Austin, Texas, Memorial for Christopher

03975561There will be a memorial for Christopher in Austin, Texas, on Sunday, June 5th, 2016, at 2PM.

Flying Saucer Austin
815 W. 47th Street
Austin, Texas 78751

RSVP: Please reply to this posting here, or send me a note on FB / e-mail if you are planning on attending, so we can get a more accurate headcount for the folks at Saucer.

Thanks, y’all.


Posted in Updates | 8 Comments

Funeral arrangements


Thank you all for your support;  it truly means a lot.  Chris is sorely, sorely missed.


Tuesday, May 17th, 2016, 6PM – 8PM.

Berryhill Funeral Home
2305 Memorial Parkway NW
Huntsville, Alabama 35810

Funeral Mass:

Wednesday, May 18th, 2016, 1PM (brief viewing at 12:40PM).

St. John’s Catholic Church
1055 Hughes Rd.
Madison, Alabama 35758


Wednesday, May 18th, 2016, 3PM.

BJ’s Restaurant & Brewhouse
401 The Bridge St #120
Huntsville, Alabama 35086

If you would like to send flowers, please send them directly to Christopher at Berryhill Funeral Home.  I have used Heritage Florist and Gifts to send flowers for various occasions in the past with excellent results.  Heritage Florist and Gifts:  +1 (256) 837-7022

If you would like to donate to a non-profit instead, or in addition to, flowers:

Please make any donations in memory of Christopher Giles.

Thank you all.

Posted in Updates | 2 Comments

We lost Chris.

My brother, Chris, unexpectedly passed away early this morning at my parents house in Alabama.  I’ll post more information when we figure out what the next step is.

Posted in Updates | 7 Comments

Trip to Texas

So my parents were able to arrange some much-needed time off again, and this year, we decided to bring Chris to a skilled nursing facility in Austin, Texas, instead of me taking care of him at my folks’ house in Alabama.

Mom and dad also planned a single day stop in Houston on the way to Austin, for a brief evaluation at TIRR and for a routine refill of Chris’s Baclofen pump.  Very early the next morning at the hotel, around 3am, Chris began having very dangerous continuous seizures, and my parents had to take him to the emergency room at Memorial Hermann Hospital.  Chris ended up in the Neuro ICU, knocked out on Ativan and monitored on an EEG cart, much like last year at Huntsville Hospital.


One of the evenings saw some staff ‘procedural panic’ set in after Chris choked on excess saliva, which lead to further complications – they scraped up Chris’s throat pretty badly and ended up causing some really unnecessary bleeding into his stomach.  Ghah.

At one point, one of the physicians was telling my parents that Chris was going to expire because of a somewhat low oxygen level in his blood.  I’d seen this same temporarily low number – 85-90% – last year at Huntsville Hospital after the seizures, but it returned to normal (99%!) after he came around again.  This observation from last year talked everyone down off the cliff…  but good grief, it was unnecessary added stress.


Chris also needed a PICC line to receive intravenous medication (folks that aren’t self-mobile tend to be difficult to ‘stick’ in the usual spots).  A few days later, he developed a fever and an infection of the central line was suspected.  Serious antibiotics.  Thankfully, blood tests revealed no infection, and the fever broke on its own ‘somehow’.

All these things continued to incrementally tack on a day or two to Chris’s hospital stay, which meant rebooking flights, and rebooking flights, and rebooking flights (props to Delta for being so accommodating).

My folks were kind of resigned to scrapping their holiday at this point, but at least Chris was OK!!!


This dude is still smiling, even after what he’s been through (again).

After almost two weeks in Houston, they finally managed to have Chris discharged from Memorial Hermann.  PICC line freshly removed and the wound covered with a bandage!  No more seizures!  No infections!

It was cutting it really close to still make their thrice-rebooked vacation flight and get Chris settled in at the skilled nursing facility – Park Bend – in Austin.  Yikes!


My parents had a weekend to get to know folks and provide some “Chris OJT” at the nursing home before they were off on their trip.

I was anxious about looking after Chris, but really glad my folks were able to GET ON THE PLANE before some other calamity unfolded!!!


I spent about six to eight hours throughout the day, every day, at the nursing home keeping an eye on things, training folks and trying to come up with fun stuff to do with Chris while he was in Austin.

