Parents evening frustration- year 8 - FASD Support

FASD Support

957 members636 posts

Parents evening frustration- year 8

Poppy74 profile image
4 Replies

One of her teachers said that she has no short term memory problems, they question the diagnosis of FASD. I felt like i was back per diagnosis where I was questioned and poo pooed. This teacher sees her for 1 hour a week. I know I should have been stronger but wasnt sure what to say in an open environment

Do they even see my precious child? Sorry rant over x

Written by
Poppy74 profile image
Poppy74
To view profiles and participate in discussions please or .
4 Replies
rachael1975 profile image
rachael1975

Hi Poppy74

I'm yet to get diagnosis for my son who is 7 and sometimes feel that I should have been stronger with the paediatrician who ruled it out because of no 'facial features'. The frustration over this has eaten me up and I've not yet revisited it. FASD is not diagnosed lightly. Just hold on to the fact that the teachers have a different agenda to you. They don't see the detail of your child that you see. They have no real knowledge of the condition and aren't in a position to question it. Hold on to what you know and keep strong. Just subtly let them know that you aren't going away and will keep pushing for what is best for your daughter. Once described to me as being a velvet bulldozer :) x

Joygirl profile image
Joygirl

a lot of people say it is harder at secondary school as you are dealing with multiple teachers, multiple subjects, more kids, bigger building....Parents evenings as well are not always an ideal place to have an indepth discussion when you have 5 minutes and they have 300 parents to see. Keep smiling and as Rachael1975 says, "I ain't going anywhere, baby.".... Try standing in the kitchen at home and banging all the pan lids together - it might help make you feel better.........

Poppy74 profile image
Poppy74

Thank you for your comments, they really do help x

Maclean profile image
Maclean

Hi again,

One of the reasons we chose to home educate. School did not see anything wrong, no language issues etc and that is with a diagnosis and reports and phone calls to school from neuropsychologist, Psychiatrist ant OT! Lots of meetings, notes back and forth almost daily, positive behaviour book and so it went on. Just got sick and tired of it all.

Not what you're looking for?

You may also like...

Advice on getting diagnosis

Hi, I'm new on here, I have a foster daughter (just in process of becoming her legal guardian), and...
lostkeys profile image

Hi - I'm new! I suspect my two have FASD and I wondered if there is any support or members in the North East? Carlisle is a bit far for me.

I'm mum to two adopted siblings (aged three and one) I fairly recently found out birth mother...
StressedMum profile image

Biological parents of babies and children with FASD

Dear all. I know a lot of you are likely to be adoptive parents of little ones whose mothers...
LJM83 profile image

No Funding!

Hello all; back in the summer we were referred to the Surrey Clinic for diagnosis and we thought...
count-to-1o profile image

Unsupported by school who refuse to acknowledge FASD as a "real problem"

Hi. I'm new to this forum so I hope I get this right. I have an adopted daughter, been with us...
echesters profile image

Moderation team

FASDNETUK profile image
FASDNETUKModerator
MB_FASD profile image
MB_FASDModerator
Sandy_FASD profile image
Sandy_FASDPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.