DEVONS UPDATE23 July 2015
Update on Devon’s Medical Condition for Give A Little
17 July 2015
Devon had a tracheostomy performed on 8 May 2015 and at that point he need the ventilation machine in order to breathe. Devon was unable to breathe independent of the ventilation machine due to two significant conditions within this trachea (windpipe).
Devons trachea collapses and flattens so that air cannot get into his lungs. This is called tracheomalacia and is an abnormal collapse of the tracheal walls. Think about breathing in and out: When you inhale, your chest expands, and when you exhale, your chest wall contracts, to help push the air out. This action puts pressure on some internal parts of the body, such as the heart, the lungs and the trachea.
A healthy trachea is supported by a series of “c-shaped” rings made of cartilage that help your airway to stay open during exhalation. Tracheomalacia means that these rings aren’t strong enough or in Devon’s case the surgeons have had to remove so much of his trachea due to a fistula and scar tissue for the orginal corrosion burn from the battery there isnt enough support left now to keep the trachea open.
The trachea needs to be open during inhalation or exhalation, and if the trachea becomes narrowed or flattened then it’s very hard to breathe. Devon has severe tracheomalacia which can be life-threatening as breathing in or out becomes impossible as the trachea narrows so much it is closed as the walls collaspe into each other.
2. Bilateral Vocal Folds Paralysis
Vocal fold paralysis (also known as vocal cord paralysis) is a disorder that occurs when one or both of the vocal folds don't open or close properly. Paralysis of both vocal folds is rare and can be life threatening.
The vocal folds are two elastic bands of muscle tissue located in the larynx (voice box) directly above the trachea (windpipe). When you breathe, your vocal folds remain apart and when you swallow, they are tightly closed. When you use your voice, however, air from the lungs causes your vocal folds to vibrate between open and closed positions.
If you have vocal fold paralysis, the paralyzed fold or folds may remain open, leaving the air passages and lungs unprotected. You could have difficulty swallowing or food or liquids could accidentally enter the trachea and lungs, causing serious health problems (such as aspirational pneumonia which Devon has already survived once).
The tracheostomy fixed the issue that Devon has with his vocal fold dysfunction however the tracheomalacia remained an on going conern.
However after the tracheostomy and over time it became evident that trache (tracheostomy tube) was stenting open his trachea. This was surprising. So as Devon became stronger and regain his health he has been able to be slowly weened off the ventilatin machine and is breathing using the tracheostomy.
At this point we were finally moved from intensive care to the Ward of Starship!!! YAY – this was hugely significant as it mean that Devon was out of imminant life threatening danger. I can not explain to you the relief this aspect was for me.
However movement of Devon from intensive care to the ward added other complications such as the requirement for a parent to be with Devon 24 hours a day 7 days a week. So I had to work out how I could manage everything with Mikayla and Brayden. I am and will enternally be very grateful to my mother (and her partner Noel) as she agreed to came up to Starship Hospital/ Ronald McDonald House to support and helped me with my other two little people (well Brayden at nearly 16 years old isnt exactly little but you know what I mean ?) .
Ronald McDonald House is a wonderful place and I think they have made a time in our life that would have been impossible manageable. The staff truly do an amazing job in support and helping family member of sick children survive the challenges.
So back to Devon’s recovery, after the move to the Ward in Starship (beginning of June) discussions commenced about what next initially we were advised that Devon could go home before the oesophagastomy could be reversed and the reconstruction of his oesophagus could commence which is roughly scheduled for commencement in January or February 2016.
However it soon became evident that this would be to risky because Devon could very easily dislodge his extra small trache tube and he can not breath at all with out (he would sufficate and go into cardaric arrest within 4 minutes). This was too much of a risk to take so it has been decided that Devon must remain in Hospital until after the oesophageal reconstruction which could be another whole year away. There is no guarantee of Devon being released even then it will deoend on how is overall medical situation is but I have to have hope of a more normal life at some stage for him.
So we are now awaiting the outcome of the up and coming discussion between Tauranga Hospital and Starship Hospital to decide where Devon will wait out the time until the oesophageal reconstruction.
I only wish Devons insides were looking as good as his outsides. He is still very much at risk with his airway being so tenuous. So there is still a very long way to go yet but we might be able to come home to Tauranga Hospital while we wait for the next stage to start.
Thank you for keeping us dated with little Devon, Our best wishes to you all, stay strong, Devon is a little fighter who will come over barriers, Hugs to you all
I and my brother both have Congenital Bilateral vocal Cord Paralysis. I don't know how but I would really like to help in any way I can!
My email is
Even if my daughter and I could paint a picture or drawing for him we would be happy to.