Showing posts with label Inspiration. Show all posts
Showing posts with label Inspiration. Show all posts

Sunday, November 24, 2019

(Video) Timeline: My Embouchure Dystonia Rehabilitation Over The Years

Time Stamps of Tests
0:04 - December 2011 - A year before this first clip, I couldn't get a sound out
2:15 - January 2012 - Tonguing Mid-to-High Register, Slowing Things Down
6:39 - August 2013 - Transitioning between Low and Middle Range Gap
10:43 - August 2014 - Downward Movement and Large Interval Control
12:18 - March 2016
13:11 - August 2017 - Fluidity in Slurs, Paced Arpeggios, Held Notes
17:09 - April 2018 - Crossing Multiple Registers, Descended Landings.
19:44 - August 2018 - Melodic Passages and Descending Landings
21:52 - January 2019 - Crossing Multiple Registers, Descending Landings, Ascending Landings, Dynamic Control, and Tongue Control
23:28 - May 2019 - Upper Register; Ascending Landings and Grasp, Stability in Dynamic/Sound
24:42 - September 2019 - Holding Out Notes; Testing Length of Grasp

By FAR one of the most embarrassing videos of my face....lots of closeups, while having dystonia over the span of several years, while aging, while rolling out of bed, while gaining and losing weight, while going into my mid-30's, and crazy life stuff in general.

Wanted to post this for those who have Embouchure Dystonia. Keep up your efforts...I know it may seem like a long journey, but you can do it! <3 I'm new to editing videos even though I post videos on my blog all the time ....so have patience, will get better over time with practice.

This is the first timeline video I've done of my playing....approx 30 minutes. Please understand, even though I'm comfortable with showing my playing because I feel it's important and for a good cause, it doesn't mean I'm not vulnerable.

There's a reason musicians don't show this disorder upfront and why it's rarely documented thoroughly as such. Auff! 📯💔 Feel free to share though! I hope to spread Musician Dystonia Awareness.

Thursday, November 21, 2019

Flautist Leslie Thompson: Determination to Continue Playing Music After Overcoming Car Accident


I love that they mention body mapping. Many music departments at universities are now offering courses or summer seminars in Alexander Technique, Feldenkrais, and Rolfing.

Happy to see a news article spreading awareness of musician injuries/disabilities, explaining how common injuries are, the importance of health education, and how adaptation is a key component in recovery (this also applies to dystonia).

Last, but not least, it's more than inspiring to see flautist Leslie Thompson share her journey of surviving a car accident and her determination to continue playing music.

She was fortunate to have Andree Martin as her professor during this time, who understands disabling setbacks all too well. Andree is not only trained as a body map clinician (Andovers Educator), but has recovered a great deal herself from focal hand dystonia and has a remarkable journey to share too.

Believe It's Possible

💕

Wednesday, November 20, 2019

Have No Fear and Embrace Life

"I am not afraid of difficulties. It is perhaps easier, and certainly safer, to follow a beaten path, but it is also dull, uninteresting and futile." --Dmitri Shostakovich

 

Friday, October 25, 2019

Philip Smith: On Upbringing, Trumpet, and Focal Embouchure Dystonia


Thank you to Alison Pesacreta (my twin sister) for sharing this! I can't tell you how many recordings I had to listen to of Phil Smith while growing up because my sister started playing cornet in the 4th grade in 1993 and loved playing along with a tape cassette of duets where he played the bottom part on side 1 and the top part on side 2. This was way before his concert studies series or hymns...don't think they publish it anymore. She actually got him to autograph the music years later through a friend and he was surprised to see it. Anyways, from then on she listened to practically every recording he came out with and I continued hearing him throughout college on a daily basis as well. His sound definitely influenced her and I hear so much of his style in her playing.

That's why it was very saddening to hear of his diagnosis with Focal Embouchure Dystonia 5 years ago. He is a legend and one of the greatest of all time.

I wanted to share an excerpt from this interview where he speaks a little about his journey. I definitely can relate here as so many with FTSED do too.

He is correct when saying to be honest there is no easy or simple explanation of what causes focal dystonia. It doesn't only occur in musicians but other fields that require high levels of repetitive accuracy, repetitive practice, and refined skill over a long period of time.

