Blog post originally written by the AllStripes community team. AllStripes was acquired by PicnicHealth in 2023.
For a long time, Jamie Barlow thought her son Bradley’s frequent illnesses were somehow her fault — she’s a nurse, and for a while, she thought she was “Typhoid Mary,” bringing home every illness there was to her child. The older he got, the worse he got, and Jamie knew there was something wrong. When he didn’t get better, she knew she had to look to her biological family history for answers.
My little boy's name was Bradley. As a toddler, he jumped off the bed and broke his leg, after several months, the leg would not heal. For someone that age, 3 ½ , a broken leg should be healed in six weeks flat. He had other issues; for a day or two at a time, he would be completely overactive. Then for two to three days after that, he would be lethargic, vomiting and have diarrhea with no fever.
As an adoptee trying to find some answers, I went looking for an adoptee search engine. On Halloween night in 1999 I found a new site. I wanted to post my story, and noticed there was an option to go public with my story. I posted my story to the public.
Soon after getting off line, I was contacted by a talk show representative for Dr. Joy Browne.
Over the next 24 hours arrangements were made for me to fly to New York to do a taping of the show. They wanted to air this special show prior to the holidays.
The taping was November 3, 1999. Halfway through my interview, while on stage, they pulled my biological mother, Paula, out of the audience. My half sister and nephew were also there. After the interview, my newfound family and I were allowed to go backstage and get to talk with one another. On the way back to the airport we got to ride together. My half sister, Margaret, wrote down a very long word, “adrenoleukodystrophy.” She said, "Unfortunately, we have a very lengthy history of this in our family, and this is most likely what's going on with your son."
I looked it up when I got home, and I was like, "Holy crap."
The next day I returned to work, I was working in pediatrics that day. After I had explained what had happened, I asked the chief of pediatrics to order the diagnostic test for me and he refused. I asked him why, he said the likelihood of that being the problem is slim to none.
The following day I was working in the OB/GYN department. I explained my story, meeting my bio family and the family history. I asked him to order my carrier status, and if I were positive then we could order the tests for my kids. The chief of OB did order the test, but he did say he didn't want to be the one to give me my results. My test came in and he handed me the envelope to read my results so he didn't have to. He had not looked at the results.
Opening the envelope, unfolding the piece of paper ... the look on my face and the tears running down my face let him know what the results were.
He was already prepared to get me to the correct place for further investigation, for my family. He ordered the test for Bradley and my daughter Candice. And even though the tests were not done yet, the chief of OB wrote a referral to Genetics.
Bradley was diagnosed with ALD the day before Thanksgiving 1999.
We went through a battery of tests, and confirmed that Bradley also had Addison’s disease (a condition many males with ALD also have). We were able to put him on medication to keep his body healthy, and we started getting blood tests and MRIs of his brain every six months. It just became part of our life.
Just after Bradley graduated high school he was assaulted, and he had to get a CT and an MRI as a result. The MRI showed that his ALD had taken off like gangbusters. After talking with the team of doctors following Bradley, we decided to pursue a bone marrow transplant.
Three days after the transplant, Bradley had a stroke.
Through additional testing, the doctors found out he actually had another genetic disease called Factor V Leiden, which is a blood-clotting condition. I asked the doctor, "Can you please put that order in for me so I can go get tested immediately?” I already felt guilty enough giving one disease to my kids. So I went down and got tested for this Factor V Leiden, and I was negative.
About three years later, just before his dad’s birthday, Bradley called from his dad’s house and asked for my help encouraging his dad to go out to celebrate his dad's birthday. I talked to his father, and he finally agreed to go out. Brad wanted sushi for dinner. We had a good time, and after dinner, he and his dad were dancing in the parking lot.
That night, we got home and started doing our normal routine before bed. Bradley asked, "Mom, will you sleep in my room with me tonight? And I said, "You okay, bud?" He goes, "Yeah, I just need you with me tonight." So I went to sleep in his room.
