes just make him melt and he’ll do anything for her the little bugger hehe. Anyway everyone gets hugs and I get my kiss too, I’ve missed him he’ll know, he doesn’t need me to say it. I explained all of my problems to him.  I’m even tired writing this so I’ll hand over to Andy for this bit gets ‘tricky’ too.
Andy here, right this is going to get distressing for some of you I’m afraid, I’m going to split this piece into two blogs, the second I will publish later tonight…
It was obvious on coming home that Julie wasn’t well, I was shocked by her appearance she looked like she had aged ten years in 3 days since I last saw her. The looks on the others faces too, Letty, Woon & Emma, they’re all concerned even without uttering a word.
Now I was home Letty needed to get back to her family, I spoke to her in private at the front door, she was extremely concerned even to the point of suggesting it might be an idea to move her bed downstairs, I know Julie won’t go for this but we all have to consider all options, at this point we are both of the view that Julie’s time is very limited now, I can’t contain my tears, my eyes well up, I’ll do whatever I need to do but I am exasperated that I cannot save myself from losing my wife, my best friend, my soul mate, its been tough watching her deteriorate and for us now to be at this so obvious stage, nothing can prepare you for this even though we’ve known this day would come, the harsh reality is painful. She hugged me like the dear friend that she is, bless her she’s suffered bereavement this year too, life isn’t good… I wiped my eyes and went back to Julie well for thirty seconds before Olivia ‘my eyes are the size of dustbin lids’ Buckley decided I needed to play with her, we should not have favourites but I have to concede this little bugger is just a cute nose in front of the other five grandchildren all of whom I love dearly.
Sadly its time for Emma, the grandchildren and Woon to go home, June has been my rock as well as Julie’s this last three weeks, she’s made some big sacrifices to support us both, I’ll be eternally grateful. Well hugs and kisses, Julie is in her chair, I had to turn away as Emma hugged her mum, I knew this was going to be heart breaking for them both, I’m truly of the view this is their last goodbye.. I left the room, I later found out Julie begged Emma not to go… Damn this awful disease. Every goodbye now fills Julie with tears, she is no one’s fool, she knows how close things have become now, the Grimsby trip was the realization tipping point since then there have been tears streaming down Julie’s face at every goodbye, I try to stay strong for her but at times our tears mix on her cheek….
Julie stayed in her chair as I saw everyone off, yes I cried walking back up our path, I know I’ll see them all again many times but I cannot help feel for everyone else who have just said their last goodbyes to Mum, Julie and grandma..
Sunday evening, our dear Friend Scouse who is on Julie sitting duty from Monday morning comes over to stay the night, Phil is still here. It’s late 9.30 ish and I am famished (again) so I suggested a Chinese take away. By 10pm we were eating but Julie had already told me earlier in the day she cannot cope with full meals now almost needing to just pick at small portions. She had two small spoons of chow Mein and within ten minutes she was telling me she needed a trip to the loo. She’s fretting about everything now, her left leg won’t work she said (though I walked her in to the lounge from the dining room and her dexterity impressed me). Given her being adamant about her leg I fetched her wheel chair, he confidence is severely shot from the last time I helped her off the sofa, it took her 20 minutes before she’d let me help her into it.
Its ten feet to the stair lift, once there no way was she getting out of that wheelchair. Her breathing is laboured, her head is down but just standing and ‘dropping (gently and assisted) into the wheelchair’ has exhausted her. I’m concerned for she needs the loo and she is feeling nauseous. I sat with her for 20 minutes and said irrelevant I needed to get her to the loo now. She let me help her but she was obviously weak. I got her to the top of the stairs and again she didn’t want to get off the stair lift, I left her to rest, ran downstairs and got the wheelchair, I got it upstairs and tested it to see if it would go through the loo door, it would but I’d be needing a paint job on the door frames afterwards but at least I know Julie won’t have to exert herself walking.  She’s still very lethargic; I’m concerned on many fronts not least for her need to visit the loo. Another twenty minutes and I explained it was imperative we got her to the loo now. Again we managed to get her into the wheel chair and with a bit of good luck the journey to the loo seat was swift though she was in panic as she stood up as I lowered her PJ’s. I left her and sat outside considering my next moves, I periodically checked on her over the next 30 minutes, despite the urgency for the loo nothing happened, it took 20 minutes or so before she was sitting outside the loo looking at the second stair lift that covers the three steps to the landing our bedrooms are on. I decided at this point and explained to her that I was going to get her to bed and call a Doctor. With the aid of June I tried to lift her from the wheelchair and you would have thought I was murdering her, bless her. She was panicking, moaning/groaning and her left leg problem was making things difficult, I managed to turn her and get her on the stair lift but she was only partly sitting on it and she was in distress. I asked if she had pain in her tummy, she said no. I then told her I’d like to check and feel it for I wanted to put the stair lift seat belt on her god forbid she slipped off it now. I gently pressed her tummy she was ok so I strapped her safely in, whilst doing this I asked June to grab the throws off the beds to wrap her in them. We covered her up she was cold, I fetched her woollen hat (we lose more heat out of our heads than any other part of the body, I heated her wheaty bag , all the time June was supporting her, Julie’s head leaning against her, I called the District Nurse service, they called a GP and ten minutes later he was pulling up. On arrival I walked him up our path briefing him about  Julie, by the time he arrived with her he was able to talk to her and start his assessment, June and I stood back as her examined her, her body temp was 36 so fine but he was struggling to get a pulse or her BP, none of his equipment was picking it up, he resorted to manually checking her BP and it was low, very low. He said he wanted her in hospital and would call an ambulance. I gave him Julie’s drug regime info as he wrote up a letter for me/her. I assembled all of her drugs in her drug box for it would need to go in the ambulance to the hospital too.
