Sorry don't think I explained myself well with the extra baggage, happy to pay for a suitcase in the hold but can't pay loads extra and his will have his weighted blanket in it. Also unsure where to look to find out what food I can pack in the hold.
Am obviously doing some research myself and trying to find out these answers, just totally rusty when it comes to travel.
@gogohmm, we use to travel with ds when he was younger, not far due to costs, but Wales, Scotland, Holland etc... and I think if that had carried on, things would be easier now. Unfortunately he had a breakdown when he transitioned to secondary school, resulting in an attempt on his life and a short stay in hospital under section. It took several years to slowly recover from that. Just as he was ready and we started looking into travel again, the pandemic hit, which obviously ruled out travel for a while and set him back in his recovery.
Ds isn't a morning person so my plan is to let him chill in the mornings, whilst I take our younger ds out to enjoy things like the pool/tennis etc.... then plan family activities for the afternoons. We have a lodge so can cook our own meals, which will hopefully help.
@Staynow thanks for all the tips, we are going to Lake Garda. One thing I'm finding confusing about Italy, is when you look at days out, they have different levels of disability discount but I can't see any explanations to work out where my ds sits. We don't need the discount, but will need help with queuing if possible, so I'm trying to work out how to find that information out.
I use to be so confident about meeting his needs, still engaging in the world and not missing out on opportunities for him or us as a family. Since his section though, everything feels very overwhelming and I'm trying my hardest not to let my fears hold him back.
I just feel like I have so much extra to manage now. Things I know I need to find out before we go.
How easy is it to navigate Gatwick, is it easy to book their sensory space?
How easy is it to take his medication? They say it needs to be in original packaging, but his liquid medication will be over the size allowed for liquids.
How much should we plan in advance? How much should we just wait and see?
Will he eat anything other than his safe foods? Will any of them be available? (Currently under investigation for an eating disorder as well)
How to balance the needs of both children, when they are so different?
What will the Internet be like? (Needs it to regulate)
Don't worry I'm not expecting answers on here to these questions, just showing you, the anxious ramblings of mine.