While it’s absolutely essential for anyone in a medical facility to always have a patient advocate,  I will say that the nursing home staff – across the board:  CNAs, LVNs, RNs, admissions, DON, facility nurse practitioner, facility administrator – outperformed many hospitals while taking care of this young traumatic brain injury survivor.


So we did some things over the course of the next month:


Taking a walk near the North Austin Medical Center, underneath the Austin Western Railroad


Spending some time in the garage, after adjusting the clutch cable on the Triumph.


Watching the Kansas State game on the nursing home’s big screen!


Chris was usually knackered after watching even half a football game, heh.


We used to go running together at the Camp Mabry track. The fall weather was absolutely perfect.


Camp Mabry, and Chris smiling at my “DON’T MESS WITH TEXAS” comment (written on the tail of the 147th Fighter Wing F-16 static display)


Chris smiling while watching an episode of “The Simpsons”


At an evening UT Computer Science Alumni Lecture event down on campus

It was bloody fantastic having my brother in Austin again, and to witness him smiling all the time.  Woohoo!

He would smile on cue at some pretty obscure Simpsons humor.

He smiled a lot during the lecture at the TACC visualization lab on campus.  He smiled tremendously while watching the Texas – Kansas State game.  He smiled while starting up the Triumph.

The smiling confirms that Chris does still have language comprehension and some amount of facial motor control.  He was also more easily able to turn his head to the right spontaneously this time, and he did so several times without being prompted (to watch a nearby television, for example).

I think Chris’s daily experience might be similar to this man’s:  VIDEO: How my mind came back to life — and no one knew.

One of our cousins recently learned of the Intel Assistive Context-Aware Toolkit, which allows a webcam-visible user to spell words simply by moving facial muscles, but the software is a tad buggy at the moment, and Chris doesn’t seem to have quick enough focus or motor control to use the software yet (for the periods when the software has calibrated to his face properly and isn’t off in some weird flashing error state).  We will definitely keep trying it, though – it’s a much more user-friendly approach than the EEG-based system we attempted last year (the EEG gel is an absolute mess to clean up).

My parents returned from what sounded like a fantastic vacation, and spent another week in Austin getting back into the swing of things again.

It was unfortunately time to say goodbye to everyone:  to my folks, Chris, and to the nursing facility and staff that really helped make this possible, too.


The two brothers and mom. Chris is sleeping, heh.


Chris, loaded up into the stuffed wheelchair van for the two day trip back to northern Alabama.


…and they’re off!

So that’s it for this update.

I’d like to think this will become an at least annual thing, bringing Chris to Austin for an extended period, while my folks take some much-needed R&R.


Posted in Updates | 1 Comment

Long overdue update

I’ve been meaning to post an update for quite a while now;  sorry folks.

P300 Speller:

I’m going to rewind to late November / early December 2014, when I filled in for my parents while they took a very-needed vacation.

The week or so they were away and the upcoming Christmas holidays provided a unique opportunity to evaluate a patient-ready brain computer interface P300 spelling system, intendiX, produced by Guger Technologies in Austria:


Chris’s wheelchair headrest strap makes attaching the EEG cap a little difficult

The system measures immensely small voltages for eight specific areas on the scalp (single ear lobe as reference / ground), using conductive electrode gel and electrodes that are pre-sewn into a mesh cap.  The electrode wires go off to a small battery-powered amplifier, and from there into a proprietary signal processing device that shows up as a custom USB device, connected to a standard Windows 7 64-bit laptop:

The other half of the magic is within the actual software itself.  The display consists of a rows and columns of letters and numbers, with a layout similar to a standard QWERTY keyboard.  You create a classifier for a particular person by “spelling” a handful of pre-selected words.  For example, using “BOB” to create a classifer:

  1. The system shows the letter “B” in the center of the screen for 1 second, to indicate the next expected letter to “train”.
  2. Entire rows and columns of letters / numbers begin quickly flashing, randomly, across the screen.  The letters / numbers of a particular flashing row or column are very briefly – milliseconds – replaced with small photos of a famous actors / actresses (probably to elicit a heightened response to human faces appearing).
  3. You simply focus on the letter “B”, and count the number of times the row or column containing the letter flashes.  The system kind of converges on the row/column response after about 20 repetitions for each letter.
  4. The system shifts to the next letter in the training, “O”, and the process repeats:

Rows and columns flash across the screen

Once you’ve created a classifier, you can begin using the system to actually spell words by simply looking at the letters / numbers on the screen.  You basically just stare at an individual letter as the rows/columns flash, and eventually it will pop up on the screen.

