With regards to companies like virgin taking charge if parts if nhs, our children's services has switched to Virgincare, and I can't say it has been great. Ds, who is 6 and disabled, has gone from seeing physio, ot, orthotics and paediatrics in one centre and SALT in school, to seeing the above in 3 centres, all of them 40-60 mins away by car (I don't drive and charity transport doesn't go this far).
At a recent appointment the therapist said she was overwhelmed because of the joining of 2 departments, meaning it would be 2-3 months before ds could be measured for splints, then another 2 months to come. Ds's splints are held together by gaffer tape and too small.
Ds's ASD referral has been lost in the changeover, and even his paed (the only professional to stay the same, at his insistence) doesn't know who to chase.
When the initial consultations were made, we voiced our fears, but were told there would be little change, therapists would stay the same, it would be a more coherent system.
Ds has lost therapists he had since birth, who know his complexities, and there seems to be a criteria of save first, see if it falls apart, then act.
Friends have had essential equipment denied or their children discharged out of the blue, others have left the area as they felt that the onus placed on 'how have you maximised saving?' Was becoming too much.
The combination of this, the chaos we have experienced at A+E, even the erosion of our pharmacy service has left me feeling even more terrified for the future for children like ds than usual.
I have written to our local mp (fobbed off with platitudes), been to the feedback meetings, voiced my anger - what else can we do? I am fucking knackered looking after my child (and my other children!)fighting for my child's education, and healthcare - but I will happily join in anything that puts a stop to this insidious erosion of the NHS.