Scheurmanns kyphosis treatment

Hello. My name is Joana...

Well... I got scheurmanns kyphosis and although it's hereditary, it started to show only when I as about 14 years old. My parents started a treatment which cost €25 euros per session, 4 x a week and of course they couldn't afford anymore of this, so after three months we stoped. My body grew and nothing can be done now. Now at 30 years old I have a curvature of over 100 degrees, hyperlordosis as compensation and a scoliosis. Dr's tell me there's nothing that can be done except a spinal fusion. And here in spain besides being extremely expensive they refuse to do it. So now im stuck without being able to work and I need money to at least try some alternative treatments. The state wont help. I dont have right to benefits unless my lung function is compromised please help me achieve a normal lifestyle.