The next morning, I was getting his coffee and meds ready. I got him comfortable on his couch. I was in the kitchen when he started yelling at me he hurt all over. I went over to him quickly. He was completely sweaty. I called 911, and we went to the ER. His vitals started dropping off, and he coded. The nurses started CPR. He briefly came to, and the second time they started CPR, I just prayed, and I said, "Just take him home, just take him home. It's okay. Just take him home." He died of a blood clot to his heart, at 2:30 in the afternoon on the 22nd of July.
There was so much care that was needed for him every day. His caregivers were absolutely amazing. They allowed me to go to work every day so I could support my family.
I could not imagine a parent with no medical training, being able to take care of their child, like Bradley, who needed so many detailed procedures done multiple times every day.
Even as a nurse, I was overwhelmed with what had to be done. So when I learned about AllStripes, I wanted to support the research as much as I could — for people with ALD and for ALD carriers, because we carriers of ALD have health issues too. I'm more than happy to give whatever needs to be done so we can stop this monster.
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List the names of all the doctors, hospitals, and other facilities your loved one visits regularly, along with those they have visited in the past. Try to go back as far as you can, striving for at least the last 5-10 years, but do your best. Even if you can’t remember them all, having a strong baseline can help you quickly identify gaps in records.
It is important to make sure that you are fully empowered to make decisions on behalf of your loved one with Alzheimer’s. Your relationship status with the patient may not be enough to legally give you access to your loved one's medical information. It is a good idea to talk to an expert about securing special legal status, such as Power of Attorney (POA), a legal document that allows an individual to name someone as their decision maker should they no longer be able to make decisions on their own.
It’s important to have all of your loved one’s medical records together in one spot. This makes it much easier for you and your loved one’s physicians to accurately map the patient’s medical journey and more easily share information between doctors. Fortunately, tools exist to make record management and access simple. A free resource like PicnicHealth helps you collect and organize all of this information. PicnicHealth’s intuitive timeline allows you to pinpoint data across the medical history, eliminating your need for keeping heavy binders filled with paper records or keeping track of multiple software portal logins.
The better you understand your loved one's medical history, the better you can advocate on their behalf. Access and understanding of this information will help you to ask informed questions with physicians. Through regular communication backed by the data in the medical records, you can help your loved one’s care team develop a more successful care plan.
Learn more about PicnicHealth’s commitment to the Alzheimer’s community and the Alzheimer’s Association
Learn MoreWhen you’re juggling appointment times and insurance claims, putting a robust support system together might not strike you as the most urgent task. Investing the time to cultivate relationships with people can turn to in times of need will pay dividends. The next time you need a last-minute ride or just someone to listen, you won’t be on your own.
There are many condition-specific support groups and support groups for caregivers generally in person or online. In addition to the encouragement and empathy they provide, support groups can be a helpful source of tips, resources, and recommendations for navigating caregiving.
The backbone of effective caregiving is organization. Keep medical information, appointment schedules, and medication lists in order. Use a planner or a digital service like PicnicHealth to stay on top of your responsibilities. This attention to detail can prevent future complications and reduce day-to-day stress.
We’ve seen incredible breakthroughs in treatment over the past couple of years, powered by patients and their caregivers participating in research. Stay in the loop about the latest in medical advancements and available resources that could benefit your loved one. Whether it’s a new therapy option or a community service that aids independence, being informed can make a world of difference in the quality of care you provide.
It may seem self-centered to focus on self-care—but when you feel good, you can be a better caregiver. Whether it’s exercise, a mindfulness practice, a soak in the bath, or just time to rest when you need it, carve out those moments in the day when you can unwind, reset, and stay healthy mentally and physically. Think of it as building up your reserves of kindness, patience, and understanding—which can only benefit your loved one. No one can pour from an empty cup.
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Learn More(from 13 patients with LC-FAOD)
38% Female
15 providers / patient
7.5 years of data / patient
(from 13 patients with LC-FAOD)
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Explore the essential takeaways from Victoria's Webinar, along with some resources that she shared.
