tag:blogger.com,1999:blog-3521947358642019977.post75668394089428508..comments2019-01-31T22:06:24.954-08:00Comments on VCFS Families: MigrainesSherrihttp://www.blogger.com/profile/17207240826243115784noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-3521947358642019977.post-48274210800429122682013-02-26T02:02:05.236-08:002013-02-26T02:02:05.236-08:00My daughter has VCFS and is 22 and has had migrain...My daughter has VCFS and is 22 and has had migraines since she was 11. She has tried so many different meds and nothing has really helped. She sees a neurologist, has had physical therapy, chiropractors, massage therapists, acupuncturists, nutritionists, mental health therapists, naturopaths...<br />She is desperate. We understand that there are anomalies with the vessels and it is a biochemical imbalance.<br />Does anyone have any suggestions from experience? PerriZinahttps://www.blogger.com/profile/07238054399803275269noreply@blogger.comtag:blogger.com,1999:blog-3521947358642019977.post-75530228051155648552010-05-20T09:30:34.225-07:002010-05-20T09:30:34.225-07:00my son asher gets (what i suspect) are migraines. ...my son asher gets (what i suspect) are migraines. he has actually been admitted three times for these, because they result in high fevers and febrile seizures, and they look a lot like sepsis and meningitis. we're seeing neurology in august... and genetics in a few months. asher is still considered "query diGeorge", with no diagnosis quite yet, but immunology is pursuing it really hard. gotta tell ya, reeeeeealllly didn't want to see this post on this blog! LOL but good to know asher isn't the only one.Heatherhttps://www.blogger.com/profile/08482109987411601315noreply@blogger.com