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It was absolutely incredible to have one of these precious cubs climbing on me and playing with me. However, the best for me personally was when I fed her a bottle of warm milk. Kandy was a very good nurser and had all ten ounces down in no time. The next thing you know she was fighting to keep her eyes open as she cuddled up to a soft stuffed animal and started to take a cat nap.

This is a segment of video where the female six week bengal tiger named Kandy was playing with me while mouthing a lot. The two little cubs are teething and the animal handlers said they are encouraging them NOT to bite. She is really quite gentle, but you will see me guide her off of biting on my socks or my jeans, etc.  I asked the zoo person what I should say;  like “be gentle” or “no bite” and he said when they get bigger all of that “goes out the window” and a handler will most likely get scratched up in those encounters. That’s part of why they are doing so much handling at this young age. One of the zoo’s goal is to be able to handle the animals for regular exams without the need to use sedatives, yet, realizing that these are wild animals and a person can get hurt. Mutual respect is practiced here.

I was so very blessed to be able to have this encounter while I was visiting my parents who lived in the area of this zoo.  There were only a very few time slots left so my daughter and I went in at different times, but the way it worked out, we were better able to witness the other person having fun and take more photos that way. : )  Plus, I discovered the cubs will actually be gone for the next couple of weeks at another zoo. So it is amazing that the timing worked out.

I talked to other zoo visitors about how it must have been like this in the garden of Eden. God had originally intended for man to live with the animals and subdue the earth. It was fun to think about. Well I can now check this special experience off of my “bucket list.”

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Next, let me say, that the video below is NOT staged. In fact it is extremely impromptu as evidenced by our lack of fine attire and makeup. Nonetheless, I think it is important to show this video to people in order to bring to light an extremely rare medical condition.

Fran found me via a local radio station who had interviewed me from time to time. “Fisher Fran” as we affectionately refer to her has  episodes of a few days with it. Her case, waxes and wanes with a good deal of normalness in between. She has other body weaknesses that resemble multiple sclerosis whereas I do not.

My foreign accent has continued for over six months now without relenting. Although, I have noticed improvement in some words as I apply tricks that I have developed through speech therapy. Another difference in our two cases is that I am able to sing in my “normal” voice, whereas, Fran cannot sing at all when she becomes accented (even though, she to sings for audiences).

Here is a video taken of me (Eastside Ellen) and Fisher Fran back in June 2009. At that point I had been speaking with foreign accented speech for a month and Fran was in day two of an exasperation of her symptoms.

This video was captured by Fran’s daughter and so is not exactly framed as well as a more experienced photographer would have done. PLUS… she and I were both in our grubbier clothes as we rushed to meet with one another without the benefit of clothing changes or make-up. We were just so happy to discover that we were not the only one with this problem that we couldn’t wait another moment. As you see in this video we are quite happy to have found one another and are enjoying our ability to joke about our situation in a unique way.

However, let me stress this. Foreign Accent Syndrome is NOT a joking matter. Rather it is an extremely rare medical malady involving the Broches’(speech) area of the brain. It is reported that only 39 medically documented cases have been reported…ever…in the whole world.  Because it is so rare, there are not many doctors who even know about it. Therein lies the problem. If they are unsure what causes it, how to fix it and it is so rare. There is not much help for a person who has it.

In fact that is the main purpose of me documenting as much as I can about it. Researchers could learn a lot about this if they applied themselves. Because it is such a rare occurrence the argument may be made that there is not much point in researching it from a cost benefit analysis standpoint. However, since it involves the study of the brain and speech/accent production, I think that this is a pioneering area that some university or speech pathology school would want to investigate more.

As one who has now endured it for six months, I am learning that I am teaching my speech pathologist at the same time she is teaching me. This is unchartered territory here. So it is going to take the willingness of all involved to recognize that we do not have all the answers. In fact, we must admit that we have far more questions than answers. Yet, since I am the one living with Foreign Accent Syndrome,  I am a self-made researcher trying to document for the benefit of medical knowledge and hopefully to bring a sense of understanding to both the sufferers and their loved ones.

