Jeff's Journey will be a place where family and friends can come to get updates on our dad's condition and progress. We have a long road ahead of us and we hope that this blog can serve not only as a place for updates but also as a journal of strength and remembrance. We have faith in our Heavenly Father and his Son Jesus Christ and we know that through our faith and perseverance our dad will be healed. Though we have been told that the chances are slim (1 in 200,000) that our dad will walk again, we will be by his side to help him beat those odds. Our dad will make it through this challenging trial and we will be there to help him every step of the way! We love you DAD & GRANDPA!!

Thursday, September 10, 2015

Day 18 - September 10, 2015

Today I (Brandi - Jeff's oldest daughter) had the opportunity to spend the entire day with my dad, so since I had first hand experience, I am going to try on my own to tell you about today's events.  I am not a writer like Julee, but I will do my best.

I arrived just after 9:00AM and found a very sleepy Jeff.  He told me he had been up most of the night thinking and pondering on things.  He said his mind was very clear and he felt great and wished he had some dictation software to use so that he could type up what he wanted to say to contribute to this blog.  And thus, my first assignment was given to me and I gladly sat down with his phone and tablet to find an app that would allow him to talk into the microphone as it would then type for him.

Not only had Jeff not gotten much sleep, but he had a fever this morning which totally wiped him out.  He was very disappointed and frustrated with the way he felt today because he so badly wanted to get right to work and give rehab 100% of his efforts.

Even though he was sleepy and as he put it "wiped out" the therapy still continued.....

First the speech therapist came in to assess his swallowing capabilities, assess speaking capability, cognitive ability, etc.  The speech therapist told Jeff that his attitude, determination & personality were remarkable.  Jeff told her about his accident and told her that because he is still here on this earth he remembers what is important.  He stated that even though he has always been a pretty positive person, his attitude now has been better than it ever has been before.  Jeff continued to talk about how he is very thankful for ALL the people that he has met and that he desires to show appreciation and thanks and to treat everyone as Christ would.  He then said, "if you treat people the way you want to be treated and love everyone the way Christ does it's a great experience!"

The speech therapist then had to ask Jeff those annoying cognitive questions that he hates.  Some of the things she asked him were, "Is a hammer good for cutting wood? Is one pound of flour heavier than two pounds?" and just like in Denver he was asked "Who's our President?" and can you guess his reply?  Yes, it hadn't changed as he blurted out "Asshole --- Obama" and the speech therapist started laughing and said, "I've had worse replies to that question." The last question asked was, "Who discovered America?" and Jeff answered, "Well that's debatable --- Columbus"

Next came in the Occupational Therapist who's name is Josh.  Josh came in to discuss what his role was in therapy.  They discussed Jeff's house and what modifications needed to be made for him.  Jeff proceeded to tell Josh all that he and his brother's and dad were planning to do to make the house ready for him when he came home.  Josh laughed and said, "I can tell your an auto body guy - just wanting to cut that out, modify that, change the color to hot pink..."  He then told Jeff, "Jeff you are emotionally three months ahead of yourself, that is AWESOME!!" Jeff told Josh that he wants to do everything possible to get his hands to squeeze.  Josh said they could work on that, but his goal was for my dad to be able to learn all he needed to learn to be independent with his current capacities. Josh's job is to teach my dad how to get in and out of bed, how to brush his teeth, how to hold a spoon to eat, etc.  Josh then had to leave but said he would be back later in the afternoon.

Next came in Cami, the Physical Therapist who would do Jeff's initial evaluation.  Cami and Josh put shorts on Jeff and lifted him out of bed into a wheelchair.





As soon as Jeff was settled in his wheelchair Josh said, "lets get you out of this gown" and asked Annette if she had a shirt for Jeff to wear.  Annette handed Josh a shirt and he immediately gave it to Jeff and said, "put it on".  Jeff was a little stunned and then answered, "you want me to do it?"  Josh said, "yes, lets see what you can do".  Jeff then immediately took the "challenge" and found the arm holes in his shirt and shoved his arms through.  My mom and I believe he probably could have gotten it most of the way on himself if it wasn't for the big neck brace that had to be maneuvered around.  All in all, with a little help, Jeff did a great job putting on his own shirt.