Within five minutes two paramedics are at the open door, and they come up, they only just missed the Dr. Their equipment would not pick up Julies pulse or BP either, this set off warning bells for me but I remained calm. Two mins later and an ambulance crew arrived. The four paramedics were superb, they explained to Julie they needed to get her downstairs on to their trolley seat and the easiest way would be using her stair lift, with the security of four of them assisting she allowed them to help her the 3 feet to it, truth be told she was too weak to object.
On getting her down, into their chair and wrapping her in a thermal blanket still wearing her woollen hat they manoeuvred her out of the house. June offered to go in the ambulance with her I would follow shortly after in my car. As the team settled Julie into the ambulance one of the team returned and spoke with me, he enquired about the side effects of the Lomustine (her chemo) for he felt she was Neutropenic, Neutropenia is where the white blood cells level drop dangerously low, yes it is a side effect… “We’ll blue light her in then” Sitting on my stairs talking to him my eyes filled with tears,  low BP, can’t find a pulse, Neutropenic, I’m scared I’m about to lose her.. He reassured with we’ll treat her with care and dignity, “Like she’s my own daughter” he said.. I thanked him told him I had tremendous faith in the paramedics but his NHS Trust CEO Mr Williams is in my view incompetent.. You'll recall the blog on the previous ambulance non-arrival, well I got a half baked response from this individual but as he failed to answer my complaint in full he is in possession of a second letter complaint demanding answers, I think I sent that THREE WEEKS AGO and STILL NO RESPONSE (By warned Mr Williams I am NOT backing down on this I will run you before the Parliamentary Ombudsman yet!) Back to Julie this is not a good place to be right now, I want this to be a nightmare I can wake up from.  I told June to wait out by the ambulance with Julie’s drug box and Dr's Letter.
I spoke to Phil who was also visibly upset, it’s his only sister but he realises the best thing he can do is remain here. I left two minutes after the ambulance but within seconds I could see the houses in the distance highlighted with blue lights bouncing off them. Whilst I wasn’t trying to catch them I was closing the distance, two close by sets of traffic lights both on red, both they took on the red light, I stayed back, cannot empathise strongly enough stay calm if you are in a situation like this no matter how distressing…  As we left the built up area although only a mile from the hospital I wanted to be there as they arrived, I am genuinely concerned Julie isn’t going to make it…. We entered the hospital grounds together and I peeled off into the car park, I got into A&E as they pushed her ambulance trolley in through their doors straight into a trauma unit with locked doors. The A&E receptionist told me to go straight in to the trauma unit waiting area where June was waiting, we were let into the family waiting room and hours seemed to pass, no updates no nothing, I’d been up since 08.00 we got to the hospital at 01.15. and its gone two, I lay flat down on the bench sets and my eyes closed I could still here people coming and going, June bless her was still awake too, someone gently pushed me it was a Nurse, “We didn’t realise you were here come on through”!! I shook my head clear and we were taken through to Julie in an almost empty trauma unit, a lovely Doctor (Hannah) asked me a few questions as I walked in to the unit, she was most impressed I’d got specific dates for events that she wanted to know about. (I’d even brought all of Julie’s hospital letters etc) I’d say to you all if you can be specific it helps and saves time.  Hannah explained they’d done tests, that they had put Julie immediately onto antibiotics and antivirals via an IV drip that initial tests were inconclusive so they were admitting her to a ward and more tests would be done during the day.
I went over to the bay Julie was in, the nurses were excellent. At 04.30 they moved Julie to a ward, I felt it wasn’t fair to walk onto a ward at that time of night with sleeping patients, I couldn’t contribute anymore so hugged Julie and kissed her goodbye, she’s in the right place but I’m still concerned she is poorly…..very poorly.
I drove home and despite having nothing more than a short power nap in the visitors room since 08.00 Sunday morning I dropped June at our house and drove straight to my office, this is my busiest week so I had to be in for a part of it. I hit my desk at 06.00 three hours earlier than normal and still in the clothes I had stepped in to Sunday morning, I looked anything but the professional business man I’m meant to be, right now I really don’t care. I wrote my boss an email I’m sure I’ll be out of here before her arrives and I did the essential work I needed to do and I was out of here, I got home mid-morning, I drove to the mouth of the Mersey to contemplate everything, I find I can clear my mind down here, it’s always been my safety net/bolt hole.
Getting home I dropped Phil off to get his train home, he knows to expect the worst, I’m glad he’s made the trip distressing as it was for him, at least he’s seen his little sis…
On getting home I told June I was going for a shower, who ever invented the electric shower deserves a medal, I made my way to our bedroom and sat on the bed to dry myself.. The next thing the door bell is ringing, I’m that dazed thinking back now I don’t know who was at the door or if I answered it or if June did…
Visiting is at two, I've not received any calls so I can but assume Julie is stable for now, at this stage I’m updating people close family I’ve put on notice that I do not think Julie has long left and to brace themselves for bad news in the near future. On my way back from my office I called Julie’s dad Bob, it’s the hardest call I’ve ever made in my life. I try to remain composed but I can’t, Bob had already picked up on my tone and he was softly wailing too, I think he thought I’d rang to say we’d lost her, Bob is in his late 80’s his wife is very poorly too, he’s in no position to drive but I need to get him over here and soon, he deserves to see his little girl one last time…
 
