Increasing Interest in Foreign Accent Syndrome

Hey everyone!  I have some great
news… first off, earlier in the year a young lady who contacted me via Twitter, then email and eventually interviewed me, wrote a research paper for class and blogged about Foreign Accent Syndrome. I will attach the link to it since it was so good.
Then this evening I had a cousin message me that a big college professor is fascinated and may be using some of my materials for his class!
This is encouraging as so many more people are helped when more educators teach the truth about that Foreign Accent Syndrome is a real, neurological, brain malfunction and press for further research and proper diagnosis and treatment.

CLICK HERE for links found on FAS blog

I really hope that the information that V and I are both eager to share with others will go beyond raising an interested eyebrow of the curious. Hopefully this will ignite further study in the medical and scientific communities, and most especially in the areas of neuroscience, brain and language. The more people that learn the truth from those of us living with Foreign Accent, the faster and better will be the scientific development of hypotheses, the greater impact that might be realized to benefit those who have FAS and those as yet undiagnosed.
On top of that I have talked by phone with two brand new cases that are now people who are feeling a bit less traumatized by instantly feeling understood by speaking with me and knowing they are neither alone or crazy.
There are so many more people to reach and teach 😉

Foreign Accent Syndrome: Important Steps Forward

Yesterday was a GREAT DAY for those of us who suffer from Foreign Accent Syndrome, the people that love them, the medical community and the population in general. Yesterday, September 3, 2013 was the long-awaited day of the airing of a documentary on Foreign Accent Syndrome that involved two of my best Foreign Accent Syndrome friends! It aired on BBC-One TV in the late evening in the World Time Zone 0 (England). Although it was available to be viewed on the BBC viewer in a few other countries, the United States was not one of them. 🙁

However, I was monitoring Twitter while my mates across the “Big Pond” were watching the documentary. Twitter was alive with postings about people hearing of Foreign Accent Syndrome for the first time. YES!! Praise the Lord! That is one of my dreams for a better world: people actually learn of something new to them so that they can show compassion in new ways. AND especially  for those  people with foreign accent syndrome (hereafter abbreviated PWFAS): when they see it being broadcast around the world in a professionally executed documentary, they suddenly realize they are not alone.

I learned today that BBC Documentary (God bless them) placed a full version of the documentary on YouTube — I will place a link at the end of this post.

I was so  excited the night before when I watched a video of a teaser clip from the documentary. I saw and heard my friends Sarah Colwill and Kay Russell both from different parts of England meeting up in a shop and talking a bit about some of the hassles  PWFAS endure every day.

First, let me tell you that Kay and Sarah are THE first two people I met on the internet who also have FAS. Therefore, these two ladies are very dear to my heart. I developed Foreign Accent Syndrome on May 11, 2009. I had enough medical experience to recognize what was happening was definitely NOT normal. Part of what I like to do to always keep learning and the web is a great instrument in not only learning facts, but also in connecting and networking. In fact I first connected with Sarah and Kay in 2010 after I saw Sarah looking like she was in a state of shock on a big national morning talkshow in the UK. The nasty remarks and cruelty they flung around, joking at her “chinese” accent, were devastating. She was on such a public viewing only ONE month after getting her FAS, yet the show had a doctor who talked intelligently to the audience about possible explanation of what was happening to her. I thought back to my journey with FAS at only one month in: “MAYBE this will just go away” and “it started suddenly, maybe one day I’ll just wake up and it will be over”. And as one month turned to two, the half year anniversary (we call them FAS-birthdays), then 1 year, then 2 . . . “nope; I seem to be stuck here.”

Instead of getting mired down in trauma of being so drastically altered as to speak as if I were a foreigner and the many different ways that people interact with me as a result; I was emboldened through growth in my faith in God with compassion to stand up for the misunderstood, seek out the hurting and ofter comfort and understanding however I can.  At my core is this >>> Truth matters! How people treat other people, especially suffering people, matters! Doctors, so-called “friends” and even family who don’t know how to diagnose it, show compassion or just brush someone off are not good caretakers. People with Foreign Accent Syndrome may sound drastically different, but we are still the same people deep inside. How would YOU feel if it were YOU? It could be, you know, because there were no warning signs given to any of us… just BAM! “this is your new voice”. YIKES!

HOW WHOULD YOU FEEL?

How would you feel when your best friend calls you on the phone and then says “Oh, sorry; wrong number” and directly hangs up on you? Of course they call you back seconds later? HOW would YOU explain it?  And what about the numerous times people raise an eyebrow at you as a “foreigner” or say “why don’t you go back to your homeland or learn to speak properly. They flat out call you stupid! They accuse you of such things as being lazy: “you could fix it if you wanted to.” There’s that horrible moment when someone you know well stands there with slack jaws after they’ve heard you speak in your “new” voice. They can’t figure out why you are talking that way. Is she in a play, been visiting or living abroad? It really is sad when total strangers treat you better (because they just assume you are a foreigner) than people who have known you for years (they just can’t believe their ears).  It is DRASTIC and LIFE-ALTERING!!

