What am I doing in this time of calm!
Well there has been a huge amount of upheaval with two moves in a month and the wait for knowing when that was going to happen. That took months to actually happen so I was completely stressed out. So in this time of calm I have started writing more and slowly but surely getting back into the swing of things.
What does that mean?
It means that I will be writing more and hopefully be more visible here. There are still days when endometriosis and cerebral palsy rear their heads and make things more difficult than I wish. That's ok though as I'm getting more help. So my mental health is stable. Although I have still got the odd bad day.
So what's changing here?
There will be a few book reviews coming in. A few more personal posts about my favourite things. I will do a few makeup looks that I can do. Meaning anyone can do them. My range of clinical depression will also be spoken about as I've only hinted about it in posts. Although my cerebral palsy and endometriosis will always be the main theme of my blog and somewhere people can learn about either condition or both. Because I feel that there is not enough taught about either of them.
The future?
The future is always uncertain but it helps to prepare a little bit. So learning about each age group of people who have cerebral palsy or endometriosis.
Why am I doing this?
I'm doing this now because I'm in a better place than I have been and feel ready for a few little changes on the blog. I also know that there are going to be more changes ahead so I want to write while I can. There's going to be another move but I don't know when. Writing while I can is another positive step forward too. Right now this feels good and I know that it's the right thing to do. Especially as I have now been acknowledged as a digital creator on Facebook and Instagram. Which is where I'll be found a lot. My Instagram name is @sweetestmoonuk.
My hope for the future!
My hope for the future is that I can be around for a lot longer although there is no set age for people with cerebral palsy.
