Re: Coronavirus - should carers allowance be increase
Posted: Fri Apr 24, 2020 2:04 pm
I think there should be an increase regardless of this virus!
I am a lone parent of two boys. My eldest was diagnosed with autism aged 3 (now 12) and my youngest (9) I have been trying to get help for for years! He was about to have the first meeting about gda referral yesterday hopefully leading to assessment for the PDA side of autism. At school my youngest is on 2 different IEP's to support his needs. One educational and one emotional!
Any way I now (like most) have both off school and we have been in self shielding officially since the 19th March but unofficially since the 15th of March for two of us (my youngest was ill with a stomach bug previous). Like most carers (dependant on age of the person we look after and their individual needs) we are now having no break or rest, being educators in school work and life skills as well as usual parental duties (in cases with children and young adults mostly), we are also coping with more mess, more demands, debt (in some cases not personally), stress, lack of sleep (I am averaging at 2 hours a day), personal anxieties (that we have to hide from those we care for as they have enough of their own), the list goes on.
Prior to this some people may have had respite or other help with the care needed. I always had meetings, appointments, etc but their school was my break from them even if in meetings about them lol. Now it is 24 hours including meltdowns and worse. All I can say is I am really glad I have a garden!
Carers should be increased! I have relatives who think my life is always plain sailing that I don't work! I do work just not in the ways they think and trained as a HELTA but cannot go out to work physically as I have to be on call for school, go to meetings, be there in the morning to get one son in a taxi and the other dressed and dragged to school because his demands stop him going, or he fights with his shoes! Then you have to be there at home time to meet the taxi, etc.
Life never stops for us! I am currently not enjoying the sun, nor am I catching up on tv (the opposite my box is filled with recordings I can't watch) and one of my kids even said I am like a slave and look like a hippo! Fantastic. Yes I see the humour but never has being a carer felt more isolating. Oh and I have to shield due to being at high risk.
Not a rant or wanting sympathy by any means. My kids are my world and I would rather we be safe than not here. They have no-one but me who understands them too so it is what it is. The Government should read these forums and see what life is really like and work out what they would pay a stranger (not that mine would go with one) to do what we do out of love!!
I am a lone parent of two boys. My eldest was diagnosed with autism aged 3 (now 12) and my youngest (9) I have been trying to get help for for years! He was about to have the first meeting about gda referral yesterday hopefully leading to assessment for the PDA side of autism. At school my youngest is on 2 different IEP's to support his needs. One educational and one emotional!
Any way I now (like most) have both off school and we have been in self shielding officially since the 19th March but unofficially since the 15th of March for two of us (my youngest was ill with a stomach bug previous). Like most carers (dependant on age of the person we look after and their individual needs) we are now having no break or rest, being educators in school work and life skills as well as usual parental duties (in cases with children and young adults mostly), we are also coping with more mess, more demands, debt (in some cases not personally), stress, lack of sleep (I am averaging at 2 hours a day), personal anxieties (that we have to hide from those we care for as they have enough of their own), the list goes on.
Prior to this some people may have had respite or other help with the care needed. I always had meetings, appointments, etc but their school was my break from them even if in meetings about them lol. Now it is 24 hours including meltdowns and worse. All I can say is I am really glad I have a garden!
Carers should be increased! I have relatives who think my life is always plain sailing that I don't work! I do work just not in the ways they think and trained as a HELTA but cannot go out to work physically as I have to be on call for school, go to meetings, be there in the morning to get one son in a taxi and the other dressed and dragged to school because his demands stop him going, or he fights with his shoes! Then you have to be there at home time to meet the taxi, etc.
Life never stops for us! I am currently not enjoying the sun, nor am I catching up on tv (the opposite my box is filled with recordings I can't watch) and one of my kids even said I am like a slave and look like a hippo! Fantastic. Yes I see the humour but never has being a carer felt more isolating. Oh and I have to shield due to being at high risk.
Not a rant or wanting sympathy by any means. My kids are my world and I would rather we be safe than not here. They have no-one but me who understands them too so it is what it is. The Government should read these forums and see what life is really like and work out what they would pay a stranger (not that mine would go with one) to do what we do out of love!!