I propose that the disability allowance be increased from the current 288 euros to at least 600 euros, because a person who has been disabled since childhood cannot survive on such a low disability allowance, which is not even enough for food per month, let alone for nutritional supplements such as vitamins, special food, various aids, etc.....
It bothers me very much that disabled people and social cases are put in the same basket, healthy people will still be able to find a job, but a disabled person will be dependent on the help of others until death and the little money he gets is not even enough for food.And you do not grant them a disability pension, you only grant them a disability allowance because they have been disabled since childhood and have never had a job or worked.
It also disturbs me that you give institutions 2000 euros a month and more for disabled people living with them who are in category 1, and barely 288 euros a month for disabled people living at home, plus a small allowance for care and assistance at home,which is overwhelmingly done by parents who have to be available to their disabled children 24 hours a day because they need constant help with everything, even the toilet, and they cannot afford to have a job, and because an assistant is significantly too expensive because the disabled person has to pay for it himself and there would be nothing left of the disability allowance and the care allowance. 
Often the whole family depends on the income of the disabled child, because the person who cares for the disabled person, i.e. in most cases the mother, cannot have a job and has no income of her own, and the worst situation is in single-parent families,
If a disabled person lives in an institution, the state gives the institution significantly more money for the disabled person, even up to 2000 euros and even more per month, without any problem, and I wonder why you have double standards towards the disabled, aren't they all equal and don't they all need the same care?
Because even those disabled people who live at home need the same care as those who live in institutions, don't they.  That is why I also suggest that you reduce the allowance for disabled people in institutions to the same level as for disabled people living at home, and you will see that the employees in the institutions will immediately rebel and say that it is not possible to care for disabled people with so little money,
So I really don't know how disabled people living at home and their parents can survive on significantly less money, even our President of the country doesn't have enough for 3000 euros a month and he said he can barely manage from month to month, so how can someone who needs constant help and care on 288 euros a month
1-Propose that you equalize the income between disabled people living in institutions and at home to the same level, by reducing the contributions for the care of disabled people in institutions and allocating the difference to those disabled people who are at home, because they are all equal, at least that is how it should be, and yet they would not have any additional financial costs.
2-To introduce some kind of record of how many disabled children and young people live in institutions and how many live at home, because institutions are now making a very good living at the expense of disabled children.
I recently heard on TV that there are about 25000 disabled people living in various institutions.
3-I would like to know how much of the money that you allocate to institutions for the care of disabled people goes to the disabled child personally, or to the age of 26 when he or she can still be in an institution, or is it all collected by the employees of the institutions?
4-To tighten up the control of the funding of disabled people's organisations and to close them down, those who cheat, who make a very nice living on behalf of disabled people, who for the most part get nothing out of it, except those who sit at the trough, and disabled people even have to pay membership fees out of their disability allowance, and the money that is collected from gambling should be given directly to disabled people, so that they at least get something out of it, rather than having to live on a pittance of a disability allowance.
As an example, a disabled person who has neuromuscular dystrophy and whose motor nerves and muscles are dying should automatically be placed in category 1 the first time he or she goes to the disability commission, because such a disease or medical condition only gets worse.
Ps also, some disabled people you refuse to grant disability benefits at all, but they are in category 1 or 2. I know of one example, he has epilepsy and is mentally retarded, such a person will certainly never be able to live independently, let alone work, and you prefer to give him a low social allowance instead of a disability allowance, and then his mother has to apply for social assistance every few months, and after the new one she does not get it because she is a part-owner of a small forest which is worth nothing and cannot even be sold.
- disability pensions should apply to everyone, regardless of when someone became disabled
www.mddsz.gov.si/si/delovna_podrocja/sociala/nadomestilo_za_invalidnos...
www.stat.si/StatWeb/glavnanavigacija/podatki/prikazistaronovico
www.stat.si/doc/pub/invalidi-2007-SLO.pdf
Please do not make excuses for existing laws again as you do with all the other proposals on this site, so I really don't know why you even want our proposals if you don't take them into account, aren't they proposals for changing existing laws for the better for all of us?