I just read another post that stated every sheltered workshop and day hab center needs to close and everyone who attends should find a “real” job. I’m not a happy mom.
I understand the reasoning behind possible laws stating every able-bodied person should be working and earning a minimum wage. Don’t they think that I would be pushing for that for my kids if I truly believed either one would benefit from it? Casey and Rob need Hopewell – it really is that simple. Does everyone that goes there need it? No, of course not, but everyone has different abilities. I just don’t understand why that is so hard for some people to understand.
Casey might… maybe… possibly… be able to go to a “real” job – with supports, for a short amount of time. If she wants to and is in the right mood and doesn’t decide that going to see Norma (a senior citizen she has developed a special friendship with) would be a better idea. Casey doesn’t care about money. She understands she needs money to buy things, but not where money comes from. (Mom’s purse! How it got there, she doesn’t know or care.)
Rob could not, at this point in his life, handle a job. It’s that simple. He doesn’t like noises, crowds, strange people or a different routine. His anxiety levels are finally leveling out (and by that, I don’t mean it’s gone – I mean he isn’t humming, flapping, squealing and stealing paper clips all day long!) He could not do it. However, if any politician wants to prove me wrong, by all means, message me. You can take him for a day – or a few hours – or an hour – whatever you can handle. Ask the people who work with him every day what they think.
Rob doesn’t care about money, either. The only thing he wants is to have 3 quarters in his pocket every morning when he leaves. He never spends them, just likes having the ability to buy a pop if the need arises. He understands that money is needed to buy things, but he doesn’t care where it comes from, either.
I do understand that there are many people out there who desperately want a “real” job and to make their own money. There are people who need that job to live on their own or help support their families. For those people, keep fighting! Demand your services and what you need. But, please, do not lump my kids into your needs. We have our own needs.
Sure, it would be great if Casey and Rob were making money and could pay for the things they want or the places they want to go. Who wouldn’t want a little extra money? But it isn’t going to happen any time soon. Maybe in a few years, they will both want jobs and I’ll move mountains to see that they get what they want. Until then, don’t take away the place we all need.
Neither of the kids have brought home paychecks in months. But – they are happy! They are going places with their friends. Rob is even interested in exploring new places and new experiences. Casey can volunteer to her heart’s content. She can have breakfast with the “girls” club (that Rob always seems to invite himself to!) and paint rocks to make others happy.
She can visit the nursing homes and see Norma or play wii or sneak a drink of pop. They are going swimming with friends. Rob will be going back to aquatic therapy soon. All of this and more is available to them because of the workshop they attend. I couldn’t do it for them. I can’t take Casey every where she wants to be and leave Rob at home and he doesn’t want to go. It just doesn’t work.
What about my job? As much as I wish I was rich, I’m not and a job is a necessity. If their lose their day hab services, what am I supposed to do? They can’t be alone and I can’t afford to pay (their waiver will pay for some hours, but not nearly enough). So where does that leave us?
I do understand what people are saying about minimum wages and the need for people with disabilities to be accepted into our communities. I fight for that acceptance every day. What I don’t understand is why it has to be an “all or nothing” situation. Why do sheltered workshops or day habs have to disappear so people can have jobs? It just doesn’t make sense to me.
We stress all of the time about looking at a person’s interests and abilities when making a plan for them, but someone who has never met my kids can make a major life decision? Yes, please, no fanks as Rob says. We would never take away a person’s therapy or medication without something to replace it – why in the world does taking away their secure, happy place make any sense?
My prayer is that all of the talk floating around is just that – talk. Rumors or half-truths that have no bearing. But, I hear about sheltered workshops closing and families being desperate for help. I know they are expensive to maintain and finding quality staff can be an issue. Casey and Rob need Hopewell – and so do I.
Keep fighting for what your family member needs. Never, ever stop doing that – but just keep in mind that our needs are different. This can’t be a “one size fits all” decision.
Jen, People who want to do away with the “special” place your kids enjoy should spend some time with them.
That’s exactly what I think! So often, the people making the decisions have never been around anyone with disabilities. I’ll let them borrow Casey or Rob anytime! 🙂