It really does feel like it happens over night and as much as you try to re-trace your steps, nothing adds up. That's because it has to do with our brain signals/wiring....you just never see it coming or crashing, especially when you're at the top of your game.

Everyone wants a simple explanation, but those of us who have lived with it for more than 10 years or even 5 years will tell you it's not like some light bulb hasn't turned on or like we're missing the answer staring us in the face or like we haven't tried everything.

Just like trying to regain the ability to walk after a stroke, knowledge does not equal understanding. Knowing how to play your instrument like a pro does not help or mean you're immune. It's not a "mental issue" or "emotional issue" or "bad habit/lack of healthy playing issue" ....it's a loss of a highly refined motor skill/brain pathway. Knowing how to walk your whole life doesn't mean you understand how to walk after losing that ability, nor even grasp how much work rehabilitation is. Some do regain close to full control, while others recover to varying degrees, and some struggle with it severely, and you can't put a time limit on recovery. However, the new pathway dug is not as natural as the original.

Phil says: Four years ago, I got hit with it, and I basically couldn’t play a note. I have had to re-teach myself how to play over the last four years, and quite honestly it has been hell.

I wish I could say what triggered it, but I don’t know. I have had people say to me “I can’t believe that you lost your lip” or “I can’t believe you lost your nerve”, and it was neither of those things. Something happened that took what I knew and wiped it off the map.

I have had to re-teach myself what to do, and in some ways, I have needed to be more ‘fundamentally’ focused, and in other ways I have had to erase everything that I thought I knew as an experienced trumpet person and approach the instrument like I am 7 years old. That has been difficult!

Wednesday, June 19, 2019

DMRF Birthday Fundraiser

I probably should have shared this on my blog and on my facebook "Living with Embouchure Dystonia" page, but didn't have time. I'm happy though that despite my lack of marketing the small fundraiser, I was able to raise $57 dollars for the Dystonia Medical Research Foundation (DMRF). I know it's small, but it counts! I couldn't be happier. Hopefully next year I can help raise more! :) Thank you so much to those who helped out. Here's the original posting:

For my 35th birthday this year (been 10 years since diagnosed with Focal Embouchure Dystonia), I'm asking for donations to the Dystonia Medical Research Foundation. I've chosen this nonprofit because their mission means a lot to me, and I hope you'll consider contributing as a way to celebrate with me. Every little bit will help me reach my goal. I've included information about the Dystonia Medical Research Foundation below.

The mission of the DMRF is to advance research for more effective treatments and ultimately a cure for dystonia, to promote awareness and education and to support the well being of dystonia affected individuals and families.

Although Focal Dystonia affects a small percentage of musicians, there is a larger amount of general Dystonia cases which are more severe and degrade people's lives severely. It truly is a complex and debilitating neurological disorder that comes in many forms.

The DMRF also oversees the Musician's with Dystonia Foundation started by former professional horn player Glen Estrin and neurologist Dr. Steven Frucht.

Thank you for any support! 💜💙💜💙💜💙



Wednesday, February 14, 2018

Mantras

Just wanted to share my mantras in both Latin and English. These give me the greatest amount of inner strength no matter when or what I'm going through. I use them during meditation or when playing horn or in prayer. One of my biggest strengths is perseverance, and these mantras accurately reflect my mentality whenever encountering obstacles/life challenges. They resonate so well with me and I always keep them close to my heart. Happy Valentines day everyone, I hope these help your inner strength shine through as well.







Sunday, February 11, 2018

New Facebook Group and Forum for Musicians with Dystonia



Hi everyone! Just wanted to chime in and share 2 new groups/forums I created for musicians with dystonia on facebook! ....

  • Musicians with Focal Dystonia & Neurologist Sharing Knowledge and Resources
      ......This group is for Musicians with FD and Neurologists. The group is focused on scientific-based knowledge, resources, case-studies, and to share personal trial/error done through scientific method of documentation and observation. This is not an emotional group or a place to advertise; no tolerating emotional lashing out or soliciting of cures (or the source of FD) without proper documentation, publication, and that it can be successfully applied to all.

