I agree. What is the point of training teachers to pick up the signs when the services to deal with the underlying mh issues don't exist.
Thank you for the thread. I shall write to my MP, again, tomorrow (tbf when dd was ill, he did intervene and switch on some services for her).
I shall also attend the CCG Board meeting next week as I shall be on A/L. I shall ask again what they as commissioners are doing to improve services and again ask why 20% to 25% (under 18s) of the population get a woeful 6% of the overall and already inadequate MH budget.
Again I shall note that I expect teachers/schools to educate and HCPs/Trusts to heal.
Again I shall ask them to estimate the cost in future taxes of embedded and intractible MH issues whereby 14-18s were denied early interventions. This compounded by parents (mostly mothers) shouldering the care burden, suffering stress and PTSD and possibly losing their jobs.
My dd got the help she needed and has recovered, been diagnosed and learnt to manage her mh. The state had nothing to do with it. She was very very lucky. I had BUPA and £6000 to spend.
It is a disgrace and I don't believe it's all about lack of resources. Much of it is about mismanagement of resources and poorly trained MH CAMHS nurses who are very out of date. The service needs fewer nurses and sw's imo and twice as many psychiatrists.