The next blog will be published this evening, all I'll say is have tissues to hand.....

Sunday 12 April 2015

Hell of a fortnight, hell of a (long) blog

Tissues Warning!......

 Well I’ve been home just a few days and I’m back at the Walton Centre already to see Alison who is removing my stitches today, 31st March. I have a head full of a beautiful blanket stitch, whoever did this (Mr Farah maybe) well it’s something a seamstress would be proud of, have a look for yourself!
I walked into the Walton Centre with the aid of Andy & my stroller and we waited patiently for Alison. She was shortly with us, I had butterflies in my tummy, this is going to hurt and I worry about pain setting off a seizure, I am petrified of these now. Alison is lovely, we sat down in her office and discussed how I was and how I was getting on, I had a bit of a meltdown, I feel so low and so useless now, the realisation of my weakness, I cannot even safely lift the kettle, I can’t cook which was a passion of mine, I feel so down about all this. Alison and Andy reassured me, Alison reminding me that barely a week ago I’d had serious Brain Surgery and that my recovery takes time, I know this but it doesn’t make it any easier, I am not fooling myself, I know I’m not going to get back to normal now… I eventually compose myself and apologise for crying, everyone is so kind to me. We’d also discussed my recent seizure; Alison went and fetched one of the registrars who decided I needed to increase my dose of Keppra (Fuzzy drug) from 1,000mg to 1,250mg twice a day. It comes with mixed blessings fuzzy drug, yes it’s meant to control seizures but it also makes me feel tired shortly after I take it.
Now it was time to have my stitches removed, Alison had a colleague to help her by shining a torch on to the stitches so she could see them properly. They have a thing called a stitch cutter; it’s like a thin Stanley knife/Craft blade with a curve on the end. Either the stitches were thick or the blade wasn’t that sharp for Alison was struggling to cut through them and every pull had me wincing. Eventually Alison took to using surgical scissors and whilst it hurt a little as she slid the stitches out within 20 minutes I was stitch free. Despite there still being some dried blood on my wound I can’t wash my head for 48 hours, note I said head for my hair is thinner than ever and my wound area, well you can see for yourself… Before we left Andy had done his usual and late the night before picked up four dozen Krispy Kreme donuts, he gave a dozen to Alison for her and her colleagues, the other three dozen were for Cairns Ward staff, I/we needed them to know how much we appreciated the care they showed me over ten days. Ha, it’s amazing how many Nurses are on diets (allegedly) hehe.
I made it into reception with my stroller but I was shaky, Andy is quite perceptive (for a man ha!) and he had me sit down whilst he took my stroller to the car and came back with my wheel chair so we could head up to the ward. Bless them they appeared short staffed, (Politicians, please note! We need more Nurses in our hospital wards!) We didn’t stay more than a minute, a card and donuts left and we waved goodbye.
By now I am as the Irish say (Andy is of Irish stock) ‘famished’, starving to you and me lol so despite the very windy day we headed to Crosby Beach, I wanted my fish finger sandwich so badly I could taste it. We got down there and disaster! No burger/butty van just the ice cream man! (Is he crackers its sodding freezing!) Disgruntled we drove over to the south side of the Mersey and were back at New Brighton, no fish finger sandwich here but having seen Andy’s recent pie and chips… Pie and chips it is (not my usual diet), t’was scrummy!
Andy took Wednesday off too as we had no Julie sitter for today, so we could chill out together, he’s amazing in how he looks after me but bless him he’s so tired. As a result in between meals he slept most of the day away, he needs to recharge his batteries, neither of us get a full night’s sleep for invariably I need the loo in the night and I need Andy’s assistance to get me up and to walk with me to the stair lift.  
Thursday Andy’s back to work and one of the Secret Agents is with me for the day J as always we have fun, Secret Agent ‘Blue Eagle’ helps me put together our grandchildren’s Easter presents, we like to be different than just giving them big chocolate eggs….
Good Friday and we chill, we went out for a drive and I needed to buy more clothes, despite my drastic drop in steroids recently the weight doesn’t fall off that quickly! I need new shoes too, something more serviceable something I can put my foot brace into, whilst I got clothes I remain ‘new shoeless’. Once home Andy packs our suitcase for tomorrow, we are Grimsby bound, this is another journey I’m not truly looking forwards to.
It’s Easter Saturday morning and we are heading for Grimsby to visit our family. I could have easily called this blog ‘We’re Sorry’…. Whilst the blog updates are always accurate when I was in hospital sadly we had to omit some information from you until we had spoken to our family, we hope you understand the need for this mild deception, reading on I hope you understand why.