It’s pretty amazing.  I tried the system out on myself, to make sure I was doing things correctly when I worked with Chris.  It was quite reliable and very repeatable – for a fully conscious, healthy person, it was extremely straightforward.  The training was short, too – it worked for me after only one training word.


No hands! I spelled “TADA!” just by looking at the characters on the screen.


The lousy part – the hospital detour:

Despite having the intendiX system from the end of November through the Christmas holidays, we didn’t really get a chance to use the system with Chris for very long…

Chris started acting a little bit weird – more absence seizure-type stuff (staring off into space) – the day or two before my parents left for their trip.  After my folks were out of town, Chris began having nightly tonic-clonic seizures.  It became progressively worse and worse as the week went on.  Initially it was one seizure a night, then two, then during the day and night, then multiple tonic-clonic seizures during the day.

After the first seizure, I started keeping a laptop next to the bed at night, to watch and listen to the camera feed from Chris’s room.  The seizures always seem to be shorter when someone is in the room holding Chris and talking to him softly, if you can scramble out of bed when it starts happening…


We went to the local emergency room to check for infection, since that sometimes seems to cause seizures for Chris.  Tests came back negative, but the tonic-clonic seizures continued to increase in frequency.  I made an appointment to see a neurologist after another day or so of this, and he had a seizure in the neurologist’s waiting room!  The nurses there had us wheel across the street to the county hospital’s emergency room instead, where things continued to slide downhill, to the point where Chris and I ended up in the hospital’s neurological intensive care unit:  status epilepticus (back to back to back to back…  seizures).

Hearing a hospital-wide neuro response team code announced, surrounded by nurses who had run out of options and couldn’t conceal the alarm on their faces, was a pretty damn scary time.

The only thing you can do is basically just knock the person out cold – in this case, using an emergency dose of Benzodiazepines.  They had Chris hooked up to an EEG for a 24 hour recording, and the seizures continued off and on, just in a non-presenting fashion.

My folks knew about one or two of the night time seizures earlier in the week, but this had progressed to the point where I finally had to let them know that I absolutely did NOT have things under control, guaranteeing the vacation THEY REALLY NEEDED would prematurely – but necessarily – come to an end.



I was bloody glad to see my parents, and I know Chris was, too.

We spent another two days in the Neuro ICU, with the neurologist running through two different choices of anti-seizure medication, before being released to a step-down unit for a few days, and eventually home.

The neurologist had no ideas about any specific triggers for this bout of seizures;  he basically chalked it up to “brain injury”, and that was that.  Chris is on a new, secondary anti-seizure medication now and hasn’t had any subsequent tonic-clonic seizures at night (and generally seems more alert during the day, which is one good thing that came out of this hospital ordeal).

We have another theory – might be daft – some of the seizures might have been non-epileptic, induced by Chris’s general panic of not having my mom around.  I remember some of the seizures at night seemed to dramatically calm down when I touched Chris, which shouldn’t happen for a “real” seizure…

P300 Speller, continued:

Getting back to the intendiX speller:  we’d only been able to use the system twice when Chris had his first night time tonic-clonic seizure under my watch.  I decided not to put any further flashing lights – the rows and columns of the intendiX screen – in front of Chris, until the seizures seemed to be reliably behind us.  That put things toward the very end of December, a few days before we had to send the system back.  D’oh.

I spent a few more hours trying to get Chris to train a few words with the system, but we unfortunately didn’t have any luck.  The Austrian company looked at one of the data sets and said Chris is having “P300 responses”, but I just didn’t have any luck at all creating a consistent classifier that we could use to spell any words with.


MATLAB: It’s everywhere!


The intendiX system is promising for the future, though, and especially for other traumatic brain injury patients that are perhaps a little further along than Chris.

The system isn’t quite turn-key enough yet for my parents to casually use – the electrode gel makes a big mess everywhere, and you have to be really careful about not moving the electrode cap around, which is difficult to do given Chris’s wheelchair headrest, and that he cannot hold his head up on his own.

We’ll probably give the system a shot again in the future, when I can spend another week or two with Chris out at my folks’ house.


