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Brian Jackson is a devoted husband and father of 2 young children. At only 47 years old, he had a cervical spinal cord injury which caused him to become a quadriplegic. He has made more recovery than thought to be possible. Now, he requires inpatient rehab at a specialized spinal cord injury facility in order to maximize his recovery and independence and to bring him home to his family.
It all started in February 2024 when my husband, Brian, had a misdiagnosed spinal cord infection. We sought medical intervention by going to many doctors and visiting the ER, only to be told it was either a muscle spasm or a herniated disc. On Februrary 22, he fell in the bathroom at our home. The fall, combined with the pressure on his spinal column, caused a spinal cord injury in the cervical spine (C1-C3).
Brian was admitted to the neuro ICU at Methodist University Hospital in Memphis, TN that day. He had an emergency laminectomy and remained in the ICU for over a month. There were many days that I was unsure if he would survive. I was told by the neurosurgeons and neurology team that he may always be on a ventilator and feeding tube. The nerves to his bowels were also severed. It was a very bleak outlook. He was septic and had multiple comorbidities, including encephalitis, severe edema, stroke and blood clot risk, and finally an exploded cecum in his abdomen which resulted in 2 abdominal surgeries. I didn’t know whether to plan for a funeral or prepare my family for the unknowns of long-term care for quadriplegia.
This catastrophic injury has been absolutely devastating to our family. All of Brian’s cognitive abilities are intact. He is a quadriplegic – trapped in his body and confined to a hospital bed for almost 3 months now. We have a 2-year-old, Isabella, and a 12-year-old, Cooper. Brian was an extremely active parent, handling many of the daily childcare and household duties. I became a single mother overnight, and now we are dealing with the inner workings of insurance, the substantial financial burdens of the future, and what the management of daily life will look like. Brian has been dealing with the reality of his condition and what that means for him as a parent and husband. I can’t fathom what he must feel like every day. He is currently in a long-term acute care hospital, and we must determine the next phase of care.
The hospital initially recommended discharge into a skilled nursing facility. Brian’s prognosis was not good. I started pushing back hard. How could my husband go to a nursing home at only 47 and with 2 children at home? What does that look like for our marriage and for our kids? Before this happened, Brian was full of life and always the funniest person in the room. Now, our lives have become a nightmare. We had to find a way to turn it around.
Despite the bleak picture the doctors painted for us, Brian has made a tremendous amount of recovery based on his initial prognosis. He is no longer on the ventilator, trach, or feeding tube. He can now move his right hand and feed himself, though his arms are still relatively weak. He can push some with his feet. Brian is extremely stubborn and a born fighter. He is doing more than anyone thought initially possible.
Brian began requesting extra physical therapy in the hopes of being qualified to go to an inpatient rehab facility. There are no Spinal Cord Injury (SCI) Model System centers in Memphis. We asked the hospital to submit his information to several SCI-MS centers, including the Shirley Ryan AbilityLab in Chicago, Illinois. After a lot of hard work and advocacy, Brian will likely be accepted at Shirley Ryan pending one more MRI of his abdomen. Final approval is not submitted until 48 hours pre-discharge, so we are starting to plan now given the very short timeframe. He can be discharged from the hospital at any time. The problem will be transportation to and from Chicago since Brian requires an air ambulance and our family’s travel, lodging, and childcare costs.
We are asking for help from our community and beyond. I never thought I would be in a position to have to ask for help, but we have no other choice. The only hope for Brian to ever come home and to maximize his independence is to get the specialized rehab he so desperately needs. Unfortunately, we do not have the resources to cover the insurmountable expense of it all.
The donations will help to pay for the air ambulance to and from the Shirley Ryan AbilityLab. Additionally, the kids and I will travel to Chicago, and the donations will help to pay for our travel and lodging costs.
If Brian is able to discharge home from Shirley Ryan, which is the ultimate goal, he’ll need specialized equipment, and we’ll need major home renovations, a wheelchair-accessible vehicle, and home healthcare. He will likely have ongoing physical and occupational therapies for an extended time after discharge.
Thank you for reading our story. It is a humbling experience to ask for and accept the type of help we need. I will share updates throughout our journey.
Sincerely,
Mary Kathryn Jackson
Family and friends of Brian Jackson are raising money for the nonprofit Help Hope Live to fund medical expenses associated with Brian’s catastrophic spinal cord injury. Brian has chosen to fundraise for Help Hope Live in part because Help Hope Live assures fiscal accountability of funds raised and tax deductibility for contributors. Contributors can be sure donations will be used to pay or reimburse medical and related expenses. To make a tax-deductible donation to this fundraising campaign, click on the Give button. For more information, please contact Help Hope Live at 800.642.8399.
