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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Monday, November 12, 2012

Protein levels

Generally they would expect Morgan's protein levels in the CSF to be high at first and gradually decrease but this is not happening.  Over the past several weeks we continued with Monday ultrasounds and testing protein levels and so much fluctuation (up and down, bigger, smaller then bigger again) it is getting very frustrating and I don't think the neurosurgery team knows what is causing it.  Her levels were 200 then 219 now even higher at 270.  They are talking about possibly doing an MRI or CT Scan instead of ultrasound next week to see if they can get a better picture and ensure nothing wrong. 

At this point we are in the ICC unit of Children's and the last major obstacle for Morgan to go home (other than her hydrocephalus resolution) is just her feedings and getting her off of the feeding tube.  I think if we were to just let her drink out of a bottle she would be able to go home soon (less exhausting than breastfeeding to her little body) but we are purposely not rushing this because we don't want them to rush into the shunt surgery.  So...we sit tight, get her breastfeeding and continue to monitor her ventricle size and protein levels.  I must say I am extremely worn out and just trying to keep trucking along to get through this. 

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