  • Musicians with Focal Dystonia Emotional Support Group
    ........This group is for Musicians with FD, and focuses on leaning on each other and connecting with others who share the same struggle of coping with this disorder. Here we share our progress, relapses, and personal journey.

    Hoping that these groups will provide additional support, connections, and resources! :-)

Monday, August 28, 2017

More Updates!

It's been a while since I've updated my blog! A lot has been happening so I'm mainly going to explain it all in photos!

First of all, I have posted a new video of my current horn playing on my facebook page Living with Embouchure Dystonia, and in the Focal Task Specific Embouchure Dystonia facebook group. You can see it here: https://www.facebook.com/embouchuredystonia/videos/1415994998449828/  . I filmed this at one of the music schools I teach at. I am warming up before my students arrive for the day.


I got to see an awesome friend, mentor, and professional horn player - Thomas Jostlein and his family again this summer! Like I've said in previous posts, I don't get to experience being in the horn playing world anymore since I'm not in an orchestra, and can't really speak to other horn players because I'm never around them. I can't explain how refreshing it is to speak to a horn player that doesn't look at me like an injured or diseased/cursed person, but instead still supports my success and boosts my confidence by reminding me that I can do it!...I can play and keep improving, and that what I am doing is good! Here are a few pictures from all the times we've got to catch up over the years.




 

I also got to meet Julie Landsman this year who is another huge inspiration to me. She said that she actually just recently donated to Dr. Itlis's Embouchure Dystonia research. It was great to hear her play with that beautiful gorgeous tone. Moved me and gave me so much inspiration.



I've started some artistic projects...check out all the drawings, wood stain art, wood burning art, and furniture refurbishing I've been up to:

















This news doesn't necessarily have to do with me. But I wanted to post a picture of my twin sister. She had the opportunity to meet up with her former trumpet section this last year. Here is a photo with her former trumpet section mates: Philip and Natalie Dungey from Seattle. I am so proud of her and miss her trumpet playing! Ally and her husband have a photography business called Sweet Dahlia Photography which you can check out here: https://www.facebook.com/SweetDahliaPhoto/?pnref=lhc . They are based in Washington state and her husband also manages a music store and lesson studio! :-)


Example of Ally and Mario's photography work! :-)

Finally, last but not least. I've started my private lesson teaching again, including several contracts with a handful of music schools around the metro area, so pretty much concentrating on doing it full-time this year and will see how it goes. I haven't completely given up teaching in public schools though...I also teach high brass at Douglas County High School/DC Downbeat band program a couple times a week!

I am looking forward to all the creative and artistic work I'm doing! Please keep sending positive energy our way. I will do my best to keep my blog updated, but am pretty busy!....until next time....happy 2017-2018! May everyone be blessed! :-)



Thursday, October 6, 2016

First Orchestra Concert in Six Years!

I had the honor of performing with the Longmont Symphony Orchestra in Colorado this last weekend. I took a risk and said yes to subbing for the 4th horn player, thinking that it would be doable with a couple easy pieces and one large more difficult piece.

But boy was I wrong about the programming! The concert included Pines of Rome, Enigma Variations, Daphnis & Chloe, and Strauss's Four Last Songs. There was transpositions in bass clef and old notation in some of the pieces and a tiny solo for 4th horn.

I had never been much of a low horn player, even before dystonia, I primarily held principal positions. It was too late to turn back now. Plus I had worked so hard and looked forward to such an opportunity for so long! I decided to prepare for it and hope for the best come rehearsal time. We only got two rehearsals and then the concert.

I was surprised that things went so well! I was so nervous about my dystonia kicking in during the long stretches of held notes throughout all of Strauss. I was scared that either spasms would violently through me off the notes (i.e. ending them abruptly), or I wouldn't have enough grasp on the notes to adjust my intonation if needed to (combined with using my right hand in the bell). But all the pieces turned out to be totally doable thanks to my mouthpiece that made things so much more comfortable.

I have been playing trumpet on a daily basis with my students. I have one class of literally 10 beginner trumpet players this year. For over a year now I've been having to play so many different instruments due to teaching; mainly flute, clarinet, oboe, trumpet, and trombone. On all of them I started out shaky, but my dystonia symptoms have receded a great deal over the year.