I’ll end this update with some really good news.  My parents have been saying this since the beginning, but Chris really does understand what we’re saying to him most of the time.  You can tell the guy a joke, or remember something funny from way back when, and he’ll crack a smile almost immediately:


This past November was kind of the first time I’d observed it, in a repeatable – no way, this isn’t just chance! – consistent fashion.

There’s still a long bloody way to go, but knowing Chris has comprehension of language is huge.

So there’s some good news to wrap things up.  Also – my folks might make a trip out to Austin soon with Chris, but we’re still working out the details on that.

The Town Lake trail – one of our favorite locations to run and solve the world’s problems – is wheelchair accessible.

Posted in Updates | 3 Comments

Update from Dad

Just a few lines to bring everyone up to date. As I think everyone knows, we are still here in Alabama (where I work), and have Chris with us of course. Chris is physically doing well albeit a little bit heavier than he was before his accident. But he is physically doing well. We keep waiting for neuro-medical breakthroughs to provide a “new hope” for helping Chris regain some function. But until that happens, he’s being well taken care of (his mother is a Saint!), and we keep searching for different things to do to help Chris. We made an “annual checkup” visit to Spain Rehab in Birmingham, AL., where we go for periodic Baclofen pump refills, and much to my disappointment, it was pretty much a wasted trip. I was expecting a bit more comprehensive approach to perhaps some new therapies or alternative treatment protocol suggestions from the Doctor, some news on the nutrition front, but it didn’t happen. They basically said, “yeah, he looks good – anything we can do for you?” I think my expectations were a bit too high going in. I contacted the Shepard Center in Atlanta Georgia, another Traumatic Brain Injury (TBI) Model System, one of 16 in the country, and although we are not candidates for an in-patient program, they have a pretty comprehensive out-patient program that may also provide Chris with some improvements. I know from experience with my dad having a stroke and severe injury from falling down the basement stairs and hitting his head on a concrete floor, the brain heals in seemingly unusual ways. There is, of course, physiological healing or mending, re-mapping of brain function, neuro plasticity, and other descriptions of types of “mending” that goes on in the brain. I know with my Dad that his lost left-side function, over time, literally came back over night when those neuro connections re-joined and those pathways were re-established. I tell Chris that we’re going to get there but it will take time. He’s a strong lad (man – but he’s still my baby) with a lot of perseverence as well as patience, we’ll get there in the end. It will take time but we’ll get there. I’ll keep everyone posted on events regarding moving toward making the Shepard Center happen and, as always, thanks for your thoughts and support- it keeps us going.

On a quick political note, push your State representatives for expansion of medicaid to allow for the uninsured in your States to obtain health insurance. We, in the United States, are the ONLY western industrialized country in the WORLD that does not provide health care for its people! The scare tactics of politicians about “socialized medicine” (and the boogeyman) are just that, scare tactics to keep you docile and dependent on your representatives! Ever seen one of these tea party rallys on Youtube where a Senior citizen is holding a sign saying, “Keep your Government hands off my Medicare!” It’s so funny it hurts! Obamacare is NOT socialized medicine, the Veterans Administration IS – but you don’t hear anyone calling for the repeal of THAT socialized system do you? Tricare for our military is more socialized than Obamacare and takes up a good size chunk of the defense budget – in excess of $50 Billion dollars a year but you don’t hear anyone calling for the repeal of that social health system! And they just pumped over $17 Billion dolars more into the VA, money that adds to the national debt ($12 Billion of it). The “real VA story” is that it’s not processing disability claims fast enough! You know, the claims for Post Traumatic Stress Dollars! Look, I was there! the number of PTSD claims doesn’t support the numbers that were actually “outside the wire” in harm’s way. The rest of us were on airbases or Forward Operating bases, you know, where you eat steak and lobster (literally) four nights a week (it’s hard NOT to put on weight during a deployment)! One more and I’ll shut up. We pay over a Billion dollars a year for retiring military veterans in disability compensation for “snoring!” Yes, sleep apnea, generally associated with obesity, costs the tax payer over a Billion dollars of scam money a year! Next time you see a disabled veteran license plate (with no handicap marking on the plate), watch the veteran when he gets out of his truck – does he look like he’s handicapped? Probably not! In fact, he’s probably a pilot for United Airlines who has to undergo a full flight physical periodically in order to fly but yet he’s disabled by VA standards. He’s diasabled for the purposes of retirement disability compensation – it puts monthly money in his pocket – but he won’t support paying a dime to a single mother for public assistance or for free lunches for kids! What a world!

