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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Saturday, January 18, 2014

temporary drain

Morgan is doing great following last nights surgery.  The temporary drain they placed on the other side of her head is not a pleasant site to see (shaved her front left side of her head to place the drain and has only clear bandage over) and very difficult to manage with a toddler since it has to remain at the same level as her head at all times.  Every time she moves or wants to sit up, lay down, be held, etc. they have to adjust and re-level the drain bag.  Her scans better now and there is no infection in her current shunt line from testing the CSF so that is good. 

They determined that her shunt is functioning fine to drain the 4th ventricle but not the lateral ventricles now.  The only resolution at this point is to place a second shunt to her lateral ventricles again.  So separate from 4th ventricle shunt.  This is not the news we hoped to hear but we really have no other options they have given us.  They will monitor and schedule the surgery for Monday evening.   I wish they could do sooner since it will be very difficult to keep Morgan mostly in the same position in her hospital crib with the temporary drain. 

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