Hi @Hannahbanana98 ,
Thank you for your post. BPD is not a very popular diagnosis in the public system - it sure does have a stigma attached to it!
Unlike your experience of the public sector (and probably most people), I have had an amazing support team spanning over about 5 years in the public system for my BPD.
I couldn't not get any help when I was living in Sydney (also probably I wasn't ready for help) where I was diagnosed with BPD in my late teens. I moved to Melb and continued my BPD struggle. After enquiring at private clinics, I was deemed too risky to accept. In 2016, I was accepted into Spectrum (public) and completed just over two years with them. At the same time, I had an area mental health treating team supporting me on a weekly basis. On completion of MBT at Spectrum, I stayed with my area mental health for another 2.5-3 years. I was only discharged from them in Feb this year. I still have a psychosocial worker (public system again) who I have regular contact with.
I have been an extremely lucky one. All in all, this year is the first time I've needed a mental health care plan to see my private psychologist (approx every 2-3 weeks, and even then, I don't pay anything out of pocket). I've followed this private psychologist from the public system because he works in both public and private.
So I guess you can say that there IS help out there? It's about where to find it.
Even then, I've had private health cover my entire life, but have not yet used anything for mental health. However, I have a limited amount for MH services.
In the public system, I have felt cared for, looked after, supported, provided individualised support, I'm not a number....if it wasn't for them, I doubt I would be here to tell my story.
Im so sorry to hear @Hannahbanana98 you are in the same boat as many others with BPD. I guess it's about reaching out to as many resources as possible until you find the help you need.
Regards,
BPDSurvivor
@Bow @Gwynn