Whilst I have recovered well from my surgical procedure it’s with great sadness we have to share with you that the day after my surgery Mr Farah informed us he could not safely remove all of the tumour for it had grown over my motor cortex to the point that removing it would have left me left side paralysed, he could only see the full extent once in theatre and had to make a difficult judgement call as the operation proceeded. I have significant left side weakness since the surgery but I still have mobility. Mr Farah is apologetic and says my surgical options are sadly at an end and he’s handing me back over to the Oncology team again now. Andy wasn’t prepared to wait for any sort of communication delay knowing every minute counts now so he made a few calls including to Dr Haylock’s secretary Coral, she knew of my case and agreed I needed an appointment asap though the man himself is on holiday now for a week; she had the bookings team slot me in for Dr Haylock’s next clinic, Thursday April 9th. I’m so thankful Andy can make things happen, it is reassuring to know where we are.
You’ll appreciate from previous blogs that Grade IV Glio Blastoma Multiforme is both aggressive and incurable/terminal. The news that there is tumour left and that my surgical options are now exhausted are a terrible blow, there is no fooling ourselves or any point in deceiving anyone on the gravity of the situation now, so we need to tell my family.
We saw Emma, Aaron & my dear Dad.  This wasn’t a fun experience, Emma & Aaron were both expecting the news especially as we had asked to see them together, they were so mature about it, I am so proud of them both. My dad bless him, telling him is a heart breaking experience for us all. I love my Daddy, I don’t want to see him sad or teary but its natural, damn you fluff!! The bad news delivered we can now ‘relax’ and have precious family time.
It’s Saturday evening & fluff (despite the increase in fuzzy drug) decided it was going to remind me it was with us and it's angry, very angry… I had a huge seizure in the hotel corridor just as we are heading out to join my Brother Mick & his wife Sue for dinner. It was so strong &  it truly scared me so badly that I didn’t want to go out now, I’d lost the use of my left hand and leg, it’s always comes back before but I fear one day it won’t. Andy calmed me down and said I should not allow fluff to hold me hostage and that we should still go for dinner, reluctantly I agreed. We arrived at the restaurant late and I broke down in tears as I apologised, I feel so useless, so helpless, I feel such a burden. Sue hugged me and re-assured me I had nothing to apologise for. We sat down for dinner, the restaurant was quiet it was all so relaxed and the bonus was my hand and leg usage came back, not before I had to ask Andy to cut up my food though, we had a great night.
Easter Sunday & we did nothing but eat, we had a traditional Sunday lunch with Vicky, Aaron and our grandchildren, Abbey, Millie & Evan and in the evening we went for a long overdue curry with Bob, Emma, Bob’s sister Jenny and his mum & dad who were also visiting. It was a great but calorie filled day!
Monday and we had invited other friends & family in Grimsby to come visit us late morning, I tire so much these days I cannot dash around like we used to. It was lovely to see them all.
After our friends had gone I was drained, I was tearful as they left, is this the last time? We still hadn’t seen the twins & Olivia, we were planning to go to their house but I worry about daft things these days, the width of corridors, the proximity of a loo and I am not feeling 100%. Andy suggested we get Emma & Bob to come to us, I agreed. Early afternoon I’m getting grandma hugs, Olivia is curious to me being in a wheel chair and my scar, Andy explained I’d been poorly and a doctor had been looking after me. The good thing with youngsters is they soon move on to the next topic and this was her showing us her catwalk walk and poses, she sure has model potential!
I’ve been enjoying the show when from nowhere I felt the start of a seizure, Fluff is really angry with me it seems. I quickly said to Andy & Emma, “get the kids outside quick”, they didn’t need to see grandma like this. Emma took them outside as the seizure kicked in, Bob stayed quietly on hand as Andy started to help me with our singing routine, although in the hotel lounge thankfully no one else was around, I am so conscious and need quiet at times like this. My leg was going and my arm was thinking about flipping, I try to keep eye contact with Andy but we can both see the arm rising. It’s like every nerve in my body is carrying electricity, they are so painful. After around ten minutes the seizure subsided and Bob fetched the kids back in so we could say our goodbyes. I’ve cried after all of my goodbyes this weekend, I realise this could be the last time I see any of them, I’m scared, very scared now.