Trumpet is the one instrument I've spent the most amount of time playing. My dystonia symptoms are actually significantly less severe on trumpet than any of the other brass instruments. Luckily I own a french horn mouthpiece designed by a trumpet player (you can totally tell if you ever get the chance to look at it) and it looks like a trumpet mouthpiece almost. The rim is contoured like a trumpets, the body is funnel-shaped, but then it is a heavy and thick/dense mouthpiece. Probably as heavy as a trombone mouthpiece.

The feeling of the trumpet rim (it's A LOT of RIM!) on a horn mouthpiece has done a bit of sensory trick for me and my symptoms don't kick in as often. I can't play very much in the high range, but that's due to the mouthpiece and it's rim contour and thickness. However, my notes are stable.

Enough about my mouthpiece! Here are some photos from my first rehearsal. Both rehearsals and the concert went smoothly. I definitely needed that feeling of playing in an orchestra again. It was way over due. I took a risk because I knew I could do it, even if it took a lot of physical effort. I was very proud of how much progress I've made and that I'm able to perform even the slightest bit or every blue moon again. There have been so many days, months, and years missing playing with an orchestra, so even having the chance to relive it once again, just once, is a dream come true!




October Link of Interest: Observing Dystonia Blog by Andrée Martin

Andrée Martin, flute professor at Columbus State University, writes a blog called Observing Dystonia and documents her FTSHD (Focal Task-Specific Hand Dystonia) retraining. Recently Andree posted a blog I found interesting on progress through the use of dowels, which I posted below. She is actually trained in Alexander Technique and Feldenkrais (http://summerflute.org/andreemartin/) which both dwell in body-mapping techniques.

This was such a great read, and I'm very happy to see a professional musician sharing their journey through recovery!!! It gives many hope and comfort knowing they are not alone throughout their own obstacles in overcoming this disorder. Thank you Andree!

Sunday, June 26, 2016

Milestones: Played Horn in A Group for the First Time in Six Years!


A few months ago I received a message from a former UNI (Iowa) classmate of mine named Michael Conrad. He is the current Graduate Jazz Teaching Assistant at UNC (Colorado)...which is one of the schools I attended in my undergraduate studies. He had asked me to sub for the horn player in the UNC Jazz group he works with. 

At first I was a bit hesitant, but remembered how much I loved playing his compositions in my undergrad. Since then he's gone on to win numerous awards for his compositions. I informed him that I still was coping with dystonia and could play as long as it wasn't anything too crazy. He sent me PDF's of all the music to check and I told him it all looked doable, so I went ahead and took a huge step/leap of faith and drove up to Greeley to rehearse with them. 


I have to say it was one of the best experiences and decisions I've made this year! I was both excited and scared. But if anything, it proved that I have come a long ways with my embouchure dystonia, and that I must not ever give up. Right around the same time I received the news that I was selected as a participant in a research study on FTSED. Going to this rehearsal made me even more ecstatic for the upcoming research. 


I'm grateful to Michael for thinking of me even though I had not played the horn in a group since 2010, and for putting so much trust in my playing...even if it was just a rehearsal...I wanted to put my best foot forward. I also was very happy to see a former classmate at a former school I attended...it brought up a lot of memories and nostalgia from my horn playing days. Which is always an amazing feeling to remember!

Oboist Alex Klein Returns to the Chicago Symphony Orchestra After Battling Hand Dystonia


It was so wonderful seeing some good news for once lately! Today I opened my browser to find news articles posted on Alex Klein returning to the CSO after stepping down in 1995 due to Focal Hand Dystonia. Here is the Chicago Classical Review Article over his new appointment in the orchestra! Congratulations Alex! This news brings so many of us hope and happiness. 

Friday, July 31, 2015

Psychological Aspects of Recovery: Mental and Emotional Obstacles Faced with Musician's Dystonia (FTSED and FTSHD).


In the past I would have refrained from writing about this area of recovery because of the tendency of others to immediately hop on the psychological bandwagon belief that Musician's Dystonia is simply an underlying psychological or emotional disorder. As I have stated throughout many of my writings that I do not support that belief whatsoever, nor do I believe it is the true cause of this neurological disorder. That is not to say that there is no psychological effect involved that must be addressed.