I am going to try to get another video with Fran and me together within the next few days. This time I WILL at least look better for the camera : P

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It was funny, because one of my friends tweeted me fearing that she had missed the time slot of the report. She usually is driving into work at that time and finds the topics we discuss interesting. It has been eye-opening to see how very many people are familiar with Eastside Ellen’s foreign accent syndrome story. They all tell me that it is fascinating, which it is. I’ve run into people at the grocery store, church, the bank and recently the hospital who ask if I am Eastide Ellen. All of them smile!! Yes! They are also so kind as to show true empathy. These people are not just listening into a report, but are identifying with it. What would they do if this happened to them? That’s part of what I love about growing up and living in central Indiana; people really care about their neighbors.

At this point I am unsure as to whether I will continue to report at WIBC on Tuesday mornings. Perhaps the story is no longer newsworthy. I don’t know how programming decisions are made. All I do know is that I am going through something that is so very rare that even mainstream medical doctors don’t know how to handle it. There is an opportunity for pioneering medical research to be made, and I am the kind of person that will share it all. I totally believe that God remains in control of every detail. I trust that there is an ultimate good that will be realized as a result of this trial and the events that are happening even now. I derive great joy in knowing that there are people who are standing beside me in both “good thoughts” and prayers, who are as perplexed as I am. and who are as fascinated and dumbfounded as even the local medical community.  We may not know the answers yet, but it is comforting to know that Hoosiers join together in an attempt to help each other.

It is for just such a reason that being on WIBC 93.1 FM “the News and Talk of Indiana” has been a great source of comfort, inspiration, intrigue and humor in a time that otherwise could threaten to undo a person. I am so very proud to call myself a Hoosier — albeit one that sounds like some kind of foreigner.  I am still a farmer’s daughter, even though my voice may stand out a bit more when calling in the cows : D

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It was with great anticipation that I went to see Dr. John Scott, my neurologist for my follow up appointment on Wednesday. I could hardly wait to hear what the EEG scribblings would show. I bet that there would be irrefutable evidence that my speech area was located in a different part of the brain than that which I used to sing. And since I can since in my “regular” voice, I thought that meant that I would be able to fully recover my normal, unaccented voice.

However, my excitement turned to disappointment when I didn’t get such a report. “Your EEG is normal,” came the report. Although that is good news in regard to connectivity of brainwaves and such, it didn’t help shed light on what is actually going on with me.

When I put the doctor on the spot with, “Well, if I just came to you with these symptoms and I had never even mentioned Foreign Accent Syndrome, what would you do with me?”

Dr. Scott told me that there simply isn’t an easy way to figure out what is going on with me. He said that in this local hospital network there simply aren’t specialists who deal with speech and how one might suddenly be stricken with a foreign accent. The closest related doctors that he could think of deal more with dementia than speech. There are also doctors who handle speech problems as it relates to psychologically based maladies, but I don’t really fit into that category either.

The bottom line of our follow up appointment is that Dr. Scott was entertaining the idea that it might be Foreign Accent Syndrome, but we are unsure of where to go from here. What testing or studies should be done. Dr. Jack Ryalls, of University of Central Florida is an expert on Foreign Accent Syndrome. My neurologist asked me to have Dr. Ryalls email him with suggestions for tests and then he will consider those recommendations and schedule them accordingly if possible. For example a functional MRI has been known to show which areas of the brain are affected, but there may not be the proper imaging tools located around here.

It is looking more and more like I am going to be dependent on some sort of a School of Medicine to launch an investigation, or include me in a study of some kind, because there doesn’t appear to be anything around here like me. Truly, I am feeling very foreign now, not just in accent, but in the idea that people just don’t know what to do with me or this problem.

There are very many people who say that I have a beautiful sounding accent. They all are intrigued by the very idea that I have this affliction. It truly is bizarre, however what to do about it? That is the question. All in all, I didn’t get the report that I was hoping for.

That is why I continue to scour the internet for more information on what may explain this. I am amassing quite a lot of documentation, but not getting to the answers yet. There is so little known about such a rarity. Still, I press on. . . there are others who are looking for the same answers out there. Still there are others who don’t know who to turn to for help. I, at least, have a group of doctors who are legitimately trying to get to the source of the problem.s

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