I have had someone recently ask me about a lift, also.  I have asked our local SLP, and got a resource in St. Louis, but looking for someone much closer to the Bloomington area.  Does anyone know how to go about finding someone that can do this?  This is a  first for me.

 

Tara Klucker, MA, CRC, LPC
Case Manager and Outreach Specialist
The ALS Association, St. Louis Regional Chapter
 
314-432-7257 ext. 7
1-888-873-8539
 
Where Patients Matter Most
 
The information transmitted (including attachments) is covered by the Electronic Communications Privacy Act, 18 U.S.C. 2510-2521, is intended only for the person(s) or entity/entities to which it is addressed and may contain confidential and/or privileged material. Any review, retransmission, dissemination or other use of, or taking of any action in reliance upon, this information by persons or entities other than the intended recipient(s) is prohibited. If you received this in error, please contact the sender and delete the material from any computer.

 

Description:
BW_vert

 

From: xxxxxx@xxxxxxxxxxxxxxxxxxxx [mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx] On Behalf Of Erin Singleton
Sent: Tuesday, August 09, 2011 1:50 PM
To: xxxxxx@xxxxxxxxxxxxxxxxxxxx
Subject: RE:

 

Thanks Tami

 

Do other SLP’s regularly suggest lifts for ALS patient’s? I have been trying to find someone in my area that does them in the event that it’s appropriate.

 

Erin

 

From: xxxxxx@xxxxxxxxxxxxxxxxxxxx [mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx] On Behalf Of Tami Brancamp
Sent: Tuesday, August 09, 2011 11:40 AM
To: xxxxxx@xxxxxxxxxxxxxxxxxxxx
Subject: Re:

 

They could be assessed for a palatal lift.

Tami

 

Tami Brancamp, PhD

Assistant Professor

Speech Pathology & Audiology

University of Nevada School of Medicine

775.784.4887

775.682.7020 (office)

 

On Aug 9, 2011, at 11:33 AM, Erin Singleton wrote:

 

Hey everyone,

 

I realize we typically focus on augmentative communication on this list serve so it may not be the most appropriate forum for this question.

 

I have had two ALS patient’s ask me this week about what they should do for nasal regurgitation when swallowing liquids. I don’t get asked this a lot so I don’t feel as though I have the best suggestions for them. The two men that asked are brothers and oddly enough have almost no pharyngeal dysphagia. Their most frustrating symptom is nasal regurgitation. It surprises me that it’s happening so often for them because their speech is only slightly nasal. If anyone has suggestions for me I’d love the advice!

 

If it’s easier to answer off the listserv my email is xxxxxx@xxxxxxxxxxxxxxxxxxxx

 

Thanks so much.

 

Erin Singleton M.A., CCC-SLP 
Neuroscience Outpatient Rehabilitation Center 
2335 East Kashian Lane, Suite 301 
Fresno, California 93701 
Office: (559) 459-6056 
Fax: (559) 459-2957 
Email: xxxxxx@xxxxxxxxxxxxxxxxxxxx

 

 

 

 

  ________________________________  

-------------------------------------------------------
WARNING/CONFIDENTIAL:
-------------------------------------------------------
This email, including attachments, may contain information that is privileged, confidential, and/or exempt from disclosure under applicable law (including, but not limited to, protected health information). It is not intended for transmission to, or receipt by, any unauthorized persons. If the reader of this message is not the intended recipient you are hereby notified that any dissemination, distribution or copying of this communication is strictly prohibited. If you believe this email was sent to you in error, do not read it. Reply to the sender informing them of the error and then destroy all copies and attachments of the message from your system. Thank you.