Friday, March 23, 2012

Video Swallow Study

When we were at Jordan's video swallow study yesterday I was thinking, "I wonder how many of these we have had done??"  I am guessing this was about the 7th, but I'm not sure.  I may just have to look into this!

Jordan was so excited about yesterday!  Every day...all day...every night...Jordan is asking what today and tomorrow are.  She uses the phrases "school day," "Julie day," "church day," "home day."  It can be very annoying to be asked the same question about 40-50 times a day, but we think it is helpful in her organizing her thoughts and anticipating what to expect.  She does best with routine and does not always handle changes with schedule or routine easily. 

Wednesday night she was asking about "tomorrow."  I was trying to come up with the easiest way to explain that she was going to have a swallow study so I told her she would be having some tests and they were going to take pictures of her eating food with her mouth.  I used the word "therapist" and yet, she didn't quite understand (even though she sees several therapists for speech and OT every week, she knows them by name, not profession).  I ended up telling her she was going to a doctor because I knew she would understand.

After that, "doctor day" was the phrase she kept using to plan for the day.  When we arrived at Mary Free Bed, we waited in the waiting room for a while and when Ellen came to get us, Jordan referred to her as "doctor."  Ellen found it quite amusing that Jordan kept calling her "doctor."  Oh well, at least Jordan understood what was going on.

The procedure for a video swallow study starts with me discussing things with the therapist and then going to have it done and then returning to discuss it and make a plan.  During our first discussion, Jordan was having difficulty sitting in the small room.  We got her a coloring book and crayons, but she just wanted to go play in the PT gym with the kids that were having "fun!!"  Eventually, we tried turning on a video, but she continued to be frustrated that she could not be out there.  This led into a screaming fit that I am sure could have been heard 2 floors above us!  It lasted about 10 minutes and although I tried talking to Jordan, comforting her, scolding her and finally putting her in a time out, she continued her blood curdling scream!  Ellen and I attempted to continue our discussion but eventually decided we needed to move on to the swallow study.

Ellen collected several different foods for Jordan to try, including the Trix yogurt that made up her diet for the past year or so.  She also made liquids of various thicknesses, honey, nectar, and thin.  Finally, she brought some cheese puffs and banana and the mesh bags we had previously used with her.  She prepared it all the barium so it would show on the x-ray and we got Jordan situated in her highchair.  Unfortunately, the recording device was not working so they had a video directly aimed at the screen recording it.  Although this is not the quality we wanted, it was better than nothing.

Ellen started with the yogurt.  Jordan had a beautiful first swallow but struggled with the residue.  This is very common with her.  She has a hard time cleaning out her mouth and throat and getting it down.  Ellen actually went with larger bites and Jordan did quite well with them.  Next she moved on to honey and then to nectar and thin.  Jordan did great on all of them!  We did 2-3 bites of each before moving on.  Then Ellen tried some cheese puffs wrapped in a mesh bag.  Jordan chewed on it and again, had a nice swallow.  We moved on to banana and the same thing.  Then Ellen decided to try something that we have not done, she gave Jordan a small piece of the cheese puff.  Jordan chewed it okay, but had no clue how to chew.  She actually chewed with her front teeth so Ellen tried to explain and show her to use her back teeth for chewing.  We tried another cheese puff and she was doing great!  We were in complete amazement and in awe of what we were seeing!  Next, Ellen took a small piece of banana and gave it to her.  Again, Jordan didn't quite know how to chew, but had a pretty good swallow.  She was still struggling with actually chewing the food completely before swallowing and then clearing the residue out of her mouth and throat.  Finally, since we had seen such amazing things, Ellen tried giving Jordan a drink of the nectar or thin (I can't remember) liquid straight out of the cup.  Jordan's biggest challenge, again, is her lack of knowledge of how to eat and drink.  She struggled with putting her lips on the cup and taking a sip, but finally figured it out and took a small one.  Ellen tried one more time and then we saw a large aspiration...and silence.

Aspiration is when food goes into the airway.  Normally, when this happens, there is a natural reflex that causes us to cough in an attempt to clear it out.  Silent Aspiration is common in people with dysphagia.  Think about when you take a drink of water and start to cough because it "went down the wrong tube."  That is aspiration.  Unfortunately, Jordan has a history of the silent kind and we saw it again yesterday.

Up until her aspiration we saw a slight penetration, but everything looked great!!  This is very promising, but shows a couple of things.  Jordan has always fatigued quickly and this seems to still be the case.  We were at about 15 bites when she aspirated and it had been only about 10 minutes.  She also struggles with the swallow process from an open cup.  This allows us to know that we need to control the delivery of the food/liquid.

In the end, Ellen decided to try 12 weeks with one session of feeding therapy per week.  Although, she said that she doesn't know that that will be enough to do much, it is the start we need.  I also discussed with her the v-stim therapy and she is going to talk to some people she knows that are more aware of it and discuss Jordan with them.  She feels that it could potentially help her with more muscle control awareness.  We know we have a long way to go, and we are realistic with our goals, but we are not going to give up!!

Please pray that we can easily schedule Jordan's therapy and that she is cooperative during the sessions.

Thank you so much!!!

3 comments:

Anonymous said...

Pulling for success for you two,

Alan Gaudette

Betsy said...

Just happened upon your blog for this year and read all the posts. What an ongoing struggle but I couldn't imagine any family trying harder. I miss working but left at the right time. Developed spinal stenosis 4 months later. Had both Knees replaced on October 28 of last year and am working hard to get my balance back. The surgery wasn't bad, but oh how I miss my balance! Good luck with every thing. I'm keeping you in my prayers!

Karrie said...

Betsy!
It's so great to hear from you! I know you would be amazed if you could see Jordan! You were such a blessing to us during that first year of therapy and figuring things out. I am thankful that we have you in our lives. I will be praying that your body heals and that you are back to your active life soon!
Karrie