Hi All,
My son has a neurological condition which causes motor planning delays. It is not a "serious" condition, or threatening to his health (by this I mean it probably falls under the category of having a mild - low moderate learning difficulty. This means he has some issues with gross and fine motor. And most significantly he has a severe speech delay.
We are currently living outside the UK and have a health insurance package which provides 2 x weekly speech therapy and 2 x weekly occupational therapy from private service providers. It also covers seeing the paediatric neurologist (whenever we feel the need). Furthermore, my husbands job provides educational grants for private schooling and additional learning suppport for my son (whatever shape or form that may take when he starts school).
My husband is keen to relocate back to the UK (in which case he changes jobs and we loose all our current entitlements with private health care, education grants etc), but I am very worried about what services will and won't be provided for my son on the NHS and within the British education system (including in nursery). I have seen other posts in the past from girls in the UK (whose children had more difficult conditions than my son) who were waitlisted to even see a speech therapist for ages, and then only got to see them a limited number of times? Also, what can I expect in terms of speech/ language/ learning support in nursery/ school?
Basically I want to gauge whether we are better off continuing as we are for my son or moving back to the UK...?
Any experiences/ advice/ tips?
Thanks
My son has a neurological condition which causes motor planning delays. It is not a "serious" condition, or threatening to his health (by this I mean it probably falls under the category of having a mild - low moderate learning difficulty. This means he has some issues with gross and fine motor. And most significantly he has a severe speech delay.
We are currently living outside the UK and have a health insurance package which provides 2 x weekly speech therapy and 2 x weekly occupational therapy from private service providers. It also covers seeing the paediatric neurologist (whenever we feel the need). Furthermore, my husbands job provides educational grants for private schooling and additional learning suppport for my son (whatever shape or form that may take when he starts school).
My husband is keen to relocate back to the UK (in which case he changes jobs and we loose all our current entitlements with private health care, education grants etc), but I am very worried about what services will and won't be provided for my son on the NHS and within the British education system (including in nursery). I have seen other posts in the past from girls in the UK (whose children had more difficult conditions than my son) who were waitlisted to even see a speech therapist for ages, and then only got to see them a limited number of times? Also, what can I expect in terms of speech/ language/ learning support in nursery/ school?
Basically I want to gauge whether we are better off continuing as we are for my son or moving back to the UK...?
Any experiences/ advice/ tips?
Thanks