The Sound of the Silent: Getting reimbursed by our HMO: status report

Monday, January 6, 2014

Getting reimbursed by our HMO: status report

Update: Our fight with the stingy HMO about funding for C.'s multi-disciplinary assessment at the CP clinic continues. We're now at "Customers' Complaints".

Not too optimistic.

No comments:

Post a Comment

About my blog

C. is the youngest of our children. She suffers from severe epilepsy, blindness, microcephaly and profound cognitive and physical impairment.

We have faced hurdles and gained insights through our encounters with the medical, educational and governmental establishments.

Nobody was there to help or guide us.

I would love to spare parents in the same predicament some of the painful mistakes and wasted efforts we have made.

I am also eager to promote greater acceptance, inclusion and appreciation of our children. The new, heightened awareness of people with disabilities tends to gloss over our children - the ones with profound disabilities. They are a forgotten minority within this minority. Still marginalized and even shunned by many "enlightened" societies, they are a long way off from achieving equal rights.

Silenced by their disabilities, this blog is their voice.

Feedback: the.sound.of.the.silent@gmail.com