Jeff was wheeled down to the therapy room for some physical therapy with Cami.  They have to watch his blood pressure really close to make sure it doesn't get to low because they don't want him passing out.


Jeff was still extremely tired and he still had the fever so it didn't help the situation, but he conjured up enough energy to give me a smile for his "first day in therapy picture".



While in a wheelchair they still need to lean him back or reposition him every 15 minutes to keep his blood pressure under control and allow blood to flow more easily throughout his body.  He was so exhausted that he couldn't hardly stay awake to listen to Cami and he kept falling asleep.  This made him so frustrated, but Cami reassured him it was fine because they repeat things over and over again.

Jeff went back to his room and was told that he could stay sitting in the wheelchair for 45 minutes, but that he needed to be repositioned every 15 minutes.  For some reason or another the nurses weren't able to come do this so my mom and I tried our best.  Jeff ate lasagna for lunch and the fact that my mom could cut it with a spoon told me that the noodles were too mushy and that my dad wasn't going to like it.  Sure, thing after the first bite he commented that the flavor was good but the texture was horrible because the noodles were mushy.

I then headed down to the cafeteria around 2:00pm to find my mom and I something to eat for lunch.  I ended up buying us a cheeseburger and tater tots (it was Tater Tot Thursday).  When I returned, Josh, the OT was working with Jeff on picking up a spoon and positioning it so that he could eat with it.  He was doing really well, but it was all my mom and I could do to hold ourselves back.  We wanted to help him do it, but realize that it is in his best interest if we don't. 


Josh then asked what I had brought for lunch and told me to bring over a few of the tater tots.  He sat them in front of my dad on his lap and told him, "eat them".  For the first time in 18 days Jeff fed himself.  My mom and I were so elated to see him do this that we made him wait to eat the last tater tot until I got out my phone and recorded the event on video.


After eating the "marginal" tater tots Jeff asked for a drink and Annette reached over to give him a sip from his cup and Josh said, "wait a minute, why are you doing that?!"  Jeff replied, "because I don't want to spill it all over myself".  Josh then put the cup on Jeff's lap, helped him stabilize it and showed him how he could hold it himself.  Because Jeff doesn't have any movement in his fingers he has to try to use his fist and wrist to open his fingers and position them where he needs them.  To me it looks very difficult, but my dad does it without a single complaint and I am so proud of him!!



Then it was time for Physical Therapy again, but this time with Alex.  Alex will be with my dad for 7 days strait.  He works 7 days on then 7 days off and today was day 1 of a 7 day stretch, so my dad will get to see a lot of him this week.  Alex showed Annette how to put on Jeff's tennis shoes and then they put him in a wheelchair again and took him down to the "workout room".



Jeff was still exhausted and feverish, but he was able to stay awake and not fall asleep which he was grateful for.  Alex got him out of the wheelchair and positioned him on a table that helps him get in a standing position. For today, because of blood pressure issues, the table was left at a 35% angle.  Alex helped Jeff work the muscles in his arms and shoulders and even though Jeff felt terrible he gave it his all and did exactly what Alex asked him to do.




After his workout, a very exhausted Jeff was wheeled back to his room by Annette.

He slept as best he could while waiting for his cousin Camille Ewell Salehi to come and give him a hair cut.  We are all so very grateful that Camille volunteered to come cut our dad's hair.  He has been complaining about it ever since he was in Denver and he is very happy to finally have it cut.  Our dad has always cut his own hair with a Flowbee so having Camille cut it for him was a real treat - Thanks Camille!!  (For those of you who don't know, a Flowbee is a haircutting system that hooks up to a shop vac.  Basically my dad could cut his hair and watch TV or work on the computer at the same time.)



When I left the hospital this evening, they still hadn't shared with us the results of the blood work and urinalysis which was disappointing because we were hoping to figure out what is causing Jeff to have a fever and not feel well.  Hopefully tomorrow we will find out.