Off my soapbox. Thanks, we love you all!

Posted in Updates | 1 Comment

Update from Dad

Just a couple of notes to “catch up.” We never did make it back to New Orleans for the Hyperbaric treatments as we wanted to. The logistics of staying there for 40 “treatment” was just not doable for us right now. However, a new alternative treatment chiropracter has come to town and also has a chamber and is doing hyperbaric. We have to be careful in terms of finding someone that knows hyperbarics for brain injury (not a medically recognized treatment), and we will but it’s another possibility for hyperbaric treatments. I’m convinced the “established medical community” may not necessarily provide the best care for the patients given the financial incentives in our system to provide medical services rather than medical outcomes. In other words, our doctors get paid for services, not outcomes. In fact, ironically enough, a Doctor can literally kill you and he will still get paid! Or he can completely botch a procedure and get paid again for the corrective procedure! So yeah, everything is taken with a grain of salt and a skeptical eye in this family. While most will say, “hyperbarics can’t hurt even if they don’t do any good,” we’ve learned that they can, in fact, bring on siezures if not managed correctly – too much pressure, too deep a dive, etc. Robert is working a brain computer interface evaluation device from an Austrian company that sounds promising to allow Chris to better communicate and have more control over his environment. More to come. We’re looking at getting Chris into an outpatient treatment program at the Shepard Center in Atlanta, Georgia, another National Traumatic Brain Injury Model System. I have visited the facility, they are very high ranked on a national scale and although an outpatient program, it fould provide about five hours of therapy per day. So that’s what we’re currently working on. And of course, I keep playing the lottery hoping for the big win to let us do some other things we can’t do limited by finances. We’re also working on some home help for Mom, she’s been going like a trooper for three years now and needs a break! Chris seems to be more aware and we can get him to smile pretty quickly after a comment or statement that he finds amusing showing cognitive abilities. We just need to get the motor neuro connections to reconnect to get him moving again. I know Chris, once he gets any movement at all, he’ll take off on his own and nothing will stop him. I’ve never know anyone with more perseverence than Chris! I’m looking at a collage of pictures we have of Chris before the accident and it brings back such great memories. What a great young man, with a warm spirit, caring heart, and a brain that will again, one day, offer us all something to be proud of in terms of his contributions to our collective time here on this cosmic rock!
All the best to you all. Thank you for your comments, thoughts, and keeping in touch.
Love, Family Giles.

Posted in Updates | 4 Comments


20041225093719Our second family beagle, Nuala, died quite suddenly Saturday morning, September 21st, 2013, at my folks’ house in Alabama.

Looking back through photos of Nuala – and her mother, Molly – reminds me of much happier times.

The more recent photos are also a reminder of the struggle that has been the last three and a half years.

I can remember picking the dogs up at the kennel in Alabama with my dad a week or two after the motorcycle accident.  Molly and Nuala were thrilled to see us, their wagging tails lifting my spirits momentarily until the gut wrenching pain and realization of the true circumstances returned.  The fifteen hour drive back to San Antonio.  The month in Chris’s apartment, our command post of sorts while he was in the STICU at University Hospital.  Packing Chris’s entire adult life into boxes…

20111010155413The shady RV park in south Austin, where my parents lived for several months while Chris was at Texas NeuroRehab.  Having the dogs at my apartment in north Austin, while Chris was at the nursing home.  Back to San Antonio, again in an apartment, near HealthSouth RIOSA.

20110530183214Losing Molly.  And Nuala spending weeks looking for her mom.  Closing out the RIOSA chapter, and the return to Alabama.

20130107122937New hope, the trip to TIRR in Houston, Nuala always along for the ride.  This time in an RV park near the medical center.

Molly and Nuala were kind of a connection to the past, and a connection to how things were before the accident.  Taking them out for walks, in all these unfamiliar places, was head-clearing and therapeutic:  much more for my benefit than theirs.

I brought Chris’s wheelchair down to where my folks buried Nuala, along with Molly’s ashes from San Antonio.  I could swear I saw a tear welling up in one of Chris’s eyes.