SUPPORT & UNDERSTANDING: DOWN WITH IGNORANCE & FEAR

I  realized that the primary reason so much of this was happening (misunderstanding, poor treatment of legitimate sufferers, and proliferation of MISinformation about FAS) was because of IGNORANCE and FEAR!  Well, knowledge and wisdom is the cure for ignorance and “perfect love casts out fear” (from the Holy Bible). So my passion was flamed way back in 2010. I started friending anyone I could find who also had FAS. Since then I started the Foreign Accent Syndrome Awareness FaceBook group where anyone can learn more about FAS and are invited to join the group to legitimately and respectfully ask questions, give opinions or experiences with FAS. Here is the link.

There is also a private group with PWFAS from around the world. There are now over sixty people there, with a majority of them sufferers or a supporter on behalf of another. The group is PRIVATE because it allows a safe place for those of us sufferers to “let our guard down” and be real without fear of injury. These two places and Twitter as well as various leads from other people have helped my FAS-Family meet and help others. Now THAT is rewarding! It gives great purpose to my suffering when I hear a new sufferer break down in tears to hear my voice across the phone or Skype because they can hear me validate them and help them feel that they are not alone. Similarly in my various writings on the web, I can die happy knowing that I am doing my best to stand up for the lowly, help educate the educators through my experiences. What makes a “specialist” a specialist! Sure, book knowledge and background knowledge help, but is it not time of actually experiencing things, living it, breathing it and learning from it what helps make a person a true “specialist”.

One of the things that I enjoy about Professor Nick Miller is that he actually involves the PWFAS in the research process while at the same time sharing his ever increasing knowledge with them to help them better manage their lives. It is a dream of mine to be able to be in partnership with his kind. However, he is in England and I in the United States where it seems to be much harder to locate people who want to research such a rare disorder.

Since the invention of the world wide web I have been so blessed . . . I can get up to the minute information. Like a good discount store, there is trash in the pile of bargains of information… but… if you know where to look and HOW to look there are great gems scattered everywhere. So I guess you’d say I am a research treasure hunter when it comes to useful information. It’s like putting a jigsaw puzzle together when I do research; a piece here, a piece there and soon I have an assembly of information that is quite helpful in finding similarities and patterns or possible causes or treatments. Of course, it is important to use reputable sources, but I highly value the personal experiences of not only the doctors who have book knowledge, but especially seek out “experiential” knowledge. Society as a whole places great value on a doctor’s opinion (as should be), however, the best doctors are those who admit they don’t know but will work WITH the patient to learn TOGETHER!!!

Cutting edge technologies have greatly enhanced my understanding of a variety of topics. However, this topic, Foreign Accent Syndrome is not just a curiosity; it is MY LIFE! I am on a mission to use my own experiences plus all that I continue to learn to help comfort, build-up, encourage, and educate others. Whether they be a sufferer, a family member, a doctor or a student, a seeker or a skeptic — whatever. We all have different ways of dealing with the bizarre and unknown. However, to those who inundate the web with MISinformation or scoff at those brave enough to step out into the public eye, I say “shame on you”. That is nothing short of cruelty! They prove themselves fools who speak without knowledge or refute what they do not understand.

WHAT IS FOREIGN ACCENT SYNDROME?

It is rare (less than 100 medically reported/documented cases in the WORLD… EVER! The altered speech is perceived by others as being foreign; sounding like the person had come from a different country or part of the country in which the language or dialect is of a different flavor. It does not mean that the person suddenly can fluently speak or understand a foreign language, only that the sufferer “sounds” as if they are foreign due to prosody, inflections, accent, and other aspects of speech production. The sufferers themselves may or may not “hear” the difference in their own head enough to help with speech therapy. A person’s speech is altered drastically after some kind of injury to the brain (stroke, past concussion, migraine, whether recent or in the distant past, or maybe for some yet unknown reason. The damage may not be seen via traditional scans such as CT, MRI, EEGs or Xrays, Yet there have been more detailed viewings via Difusion-Tensor MRI (DTMRI) or Functional MRI’s (fMRI) HAVE shown damage at the nerve level that did not show up on the more frequently utilized brain imaging techniques. However, since these machines are so very expensive there are not many places that perform the scans and insurance doesn’t cover their use. Oh, and one more thing, many people on Twitter proliferate the falsehood that Foreign Accent Syndrome is a Psychological or Mental disorder. The truth is that FAS is a “neurological” disorder. This is a very important thing to correct if you see it. I have written to the writers of the articles that falsely stated this, but no retractions or corrections were made to my knowledge so the MISinformation continues. It’s up to those of us who care for truth to correct when we see it in order to promote true understanding.

PURPOSE

I have a PURPOSE in having such a rare thing as Foreign Accent Syndrome. Namely: I must tell everyone, Foreign Accent Syndrome IS REAL!

