Do you happen to know if there's a standard form? Im not sure he would qualify or what the criteria is. Hes in mainstream school, sat his exams but needs to be remindee to shower, eat and has a lot of anxiety. He wont answer the door if there's a delivery for example. I cant see him taking on any type of work for next few years, but msybe as he's older and has continued with therapy.Incapacitated child credit info is here. Your doctor has to sign a form to say that the child wouldn't be able to maintain themselves after they turn 18.
Thank you. Its a relief to have a diagnosis and im hoping that will help him understand himself more. Hes still gling to Pieta due to the self harm and i think later in the year I'll send him to therapy as pdychologist mentioned he is avoiding dealing with his feelings and has difficulty in this area.Hi dubdub,
The incapacitated child credit is a tax credit, not means tested to assist a family which has a child with a long term disability.
It is granted to the parent and reduces their tax bill.
Congrats and comiserations on the diagnosis and well done for supporting your son.
Do you happen to know if there's a standard form? Im not sure he would qualify or what the criteria is. Hes in mainstream school, sat his exams but needs to be remindee to shower, eat and has a lot of anxiety. He wont answer the door if there's a delivery for example. I cant see him taking on any type of work for next few years, but msybe as he's older and has continued with therapy.
Im so confused whether he fits the criteria and if i should apply.
Anyone know what the steps are?
Please Get help with the Disability Allowance form from citizen info as they are very used to the forms, sometimes T.D.s eg parliamentary assist are excellent with advice and filling forms and tracking the application. Also I.N.O.U. Dublin very good. Robbie Lynch information section. If denied first time (very common) appeal, ask for written reason that application refused eg not enough medical information and reapply and you can either ask for a review or appeal the refusal. Appealing the disallowance might be an advisable route. This appeal is held outside the department and they are independent of DSP The higher the specialist who assessed I believe the most value is ascribed (my opinion).Great thank you so much. Any idea if it should be the psychologist or our GP to sign off? Im awaiting full report.
Ive printed out the disability allowance form and starting to go through that as well and there's a medical section in thete as well.
Would be huge peace of mind to get some support for him.
Thanks so much
Thank you so much.Please Get help with the Disability Allowance form from citizen info as they are very used to the forms, sometimes T.D.s eg parliamentary assist are excellent with advice and filling forms and tracking the application. Also I.N.O.U. Dublin very good. Robbie Lynch information section. If denied first time (very common) appeal, ask for written reason that application refused eg not enough medical information and reapply and you can either ask for a review or appeal the refusal. Appealing the disallowance might be an advisable route. This appeal is held outside the department and they are independent of DSP The higher the specialist who assessed I believe the most value is ascribed (my opinion).
G.P. section on D.A. form vital the G.P. fills that out with full knowledge of your sons condition how it affects him. Reports are very important to confirm the diagnosis and explain as the person doing the desk assessment may not understand neurodivercity. The mental health and physical aspects and affects should be outlined fully and any medication prescribed, lists can be printed from chemist. psychologists, counselling, school reports etc. can assist the Medical officer assessment. The D. A. section in Department can be very helpful and emphatic if you can get through.
Good idea to document day to day impacts and I think detail is good in clear languageThank you so much.
Im waiting to get official report and I was going to put together a few pages stating his day to day issues.
Hes attending counselling with Pieta House. Was previously at a psychotherapist but i cant get a response from him but he didnt provide a written report.
I have an OT report and hes been to MDT and disgnosed with autism.
We recently moved house abd have new GP and ill chat with her. She is aware that he was self hsrming and wrote letter to Lucena (he is waitlisted there)
Where do i find any of those supports you mentioned? INOU, Robbie Lynch? Would be great to get some help.
Thats really helpful thank you so much. We are based in Dublin.Good idea to document day to day impacts and I think detail is good in clear language
I.N.O.U. welfare assistance team (01) 8560088 www.inou.ie or you can leave an email re welfare rights.
Citizen information phone service 0818074000 Mon Fri 9am to 8pm www.citizensinformation.ie that's where I am getting the information very good site
or you can go to your local centre or contact by phone or email. I think its better to have face to face appointment depending where you are living you could phone them perhaps to make appt or call in. When you phone leave a message and they will get back to you. Most offices now are very busy but the will phone you back.
Disability Allowance Section dept of Social protection is based in Longford
Tel (043)3340000 or 0818927770
email: DA InetInfo@welfare.ieDisability Allowance
Disability Allowance is paid to people with a disability. You can get it from 16. The maximum weekly rate is €208. From January 2023 it will increase to €220. You can work and receive a reduced rate.www.gov.ie
Be prepared for long wait times on phones but persist and you will get through or email
keep copies of all applications and timeliness. Don't do this on your own as the support will he required you have enough on your plate
Let us know how you get on
There is also community law and information there is an office in Dublin. Where are you based
My son was diagnosed with Asperger's when he was 9. The school was utterly useless but we did get limited support privately.
He's in college now and he's agreed to be reassessed as an adult. I'm getting myself assessed as well as I see lots of behavioural traits that we have in common.
I haven't claimed for the incapacitated child tax credit because I don't believe that he will never be able to live independently so while I might get it, in good faith I can't
Yep, they didn't pick it up off the stones, as my Granny liked to say.Myself and son have a very similar outlook on things and looking back on my own behaviour, I suspect that Im also autistic. At some point I may seek diagnosis, but right now thats ok.
It is and what's the reason for the reassessment. I lot has changed since he was 9 and a re-assessment means that he can take ownership of it now. If he's involved then there's a better chance that he'll get the supports he needs. Of course there's no public funding for an adult assessment, how could there be, sure we only have one of the best funded healthcare systems in the world.Well done to your son - the college environment can be quite overwhelming.
Do you mind me asking reasoning behind further assessment? Is it to identify additional supports?
I found the schools at both primary and secondary level almost totally useless. Other than the insincere gushing that every parents gets at parent teacher meetings they had no interest in him.Im feeling bit adrift in thst we have diagnosis for him (pending report), but outside of asking for movement breaks Im not even sure what we can request in the school.
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