Speech therapy experiences
Hello,
My name is Tate Smith, and I am a graduate student studying Speech-Language Pathology (SLP). If you have been in speech therapy, I would love to know more about your experience. Did you enjoy your SLP/SLPA? Did they make a difference in your perspectives or personal goals in the realm of communication? Why or why not?
Thank you!
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Thank you for these excellent questions, Tate!
For me, an attempted response would be complicated and lengthy, since I have gone through SO MANY therapies, of different types, and with different kinds of results. These also led to differences in perspectives and personal speaking goals over the years (and decades).
But I will attempt a summary. Please be patient, as it will necessarily be a long read. Hopefully, you and other readers will find this account to be helpful.
I began stuttering at about age 3, and began to have speech therapy at about age 4.
From about age 4 to age 23 (late 1950’s to late 1970’s), I had at least some therapy at each age. Then later, I had fluency shaping therapy and refreshers periodically through most of my 30’s (mid-1980’s to early 1990’s).
I estimate I saw about 35 therapists for stuttering during the periods above. Of that number, I count 7 as being significantly helpful. And of those 7, there were 4 who were very helpful
All the therapy I had during my childhood, before age 17, was totally useless. To be fair, knowledge and therapeutic understanding of stuttering back then (55-65+ years ago) was much less than it is today. Most of my childhood stuttering therapy consisted of either talking about various aspects of my life, or practicing articulation (which was not my problem at all – stuttering is a fluency disorder, not an articulation disorder). The therapists really did not understand the problem of stuttering.
At the age of 17, I had the first helpful therapy of my life, in which I learned pullout techniques – and those very much reduced the length of my blocks (which had been measured up to 45 seconds), though not the frequency of blocking (which occurred on most words).
During my first three years of college, I had therapy from a speech pathology professor who stuttered himself. He tried traditional approaches with me – reducing avoidances and secondary symptoms, and trying to reduce my speech anxieties. This didn’t help my speech at all.
BUT this therapy did very much improve my social life, as under his guidance, I began talking with many fellow students on my college campus, regardless of how severe my stuttering happened to be. I quickly made many friends who – to my great surprise – didn’t care at all how disfluent I was.
Because of how he helped me develop my social life, I count him as one of my very helpful therapists.
My next therapy was a mysterious one, based on an experimental approach of successfully responding to commands to be fluent – beginning with single words, then advancing to sentences, paragraphs, and increasing periods of time (for example, “for the remainder of this therapy session”). Soon I was fluent for entire therapy sessions, and this expanded into my everyday life, as I learned to give myself commands to be fluent.
I began to experience a sensation of being enclosed into fluency bubbles (“fluency feelings”, I called them), perhaps a form of self-hypnosis. I was experiencing the first fluency of my entire life at age 21 (I remember my first fluent phone call, for example, in November 1975.) During a “fluency feeling”, I felt completely immune to disfluency.
Soon I reached a point of fluency in about a third of all my situations, and improved speech in another third of my situations.
For the first time in my life, I learned that I could indeed sometimes talk fluently.
But eventually that all collapsed. About a half-year after it began, there were no more fluency feelings, and I could no longer get fluency by self-command.
I next tried a behavioral therapy program at the University of Chicago (where I was then a grad student), run by the psychology department, and developed by Dr. Israel Goldiamond (now deceased). The premise behind this program was that one stutters because one “gets something out of it”, i.e., that one receives some hidden advantages from stuttering. The idea seemed like total nonsense to me; but since they claimed a 98% cure rate and I was desperate for help, I tried it. They taught a simple technique inside the clinic (based on breathing and phrasing), and I managed to speak fluently inside the clinic. But I could not apply it in the outside world. My clinician (a psychology grad student – I never actually met Dr. Goldiamond) spent hours with me, trying to figure out what (alleged) hidden advantages I was receiving from (allegedly) “not choosing” to use their technique in the outside world.
Total BS. I knew I wasn’t “choosing” to be disfluent, and wasn’t receiving any advantages from stuttering. I just couldn’t apply their simple technique, that’s all – my speech stresses were too great.
In the end, they told me I was among the 2% who had failed their program. (In retrospect, I don’t believe their statistics.) That damn program cost a huge amount of money, a total waste.
My next therapy was the famous airflow program of Dr. Martin Schwartz (now deceased), a speech scientist who had offices in Manhattan
His therapy was a relaxing airflow, with thoughts only on the flow while inhaling; then a little sigh at the top of the exhalation, followed by speech and a stretch of the first syllable. There were two others taking the week-long therapy at the same time I was (back in 1977 when I was 23). I was quite severe in my stuttering, and one of the other clients was even more severe than I was. But within a few minutes, we were all speaking fluently using Dr. Schwartz’s technique.
I could use the technique inside the clinic. The other two also found success with using the technique in talking with strangers, store clerks, and waiters in Manhattan. But not me. I could only use the technique inside the clinic.
