ANA Discussion Forum

Treatment Options => Radiation / Radiosurgery => Topic started by: crazyauntjules on April 28, 2010, 12:02:06 am

Title: 8.5 years post FSR at Hopkins--doing great, still!
Post by: crazyauntjules on April 28, 2010, 12:02:06 am
Hi all ANers-

8.5 years ago i was posting and reading on the then, "AN Guestbook."  Got great help, and support and info.  And so, I am back to say I am sorry I have stayed away so long, and not reported back as much as I might have. 

I had my FSR at Johns Hopkins in Dec 2001.  Initially my tumor (7mm x 9mm) swelled a bit, but went back down to 8mm x 9mm.  I have had MRI follow ups for a couple of years at every 6 mos, then went to two year follow ups, and still doing well. 

I retained quite a bit of hearing, tho I do have some loss and tinnitus (i thought everyone just had that screeching in their ear, thought it was normal and had it quite a while before my diagnosis).  I had no other side effects from my treatment, indeed, sightseeing in DC and Baltimore with my family each day after treatment.  So, as you can guess, I am a proponent of FSR when it is an appropriate treatment.  My local small town ENT felt strongly that I should have surgery.  I did the research, and made a different choice...I chose radiation.

I wish you all good success with any treatment option you pursue.  No matter what treatment we choose, we will never know if another treatment would have been "better" or "worse."  We make the best choice we can and roll with the punches.  Hang in there, everyone, there is life after AN!     
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: goinbatty on April 28, 2010, 03:01:07 pm
Great to hear you're doing well.  I was like you and went sight seeing every day after treatment.  I'll have to admit, it made dozing during treatment a bit easier being tired from all of that walking around DC. 
You're so right about making the best decision for oneself.  Deciding on the treatment option was the toughest part for me.  After that decision was made, it was like a huge weight had been lifted.  Only time will tell if we made the correct decision.  It was great getting to a point where I didn't focus on it every day.  That's not to say the tinnitus doesn't get irritating at times as well as hearing issues but life is good.
Sandra
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: Jim Scott on April 30, 2010, 01:09:26 pm
'Crazyauntjules' ~

Congratulations on your long-term FSR results!  Thanks for sharing this pertinent information with other AN patients.  As another AN patient who underwent FSR - with excellent results - I wish you continued success.

Jim
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: NancyMc on April 30, 2010, 02:12:13 pm
Your post sure brought back memories.  I was diagnosed Sept 19, 2001.  I was on the AN Guestbook as well.  My doctors wanted surgery, but I researched as you did and decided to have FSR at JHU as soon as any growth occurred.  I suppose you were one of the fortunate ones who had Dr. Jeffrey Williams treat you.  My MRI films were on his desk waiting for review when he went to the hospital gym and never came back.  Truly sad.
Congratulations on your excellent outcome.
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: Cheryl R on April 30, 2010, 02:46:34 pm
My day was told AN for sure was August 14th,2001.    The MRI report said AN vs neuronitis.   My dr just came in and started talking about my tumor when hadn't yet been told it was for sure.   His bedside manner has improved.       I was on the guest book too.   Does this make us oldies but goodies?           Surgery wasn't till Nov 1.         
                                                          Cheryl R
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: sgerrard on April 30, 2010, 06:25:49 pm
 Does this make us oldies but goodies?

Yes it does!  :D

Steve
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: JimmyD on May 20, 2010, 12:05:59 pm
Your post sure brought back memories.  I was diagnosed Sept 19, 2001.  I was on the AN Guestbook as well.  My doctors wanted surgery, but I researched as you did and decided to have FSR at JHU as soon as any growth occurred.  I suppose you were one of the fortunate ones who had Dr. Jeffrey Williams treat you.  My MRI films were on his desk waiting for review when he went to the hospital gym and never came back.  Truly sad.
Congratulations on your excellent outcome.
I had my FSR at JHH buy Dr Williams in December of 99'.He was the reason I chose FSR over surgery.I figured being a board certified Nerosurgeon and Radiologist he had nothing to gain either way.When I drove down there to drop my Films off to Tammy Cuda I ran into him in the hallway.He was with several other Doctors,he stopped what he was doing shook my hand and looked at my films right there in the hallway.I was sold right then.It was tragic when I heard the news of his death.
Jim
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: NancyMc on May 27, 2010, 07:04:21 pm
I'm glad you benefited from his skill.  I remember Tammy as the contact person as well.  I felt very sad for his fiancee.
Stay well.
Nancy
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: moe on May 28, 2010, 08:13:30 am
  My MRI films were on his desk waiting for review when he went to the hospital gym and never came back.  Truly sad.

So what happened to Dr. Williams?? I gather something happened in the gym- aneurysm, heart attack????
How tragic :'(
Maureen
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: NancyMc on May 30, 2010, 09:58:05 am
I've always assumed heart attack.  Yes, very unfortunate.
Title: Re: 8.5 years post FSR at Hopkins--doing great, still!
Post by: MLB57 on May 31, 2010, 07:02:47 am
Hi Crazyauntjules,

Always glad to hear positive follow-ups from FSR patients from several years gone by.  It certainly makes me more than hopeful that this time, choosing FSR, was the right treatment to combat my AN...and it's great news for all others exploring their options for treatment..

As you said there is certainly life after AN...

Best wishes always,

Mary (one of Phy's Maxwell Silverman's Brunch Bunch)   ;D
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