Jeff had cousins come visit him this afternoon and tonight and we are grateful to them for coming and showing their love and support for our dad!  We found out today from the therapists that everyday will be as busy as today if not more busy than today. Because our dad is going to be so busy during the day working with the therapists and learning all that he needs to learn we ask that if you would like to visit that you please call Annette to make sure it's okay that you come and to also plan on coming after 4:00pm.

Finally, I would just like to say that my mom is awesome!!  The way she cares for my dad is remarkable and I am so grateful that the Lord is strengthening her and providing her with what she needs, both physically & emotionally, to help my dad.

Then there is my dad, I am so very thankful I am his daughter and that he realizes that our family still needs him.  I am grateful that he feels that he still has a purpose here on this earth.  He is so positive and patient and I love sitting and listening to him talk with the Nurses and Therapists and share with them his views on life as he now sees it and then asks them questions so he can get to know them better.  I too want to learn how to treat people and love people like Christ would and I know that I can learn this through watching my dad and following his example.

I just want everyone who is reading this to know that if you are going through a trial in your life please go to God for help, support and strength.  I can't imagine going through this type of family trial without the Lord at our side.  Having his spirit with us gives us so much strength and hope for the future that it is incredible.  I know that through this trial my dad will experience JOY like he has never experienced before and he will be an example to others through his words and actions.  The light of Christ will shine through him allowing him to share his testimony with many, many, many people.  I am also grateful for the peace that the Lord has given me to know that no matter what my dad is capable of in the future, he will be happy, find joy and be content with whatever situation he is in.

Please continue to pray for our dad, our mom & our family. Your prayers help strengthen all of us and we are so grateful for them!

Day 17 - September 9, 2015

Jeff is now officially in Neuro rehab! The grueling hard work starts tomorrow and he is more than up to the challenge. There's no doubt that the Lord has heard our prayers.

The plan is to take things slowly and build up to more vigorous and more frequent therapy as he tolerates it. This phase of recovery is critical for developing the skills and abilities needed to return to a regular way of life. We know that while he may be limited physically, in time he'll be able to drive, be the brains of his business, and get back to the busy lifestyle he's always enjoyed.

We expect tough days ahead as he learns how to maneuver his body and relearn skills that used to be as easy as breathing. He will need all the encouragement and support we can give him. We are so grateful for the incredible network of friends and family who have shown their love for Jeff and our family, it is truly humbling.
 
Yesterday Annette came home from the hospital with a list of things Jeff would need for rehab.  One of the items on the list was 5 sets of comfy clothes. As Annette & Cherie were looking through Jeff's clothes they realized that Jeff didn't really have any good shirts that would be comfy and breathable not to mention that the neck needed to be stretchy to fit over the neck brace and all his t-shirts were cotton and not fit at all for rehab.  So, Cherie & Blake went to Target and bought Jeff three loose fitting breathable shirts and a pair of basketball shorts and took them to him at the hospital.  When they showed Jeff the clothes they had bought he said, "those will work, they look like my style".  This means that Cherie and Blake did a good job at choosing out the right clothes.


Jeff tried a wrap for lunch today and he said it was good, but he wouldn't get it again because it was the size of a softball and difficult to eat and Annette had a hard time cutting it up and keeping it all together.

Grandpa & Grandma Green (Annette's parents - Clifton & Joyce) came for a quick visit today.  After Jeff ate lunch he was tired and wanted a nap so Cherie, Blake, Aliyah, Annette, Grandma & Grandpa left and went to lunch at Rumbi's while he slept.

The people in Rehab say that Jeff will be there for 6-8 weeks, but Jeff says he is shooting for 4-6 weeks.

Cherie said that it was really great to see her dad and see him continuing to make progress.  It is also great to see him ready and eager to get going in rehab.

