Hi Allie, welcome to the forum.
Are Social Services giving help with the children?
Benefits sorted?
Aware of the Family Fund?
I can relate. I care for my little brother with open defect spina bifida. Hence I have attended a lot of appointments with him. I have also contested decisions on his behalf for the maximum rate of the mobility component of the DLA as well which was definitely tiring to say the least.Allie_1411 wrote: ↑Thu Mar 05, 2020 4:30 pmHi guys, thanks for your replies
Social services - no
Benefits - no
Family fund - I’ve heard of it.
4 of my 5 kids have ongoing medical/SEN appointments. Juggling them with working part time and the usual domestic stuff is such a challenge. I often feel like I don’t know where to start: which form, for which child, should I attempt to fill in first?!
I’m currently summoning up the energy and courage to, amongst other things,
- ‘fight’ my ASC sons school for an EHCP for him - where do I start?!
- waiting to receive latest assessment report for youngest daughter’s SEN to decide what to do next
- decide whether to push for my eldest daughter to be admitted to a psych ward. Not sure I can keep her safe any more but she doesn’t want to go...it’s that thin line between her being safe and not...she’s getting professional help but it’s so under resourced that I frequently need to ring them and chase things up. I know to them she’s just another patient, another set of boxes to tick. Sigh.