It has been a long time since I wrote a blog. Lots of reasons, both practical and less so. One reason is that two months ago we left the UK behind and made the permanent move to Italy. That’s where this blog begins.
Moving abroad was, in many ways, much easier than you might think, and in other ways very difficult, but regardless, it is stressful. Sorting out all the life admin stuff, transporting five pets, selling the house in the UK, and timing everything! We already had the house in Italy and it was liveable, which helped, as we didn’t have to rely on the movers getting here for us to be able to live in the house at least. We had also bought an Italian car already, which we would drive across with the two dogs.

The stress before we moved had been mounting up. We both had to become self employed, for legal and tax reasons, as we were going to be Italian, rather than UK, tax payers and residents. For me this meant completely new working arrangements, consultancy contracts, tax and legal advice from Italy and the UK.
We had to get all the pets checked, vaccinated, and ready to travel. I had to have various medical appointments for prescriptions and health checks so I had time enough to make the transition when we arrived in Italy. We had various get togethers to say our goodbyes. Then of course paperwork, movers, more paperwork etc,.
My lists just kept getting longer and longer, as did my worries of course. What had I forgotten? Would the cats be ok flying over?Would all our stuff get here in one piece? Would my work still be there for me? Had I cancelled all the UK bills? Was there anyone I had forgotten to tell? And so on. And, although there wasn’t that much keeping us in the UK, sadness, nostalgia and tears at leaving friends, and my little home.

The stress also meant that my husband and I were individually stressed too, which can make for being snappy and irritable and not having time to spend together. My mental health was not brilliant, and in addition to depression and anxiety and type 1 diabetes, I’m peri menopausal (HRT has helped), and as a result my physical health was being left at the back of the queue. It is always the first thing to go when my mental health is poor, looking after myself, and as a type 1 diabetic, this is dangerous. It’s almost a form of self harm, as though I’m not worthy to be taken care of, as well as thinking, if I just power through *this* I’ll start to take care of myself afterwards. The problem is, there is always a *this* to power through.
Anyway, we made it. The highs and lows of the process and journey will be for another blog. Friends had decorated the house as a welcome home, we had meals and drinks, and were planning for Christmas and beyond with our new life in the Italian countryside. One week into our Italian life, it all came crashing down, and my self neglect and the stress meant my immune system said enough.
It started with stomach ache. But not stomach ache like I’ve ever known it. Nothing helped and it was excruciating. I wondered about appendicitis or an ulcer, but then thought, bollocks, DKA. All the symptoms pointed to DKA.

We drove to A&E, all the while the pain intensified. In the waiting room, I was in a wheelchair, and the agony increased, that’s when they rushed me in for treatment. I don’t remember all of it. I had an EKG, a scan, a catheter was fitted and my stomach pumped. I remember bits of it, like pulling the tube out twice, and being incredibly thirsty but unable to drink, and screaming in pain. My husband says after that I was totally incoherent.
I was in hospital for just over a week, on various drips and constant poking and prodding and needles everywhere. It was about three days before I was aware of where I was and what had happened. Turns out I nearly died. The staff and my husband spent twenty hours frantically trying to keep me from slipping into a coma. I didn’t appreciate how close it was, or how frightening, until days afterwards. At the time I had no idea, aside from the occasional doctor or nurse coming to make sure I was still conscious. It’s terrifying in hindsight.




I had to give up the idea of going back to work for a month. I had to recover. For weeks I couldn’t do anything much except rest. We went back to A&E once because the treatment I had had made me swell up after I had been discharged. I had to go to appointments with various consultants for various things and procedures. I still have to go for an endoscopy. Christmas was a fairly sedate affair and my husband’s mum joined us for a couple of weeks, which was nice because it meant I got out of the house, even if only to see some nice scenery. I had plenty of rest days in between. For the first time in a long time, I listened to my body and stayed home when I needed to, instead of my usual ‘I’ll be fine, let’s go’ attitude, whilst knowing full well I wouldn’t be.
Since then however, there have been further disasters and crises. I have been sick again, despite following doctors’ orders. One of our dogs became really ill whilst my husband was away and it looked as though she wouldn’t make it. Lots of other little things that could go wrong, did go wrong. My mental health reached breaking point. I haven’t been able to go back to work, which was one thing I was holding onto for a bit of normality and routine. But I have to listen to what my body and mind are telling me.

One thing I did do, for the first time ever I think, I reached out. I asked for help. My husband came back from his trip, friends took over some chores for me, I talked to friends about how I was feeling and that I was at breaking point. And, who knew, reaching out and asking for help, helped! I was not as alone as I felt. It’s still hard because I feel like a burden, and I feel guilty, and of course I feel like I should have been able to deal with it all on my own.
The truth is, since arriving, because of all of the various disasters, I have yet to feel at home here. I feel unsettled in myself and in my relationships. I haven’t been able to establish any sort of routine, or so many of things I intended because of my poor health. Everything feels harder than it would if I were well and things were normal. It’s not about being in a new country, or that I don’t have a support network here; in many ways we are more at home here than we ever were in the UK, it’s the upheaval of my mental and physical health which has thrown me off kilter. That and the fact that I haven’t been able to do the things I wanted to. I get frustrated when I am feeling well enough to know what I could be doing but not well enough to do them, and it feels as though I am wasting precious time.
However, I also want to live a long and happy life here. My neighbour is my role model. She is 85 and still chopping her own firewood, I want to be that able when I am her age. In order to do that I need to let my body work at its own pace. I want to get strong again, but if I force it, it will have the opposite effect. Irony thou art a heartless bitch …
So, here we are. Not the best start to a new life, one which I expected to be interspersed with some difficulties, just not that many, or that hard, or all at once. No doubt there will be more, but if I listen to my body and mind, ask for help, and keep talking to people, I might just be strong enough so that they don’t seem as challenging as they otherwise might.






























