For the next several weeks, give or take, he'll remain in his current room.
The address to send him your well wishes is:

IMC, Pt. Tower, Rm. 1209
In care of Jeffery Page
5121 Cottonwood St.
Murray, UT 84157

We pray for continued progress with high hopes and unwavering faith. The Lord has a plan and in time His wisdom will shine forth like a beacon of light and we may gain a better understanding of why this has happened. Until that time, we will stay strong together and lift each other up through the long days ahead.

Tuesday, September 8, 2015

Day 16 - September 8, 2015

Jeff got moved out of the ICU today! The room he was moved to will not be his final destination. It was more like a rest stop without the rest. His room on the inpatient rehab floor is calling his name and thankfully his reservation is set for tomorrow.

When he's settled in his permanent room (for the next phase of recovery) we'll get the address and post it on this blog for everyone who desires to send him well wishes.

They changed out his neck brace again to try and help him be more comfortable. The one he has now is larger, but better because it has more padding.

Grandkids and grandpa were finally reunited! Sierra and Talon were both shy at first and more interested in the gadgets around the room than anything else. Jaxon and Kaisy had a lot more questions about what grandpa could and couldn't do and what is expected as far as recovery goes. Tylee was all smiles. They've missed their grandpa and despite them seeing him "messed up" as he calls it, it was a very sweet reunion.
 

Annette took a much needed break to get her hair done this evening, but even as she left she was hesitant to go saying, "I should just cancel it." Her love and attention for our dad is immeasurable and we know that with her help our dad can accomplish anything.

Jeff's biggest hope is to regain the use of his hands. He then said, "If I could get my hands back and the use of my stomach muscles, I could do anything!"

While we continue to pray for a full recovery, we know it's in the Lord's hands. The healing process has just begun and the possibilities are endless at this point. We remain optimistic and count each day a blessing.

It was great to see Jeff interact with friends and family. Even when he was in pain he was animated and passionate about all the same things he used to be. A huge thank you to everyone who has come to visit so far. The words of encouragement and distraction are much needed and appreciated.

We may seem redundant with the thank you's, but it's only because we are so overflowing with gratitude for all of the blessings we've received... For every kind word of concern and love, every encouragement, every financial help, and every moment we've been blessed to keep Jeff on this earth. With so much to be grateful for it's difficult to express our overwhelming appreciation fully.

We pray that the Lord blesses you all for your kindness and love toward our family in our time of need.

Day 15 - September 7, 2015

Today marks the two week anniversary of Jeff's accident. It's been a very long and difficult two weeks. We are extremely happy to report that Jeff is in stable condition and if nothing changes he will be transferred out of the ICU tomorrow. That means more visitors at a time, more physical therapy, and more progress!

The physical therapy regimen will be extremely vigorous, for which Jeff is grateful. He says they told him it will be an 8 hour day, like a full time job. The doctors are all impressed by how motivated he is to get going.

They used a special board today to get him into a standing position for the first time and he did really well!





We are so thankful for everyone who has visited so far! His therapy will be on a schedule so it will be easier to schedule visitors once that's been established. Just give Annette a call to know when is best. Jeff and Annette look forward to the time they get with all of you!

As things have become more predictable and everyone now has the option to visit with our dad, we will only be posting updates every two to three days from here on out. If you ever have questions you'd like us to answer you can post it under the comments on this blog or contact Brandi or Julee.

Of course if anything big happens we'll post it! We're going to continue to track his progress on this blog for his benefit, our benefit, and anyone else who is interested. We are grateful for such a readily available way to keep everyone up to date and involved.

So very very grateful for everyone who has donated financially to help our dad! Your kindness is overwhelmingly appreciated! We are just barley over half way to our goal!! Every penny counts & even the smallest amount is appreciated. Our hearts are full and whether you gave $5 or $500 it means so much!  If everyone you knew and everyone they knew and so on only donated $1.00 I know we could meet our goal and beyond. Please help us share our dads story - http://www.gofundme.com/7s2p4cpk.  May God bless you as much as you have blessed us!!!

For everyone who has already given of their time, financial resources, and moral support... you have no idea how much you've helped us all. Words cannot express our gratitude!