Pev

Brumi

Hi does anyone have the answers yet. Thanks

crawleygirl

I would really like them too, i thought that they were meant to be out by the 2nd but can't see them anywhere.

jewels.p

The answers arent posted on the AAT Website until the results are out. The only other way people get the answers before that is if someone who knows what they are doing in each subject attempts the questions for us.

(Didnt mean we dont know what we are doing)

SandyHood

I've completed my answer and have a copy to send out
It is on the auto reply so if you want a copy let me know [size=+1]by email[/size] (not a pm) and use the subject line: [size=+1]PEV J10[/size]

Now a plea for charity:-

My son is Mark Mayer. He has a form of Cerebral Palsy called Worster Drought Syndrome. WDS affects speech and eating. He is also Hard of Hearing and has to use Hearing aids. He has a wheelchair that he has to use as he can not walk long distances.

Mark has become chairperson of the Worster Drought Syndrome Support Group. This organisation supports children and adults with WDS.

Each year the group hold a family day where the children, parents and people who have WDS can meet up and share their experiences. The day gives a great support to all the WDS suffers but relies on donations to enable it to go ahead.

If you find my answers help, or wish to show appreciation of any support I’ve given you, please consider making a donation to the Worster Drought Syndrome Support Group; http://www.justgiving.com/WDS-SG

Thank you
Sandy

beaneygirl

SandyHood wrote: »

I've completed my answer and have a copy to send out
It is on the auto reply so if you want a copy let me know [size=+1]by email[/size] (not a pm) and use the subject line: [size=+1]PEV J10[/size]

Now a plea for charity:-

My son is Mark Mayer. He has a form of Cerebral Palsy called Worster Drought Syndrome. WDS affects speech and eating. He is also Hard of Hearing and has to use Hearing aids. He has a wheelchair that he has to use as he can not walk long distances.

Mark has become chairperson of the Worster Drought Syndrome Support Group. This organisation supports children and adults with WDS.

Each year the group hold a family day where the children, parents and people who have WDS can meet up and share their experiences. The day gives a great support to all the WDS suffers but relies on donations to enable it to go ahead.

If you find my answers help, or wish to show appreciation of any support I’ve given you, please consider making a donation to the Worster Drought Syndrome Support Group; http://www.justgiving.com/WDS-SG

Thank you
Sandy

Hi Sandy
I'm not sure whether you got my last emails but I felt terrible as I felt I plagued you with the PEV answers request. I thought that your email was purely automated and that you wouldn't have to be personally bothered so just tried on the off chance when I could. I gave to your nominated charity today anyway and just wanted you to know how truly grateful all of us studying AAT are for you going out of your way to put our minds (or curiosity) at ease by taking time out to do this for us.
You're a total star.
Thanks again.
Lou
x

SandyHood

Thank you Lou