 I’m drained and this episode had delayed our trip home by a couple of hours, we are going home but not alone, my amazing, truly amazing best friend of over 34 years ‘woon’ June, one of my sister-in-laws from my first marriage is coming with us to ‘Julie sit’ me until the end of April! This is an incredible gesture on woon’s part, its taking her away from her daughter and adorable grandson Charlie for a long time and her other half (Also Andy!). We are both so grateful for this gesture. The one thing I can be certain of the next few weeks despite the clouds of gloom overhead it will be fun filled lol we are terrible together hehe, Andy beware!
Moving on to Thursday 9th and I see Dr Haylock, I have to admit I am scared and I am now becoming tired of the fight, I haven’t told Andy how scared or how tired. I am questioning myself now as to whether I want to fight fluff any longer, I know despite what everyone says (that I’m not), that I am a burden, we both have disturbed sleepless nights, I cannot be left alone any longer, my slowness concerns me in terms of my dignity in going to the loo, I’ve had no accidents but I worry, showering now scares me, travelling the stair lift worries me, Fluff has turned me in to a nervous & scared wreck. Whilst a lot of this is obvious to Andy & to June other than Andy seeing my fear when my surgery was first cancelled no one has picked up on how I am considering ending this battle now. With no further treatment I know my time left will be short, life expectancy for patients with an untreated GBM IV tumour is around 14 weeks, we know fluff has been here for six, if I do give in it won’t be long to the end of the suffering, I really cannot go on forever fighting, I’m sorry…
We, June, Andy & I arrived at Walton, Alison came and gave me a hug, and said she’d tell the boss ‘Dr Haylock’ we were here, we are first on.
I’m in my wheelchair and we’re greeted by Dr Haylock, he has an amazing way about him in terms of the Doctor and patient relationship. We chat generally about how I am and how I am feeling post-surgery. He also, although I didn’t realise it, was indirectly asking me if I wanted to continue with any treatment. Andy not knowing how I was truly feeling spoke to Dr Haylock, “We have discussed where we are now we are post-surgery, we fully understand the implications of the tumour still being there but, in general Julie’s recovery is going well and she feels strong enough to at least continue the fight”. I sometimes get lost in conversations these days and didn’t realise the full extent of what was said. Dr Haylock then went on to explain that my options were indeed limited, we discussed the drug trials and although he needed to read up further on the entry conditions he felt that as this was my third tumour and most trials take place after the first’s removal, that I have Rheumatoid Arthritis (an auto immune desease) and I have had ‘recent’ (My SRS) radio beam surgery AND I am still on a high dose of steroids the odds are very much against me, Andy asked Dr Haylock about Lomustine, the chemotherapy we had previously discussed. He suggested this might be the best hope for me but again he would need to see if I was well enough to have it. “If I can get blood tests done here today for you, can you come and see me tomorrow morning at Clatterbridge I’ll have time to check out your options, my appointments are full but I will see you at 10.00?” Andy said, “We’ll be there”. As he filled in blood sample request forms Andy asked me if I was happy with what we had just discussed. I answered “I’m not sure, you know how these things sometimes confuse me, you can tell me later”, Dr Haylock left the room with the blood forms. Andy chatted to me, “It looks like you will be good for the Lomustine Chemotherapy hunny”, he kissed my forehead, I looked at him and asked “So do you want me to carry on fighting this?” His eyes welled up, for the first time it dawned on him that I’d had enough; I’m too tired to fight now. As he cried he said “of course I want you to fight this hunny” I touched the side of his face and he wiped his tears away before Dr Haylock returned and then took us the short distance to the nurse’s station to do my bloods. As Andy wheeled me past Dr Haylock’s room Andy just confirmed we were done and that we would see him at 10.00 at Clatterbridge tomorrow.
We grabbed June and headed to the CafĂ© for a Costa Coffee, I need my fix. As we sat there Andy asked me to confirm the conversation that he and I had just had to June, I just explained I didn’t think I could fight this any longer, “None of you truly know what I am going through and living with”. June always a voice of reason added, “Julie, you’re a brave lady, you’re stronger than you think, you have fought illnesses in the past, you cannot give in to this yet”, Andy reiterated a similar view as he held my hand but he also added “You have our full support hunny, if we thought it was right for you to give up the fight we would tell you but for now we feel you are recovering really well, you’re forgetting it’s not been a month since your surgery, serious brain surgery and you are coping and showing some improvement, ultimately you and you alone need to decide though when enough is enough and we will support your decision, but please for now consider what we’ve said”. I think a lot of it is I am scared and I know I have deteriorated and I needed assurance from others, I told Andy as much. We left with the conversation still ‘open’, I am still not decided..
