What I’ve discovered in my PTSD journey.

Despite suffering intensively with the flashbacks and the brain changes, I went into episodes of bursts of laughter pacing, losing my memory, constant thoughts of feeling stuck and wanting survival in my head.

People just say “it looks like BPD and we can’t be bothered with attention seekers” hence I have no support network.

And that’s why I don’t socialise, work, and avoid friendships and relationships. To be honest I’m not in a fit state to go back to work yet, I can’t wait to so I can finally live a normal life.

I never asked for PTSD or CPTSD/?bipolar (put ? As I’m undiagnosed with bipolar).

Neither did I want it.

I just have to suffer with it. But yes America refers to BPD as CPTSD.

It’s not the same in the UK.

It’s a different illness altogether.

Just listen to Sia’s songs and you’ll understand.

BPD or not; I’m still the one that has to relive my traumatic memories and suffer in silence so if I can make it out of that, I’m pretty much invincible.

I need to get better to go back to work, save up for dentist because I’ve messed my teeth up during a PTSD crisis which is £3200. Then I need to wait 6 weeks for the sertraline to work again.

And then I’ll be dissociative again. I won’t remember a thing. Hence I kept a blog. So I know what to expect if it ever came back. Even I confuse the labels and I’m suffering from the conditions.

So tbh how would I expect anyone to understand? I can’t. No one can.

When you go through prolonged trauma it feels like a brain injury.

It’s just the emotional flashbacks where you age regress was new, that’s why I thought – oh no. The PTSD has become CPTSD but then how can you have CPTSD when you were pretty much had CPTSD since you were 9 months old?

See what I mean? That’s the price you pay for living your life swimming in trauma.

I’m literally textbook PTSD. At a high level.

I always say if a clinician suspects BPD in someone, assess them for ADHD first – people with ADHD have RSD.

People with real BPD have dissociative PTSD which is now known as CPTSD.

2 responses to “What I’ve discovered in my PTSD journey.”

  1. “When you go through prolonged trauma it feels like a brain injury.” It IS a brain injury, and a very complex one. And they don’t warn you about how lonely it actually is, and that very complex brain injury can make you VERY vulnerable to those seeking others to exploit, and making the injury worse.. and the hardest part to understand is that others see it long before we do. … I just wanted to leave a comment letting you know that you’re not alone. Stay focused on your journey. Walk the path and work the systems, especially when it’s hard, because that’s how we forge new neural pathways that allow our brain to change and abilities to expand. (Think baby steps, then you learn to walk, then run, etc. It’s just like that!) And be kind to yourself sweetheart, talk to yourself like your best friend, because the world won’t. It took me several years of therapy, but I changed my entire life for the best.. and I’m not special — you can, too! Have faith you’ll find more (in its right timing), and you will. I promise. 💖

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    1. That’s exactly what it feels like, and at the same time the people who are supposed to support you tear you down even more. I’m so glad in you’re in a better place now. 😃 I was refused therapy by the mental health team but my GP knows I have CPTSD and saw one of my PTSD attacks today. Unfortunately, they just like to use the BPD label against people, for reasons unknown which doesn’t give us the chance to get therapy before things get worse, thank you so much ☺️ you give me so much hope. Sending you love and care. ❤️

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