Megan Manuel

This is for my daughter Megan Manuel.  She has been diagnosed with RSD,EDS, POTS, hypermobility syndrome, juvenile fibromyalgia, and peripheral neuropathy.  All of these together cause great pain in her body.  All of this began for her in Sept 2008.  It has taken nearly 5 years for her to be diagnosed.  She is 15 years old.  Megan has a chance to get a spinal cord stimulator, this may very well be the first and only chance to get some relief of her pain. She has seen many drs and we always leave hearing the same thing, there is nothing we can do, she is a mystery. We have finally found a Dr that feels like he can help and now her insurance will not pay for the procedure. Megan has spent all of her teenage years unable to do what other girls can. This stimulator may give her life back to her. She has an invisible illness that most people don't understand, but this stimulator may be her best chance to a "normal" life. I pray you read her story and find it in your heart to help us.

GOD BLESS
Tina Manuel