Dr Haylock added a new drug to assist ‘fuzzy drug’, its called Clobazam. I have to take it at night, I’ve read the side effects which include you may stop breathing, I said to Andy about this and I didn’t want to take it just in case… The odds against this are so slim but I am scared all the same, this illness has knocked my confidence, I took the tablet and lay down, the drug can also make you feel tired, apparently not I though! Wide awake half the night.
 Friday 10th April and Andy thinking he was doing a good thing let me/us have a lie in, as I awoke the smart ass said “I see you’re still breathing hunny”, bless him he cannot do right for wrong right now. I panic that I am not up and downstairs to take my steroids at 08.00 with breakfast, today it is going to be nearer nine and this is freaking me out, so much so I feel unwell. I feel I am being rushed even though I am not and I am worrying we won’t be at Clatterbridge on time.
Well I had my breakfast, cup of tea & drugs, and we made it to Clatterbridge dead on time, As we booked in Andy waved at some newly found friends also on this same journey, Andy had chatted on twitter and Facebook to them as they were reading the blog and their Father was diagnosed with GBM IV last August. Andy knew they would be here today and arranged for us to say hi. There is an instant warmth and in a way a relief to meet others who understand up close our journeys. Bill is an incredibly brave man, he has a loving family supporting him in wife Eileen & Daughters  Adele & Clare, I won’t go into detail for it is their story not ours but to demonstrate again how important it is for a family to look at all options and to challenge, Bill was initially told by another team at a different hospital that his condition was inoperable and his future would be short, a brave daughter challenged this and asked for a second opinion, One of the Clatterbridge Team saw Bill and agreed he would give it his best shot to remove the tumour, suffice to say 8 months on and well beyond the initial prognosis this family are united and are filled with positivity, we all agree this helps keep the beast in its place, we take our hats off to them and we hope their journey lasts at least as long as I have been ‘fortunate’ to ‘enjoy’!
Soon we are called in to see Dr Haylock, we’ve caught a glimpse of Helen and she is busy with other patients, we swapped waves, today Dr Haylock has a nurse called Lisa with him, she too is lovely. The conversation starts with, as thought I am not going to qualify for any of the drug trials though I could be put back onto my first chemo drug (Temodal (brand name)- Temozolomide (generic drug name) - same thing- pronounced TEMO- ZOLO-MIDE) again with the Sativex or, as my blood results were good he could put me on to CCNU or Lomustine as it’s named. Andy again mentioned he had little confidence in The Temodal/Sativex plan due to Temodal’s previous ‘failure’, Dr Haylock concurred and said were the choice his he would opt for CCNU. Both looked at me for a response, Dr Haylock unaware of our conversation of yesterday, Andy holding his breath wondering what my response would be. “OK let’s go with this one if you think it will help”. Andy as you would expect was so thrilled. At that its explained its four capsules one each night for four consecutive nights each month, that there are risks, the main one being my blood count dropping and the risk of infection, it could also give me nose bleeds and it will certainly make me tired, very tired. I had to sign a consent form to start the treatment, I’d also need anti-sickness meds (Domperidone) and I would need a scan shortly. Whilst I had a scan immediately after my operation we learned there is no use in a scan in the next three weeks for it could show swelling as opposed to the actual tumour and its site. We need a ‘benchmark scan though’ and I’ll be scanned regularly also monthly blood tests for the foreseeable future. Andy asked Dr Haylock how long the Chemo could be taken for, we all know this is an impossible situation to gauge, each patient is different and so it wasn’t surprising the response was vague but it was said that he would review things monthly but after two to three months would give us a better idea. 3 months is way beyond where I would be in declining treatment, hopefully It all goes to plan and I remain healthy enough to enjoy it, I’ll say to you all now though if it gets too tough now I am likely to call it a day, I feel I have reached a tipping point in my journey.
Special thanks this blog to Alison (again), to the Management & Staff of the Humber Royal Hotel in Grimsby who gave a lot of thought to their disabled resident guests and for being prepared to invite feedback on how they could improve their disabled guest’s stay.  Special mention to Woon, to Bill, Eileen, Adele & Clare for taking time out to say hi… To all the friends and family we saw at the weekend, we’re so sorry for upsetting you all.