It is what I consider one of the 3 major stages of rehabilitation; (1) Educating oneself on the disorder, treatments, rehabilitation methods, other related injuries/areas, the body (movement and anatomy), and literally anything involving musician's health. (2) retraining the mind (psychological cognitive restructuring). (3) Rebuilding Neuro-pathways (Physical Rehabilitation). 

These are my own opinions. However, it is safe to say that without a doubt anyone who has been marked with a major physical setback or injury naturally inherits emotional hurdles afterwards. As it takes a huge blow to ones self worth, it leaves us with doubts in our capabilities, dislike in our concept of sound, we start to over-analyze out of pure confusion and trying to fix what is going wrong with technique, and it leaves us overwhelmed and lost in the stages of grief. Sometimes we don't even realize that we are in grief or are in denial of it.

It is best to address the psychological aspects first and foremost before any musician tries to start physically rehabilitating. I believe they should be in a healthy frame of mind and emotionally stable. Many musicians who are hit with this disorder panic and want answers right away. They are very confused and don't want to accept the current state they are in. The only problem is that part of the answer IS embracing the current state. Mind you that embracing a temporary state/setback does not mean it defines you or that you're giving up. The disorder does not define who you are or who you will be. There is a difference.

Being diagnosed with what is considered a career-ending disorder is scary and devastating. It is hard to see the silver lining when it seems there are vague answers and not just one solution to overcoming it. It takes a great deal of courage and optimism to look at it in positive light, and no one is ready to do that until they've allowed themselves to grieve and face the possibility of their worst fears.

But I look at it as facing ones fears and saying, "Even though I believe I will beat this disorder, I'm not scared of the worst that could happen because here are the good things that can come out of it...." It's like facing your fear in order to overcome it. Once you experience it, it no longer holds a death grip on you.

I can already hear my musician friends saying, "What good could come out of this awful situation?" In order to come to that point, you have to go through the stages of grief. You must cry over the misfortune, get angry, yell, curse others, become bitter if you have to, go through highs and lows, desperately ask for help, ask "why me?"...whatever it takes to heal no matter how bad it feels. But then there comes a time where you do feel you have a choice; you can continue mourning or build up the courage and say, "I'm tired of being sad. I'm tired of hating the way I sound due to the spasms. I'm tired of fearing my instrument, being frustrated, confused, fearing the worst, and living like this in misery." Then you find the strength to fight. Once you are ready, there is a lot you must change about the way you think, and in a big picture type of way...


  • The first and most important thing I have found is learning to separate your worth from the instrument and center yourself.
We are gifted with the love of (sharing) music. It initially started off as a feeling and transferred to an instrument that resonated with us personally. Yet this gift of the love of music is still with us, even if we can not play for the time being. The instrument does not define who we are or our gift, just like our disorder does not. We must believe that our knowledge of music and passion is meant to be shared, that all we've done in the field is not for nothing. Being gifted with music means we have the choice to share it in more ways than just one. Focusing on another area of music or field/activity that reminds us of that love surprisingly allows us to still remain connected to the gift. It may not give us as "full" of a feeling as we had before, but it can as time goes by and we find our confidence returning in something music or non-music related that we didn't know we had a talent for.

Having Dystonia allows us to focus on other areas of our lives that we didn't get to do while focused on performance. We have more time to build relationships, explore new areas, work on our health, study something we never got a chance to do.  Some are too afraid to try to live again, to seek out something similar out of fear that it won't be the same.

We are literally brought back to the major question of "Why do we love our instrument so much? and where do our priorities fall? It also makes us question what is success? Did we love our success more than the music? Dystonia really grounds us and brings us back to why we love music. Success and failure are one and the same. There are no rewards/praise for success. The reward we found in music when younger was that feeling of exploration. We could make a million mistakes and still love the way we sounded. Yet the more advanced you become you lose that sense of exploration, creativity, curiousity, and unconditional love and acceptance of how one sounds.

  • That leads me to the second thing. You must embrace the way you sound and love it.
I am dead serious when I say it is vital that you revert back to that childhood state of mind in order to embrace your dystonia. Dystonia must be confronted with that same feeling of exploration, curiosity, and unconditional love and acceptance of how one sounds.



