Finally. After all the pandemic restrictions and my recent health problems, it’s such a joyous relief to be out and about properly again, doing the things I enjoy.
So there’s quite a lot to mention in this month’s post and video, as I’ve been attending theatre shows for the first time in ages, taking nice walks, and enjoying a mixture of films, dramas, comedies and music at home. Plus I bought the new iPhone 13, which I’m very happy with as explained in my review, so the photos and videos you see going forward will be taken using that.
Apart from the theatre show States Of Mind, for which I was given complimentary tickets to go along and review, nothing else in this post involves any gifting or sponsorship. And all opinions are my own throughout. So I hope you enjoy!
My trusty iPhone 6 was an excellent friend and assistant for 6 years, and only needed one battery replacement in that time. But with that second battery now dying and an increasing number of apps not being supported or updated any more, it’s time to move on.
Therefore, I’ve now bought Apple’s new iPhone 13, so I’m fully up to date at last. I’ve got the Blue 256Gb model, which looks and feels really nice, and is working really well.
With 7 generations between my old and new devices, there’s a world of difference between them, which isn’t remotely surprising. It’s a big leap forward in every respect – the screen is bigger and brighter, the audio’s better quality, the camera takes clearer photos and videos, and it’s much speedier at opening apps and doing tasks.
There are already lots of reviews and videos out there about the iPhone 13 and related models, by people who are much more professional and technical than myself. So I won’t go into detail about the technical specifications and all the features. I just wanted to share my first impressions as a regular user, after having it in my possession for a few days. I’m sure I’ll discover more about it as I continue to play with it.
So I hope you enjoy my overview and find it of interest. This isn’t sponsored by or affiliated with Apple in any way, and all opinions are my own. And feel free to let me know if there’s anything in particular about the phone or any apps that I should check out, as I’m looking forward to getting very well acquainted with my new companion!
Hello again. Miraculously we’ve made it past the halfway point in the year, although admittedly it feels like a lot more time has passed. Months effectively haven’t existed for a little while now, with all the weeks just blurring into one continuous sequence.
It’s also strange to think that we passed 100 days of lockdown in week 15. That seems to have gone by quicker than I’d expected, although I know for many that time will have dragged terribly, and certainly early on I found it difficult like everyone else. But I’m glad I’ve been able to settle into a new routine and adapt during that time. Connecting with friends, homeworking, blogging, music, TV and film have all got me through it, and are continuing to do so.
Regular readers will know that my mother and I have been voluntarily shielding, even though we’re not explicitly required to do so, for my mother’s safety in particular. In recent weeks I have been getting out a little bit more though, and Mum’s been at once, as I explain during this post. It’s just around the local area though – I still don’t intend to use public transport for the time being, even though there are safety measures in place for train travel, as the risks still feel too great and there isn’t anywhere that I need to go.
So here’s my latest update on the things I’ve been doing and enjoying over the last few weeks, with accompanying videos for weeks 13-14 & 15-16. None of it is sponsored to appear here, but I was paid to attend the CXcon event as you’ll see. I hope you enjoy looking through it all!
Update (March 1st) – I won the challenge, much to my surprise! Thank you so much to Rare Disease UK! It was great fun being involved, because I loved the theme of the campaign, and I really enjoyed seeing other people’s photos. So very well done to all involved. We can all be proud of our efforts to raise awareness during the month! 🙂
Today is a wonderful international opportunity to raise awareness of rare diseases, conditions, disabilities, etc, to educate people and highlight the need for greater funding and research. Here in the UK, it’s led by Rare Disease UK. But there are events taking place worldwide, so there will be related organisations in many countries.
1 in 17 people have a rare disease, meaning it’s a lot more common than you might think. So even if you don’t have one yourself, chances are you know somebody who does. And if you do have a rare condition, you’re certainly not alone.
There are over 6,000 rare diseases, affecting over 300 million people worldwide (including 30 million in Europe). That’s a huge number! So this is a day for all of us unusual rarities to get together, along with anyone and everyone who supports us and the cause in any way.
This year, the theme is “Show your rare, show you care”, and everyone can get involved, regardless of whether or they you have a rare disease. So that includes patients, families, carers, medical professionals, policy makers and members of the public.
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