After returning home to Massachusetts, I practiced intensively, an hour or more each day. Finally the technique started to come together for me, and soon I could use the technique successfully in more and more situations.
I soon resumed grad study in Chicago, and continued to make progress. Pretty soon I was fluent in about a third of my situations.
Then speech disaster struck. A young uncle of mine passed away from cancer, and I rushed back to Massachusetts for the funeral. My speech completely fell to pieces, worse than it had been before I began Schwartz therapy.
Despite many efforts over the coming months, I could not get back my previous successes with Schwartz airflow.
Frustrated with the whole therapy scene, I didn’t have any therapy at all for the next seven years – until age 30.
Then in 1984, I became involved with the program in which I found the most success, the Precision Fluency Shaping Program (PFSP – later called the Hollins Fluency System), devised by Dr. Ronald Webster at the Hollins Communications Research Institute (HCRI) in Roanoke, Virginia.
(Neither the therapy program nor the institute is still around.)
It was a three-week intensive program (later shortened to 12 days), which trained clients in the use of a relaxing diaphragmatic breathing technique, gentle onsets, a loudness contour through syllables, and stabilizing articulators through slight stretching of the first vocalized sound in each syllable. The technique is complex, and is learned in stages – first with 2-second-long syllables, then with speech gradually speeded up until one is speaking at a slow-normal rate (or in Hollins terminology, slow-normal syllable durations).
I learned the technique very well, and could apply it successfully inside the clinic. Most of the others taking the program at the same time I did went home after three weeks speaking fluently in all situations.
Not me. As in several previous therapies, I couldn’t immediately apply the technique in the outside world.
But after coming home, I practiced really intensively, an hour or more each day. And there was gradual improvement. I was speaking fluently in more and more situations.
Finally – after three months of intensive practice – I reached my ultimate goal!
I WAS FLUENT EVERYWHERE!
It was a dream come true!!
I thought I was totally cured! WOW!!
I remained fluent for many months. I reduced my daily practice, thinking it wasn’t as necessary as it had been before. Four months after reaching total fluency everywhere, I attended a reunion at Hollins. My former clinician warned me that, even though I was speaking fluently, my techniques (called “targets”) were weakening. Sure enough, a few months later, I began to experience disfluencies again. A month after that, my speech fell apart totally.
I went back to Hollins for a week-long refresher, and my total fluency returned. I maintained fluency again for quite a few weeks. But it required a great deal of practice to maintain (an hour or more daily), and I didn’t always have the time to practice. Eventually my speech fell apart again.
In 1988, four years after first attending the Hollins program, I tried therapy somewhere else – also a Precision Fluency Shaping program, run by Ross Barrett (a speech pathologist who stutters, who is a master of the Precision Fluency targets he learned at Hollins). This program took place at the Eastern Virginia Medical Center in Roanoke.
Ross has an advantage over the fluent clinicians at Hollins – he uses the fluency targets himself, and has additional insight from his own personal experiences with stuttering and the Hollins techniques. Therefore, his program was a slight bit different from Hollins.
I started to periodically take one-week refreshers from Ross, one or two a year. I found his therapy to be really excellent, and his personal insights very helpful. During every refresher with Ross, I returned to complete fluency within a matter of hours. Then after a week, I maintained my fluency for weeks or for months, with intensive daily practice.
But still my speech eventually fell apart each time, and I kept returning to Ross for more refreshers.
Meanwhile I went back to graduate school to study speech-language pathology (very different from my previous graduate program, music composition).
Afterwards, I became my own therapist, and conducted Precision Fluency refreshers for myself and others in Massachusetts and nearby states.
I continued the same pattern – reaching total fluency, and maintaining it for quite a while with continued intensive practice. But eventually, my speech always relapsed, and then it was back to conduct another refresher. This occurred many times throughout the 1990’s.
Up and down, up and down, up and down.
I eventually got tired of this yo-yo effect.
About 25 years ago, after moving to Norway, I decided to pull the plug on Precision Fluency. I now simply, peacefully, and calmly accept the fact that I happen to be a person who stutters.
And life became much simpler, less stressful, less pressured.
Yes, I still stutter severely. But it’s okay. I accept it. My speech is a difference. I no longer have the fluency I enjoyed for many long periods with fluency shaping techniques – but I no longer have the wild relapses either. I stutter severely, but I don’t have the really wild swings in both directions that I used to have.
And it’s all right. My life is happy, even though I’m not the most fluent person in the world. I accept myself as I am.
Best of luck in your future career.
– Paul
Thank you for this question.
