Helpline 07939 046 030

Kathryn’s Story

23 July 2019

Kathryn's Story

Here Kathryn honestly opens up to us about her journey and experiences with NF2:

"I was diagnosed with NF2 when I was 16 years old. One night I woke up with ringing in my right ear and a deafness in my right.

We went to the doctor the next day and after discovering that my eardrum looked healthy they decided to do an MRI. There results of the MRI found two bilateral schwannomas on my left and right auditory nerve near my brain stem.

After a lot of deliberation, my doctor decided to try to get me into a medical study that used chemotherapy to try and shrink the tumor and restore my hearing, it was the only treatment available at the time. I was in chemo for two years with quarterly MRIs scheduled. My right side tumor Stabilized but my left side kept growing. In 2017,  I flew to California to have my left side of my tumour removed as it was pressing dangerously on my brain stem.

I was having vertigo problems with my coordination and balance facial nerve ticks and tinnitus. To have my surgery I went to the house clinic in California, the tumor had grown to over 6 cm meaning the surgery was 19 hours, I also received an AVI. 

As a result I was fully deaf in my left ear and had partial facial paralysis from damage from the surgery, howeveer since my right side tumor had been stable I felt like I was in the clear. I had a few follow up MRIs after, before an MRI  in August 2018 showed that my left side tumor had grown substantially.

Unfortunately somehow there was a lack of proper communication between me and my California doctors, meaning that I did not find out that the tumor was growing until December 2018. In January 2019 my right ear, my remaining hearing ear, had a major hearing loss drop. I have a loss of hearing of lower pitches and a 4% word association as well as tinnitus in both ears. The doctors are deliberating if I should fly to California and have a whole removal or if I should have a debulking surgery getting rid of the tumor near the brainstem and then having a few rounds of radiation to try to shrink the tumor near the hearing nervous in order to attempt to restore or retain as much hearing as I have left.

My eyesight has gotten worse as well my balance and coordination. I am still in the middle of my journey, I am learning how to cope with extreme hearing loss and learning ASL. My remaining tumour is about 4 cm now and growing into my brain stem. I have a little time to decide the next step but I am sure God will make my decision for the next step clear to me." 

Filter News

Filter by Date
Category
Reset

Second Face Equality International Week

Find out more & how you can take part

Read More

Shine a Light 2020 Success!

Check out some amazing blue buildings that took part in our Shine a Light On Neurofibromatosis 2020 campaign

Read More

Sarah’s Story as told by her Father Clemence

Read more about Sarah's story and her Shining a Light on NF from home for World NF Awareness Day!

Read More

Statement by Helen Tomkins our Specialist Neurofibromatosis Nurse UK

A statement on coronavirus by Helen Tomkins specialist Neurofibromatosis nurse in Devon & Cornwall

Read More

Courtney’s Story

Read more about Courtney's NF Story and how she overcomes her difficulties

Read More

Shine A Light on Neurofibromatosis 2020

Find out what we're up to for our Shine A Light campaign this year!

Read More

Statement by Michael Fry our Chair of the Board of Trustees

The impact of the corona virus on the charity sector and Nerve Tumours UK's continued support to those affected by NF

Read More

NF1, Plexiform Neurofibromas Market Research Study

Find out more about an NF1, Plexiform Neurofibromas market research survey

Read More

Statement by Rachel Jones & Rebecca Rennison our Specialist Neurofibromatosis Nurses UK

A statement on coronavirus by Rachel Jones & Rebecca Rennison specialist Neurofibromatosis nurses in the North East & Cumbria

Read More