People Have the Power

Individuals with SZ are seen as interchangeable with no identities of our own apart from the illness and its symptoms.

The reasoning goes: we’re not able to recover so why bother trying to help us do this if it’s impossible?

NO. That thinking doesn’t fly with me.

We should be trying to help people recover.

I don’t accept chronic disability as the fate of any human being.

My point exactly is that getting the right treatment right away can enable an individual to bloom–to do better–to be able to have a full and robust life.

I’m not a fan of the all talk and no action to create solutions MO of so-called normal people. They don’t have a vested interest in my life and health and in yours and other people’s who have MH issues.

I titled this blog entry “People Have the Power” because we have control over the dialogue. It’s also the title of my favorite Patti Smith song.

I’ve written before that I think no one we elect in government can ultimately ever do things to remedy societal ills.

So it’s up to each of us to take action to create the kind of life and health we want for ourselves.

It’s up to each of us to help each other.  Martin Luther King called this creative altruism.

I ask you:

Are you willing to remain silent?

Are you willing to accept chronic disability?

Are you willing to accept the status quo?

I’m NOT able to buy into the myth of helplessness and hopelessness.

There’s a better way: having the courage to speak the truth to power. Telling our stories.

Doing something to help those of us who WANT to recover have the OPPORTUNITY to recover.

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