Seeing other people play music, even small children, reminds me of what a tremendous blessing music is in this world. It's meant to be used as a form of expression whether or not it sounds good or bad...it has meaning and that is all that matters. Technique no longer matters, all the blabbering about breathing, hitting the notes, using articulation, etc. All that matters is embracing the love of music and letting go of the ego, the success, or judgement, and really appreciating what a gift it is to have music in the world. I imagine my feeling is similar to that of someone who has lost one of their senses like sight or hearing. We don't realize how truly miraculous something is until it is gone. We appreciate it more, aim to protect it, and love it in a way that is no longer criticizing, demanding, or taking it for granted as we did before.

I'm serious when I say I absolutely love hearing beginning band students play.
I believe that is the kind of love it takes; to embrace music with no judgement, or at least an appreciation for it that is much deeper than before.

  • Third. Shift your focus from the performance mentality to relaxed awareness. 


I learned to not fight my symptoms or judge them, but to let them happen and just relax into a state of awareness. (ex. "I'm noticing that it's easier to grab an F than a G, and the angle of my mouthpiece made a difference today"). That way you are focused more on feeling things out than fixing things with technique or judging the way you sound. Your body knows what to do and is trying to tell you something, so listen to it and get to know the symptoms well. I started taking an inventory of my symptoms and recording myself. The more I played with an open, loving, and aware mind, the more I discovered and adjusted my playing over time and saw improvement.

Performance mentality focuses on analyzing technique, physical agility, skills and accuracy. Relaxed awareness is what is needed instead. Focusing on embracing the symptoms, getting to know when they happen, looking at them with curiosity, exploring ways to lessen them through adjustments and modifications.It seems pretty simplistic and basic, but it works if you have patience and don't rush the process of recovery.

Though this may sound odd, there are some other things I did to help embrace my dystonia sound; telling my horn thank you and that I loved it no matter how it sounded, recording myself and listening to it with love, sympathy, and curiosity. Also practicing mantras, visualizations, building self-esteem, and treating myself like a survivor and not a victim were other major factors in changing my state of mind. Also farther down the road I liked listening to recordings of the horn before I fell asleep and visualized that my playing felt just as smooth and effortless. Pretty soon I started having vivid dreams about playing easily and this boosted my energy and happiness the more it occurred.

I started off practicing in a practice room with a piece of paper over the window. As I got more comfortable with accepting my sound, I removed the paper. Eventually I moved into a larger classroom, and then a stage. I adapted myself so that I did not fear the way I sounded in front of others. Whenever the thought that someone might be judging me popped up I would tell myself, "They are not judging me, I must be judging myself harshly to assume so. Even if they are, they do not know what they are doing. If they are, I feel sorry that they have been brainwashed to look down so shallowly on the act of making music which is a beautiful thing. I must remember I am now at a higher state of mind than what I had before and I love the way I sound no matter what. I must let go of the inner critic. I love myself. I love my sound. I accept it."

  • This leads me to the fourth thing that I have learned. It is important to surround yourself with people and environments that help promote a healthy state of mind.
Teaching beginning band students helped me a lot, and this is actually why I'm going into teaching. I love working with students who are just starting to learn music because that is when I most clearly see the importance of music. In a way it is living my life up to my ultimate rule...that it's always about the expression of music and imagination more than anything else. It is similar to developing strong morals and values and sticking to them, living them, breathing them, becoming them.

My students never judged the way I sounded and instead thought it was the best thing on earth. It reminded me of how children are much more centered (mentally and emotionally) than adults can be. They are in that state of daydreaming and imagination all the time. I am happy to influence them in a positive way and help them find balance in not only their abilities, but way of thinking/approach too. It was much healthier for me to be around children with this state of mind than performing in a group full of adults that are way too hard on themselves and others.

Many Dystonic musicians who talk to me usually ask me how I feel about playing in a group. They hate it when I tell them that I am against people playing in an ensemble of high caliber or even of musicians that would not understand what they are going through. I think it is important at the beginning of rehabilitation to focus on yourself and spend time playing alone and not aggravating things. Later on as playing gets better, then maybe if psychologically prepared for it, but playing in a group can add even more anxiety, pressure, demands, fear, frustration, and stress that you already deal with when facing the dystonia symptoms; not knowing if things will come out correctly, or if you'll be able to play a passage, etc. Live concerts are the worst because it adds in adrenaline, and the adrenaline heightens the dystonic symptoms just like loud noise heightens or triggers a migraine. It's best to remove oneself from anything that worsens the symptoms for the time being.