I was born in a small town in Northern India, and nearest big city was a few hours away, so I did not get the ‘traditional’, or research based speech therapy which is quite common in the west. My family beleived I will ‘grow’ out of it, when I was a kid so they convieniently skipped the ‘therapy’part. When I did not ‘grow’ out of it, and it became quite visible when I was 11/12 years old, my family started asking around what shoudl be the way going forward. It was early 2000s and internet was not avaialle to us, so lack of knowledge is also a factor in me not receiving the therapy on time. I was sent to few ‘therapsists’ or doctors who would suggest the physical exercises to deal with it, like blowing a baloon, reading in front of a mirror loud , etc- which have proven beneficial in some cases I have heard. No one touched the psycholological aspect of it, hence it my speech did not get ‘corrected’. It became worse, as I enetred into my late teens. When I got hold of internet and started reading, I found a speech therapist in a nearby big city (Delhi) and I enrolled myself with their speech therapy program where I stayed at the hostel provided by the centre (another nightmare, as I was living with complete strangers and was homesick to death). As expected, the therapy did not workagain, as they were also focussed on physcial aspect of the speech and not the psychological one. They treated us like patients and I left ater a month. That was it for me in terms of speech therapy. I did some more research and found TISA (The Indian Stammering Association) and it was a huge step-up for me in terms of moral support and mental health. I really beleive in the power of community, the stammering community has been a blessing to me. I still stammer visibly but with much less shame and much more confidence.
Hi Tate
When I was you, stuttering was taboo. Nobody talked about it. Not at home, not at school. Noone told me there were others. When I was in my late teens my school wrote a letter to my parents (which I found out many years later) that I should see an SLP. This didn’t go well (private story), but a few years later I tried another one. This didn’t go well either and I lost all trust in SLPs. I even other tried other therapists, f ex healing, hypnosis, etc. Long story short, they were all focused on my breathing and fluency. I can breath. I play the saxophone. Stuttering? Wrong. the only goal was fluency. If their methods didn’t “work”, I was to blame. I was lazy. I didn’t want to be “cured”.
Later on in life I found a support group where we practiced public speaking. THIS became one of my keys to freedom. I could speak. Just not fluently. I also found other fantastic, dedicated SLPs who were no longer focussed on fluency, but on making clients talk freely again. I also found Mindfulness and NLP. More keys. And I found the stuttering community. The biggest key of all.
Unfortunately there are still SLPs who’s goal is fluency and less stuttering syllables. Fluency? Is it the SLPs who wants it? Parents? teachers? Employers? If it’s something others want, it’s doomed to fail. Even worse, it can lead to silence, covert stuttering, fear, shame, low self-esteem, or even worse…
So start with listening. Ask questions and listen, before you even think of starting therapy. As we all bring different things to the table. Background, culture, religion, family, age, gender, and our many different experiences. This goes for clients of all ages. You may find out that not all clients come for total fluency. Some want answers, some want a family member to know more, some want some tools to speak with less tension, some want to practice job interviews, some are there because the parents want the child to be fluent while the child just wants to speak freely, some want help with self-esteem, etc etc. When you get a picture of the client and what they want (at that moment, as it can change along the way, and if that’s reachable of course), you can start offering a smörgåsbord.
This can be all from speech training to refer to relaxation, mindfulness, NLP, speaking circles, theatre, art, presentation techniques, yoga, swimming, singing, and maybe even a combination.
Also show the way to the stuttering community. This group is not instead of, but can be a great addition to therapy. People who walked the walk and literally talked the talk. They can help with exercises, help to speak in school or at the workplace, support outside the therapy room, etc. They often have gatherings, camps and some even have virtual meetups, even international ones, with meeting friends and simply playing games together.
With acceptance being the safety net, you can start the journey of practice, challenging yourself, and go for your dreams. Acceptance doesn’t mean you’re done. It means you catch your breath and get ready for the next step, whatever that step may be.
And help me to find my true self, and my self-worth. Show me what I’m good at, and that stuttering is not bad and fluency good, but that stuttering just IS. And that it’s not up to me to make my listener happy, but maybe instead up to the listener to simply… listen. Help me to see there’s more in life then fluency. And that I’m good enough either way. But to also help me to find tools that fit me and my stutter, ways to explain to others what stuttering is, ways to meet bullies and other people not getting it. Ways to speak to my teachers. And show me the way to stutter camps, where I can be me, speak freely, without any therapy, and where my parents can come and speak with adult PWS. As the more we understand, the more we feel good enough, the more we lose the shame. So be a friend.
Most of these advices can work with both adults and children. With children however, make sure you listen to the child and not just to the parents, as they can have different goals, and the child might tell you what s/he thinks others want to hear. So have them both together and seperately. Also group meetings are good, to show they are not alone, and do exercises together, the same for parents.
Lastly: stop the counting syllables. Just because someone stutters less, doesn’t mean things are going great. It can also mean the iceberg is getting under the surface, and thus way harder to notice, and to treat. So listen not only with your ears, but also with your gut, to what’s not been said.
Sounds tricky? I promise you that, as soon as you gain your client’s trust, you’ll have an exiting road ahead, walking and working together, sharing ups and downs, and enjoy the progress, whatever this word includes for that very client.
Keep them talking
Anita