I have gotten a lot of questions about Brian lately. I am truly sorry that I haven’t updated the campaign page. Each day is a lot. Each minute is a lot. Brian has been in Memphis since July 31. He is at a hospital, and I am working with the hospital case worker to get him into a skilled nursing facility. He has been clinically denied at every place I requested a referral be sent to… all the “best” nursing homes. So, we’re down to 5 options. There was only 1 with a private room, and that’s important to Brian. We’re trying to get into that one, but there are more insurance issues. Brian’s age is a problem to get him approved for state programs. The hospital is trying one more time to get approved with insurance. We will see. I am not optimistic about it. At least at a skilled nursing facility, he will be able to bathe and get out of the bed for PT and OT. Right now, he is bed bound and unable to shower. Who knew a hospital wouldn’t be accessible for an SCI patient? I was hoping to wait to report on the campaign page until I actually had news to share, but we’re in limbo right now. Brian is okay. The kids are okay. I am okay. Isabella started ballet this month, and she’s really enjoying it! She is also doing to full time daycare 3 days a week, and that has made my workload and household chore load easier to manage. Cooper broke his arm last week, but even he is mostly in good spirits. I think all of us are burnt out from the hospital, and I can’t imagine how Brian feels and handles it most the time. But here we all are, going forward each day. I am amazed at these kids, especially Cooper. He is wise beyond his years and incredibly kind, particularly for someone only 12 years old. I don’t know what I’d do without him! I promise I will update the page as soon as I have more to report. Please continue to keep our family in your thoughts.
The kids and I visited Brian in Chicago for five days. They were all so happy to see each other! While we were there, we took Brian to the aquarium and on the river cruise. He had only been outside of the hospital a couple of times. It was nice doing something normal together. Brian was in better spirits when we were there. I will post some pictures in a new album shortly.
The hospital had me participate in caregiver training. They are working on slide board transfers, which is basically using a wooden board to help Brian scoot (with assistance) from the hospital bed into his motorized wheelchair. He's made a lot of progress doing small things by himself, but he will need someone with him a lot of the time to help get him in and out of the bed (hopefully using the slide board and not the lift all the time), for bathing, etc. His cognitive issues have improved some. He is able to sort his own medications. He gets really tired after rehab. The kids definitely wore him out while we were there!
Over the past week, I have been dealing with more insurance issues and trying to work with the hospital to determine the next phase of care. Unfortunately, the in-patient rehab benefits have been depleted. We are completely out of benefits starting this Friday, July 26. The hospital was planning to transfer him to a step-down spinal cord rehab facility, and there is one that may possibly bill a different way. If that doesn't work out, I will have to get a little creative to get Brian back to Memphis and figure out where he will go once he's here. He still needs intensive rehab. It is unfortunate and disheartening that we are at this point - where continued intensive rehab may not be possible due to insurance limits.
I am beyond frustrated and exhausted on so many fronts. There are a lot more things that need to happen in order for Brian to come home. He has only just started the bowel program, and he will continue to require nursing care, physical therapy, and occupational therapy. There are no renovations on our house, and I frankly don't know if we will continue to live here if he is discharged home. There isn't much room here to accommodate a hospital bed and lift. They are recommending a wheelchair-accessible van, which, of course, we do not have. They cannot send any equipment (like the lift or his custom electronic wheelchair) unless he is home - kind of the chicken before the egg conundrum.
I will keep everyone posted once we know where he is going. It will either be a facility in southern Illinois or back to Memphis. Thank you for the continued well wishes and to everyone who has reached out to us.
Brian continues to do therapy for 3+ hours a day 5+ days a week. Unfortunately, he has yet another infection that requires IV antibiotics. I am virtually meeting with his medical team on Thursday to understand more about his long-term prognosis and discharge plans. Developing the list of questions for his medical team over the last couple of days has been disheartening and overwhelming, but here we are... trudging through day by day.
He went outside for the first time in over 4 months this past week, and that seemed to help his depression somewhat. He is having more issues with short-term memory, and they can no longer work on bathroom training (or even begin to talk about things like toilet transfer) until after this new infection clears. He started gait training, and he has increased movement in all 4 limbs. He is unable to sit up on his own, though, and cannot support his body weight. He is unable to turn his body from side to side and requires repositioning and cushions to avoid new pressure sores. They have a lot of crazy equipment there, so it is promising he's regaining some strength and hopefully more independence. I got Brian a new magnetic charger and stand for his phone, and that seemed to help him quite a bit. It's the small things :)
The kids and I will travel to Chicago on July 10. I will have 2 half days of family training. I'm sure Isabella will be super helpful lol. The hospital refers to me now as "caregiver," which is a lot to process on its own. I don't know what a month from now looks like, let alone 6 months or a year. The goal is for Brian to return home, but a lot of it depends on his prognosis and the level of care he will need at discharge. I will keep you all posted as time and my own capacity allows.
Thank you everyone for your continued support, thoughts, prayers, and positive vibes. I honestly don't know what I would do without such a strong support system, especially my siblings.
The kids and I had to cancel our trip to Chicago. Brian was admitted to Northwestern University Hospital on Friday, May 31. He had another growing abscess in his abdomen. He thankfully didn't require another surgery or a drain. They finally removed the feeding tube, and they will continue to watch the residual abscesses in his cervical spine and abdomen. He was readmitted to the Shirley Ryan Ability Lab last night, June 10. Therapy assessments began again today, and we'll receive another discharge date soon. It has been a lot for me to juggle and keep track of, along with the kids and work. I'll post some new pictures of Brian in the coming weeks and will share updates as much as I can along the way. The kids and I will likely visit Brian in July.
