โ26-09-2020 07:41 PM
โ26-09-2020 07:41 PM
I'm writing here because I don't know how to start again or where to write.
Recovery as it turns out is a long and winding road.......in my case there is no road, just woodland to forge a path through.
So here I am feeling incredibly vulnerable and scared. I don't know how to be in real life or the forum. I am feeling a strange distance with my close irl peeps and I guess on here as well. It is not anyone else but me and my brain, my very insecure and confused brain.
Last night I had a very therapeutic call with the helpline here. I am so grateful to have this service when I need it. I needed putting back together in a big way. Therapy has been confusing and somewhat disorientating of late.
So my reflections go somewhat like this. A change in diagnosis or being newly diagnosed is much bigger than I ever anticipated. It's a bit like learning to walk and talk again. It takes so much time to honestly digest the things you need to learn about how your brain works. It's like looking at everything through a new lens, but everytime you look through that new lens there is more to see. I didn't think I could get much more broken and scattered than I was, but I was wrong.
For so long I've been saying that I need to learn what I can do. I think I am just beginning to understand why it felt this way for the longest time. I know that I will need to understand 'my' brain, not in the terms of a generic diagnosis but how 'I' and my brain work or don't work. I had become obsessed with the main tick boxes of a diagnosis which I would own or disown always creating extra confusion for me about never fitting into boxes and always feeling like the outlier that didn't belong anywhere.
Ive been listening to podcasts from experts and lived experiences. I finally have begun to realise that within any diagnosis the combinations and possibilities of traits are endless. Saying this I am beginning to understand that if I'm ever going to learn to drive this brain I really need to understand and own my particular traits, the ones that create great difficulties and the ones that can be strengths.
It's easy to obsess with 'how to fix oneself' but much harder to learn to live with and work around the behaviours that can't be changed. They will always be there and my behaviour choices will help or exacerbate them.
Who knew self care in every part of your life can make the smallest differences that can help live a better life?? ๐คฆโโ๏ธ. I think self sabotage will always be part of my go-to-not-very-helpful-coping-strategies. The trick will be to recognise it and change those behaviours. I have just been on an unhealthy emotional sugary food eating tour over the last few months that I am now correcting. I hope that over time I will get better at recognising it and turning the titanic sooner :face_with_rolling_eyes:. I feel much better for eating healthily again even though my circumstances haven't changed much.
So the vulnerable part is that I know my challenges are very different to many others. I've let that become a great source of comparison and shame. I've spent decades masking and hiding it. I just learned that it is fairly common for us to mask and avoid and hide the real person underneath. For me I am terrified of learning who that person really is. I don't know yet because I've spent so much time hating her and having no respect for her. Society doesn't respect her traits so I learned to disrespect her traits too. It is really hard to find a way to live with traits that are not desired in society, especially when you see all those you love also not respecting them. It is easy to hide rather than be you, it's easier to become a chameleon for me than to learn and stand up for who I am. I am scared because I still struggle to see the light at the end of the tunnel where things will be ok again but I draw strength from those I see or hear about going through it as well.
I have written this as an intentionally vague post because I have come to think that a specific diagnosis isn't the central part, it's how we deal deal with the stigma of having different brains (either through genetics or life experiences where our brains have been changed), and how we then do the living with our specific challenges.
These are just my current thoughts. I'd love to hear anyone else's thoughts about how you feel about learning to live honestly with your diagnosis or set of challenges.
โ26-09-2020 07:43 PM
โ26-09-2020 07:43 PM
โ26-09-2020 07:56 PM
โ26-09-2020 07:56 PM
Thanks @outlander ๐๐ค๐
โ26-09-2020 08:03 PM
โ26-09-2020 08:03 PM
โ26-09-2020 08:27 PM
โ26-09-2020 08:27 PM
Gentle Hugs @Teej
I could relate to a lot of your post.
Sadly RESPECT is in short supply in current times.
I have had been indulging in a sugar tour too. Unusual for me, and not in excess, going with the having constant supply for a bit, tho will eventually tire of it I think. Anyway it means I browse freely at the supermarket and bring a little variety to my days. I have to cut salt, so something had to give ... excuses excuses.
Your the first person I did pokey out tongue with.
Love seeing you Bella Teej.
โ26-09-2020 08:36 PM
โ26-09-2020 08:36 PM
I love that response @Appleblossom ๐๐ค. Feeling a bit honoured that you poked your tongue out at me in cheekiness. ๐
Im trying to get my sugar fix in a piece of fruit now. Salt is another hard one......I am also a salt fiend. :face_with_rolling_eyes:
โ26-09-2020 09:03 PM
โ26-09-2020 09:03 PM
@Teej Yeah. I thought I was good about added salt, but it means no olives, and then I realised no ham, no bacon. Cat was lucky I gave it to him.
โ26-09-2020 09:10 PM
โ26-09-2020 09:10 PM
Thank you for sharing so many of your thoughts regarding diagnosis and reality.
My straightforward answer is I canโt live with my diagnosis. Right now itโs too hard considering I have faked it for so long.
i truly admire you for sharing so truthfully and wanting to be who you are. Unfortunately I am not in that place yet @Teej
โ26-09-2020 09:59 PM
โ26-09-2020 09:59 PM
One of my issues is that nobody has wanted to commit to a diagnosis at least to my face. First went to a pdoc when I was 17. This is going to get tested as the NDIS want reports, but my psychiatrist has been AWOL or MIA. I cant get through on the phone and he has not responded to my contact form on his website. He also "forgot" to email my Gp last year about my diagnosis. I am forgiving as usual. Well it will all come out in the wash ...
โ26-09-2020 11:17 PM
โ26-09-2020 11:17 PM
Thanks for the reply @Eve7 . I think the first step for me was accepting my diagnosis. I spent time dialing with acceptance and denial. I'm kind of scared to mention time frames but this is my 9th year of dealing with my mental health. Part of that was because I was misdiagnosed. It wasn't until I had a psychiatrist I trusted that I've been more accepting and then researching. I've been taking medication for this diagnosis for more than a year now so it's been a long time working through accepting and now understanding.
It's ok not to be in the place where you can see a light. I have lots of days I think that I don't want to stay alive with all that's ahead of me. There are days though that I strive to make things better. It took a lot of me making things worse (sh and s attempts) before I have been in a headspace to be able to make things better. It's all just part of the wild ride of recovery. I don't know what comes next either.
Take good care of you. Remember that we all go through things in the best way we can. Everyone's path to recovery is different......and it's a life time of work. Perhaps, as the saying goes, that it's the journey that is the most important part, and not the destination. ๐๐ค
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