My Journey with hydrocephalus and Cerebral Palsy

Morgan Grace was born 3 1/2 months early on Aug, 21, 2012 weighing just 1 lb 7 oz and 13 inches long. Morgan was hospitalized at Children's Hospital NICU in Minneapolis, MN for 108 long days. During this time she encountered many medical challenges common to "micro preemies" but most devastating was to hear she had suffered from grade III/IV Intraventricular hemorrhage (IVH / brain bleed). We were told she may never walk or talk and they would not be able to tell the severity of the damage until she is older. The IVH resulted in Hydrocephalus, a condition she will have for life. At two, Morgan was also diagnosed with Cerebral Palsy.

I have found it very difficult to find information online - stories and information on hydrocephalus, shunts and people's experiences - so decided to write this blog to share what we have been through. I hope some day that Morgan can take over writing from her perspective. More importantly I hope maybe it can shed some light for other hydrocephalus and Cerebral Palsy patients and families. We welcome comments and questions.


From Wikipedia, the free encyclopedia:

Hydrocephalus is also known as "water on the brain", is a medical condition in which there is an abnormal accumulation of cerebrospinal fluid (CSF) in the ventricles, or cavities, of the brain. This may cause increased intracranial pressure inside the skull and progressive enlargement of the head, convulsion, tunnel vision, and mental disability. Hydrocephalus can also cause death. It is more common in infants, although it can occur in older adults.
The cause of Cerebral Palsy is a brain injury that occurs while the brain is developing. As a result of the brain damage during brain development a child's muscle control, muscle coordination, muscle tone, reflex, posture and balance can be affected.

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Thursday, November 13, 2014

Follow up

Had a chance to speak with Morgan's neurosurgery office today and were discussing the "intermittent Shunt Blockage" theory which he said is unlikely for her to be experiencing.  Apparently this is pretty uncommon but when it has happened usually the patient is slower to recover since the CSF build up and release via the shunt isn't a "burst" of fluid but more slow and gradual.  Morgan seems to snap out of it much quicker and feel better suddenly.  He does think the vomiting/lethargy episodes are very likely related to the shunt or other neurological issues though and we are going to do further follow up. 

I also asked him about slit ventricle syndrome (yes, I have been googling) since her symptoms seem very close to the description- intermittent intense headaches, varying degrees of lethargy, with or without nausea, and vomiting that last anywhere from 10 to 90 minutes.  Based on her last scans he doesn't think either because her ventricles are still quite large.

So...next week another MRI to take a look and setting up an appointment to see a neurologist with her neurosurgeon also to check out if she is having any seizures that may cause. 

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