Wednesday 1 April 2015

Homeward bound!


Continuing on from my last blog.
Mr Farah wanted to send me home Monday afternoon or Tuesday, Andy wasn’t happy about this as it was clear I needed assistance at home now such as, walking frames, something to sit on in the shower as I cannot stand unassisted for more than a few minutes now.  The hospital has an occupational therapy (OT) team that assess you and then supply such items but it takes a day or two hence why Andy didn’t want me discharged until these items were set up home, he'd had two stair lifts installed ready for my homecoming.  (Andy here quickly)  The above few words and acts when you are in the position of ‘patient & family/carer’ are unsettling. I’d say to NHS staff, you do a fantastic job but you need to communicate things better to ‘us’ (all patients). The situation was this, Mr Farah says you can go home Monday or Tuesday but no OT provision had been made. When raising it later with Alison our specialist Nurse she points out that the Surgeons don’t necessarily understand that other things need to be actioned before a patient is discharged but as a patient how are we to know the Surgeon’s word isn’t final? This caused us significant stress, avoidable stress IF the following had happened.

IF during the days post-surgery  someone had said to Julie or myself during the recovery period. “Ok at sometime you’ll be seen by Mr Farah who will agree a discharge date however this in effect means he’s finished with you for now and is happy for you to go home, WE still have to assess you and sort out physiotherapy and Occupational Health equipment for you if needed and ALL this WILL be sorted BEFORE WE SEND YOU HOME” Not that difficult is it really? Please I beg, give this some thought..

OK, I’ve wrestled the laptop back from froggie ;}

Late Monday morning, I’m wheeled down to OH where they have a room of equipment, I needed quite a bit. I needed the following:

·        A frame for around the loo to enable me to push myself up.

·        A walker/trolley that allows me to move drink and food from the kitchen safely to the lounge or dining room.

·        A shower stool

·        A frame to clamp on to the bed so I can push myself up off the bed and to help me turn over in bed.

·        A walking frame for on the first floor

·        A walker to help me when I’m outside on any short trips.

·        Risers for the sofa legs to help me with getting up and standing

Quite a bit and it’s only when you get to the stage I am at that you realise how dependent you are on items like this to have a quality of life. The alternative would be to be stuck in bed, maybe a commode that someone has to ‘deal with' after.  As fit and healthy people we take so much for granted.

Later in the day the physiotherapy team made me a support/brace for my left leg to try & help what is now being referred to as ‘Drop Foot’..

Tuesday, I got hit with another seizure! I hit my bell Nurses came running, this was scary again for them as well as me, this time it’s a whole different team so again they have no idea how to deal with the seizure or with me. At one stage there were five Nurses, I had to shout for some of them to leave and to stop messing with the blinds/window. If you are reading this and were one of the Nurses, I’m truly sorry but I could not cope with the ‘fuss’ and noise, for me I need quiet and calm not to feel a sense of crowding and panic.  It’s scary that the seizures are still here after my surgery, perhaps now this is after all Epilepsy, I don’t know, I know I am scared by them.

Wednesday morning comes and Andy calls me around 8.30, all of the OT stuff has arrived. “You’re coming home tonight hunny” he announces he was collecting on his way home from work.

Wednesday evening and another amazing Staff Nurse, Joanne, was looking after me. In an 'Oliver like' approach Andy went to the Nurse’s station “Please may I have my wife back?” he said with a grin. My drugs needed sorting out first, not long to go now.

Andy filled my case with my belongings. He took a couple of trips to the car so he could focus on me when I could be finally discharged. Joanne was sorting out my drugs for me and explaining my dosages. Not much had changed except for the infamous steroids. I was to be weaned off them! YAYYY! Goodbye steroid bloat

So all drugs on board, I got a hug from Joanne, she tells me I’ve been the perfect patient and I’ll be missed. Andy had me sit in a hospital wheel chair he’d procured (don’t ask) and he wheeled me down the corridor as I said goodbye to other staff. I’m excited to be going home but I’m also frightened of losing the comfort blanket of Cairns Ward. We get outside and OMG its BLOODY COLD!! Thankfully the car is warm and I manage to get in it with no real problem. Andy left the engine running and the heater on to keep me cosy as he returned the wheelchair, as he got back in the car we hugged & had a kiss.

As we arrived at ‘Shute Manor’ I felt a sense of comfort but I needed to be inside on my chaise! Andy supported me and helped me in to the house, we have a few steps up into the house, I’m already thinking this is going to be an ongoing challenge. With Andy's assistance I’m soon on my comfy  chaise looking at a room full of OH aids, the Chaise had been raised around 3 inches to assist me getting off it, it’s great, I have a better view outside now!

Aaah my first cup of tea, Andy shopped on the way to the hospital, it's bad news when he shops, he buys more than we need and stuff we might never use or eat. I normally send him shopping with a list like a school boy hehe. (Can’t be trusted). Anyway he leaves me with my cuppa and cosiness whilst he unloads the car.

