Has anyone else with epilepsy been diagnosed with Raynaud's Syndrome/Phenomenon? My 7 yr old has complained of issues that relate to Raynaud's since she was able to communicate. She would either blow on her hands and/or feet., or say they hurt/burned/tingled. Or have one of us blow on them or rub them for her. It help some but nut a complete fix and I worry I may spark a seizure from over-stimulation. We live in New York state so it's not like the temperatures would be consistent year round. I'm curious if anyone noticed more or less seizure during the time when their Raynaud's acted up. Any and all help is greatly appreciated. My daughter is newly diagnosed with epilepsy as of late November 2011. But I suspected it since she was an infant. Took over 6 years and several trips to Pediatric Neurologist that did not before I insisted on change and got what I asked for. Now we are finally starting to get answers so some of the questions, but some are best answered by those that have lived it. Again, thank you for any info you can provide!