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Completely exhausted, any ideas?
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Ahh my boy loves holidays, but only with us, or his grandparents on his dad's side - he can't stay with anyone else... he's very lucky because this time he's going with granny and grampa (while me and my husband go camping!), and they are very structured and routined, and strict in the best kind of way... He's strange because sometimes he loves new things! Although it's almost like he feels he has to say 'I like to eat new kinds of food.' a few times before he goes for it ![]() He's been singing happy birthday to me today, on loop, again.... all day.... lol |
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#6
07-29-2010, 07:55 PM
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matt wont try new food at home when we make it for him yet he has things at college or respite that surprise us yet he did nick my saus sandwich that i put brown sauce on cause he doesnt like the smell and scoffed it. he has to smell all his food and if he approves he will photograph it before he eats it lol its good that our Children can make us laugh just when we need it
There comes a point in your life when you realize:Who matters,Who never did,Who won't anymore...And who always will.. So, don't worry about people from your past,there's a reason why they didn't make it to your future. |
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#7
07-29-2010, 07:58 PM
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(07-29-2010 01:47 PM)Blueberry Wrote: Hi, I'm brand new.. I joined today because I reached a point of desperation yesterday and I've been googling for help! hi sorry but other reply was wrong. i was just writting to say have you got homestart in your area this is a great chariety that will give you support mentally and physically for a few hrs a wk so that you can recharge yourself can get refered or self refer by Health visitor. hope this is an idea to go down the best of luck and hope you get the help and rest you really need zoexxx (This post was last modified: 07-30-2010 07:50 PM by zoem474.) i have 4 special children emily 9 thomas 3 and id twins who have gdd who are all the greatest |
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#8
07-30-2010, 07:44 PM
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Homestart are a great charity offering support both in the home and outside the home and also run numerous disability groups for parents.
We go to one and its great ![]() Members should check if they have a local group as its been great for us to have adult conversation and they even have a playworker at our group so the adults can chat and the playworker plays with the Children
![]() Our Irish members can also use our new website for Ireland which is |
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#9
07-31-2010, 07:16 PM
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Hi it took me from year 2 until year 6 to get someone to see Liam, they diagnoised him just as he was leaving junior school to go into high school. The school was brilliant and were trying everything to get him seen by someone, they even got him referred to the nspcc as they said they needed someone big behind them to listen(but they said he was over there heads and they couldnt do anything to help, even told me not to tell anyone they had been involved because if cahms found out they wouldn't see him) . In the end it was the paediatrician (that i self referred him too) that managed to get cahms to see him. I have just tried to refer my daughter myself to the paediatrician like i did with Liam as she is exactly the same as her brother but apparently the system has now changed and it has to go before a panel before they can accept her.
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#10
08-01-2010, 07:27 PM
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would it be worth calling social services?! I really don't know.. sorry for the huge message..
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