Instead, surround yourself with a network of people who understand; whether it be the musician's dystonia group on facebook, write or visit with other musicians from the group or who you've come across online with dystonia, lean on a supportive teacher/mentor, etc. If you feel comfortable with talking to me, then by all means call me or message me if you need to. It's the least I can do for others.

If can, speak out about your dystonia. It is oddly relieving. Not everyone is comfortable with that, but for me it is a way of healing. Knowing that I am informing others (non-dystonic people) about this disorder that is rarely spoken of, makes me feel like I'm not wallowing in pain while keeping my mouth shut. I want others to know so that some day others who are in the same boat won't feel as alone or outcast. Yet, I always speak positively of it; never victimizing myself, but instead aim to promote awareness and understanding of the disorder.

I know this is not how everyone feels, but I believe that my dystonia was meant to happen for a reason. I may not understand the reason, but I choose to believe that it is because I am strong enough to handle it and navigate the tremendous loss, and that I am to help others and promote awareness about this disorder. I believe that what I'm experiencing is unique and it is rare to see anyone share their experiences about this disorder, so it must be done for the sake of healing and helping. I see a lot of injured musicians do this, and it makes me happy to see them channeling their love and support to others in need before themselves. This leads me to the importance of belief or hope....
  • Last, but not least. Do your best to find the silver lining and say it out loud.
Physical rehabilitation tests your patience unlike any other. There are many days where you will get better, then relapse. There are many days where one adjustment might work and the next not. There are even more days where you just plain sink into depression again. The wound from losing what you love never truly goes away. It is not easy to stay optimistic about it all the time, and I don't suggest that anyone avoid their emotions; whether it be sad, angry, happy, excited, etc. It is important to go through the motions and let whatever you feel happen so that you can heal.

Creating some strong beliefs in yourself and your recovery will carry you further and support you when things get tough. When you are able to find the silver lining...even if it's not something you necessarily completely 100% believe yet...say it out loud no matter what. It could be something as simple as, "Maybe not today. But tomorrow." or "Can't have progress without some relapses." I always say it out loud, whisper it, or say it to myself in a mirror because it somehow feels more grounded and reassuring. I know I sound crazy for doing such things, but it makes a difference and that is all that matters. Whatever gives you strength, believe in it and hold onto it....not matter how ridiculous it may seem, look, or sound to others.

The psychological aspects of recovery are a huge obstacle to overcome! It is probably the most difficult part of rehabilitation. I see these psychological aspects as a very heavy fog that blinds us from the physical obstacles beyond that. Once the fog is lifted you can focus on the dystonic symptoms and alleviate them through physical therapy and rebuilding the neuro-pathways slowly over time. But first and foremost you have to be willing to embrace what is right in front of you and keep tremendous patience. Not everyone is ready to do that or needs help with it. Some good options to help find what centers you is meditation, hypnosis, or it could be something spiritual or religious like going to church, it could even be helping others...whatever allows you to reflect inwards and face the grief at your own pace and allows you to think about a meaningful purpose of this experience. The good news is that you will see progress without a doubt, and time really does heal both the mind, body, and soul.

Thursday, July 23, 2015

Good Times: Friends, Horn Players, Traveling, and TENS unit therapy!

I've had a busier month than expected! A lot of great blessings despite several car problems. I currently work in Denver while living in Boulder. It's quite the commute, but I don't mind since I love driving long-distance. However, my car has broken down three times in the last month....let's just leave it at that and hope the terrible 3's are finally over. I'm so thankful for the many friends and family that have helped out throughout that stress-ball.

Back to the positive stuff! A fellow FTSED musician lent me their TENS unit to use! My neuromuscular dentist wanted me to undergo several sessions of using the TENS unit since it showed signs of improvement, yet I couldn't afford it. I'm literally a broke college student again. Boy am I grateful for this generous person to let me borrow their unit!!! It's helped tremendously. I'm already experiencing less pain. Even when the pain does happen it goes away quicker. I just have to make sure that I keep up the ice/heat packing and the TENS unit consistently especially after practicing.