Being such a rare thing means that more people haven’t heard of it than have. And that includes “specialists” such as neurologists, hospital ER staff, family doctors, psychologists, clergy, college professors, etc. ###You can quote me on this: “Just because you have never heard of something before or can’t see it or have no experience with it, does NOT mean it doesn’t exist!!” Every inventor, great scientist, and the wisest of students and educators as well as cutting edge researchers have learned: the greatest thing about “knowing” something is to realize we can’t ever know it all!

Given my background, my talents, and my years with this rare disorder, I am always increasing in understanding more and more about it. I believe that my passion has always been communication, artistic and interpersonal: caretaking people or animals, science, especially physiological and  behavior, God-loving, nature-admiring, art, poetry, music, photography, film, — all of that.  I have learned how to use all of these skills in the New Media I now see how God allows me to use all of that to help others and it is humbling and exhilarating at the same time.

WHAT NOW?

I would like to encourage you to read more on my site here about Foreign Accent Syndrome? I am going to go forward with creating a site specifically for Foreign Accent Syndrome that can act as an aggregate depository and interactive location for anyone around the world, but in the meantime you can just type FAS in the search box above and see several postings specific to reports of living with it, thoughts, experiences, etc. as well as links to other media. I would really like to work with scientific research and especially as the field of neuroscience is growing. I am encouraged by our U.S. President Obama’s announcement this year of “The Brain Project” in which the government is encouraging more study in the area of brain function and dysfunction. I do hope to be included in a reputable research program and especially have them to view me with fMRI to see how my brain functions when talking versus singing. (I am able to sing in my normal voice).  It is invigorating to connect with other people who are passionate about helping others. I pray that God will grant you the joy of knowing you are unique, no other person can be you as well as you!

Love others as you wish to be loved. Correct lies. Promote truth and compassion. Enjoy living in whatever your circumstances with the sense of purpose. It is a great way to live!

PLEASE DO LEAVE A COMMENT BELOW… it really helps me to know what others think about what I write here. And if there is anything I can do to help you along your journey, just ask. All legitimate inquiries will be answered.

Finally, here is the link to the GREAT Documentary on Foreign Accent Syndrome that just came out called The Woman Who Woke Up Japanese:

Foreign Accent Speech Changes with Video

On May 12th of 2012, I am celebrating the anniversary of a milestone in my life, namely just completing my third year with Foreign Accent Syndrome. It was such a dramatic change in my life that I am thankful I have some audio/video captured to show a bit of the journey for the sake of medical documentation as well as public information.

For those who have not heard my “old” voice (a.k.a. “normal voice”, “real” or “original” voice) here are a couple of pieces wherein I am being interviewed, and another where I am the interviewer as well as much more normal speech patterns.

February 3, 2007 –Before foreign accent: This is a video of me being interviewed after giving a seminar on using new media tool of Flickr and tagging photographs for better communication across the world wide web.

 

May 24,2008 — Here I am both interviewing AND filming a piece about a local ministry that accurately reflects my normal speech BEFORE I got Foreign Accent Syndrome:

THEN IT HAPPENED — MAY 12, 2009 — FOREIGN ACCENT SYNDROME changes my speech and a big part of me is gone!

May 26, 2009 — 2 weeks – my first radio interview in which I actually tell about how I got it and with my brand new voice!  http://ellen5e.com/wp-content/uploads/2009/05/wibcinterview090526.mov

June 15, 2009 — 1 month after onset of Foreign Accent Syndrome: here I had an impromptu meet-up with Fishers Fran who occasionally has “bouts of Foreign Accented Speech” when she goes through multiple sclerosis type symptoms. She coined the phrase “flipping” for those times when she goes through it. Most of the time she is normal speaking. She found me via the Indianapolis radio station where I was routinely interviewed.

The June 19,2009 (1 month) video greeting is glued to the top of my Ellen5e.com web site.

 

November 12, 2009 –6 months after onset:

 

May 13, 2010 — at the One Year Mark with Foreign Accent Syndrome:

 

November 13, 2010 — One and a half years with FAS:

 

November 20, 2011 — Two and a half years with FAS (I am behind the camera asking the questions):

 

This is a pretty good library of audio/video documentation for now. I shall have to record some newer material for my actual “FAS birthday”. So you’ll just have to check back later.

I know that part of it is getting more comfortable with unusual sound and speech patterns as well as my avoiding using those words that I know are my “bad” words. Those being the particularly heavy accented or hard to pronounce words that stop a listener from hearing what I am trying to say because they are so hung up on its sound that they are busy figuring out from what country I originate.

In the meantime, I would greatly appreciate your observations about what you think of this bizarre Foreign Accent Syndrome. How would you describe my speech? What language do you think dominates the accent? Do you notice a change over time?

Please allow me to thank you in advance for ANY observations you have. Because your unfiltered input helps me better gauge how the general population views those of us with such a rare condition that takes away a part of our identity by making us sound like someone else.