1998 – 2013

Posted in Updates | Leave a comment

A Little Hospital Stay

A quick update. Chris had to go into hospital for about four days two weeks ago, unnecessarily, as it turns out. What a palava! We took Chris to see his family Doctor for a very low grade temp. Something was “off’ a bit and we worry about siezures. Seizures, it seems, can be triggerred by anything! We suspected a urinary tract issue and the Doc took a urine sample and sent it off to the lab. We didn’t hear anything back for about a week and a half when the doctor called the house late on a Friday afternoon asking how Chris was. We told her he was fine and her reply was, “No he’s not! He has an infection that I can’t treat with oral antibiotics and he needs to be in hospital on intravenous antibiotics!” “He already has a room at Crestwood hospital. Get him down there and checked in!”  The antibiotics they put him on are very strong antibiotics and, apparently, are very hard on your kidneys!

So off we went to Crestwood hospital. This was our first experience at Crestwood, one of two hospitals in Huntsville, Alabama – three if you count the new hospital in Madison that’s also affiliated with Huntsville hospital. We did NOT have a good experience at Crestwood. It’s a Doctor-owned hospital, they give you a list of about fifty doctor/owners when you check in…….hmmm, cheap bastards interested in the bottom line it seemed more than adequate care for the patients. oops, I didn’t just say that about Doctors did I?

Of course, Chris is not your normal patient and requires supplies that are a bit diferent than most, condom catheters, urinary bags, feeding bags, etc. But the supplies they used there were about the cheapest you can get – we know, we buy them for home use all the time. We ended up supplying the hospital with supplies while he was there! Long story shortened, we won’t be going back to Crestwood anytime soon! After four days of being there, they ran another urine sample and the Doc said it came back clean (a different Doc, not the weekend staff), and wondered why we were there!

Good news for us though. It took us about a new York minute to get out of there! We subjected Chris, as it turns out, to an apparent unneccessary hospital stay! On the upsaide, better that he didn’t have anything wrong with him I suppose thatn the other way round.

The take-away was that we now have our own sterile urine collection jars to take with us to his family Doc so we avoid taking a sample from a urinary bag that’s been on for awhile. They normally last about a week, give or take. But it obviously needs to be a “clean catch,” or you’re liable to grow all kinds of nasties in the sample that will cause a misdiagnosis.

Chris is fine (in terms of the urinary tract issues) and we’re at home and back to our abnormal “normal” routine.

Still working on the logistics for hyperbarics in New Orleans but I’m having a knee replaced here in a few weeks so that will postpone the New Orleans trip and hyperbarics for a few more months. Getting old kind of sucks! As the saying goes, “if I’d known I was going to live this long, I’d have taken better care of myself!”

When you discharge from a hospital, “the system” wants to make a few more bucks by offerrring “home health.” Since it’s free, or I should say no cost to us as we all pay for it in our taxes, we take it because something is better than nothing, although, the therapists they send out really don’t do much! We did get a good lead for home help from the social worker they sent out and the Physical Therapist (the most helpful of all) lead us to an Alabama brain injury resource site that his wife has been involved with and we have also attended a monthly brain injury meeting at the local Healthsouth facility where you get to meet other brain injury survivors and care takers and change stories, ideas, gain some leads here and there, etc. So although we were in hospital unnecessarily, it did produce some posuitive results by way of the social worker at Crestwood who started the ball rolling that led to this lead that led to that lead and so on. Funny how it all works out sometimes!

I’m working on transfer of guardianship for Chris to the State of Alabama (from Texas), another whole different set of legal details and issues, a hassle but a necessary hassle! I remember the first week after Chris’s accident in San Antonio. I called Met Life as they held a disability policy through Chris’s work and the very nice lady on the phone (I’m being facetious) told me she couldn’t talk with me because I was not Christopher. As I explained that I was contacting them on Chris’s behalf since he was currently in intensive care fighting for his life, she asked me how I knew they had corresponded with Chris, to which I replied, “I opened his mail.” She responded with, “that’s illegal!” Of course, the reply they were looking for had a suspense on it that Chris obviously was not going to meet (and I was afraid the policy would be voided without a reply within their time limit). Doing what you would think is the right thing considering the circumstances resulted in some Beeee-atch on the other end telling me off for opening Christopher’s mail! God Bless her little heart as they say in Alabama! And it seemed everyone I talked to on Chris’s behalf (except the hospitals) wanted to know if I had a Power-of-Attorney to act on Chris’s behalf. And of course the answer is no because a power-of-Attorney is something you grant to someone else and of course, Chris was in no condition to grant anything! So off we go down the guqardianship route and some facilities still wanted a Power-of-Attorney even though I told them I had legal guardianship because they didn’t know what guardianship is or how you get it or what it means. Note to self (and I still haven’t given power-of-attorney to mom and Robert), give Power-of-Attorney to someone because it’s too late after an accident, or stroke, or other life-altering event!

