A New Me Blog

# 34 Post Treatment
Monday, February 3, 2025 by Deb Vellines

All went well with the treatment. After so much study of treatments, it was almost anti-climatic. I had my three days of treatment and we flew home to Illinois. No problems. I did feel extra tired and needed extra naps. Other than the tiredness, I felt good.

I was excited to see future MRI’s. Would they show the tumor getting smaller and dying? I would have to wait. It’s hard waiting. Any little symptom and I worried the tumor was growing, or I might have swelling from the treatment. I prayed more often and my trust in God grew by leaps and bounds. Whether the tumor died or not, God would be with me.

After six months, I finally had a post-treatment MRI. YES!! The tumor is dying and has gotten smaller. The original size was 1.3 cm by 7 mm by 5mm. Six months following treatment the size measured 1.2 by 6 by 4. Now, this might not sound like a big difference, but it meant the world to me. There isn’t any extra space in our brains for tumors.

By the way, I have had my follow-up MRI’s in Illinois and Missouri. Different radiologists and neurologists can look at the exact same MRI and read it a bit differently. This used to confuse me. When the MRIs were big pieces of film, I learned how to read and measure them myself. That’s a whole lot harder to do with a disc. In fact, I can’t. I used to mail the films to California for their readings and was always amazed when they read them a millimeter or two different from each other. Now I don’t have to mail films. It all happens electronically.

My treatment was in 2005. Now, not quite thirteen years later, my latest reading is 8 mm by 4 mm by 5 mm. Yipee. When I asked if I need to continue getting the MRI’s, the answer was I can wait three years for the next one!! More good news.

Now for the bad news. Six months after receiving the radiation, my hearing took a nose dive. With prednisone, some hearing came back. I wanted to continue on the drug, but the doctor said no. Too many side effects with that drug long term. I didn’t care. I wanted the drug, but he said, “No. too many side effects.” If it were up to me, I wanted to stay on the drug. I couldn’t talk him into it.

Most often, someone diagnosed with an acoustic neuroma has had a hearing loss in one ear only – Single Sided Deafness – SSD. It can be a sudden loss but usually is slow. Because my tumor was mostly on the balance branch of the 8th cranial nerve, I had good hearing. My problem, as you might recall from an earlier post (#2) was balance, not hearing.

From: American Hearing Research Foundation.  This website has lots of good hearing information.

Without the prednisone, my hearing continued to decrease. Today, I’m deaf in my right ear. Would I have had the treatment if I had known I’d lose my hearing? Yes. It’s a good feeling to know the tumor is dead. That knowledge is worth the loss of hearing – to me.

I would hate to have not had the treatment and lose my hearing. Then my question would have been Would I still have my hearing if I hadn’t had the treatment? That question would have been a tough one. I’m glad God directed me and nudged me to the treatment.

I once heard someone at a symposium say, “Hey, with an acoustic neuroma, you lose your hearing. With or without treatment. Doesn’t matter.” From everybody I have talked with, this is true.

*****

Readers, do you know someone with an acoustic neuroma who has good hearing on the acoustic side?

*****

Dear God,

You tell us to ask for what we want, so I will come right out and ask for my hearing to return. I thank you the treatment killed the tumor, but did it have to take the hearing?

Forgive me for trying to second guess your ways. I’m trying hard to trust you. I know you didn’t promise it would be easy to trust. But this is hard. I have two ears. One of them works and that should be good enough for me, but it’s tough having this SSD. With you beside me, I can handle it. Amen. 

God is our refuge and strength, always ready to help in times of trouble. Psalm 46:1


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# 77 – 21 Stress Busters
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#72 AN Awareness Week
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# 71 Hearing Loss
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#70 Understanding Changes
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#69 Is It Growing?
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#66 Decisions & Stress Busters
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#62 Three Ways to Connect
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#61 Reminders
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#55 Hints for the Holiday
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#53 Headaches
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#51 ** 5 Ways to Prevent Falls
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#48 Networking8 Networking
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#46 4 YouTube Videos
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#45 Get Connected
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#44 Signia Hearing Aids
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#43 Improving Balance
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#42 Treatment of Depression
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#40 ** 7 Ways to Fight Brain Fog
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#37 Phonak CROS Hearing Aids
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#36 Hearing Devices
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#35 Single Sided Deafness
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# 34 Post Treatment
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#33 Treatment
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#32 A Hit Over the Head
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#31 National Symposium
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#30 Knots with Purpose
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#29 A Time to Kill
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#28 A Letter
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#27 Peace With Trust
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#26 Joy is a Choice
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#25 Flat Emotion
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#24 New Thoughts
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#23 Acceptance?
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#22 Help!
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#21 Crying
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# 20 Full Plate
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#19 Concentration
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#18 Worry versus Trust
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#17 For Healing
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#16 Who’s in Control?
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#15 Depression
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# 13 Doctor (specialist)
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#14 Different Treatments
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#11 Support Group
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#12 Thank You
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Step # 10 Questions
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Step # 9 Bargaining
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Step #8 Energy
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Step # 7 – Reactions – of others
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Step #6 – Do I share my News?
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Step #4 – To stay calm waiting for test results
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Step #5 – Why?
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Step #3 – Courage – to make an appointment for a test.
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Step #2 – Wisdom – for the doctor
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