We made it to Chicago! After much discussion, Brian was able to go to Chicago via ground ambulance, and the plan now is for him to return via ground ambulance. It was a long and rough ride for him, but he didn't get any new pressure sores. He left Memphis around 4 a.m. and arrived in Chicago around 12 p.m. on Saturday, May 25.
The next 2 days were full of evaluations and assessments. Even though it is capped off now and not being used, Brian's feeding tub is still in his abdomen. It causes quite a bit of pain. We hope that is removed this week. By Wednesday, May 29, he had already started a full day of therapy, which included physical, occupational, speech, mental health, and cognitive therapies. Occupational therapy will include grooming - brushing teeth, washing hands, and showering - so we are both excited about that. The goal is to reach the highest level of independence possible. It will be a lot of work, but Brian is really trying to push past the exhaustion and get it done!
My sister, a doctor of Chinese medicine and acupuncture, connected me with another doctor in Memphis who specializes in neuro therapies. She gave me a special pad that hooks up to a phone app for frequency-specific microcurrent (FSM) therapy. She created a few different FSM programs within the app specifically for Brian's issues - nerve pain, spinal cord repair, infection, etc.
The kids and I will return to Chicago next week. Cooper is very anxious to see Brian in this new, high-tech facility. Brian thanks everyone for their support.
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A special offering from the congregation of the First presbyterian Church of Rosemark
special offering Rosemark First Presbyterian
Praying for y’all during this trial. May God bless you with His presence.
Virginia Davis
Wish you a speedy recovery!
Sagar Khadka
We are praying for Brian and all his family
HARRY DAVIDSON
Brian/Mary Kathryn -
Wishing you strength and steady progress!
Janie Thompson and Bill Thompson
William Thompson
Wishing you all the best!!
Shaun Southern
Stay strong! Wishing you well and speedy recovery!
Anonymous
Jennifer Johnson Little
Jennifer Little
Stay strong!! Sending thoughts and prayers for your recovery.
Anonymous
Sending thoughts and prayers from our entire team!
Monique Stitts
Sending prayers for continued progress, Brian!
Alison & John Barnum
Praying for your family
Denise Wood
The Lord tells us in Isaiah 41:10, \"So do not fear, for I am with you; do not be dismayed, for I am your God. I will strengthen you and help you; I will uphold you with my righteous right hand.\"
We are praying for you and your family!
David Chigne, CCP PSP CEP
We will continue to pray for Brian and his family.
Judy & Daniel Horning Amsler
Daniel & Judy Horning Amsler
In hope that Brian can receive the best of care and in loving memory of Mariellen Thompson.
Linda and Lee Davidson
Sending love to you and your family. Ansley (George’s mom)
Ansley Murphy
Sending love and support to your family, Mary Kathryn and Brian. - Janice Johnson
Janice Johnson
Brian, we are both sending up prayers that you get the professional care that you need in order to return home to your family. God Bless you and yours during these difficult times.
Paul and Pat Glidewell
You remain in my thoughts and prayers, Brian.
Jennie Amos
More prayers for Brian and the family.
Jim Krebs
Brian wishing you a smooth recovery.
Chelsea Calhoun
Get well soon Brian :-)
Lucia Vernon
God speed on your journey!!
Jeffery Stimpson
Our thoughts are with you,
Kelly Gray and Jim Dietz
Kelly Gray
All the best in your recovery
David Mallett
Thinking of you and your sweet family and hoping for a quick recovery.
Linda B Sowell
Sending my heartfelt wishes for a swift and complete recovery to your husband, Mary Katheryn! My thoughts are with you and your family during this challenging time.
Felipe Gutierrez
Prayers for the family and a full recovery for Brian
Debra Dunavant
Brian, thinking of you so much and praying for you everyday. Hope to come and see you very soon. Miss hearing your laugh and seeing you smile. Lots of love from us all.
Marlana Rose, Keith Turk, Riley Higgs
Sending love and hugs to you and your entire family!
Anonymous
My prayers for a speedy recovery!!
STEVE WARHOE
We'll keep your family in our prayers!
Dan Gilmour
Praying for your family
Jessica Colbert
Best wishes for a your continued treatment and recovery!
Larry Dysert
So good to hear that Brian is improving! Hang in there.
Christian Heller
You all are in my heart and prayers
Carol Tuggle
Sending lots of love and support to all of you.
Carol Ross-Spang
Hoping the best for your amazing family. Brian's progress is awesome. Hoping things improve steadily for all of you.
Greg Carte
I continue to pray for your family. Sending all my love from our family. Audrey, Ben, and Vance
Audrey Stimpson
Our prayers are with your family!
Marshall’s parents
Melody McAnally
Make checks payable to:
Help Hope Live
Note in memo:
In honor of Brian Jackson
Mail to:
Help Hope Live
2 Radnor Corporate Center
Suite 100
100 Matsonford Road
Radnor, PA 19087
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