I’m tired and already dozing so Andy suggests we try out the stair lifts, I agree but with a degree of apprehension, I don’t like the thought of being out of control even though I know climbing the fourteen large steps would be like me trying to climb Mount Everest right now.  There is a seat belt on the stair lift and its swiftly fastened. Andy gives me a crash course on using it, seatbelt on and I am gliding to the first landing. The stair lift seat swivels so I am now facing the wall but its difficult to get out of, I grab the banister rail and reach for the wall in front of me but I am not going to reach it unless on my feet. Andy had to help me. Holding the wall and door frame I entered our loo, Andy had already put the loo frame in situ. It turned out it was too high but its easily adjusted. The relief of being able to stand up with ease is a great comfort. As we left the loo, I looked at the second stair lift which goes up just three stairs and think to myself we can soon get rid of this when I’m better. Within a few days I now realise three steps or not this is vital to me for now, it makes my life so much easier. Yes I hope I’ll improve enough to cope without this but for now, I’m pleased it’s here.

Yay! I’m on the bedroom landing and there is a walking frame here waiting for me, I struggle off the stair lift seat and grab the frame.  We go in to the ‘Red Room’ yes lol all the bedrooms in ‘Shute Manor’ have a name and a name plaque on the door, it’s me, I’m quirky ok lol, When we have no visitors this is our dressing room, we have wardrobes in here, we have none in our bedroom (The Green Room). So I undressed with Andy’s help, I cannot take off or put on my left slipper/Shoe/Boot so Andy has to help me. I’m soon ready for the next part of my decathlon, now it’s the walk (with the frame) from the red room to the green room and MY comfy bed!

It took around five mins to complete this manoeuvre and Andy had to ‘lift’ my left leg in to bed, I have no strength or control over it in this position. I’m soon covered in our quilt, Andy took all of our worn clothing to the laundry room on the next floor up and put another wash on. I know I am going to have to make some recovery to make the 14 steps up to the top floor but I WILL make it one day!

Andy came down and slid into my comfy bed, I was dozing already, and there is no place like your own cosy bed! I put my arm over him, told him I loved him and I thanked him for all he’s doing for me. I get told to shush as he kissed me and told me he loved me, I’m as close to heaven as I want to be right now thank you.

Next morning the first of my Julie sitters was with me, one of the secret agents haha, she arrived at just gone 7.45, Andy is off to work. We have fun but also chill on the sofas in the lounge.

Friday it’s my amazing friend Xena who travelled from the outskirts of Liverpool to be our side of the Mersey by 07.00! Andy collected Xena from a nearby train station, I’m alone for five minutes, an extremely scary five minutes! I had my panic alarm buzzer & phone but I still felt vulnerable. Andy went off to work, we had fun watching DVD’s and snoozing. Andy came home and we drove Xena home, again I’m scared to go out, Andy though is committed to ensuring I am not alone and that I’m to live as normal a life as possible.

Friday night I confessed to Andy that yes, I did need a grab rail on the top of the stairs so I could pull myself off the chair lift. “We’ll sort it tomorrow hunny”. Ha that normally means in four months with Andy hehe.

Saturday came and we are still up early because of my steroids plus Andy wanted to get his hair cut, he looks like a mad professor again now so we need the barbers. I love the girls at this barbers and yes the lower part of the salon is a lady’s hairdressers. Jen one of the team came to my wedding and did my hair for me, we are great mates. Anyway breakfast long done, we need to shower and dress. Next stop is BarberAnne’s, as we approached the busy road outside was full of parked cars despite the yellow lines. Andy said “We’ll come back”, Our next destination I hadn’t a clue about. Andy took us to a close by mobility aid shop on the pretence of getting the grab rail. Ultimately it was to sort me out with a wheel chair, I realise now just how weak I am and whilst I can walk very short distances it would not be fair on me or anyone else with me to walk around town with my stroller, I can barely cover 10 yards at the moment, I want to improve but right now truthfully I am not convinced I can or ever will. So we try a wheelchair and test ride it around the showroom picking up a grab rail and a cushion on the way. The wheelchair is lightweight with smallish wheels on it, I have to be pushed in it. I smile ironically as Andy is paying as we are told items are VAT exempt if you are terminally ill….. So I saved us around £40..

By now lunch time was approaching, I said to Andy that I would like fish and chips in the car on the sea front, so we headed down to New Brighton and spent a couple of hours eating our lunch in the car 'people watching' and watching the ships enter and leave the Mersey. I’m cosy and with my wonderful man in the warm with great views, today I’m happy.

A quick trip to Wilkinson’s in the town centre to get some things I’m putting together for  our six grandchildren, next weekend we are going to Grimsby to see them all and so that I can have ‘Daddy Hugs’

We headed back to BarberAnne’s and with my stroller I made it in to the salon to lots of hugs whilst the mad professor had his hair cut, It’s lovely to see the girls. Life is still good despite all the ills in my life.

We headed home to the sofas we were both so washed out our eyeballs were soon looking at the back of our eye lids. Life isn’t that bad you know…..