They lent me four electric pads, so I've been using it on my face and my back shoulder and neck. My jaw is popping less, but still just enough to keep me worried. However, I have to say that my jaw feels more sticky in a good way...before I felt like it would pop or crack so easily by the slightest touch, and now it doesn't feel as loose or crackly or off. It's weird, the more I use the TENS unit along the line of my shoulder blade in my back, the more relieved I feel.



Another risk I'm taking is bringing back slight playing into my daily activities. My friend Thomas Jostlein the associate principal of the St. Louis Symphony is here in Boulder for the CMF festival and wanted to see where I was at playing-wise with my disorder. I'm VERY picky about who I play for because it requires a deeper understanding of the complexity of what I'm dealing with (a combination of injuries and disorder), and also an unorthodox approach vs standard lesson approach when giving advice or suggestions. But I trust him as a mentor.

The best thing is that I feel like I've contacted my inner horn geek again...which I've missed a lot! hahaha! It's therapeutic in a way feeling like I'm included in the horn playing world even if it's just talking to another horn player. Even better, one who isn't afraid of my disorder and is genuinely interested.

Many years ago when starting my (horn performance) grad school audition process by visiting campuses, the University of Illinois (Champagne-Urbana) was on my scheduled list. After visiting Thomas, I realized I favored his horn pedagogy and approach to music best out of any other schools, so U of IL became my top choice for schools to apply for. I liked that he wasn't like other typical professors; lost in technique or standard methods of solving playing issues, nor taught by the textbook....he had a unique and innovative approach due to his former teacher, Arnold Jacobs' influence. However, grad school on horn never happened due to my injury and then disorder. However, I consider him one of the best horn players of our time (if you haven't heard him, you need to...he really needs to make a solo recording), so it means a lot knowing he believes that I'll make a full recovery and has been supportive of all the hard work I've done to rehabilitate.

 I also had some of my closest friends in Colorado this summer! I went and visited my friend James at the Aspen music festival. He use to play principal clarinet in the orchestra I was in, and we played in a woodwind quintet together. My best friend Lizzie, also from my undergrad, visited me in Denver. She's working on promoting her artwork and trying to make it as a solo artist. I know she will because she has such a diverse set of skills!



For the first time in MANY years I felt complete....like myself again. Just being around people who get me, who have known me throughout my music endeavors and all the challenges, changes, and growth in life...it brought me a sense of relief being around what feels like family. My friends are family...even if I'm not the best at keeping up, I would do anything for the few close friends I have. Even my own family (except my twin sister) hasn't attended any of my concerts, recitals, performances, or tours after I left high school.

Music has always provided the family, support, and sense of purpose I strived for and needed. Even if I could play, it wouldn't mean as much if I didn't have others to share my pursuit of music with. I miss performing with friends, people that I love, and sharing good memories. No, the performance world is not always pretty, there can be drama, but in the end when I look back, it's my friends I miss the most. I proudly watch them grow into professional musicians, already establishing their names and professions. And while I wish I could share in the same things, I can't complain too much....it brings me tremendous joy seeing them shine and accomplish their dreams.

On a completely different note and change of subject, I'm in a committed relationship; something that is a huge milestone. It's taken a lot of courage on my part, but so far I feel like my heart has healed a lot and I'm ready to see the world through a more positive lens again and embrace whatever comes my way without fear.

I'm still learning how to let go of control and to not fear the worst, but I've come a long ways since then. In a way I felt like all these wonderful reunions with musicians I admire and friends I care deeply about, was a gift from God as a reminder of who I am, that everything that's happened in the past, all that I've accomplished, the gift of music I was given....it wasn't all for nothing, and it really did happen. I really could play. Just when I thought the former me was dead and gone, I was reminded that passion and fire inside is still alive. I just needed a jolt to wake me up again. I honestly haven't felt this alive in a very long time, and I'm grateful for it. I can daydream about the future and look forward to every day with the faith that my talent and skills will serve a purpose again.