Coping With HydrocephalusThis section is a place to share stories about Coping With Hydrocephalus. Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation. You may also Help others by sharing your story. To quickly access health information from your website's browser, download 15 years post-shunt placement I am a 55 year-old female who was diagnosed with hydrocephalus in 1993 at age 39. My symptoms included severe headaches with extreme pain in my eyes, morning nausea, confusion, and numbness and tingling of the extremities. After confirmation of hydrocephalus by CT and MRI studies, I received a VP CSF shunt in 12/93. I was told by my neurosurgeon that my hydrocephalus was most likely congenital and my body began “decompensating” for it due to the aging process. I have had no problems with the shunt during the past 15 years. Upon my last exam by a neurosurgeon, I was told the shunt was working fine and no need to return unless their were problems. I am asking if anyone has had similar experience–diagnosed in mid-life with congenital disease. If so, how were you diagnosed, treated, and what is your current status? Thank you. Comments
December 2008
|
|
Archives:
The submissions from our site visitors do not reflect the opinion of Healthcommunities.com, Inc. (HC). The Content of HC's sites is intended for informational and educational purposes only, and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. HC does not provide medical advice. Never disregard professional medical advice or delay seeking it because of something you've read on an HC website. Always seek the advice of your physician or other qualified health care provider regarding any medical question or condition. (See also: Website Disclaimer) |

