Spoke to the physio who was dd1's physio yesterday - bad news.
Dd1's therapy has been rather patchy this year but consistently we have had speech therapy - something dd1 is jsut going great guns with.
Until - her speech therapists goes to a job closer to home ( can't blame her - she has been very ill and travelling long distances to get to work making it much worse)
What me is that they are not replacing her with another speech therapist - so our equivalent of CDC - has one part time speech therapy to cover a huge area.
Dd1 has just started a program called prompt which needs a trained specialist SALT to deliver - and we have only done two sounds!!!! Her rapid increase in use of speech and her desire to speak is being put at risk by having no speech therapy.
So now I have to find a great deal of money to have dd1's therapy needs being met by private practitioners.....
I have overnight ( found out yesterday) written to the following:
Manager of CDC
state MP
Minister for disability services ( dept provides the services)
CEO of disability services.
So tired of having to fight for things that would just make life a little easier for all concerned.
It is not just dd1 who will be missing out but other clients of this SALT - and no one - that is the admin has bothered to actually tell us she is not being replaced - heard this from another therapist on the team.
too tired......