OK, enough rambling. We’re out of the hospital and back home! Chris is doing well. He smiles a lot more now and it melts your heart when he does. He’s such a wonderful person and still finds a way to smile even in the face of his situation. He’s a great young man!

Thanks to all for keeping Chris in your thoughts – it helps more than you’ll ever know!

God Bless.


Posted in Updates | Leave a comment


The morning routine around the Giles’ house is a bit different than most. If it’s a weekend, I try to give Mom a little break by taking care of Chris in the morning around seven-ish, at least getting him turned and getting his food going (of course, the dog gets us up to go out around 5:30 or 6:00 and then wants to be fed). The routine consists of repositioning Chris in bed, off his side and on to his back, telling him good morning, we love him, giving him and hug and kiss and telling him how great he looks. Chris usually does a morning stretch and then verbalizes a bit as if to say, “leave me alone. Can’t you see I’m trying to sleep!” And he usually has a little “bed-head” going on. He looks great!
We get the food going (two cans of Jevity 1.2) and morning meds, turn on NPR so he gets to hear a bit of what’s going on in the world and then we usually have a cup or two of tea while Chris is having his first feed of the day. I usually go back to bed while he’s eating and Mom takes over giving meds, shaving him, washing his face. He hates getting his face washed. If it’s a bath day, the bath comes next beginning with a shampoo and moving on from there. When we finally get Chris up, he’s fully dressed, has been fed, and looks great! Mom, mind you, is doing all of this on her own during the week!
Chris goes on his exercise bike (Motomed) every morning for an hour. We wheel him up to the machine, strap his feet into the feet pads and then off he goes on a spin class as Mom calls it for about an hour – usually about twenty kilometers worth. On weekends we’re usually having breakfast while Chris is on his bike. As a nice sidebar, I’ve gotten a full Irish three weeks running now! The works, eggs, Irish Sausages, bacon rashers, black and white pudding, fried tomatoes, toast and jam and, of course, a glass of orange juice and tea! Yum!
Chris gets wheeled into the sitting room after his motomed session and we usually put the television on, usually PBS with the beginning of the Saturday morning line up of DIY shows. Mom was off doing the morning chores this Saturday and I had left the room for something. Chris will sometimes pull his head out of his headrest and it results in his head lying forward on his chest, looking down. When I walked back into the sitting room, there he was with his head lying forward on his chest, having pulled his head out of the head rest. It was the top of the hour and as I walked over to lift his head up for him I noticed the “Create” program was just changing to a new program. As I lifted Chris’s head up I said, “Chris, what are you doing?” Glancing back at the TV I went on, “how can you watch “Sewing with Nancy” with your head on your chest?” Chris gave me the biggest smile I have ever seen! And from both sides, not just the left side that he favors when he normally smiles! I pushed a bit with, “how can you learn to sew if you’re not looking at the TV?” His smile got bigger! He was really enjoying my teasing him and it melted my heart! I gave him a big hug to show how happy he had made me (and to hide my tears), but I was absolutely overjoyed! We’re on our way to good things! That’s the normal ribbing we would have done before his accident. And it’s great to know he still enjoys it!
This Monday morning as I left for work, as I usually do, I go into Chris’s room to tell him goodbye and wish him a good day and to remind him to “practice” moving head, arms, legs, feet. This morning as I grabbed his left hand and gave him a hug and told him to remember to practice movements, he pulled my hand up to his chest with his left arm and then put it back down to his left side, giving a slight “whew” as he completed the movement! He made my day – again! He wanted to show me that he can move and has obviously been practicing, or at least, thinking about the movement. He puts me on cloud nine with the progress knowing that we’re moving in the right direction and that he’s there and trying hard! I feel like we’re on the verge of good things. Chris gives us hope when you least expect it! In the midst of his great personal tragedy and adversity, he finds the strength to gives us hope and to continue fighting! What a lovely young man and what strength of character!
Hope you all have a great day too!
We’ll get there!

Posted in Updates | 2 Comments