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Courtney Sanders Hydrocephalus Journey
Courtney Sanders Hydrocephalus Journey
Courtney Sanders Hydrocephalus Journey

Living with Obstructive Hydrocephalus

7 Brain Surgeries and 7 Shunt Revisions Since 2012

my
story

I was diagnosed with Obstructive Hydrocephalus at the age of 18, from a traumatic brain injury (TBI).

I was not born with Hydrocephalus, as most are.

Unfortunately, this disorder is not curable but can be maintained by a medical device known as a Ventriculoperitoneal Shunt, (VP Shunt).

I started recording my journey because after being diagnosed with Hydrocephalus with the implantation of a VP shunt at 18 - I wanted to record what I dealt with.

Since my last round of surgeries in 2019, I continue to experience migraines and headaches. As of August 2024, my shunt is still operating well and is in good health. (Shunts have a higher failure rate than other medical devices.)

Symptoms I Experienced:

  • Numbness in extremities

  • Headaches / Migraines

  • Could not wake up easily

  • Always tired

  • Fatigue

  • Blurred vision

  • Double vision

  • Sensitive to light

Courtney Sanders Hydrocephalus Journey

My traumatic brain injury does not define me.

What caused my Hydrocephalus? Traumatic Brain Injury (TBI)

What was the TBI from? Domestic Violence resulting in a head injury

The TBI occurred on June 14th, 2011, and the discovery of my diagnosis was not discovered until April 12th, 2012. 

After my headaches gradually turned into constant migraines, I knew something was not right. I could not wake up when my son would cry. Oh yeah, I was 8 weeks pregnant on June 14th, 2011, and had my son in January 2012. 

Because my body had gone through so much, I believed I was in chronic stress and trying to recover. Shortly after Noah was born, a CT scan was issued. 

Side note: I did not disclose the situation out of fear and not knowing the repercussions. After my second brain surgery in 2015 due to my shunt malfunctioning - I knew this was my life from then on. Always needing a shunt revision sooner or later. There is no cure. 

I started speaking out. 

It is not easy living with Hydrocephalus. 

Despite the periodic headaches, I am able to live a healthy life. I do have restrictions which is probably a good thing because I am a thrill seeker. The rollercoaster rides and bucket list to skydive is no longer obtainable but we can get the adrenaline pumping other ways - for instance, let's conquer my fear of deep water and confined spaces. Cave crawling? Yes! Swim hole with friends? Yes! Hiking 20 miles? I am doing it!

Courtney Sanders Hydrocephalus Journey
Courtney Sanders Hydrocephalus Journey
Courtney Sanders Hydrocephalus Journey
Courtney Sanders Hydrocephalus Journey
Courtney Sanders Hydrocephalus Journey
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