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Congratulations, You Don't Have MS: How Christina Applegate's Story Affects Us All

Health News · Neurology
After years as one of the best-known faces of MS, Christina Applegate learned from her doctors that she does not have the disease, and her symptoms remain. Her story shows how real multiple sclerosis misdiagnosis is: in one 2019 study, nearly 1 in 5 patients referred to two MS centers with an MS diagnosis likely had another condition.
Since 2021, Applegate has been one of the most recognizable people living with a multiple sclerosis diagnosis. She wrote a memoir about it. She co-hosts the podcast “MeSsy” with actress and fellow MS patient Jamie-Lynn Sigler. She left her Netflix series “Dead to Me” as her health got worse. By her own account, she and Sigler had become “the poster children for MS.”
This week, Applegate returned to the podcast after seven months away, while Sigler had been hosting alone. Then she shared news from a recent doctor visit. Her doctor walked in with new test results and said: “It’s hard to say, but she came into my room, and she said, ‘Congratulations, you don’t have MS.’”
Most of us would expect relief. Applegate felt the opposite. “I was like, not happy at all. Everybody else was so happy.” That sounds strange until you hear the rest.
Back at Square One
A diagnosis is more than a label. It is an answer. For Applegate, MS had explained years of tingling and numbness, poor coordination, balance trouble, and problems walking. Losing the diagnosis did not make those symptoms go away.
“I haven’t gotten better, Jamie! If anything, I’ve gotten worse,” she told Sigler. “So I’m back at square one where I don’t know what’s going on with me.”
She still uses a wheelchair when she goes to the doctor’s office. According to CNN, recent testing using new technology led to the conclusion that she does not have MS, and her doctors are now working to figure out what has been happening since 2021. “Nothing magical happened when she said, ‘You don’t have MS,’” Applegate said.
That is the part of her story many patients will recognize. When symptoms are real but the name for them is uncertain, the goal is the same one behind managing symptoms rather than just masking them: keep looking for the cause, not just a label.
How Often Multiple Sclerosis Misdiagnosis Happens
More often than you might think. In 2019, neurologists at Cedars-Sinai Medical Center and UCLA reviewed 241 new patients who came to their MS clinics already diagnosed with MS. Nearly 18% did not fully meet the diagnostic criteria and had another, more likely diagnosis: 17% at Cedars-Sinai and 19% at UCLA.
Those misdiagnosed patients spent an average of four years being treated for MS before getting the right diagnosis. That added up to about 110 patient-years of unnecessary disease-modifying therapy. Four years, for a disease they did not have.
So what did these patients actually have? The most common alternate diagnoses are among the conditions mistaken for MS most often in clinical practice:
| Alternate diagnosis | What it is | Share of misdiagnosed patients |
|---|---|---|
| Migraine | A headache disorder that can cause neurological symptoms and small spots on brain scans | 16% |
| Radiologically isolated syndrome | MS-like spots on an MRI in someone without typical MS symptoms | 9% |
| Spine disorders (spondylopathy) | Problems in the spinal bones that can press on nerves | 7% |
| Neuropathy | Damage to the nerves outside the brain and spinal cord | 7% |
The study’s lead author, Cedars-Sinai neurologist Dr. Marwa Kaisey, called the diagnosis of MS “tricky” and said, “You have to rule out any other diagnoses, and it’s not a perfect science.” She also described the human cost:
“I’ve seen patients suffering side effects from the medication they were taking for a disease they didn’t have.”
— Dr. Marwa Kaisey, Neurologist, Cedars-Sinai Medical CenterThe findings come from a retrospective review at two academic MS centers, so the exact rates may not apply to every patient or care setting. You can read the Cedars-Sinai MS misdiagnosis study for the full details. Here is the kicker: Kaisey was a guest on Applegate’s podcast this week.
Nobody Is the Villain Here
It would be easy to turn this into a story about bad doctors. It is not that simple.
On the podcast, Kaisey described what she called the “push and pull of the diagnostic process.” Doctors want to diagnose MS early, because starting treatment sooner tends to lead to better long-term outcomes. At the same time, they have to be extremely careful to get the diagnosis right.
That is the real tension, and doctors face it every day. Wait too long, and a person with MS may lose ground. Move too fast, and someone without MS may spend years on the wrong path.
Diagnostic error is not unique to MS. Missed and delayed diagnoses happen with many serious conditions, as the chart below shows. The MS figure comes from a different kind of study than the others, so it is not a direct comparison, but the takeaway is the same: diagnosis is difficult, and a second look can matter.

That is why questions matter, especially when you are asking how MS is diagnosed or whether another condition could fit better. A careful MS differential diagnosis weighs the conditions mistaken for MS before settling on an answer. Which brings us to the one person who sits through every visit, every test, and every prescription.
You.
The Most Invested Person in the Room
At The Wellness Company, we believe nobody values your health as much as you do. Your doctor has many patients. You have one. That does not mean you have to do it alone. Find a doctor you trust, and stay involved:
Keep a symptom log
Write down dates, triggers, what helps, and what does not. Details beat memory.
Ask what else it could be
Good doctors weigh the conditions that can look like MS before settling on a diagnosis.
Ask what would confirm it
Which test, scan, or finding would rule it in, or rule it out?
Keep your records
Keep copies of your records and imaging. Other doctors can only review what you bring.
Get a second opinion
Especially for any diagnosis that means long-term medication. Fresh eyes at a specialty center can catch what a first look missed.
Research your options
Before changing treatment, talk with your doctor about the evidence and your choices.
You may be wondering whether your doctor will be offended. A solid diagnosis should hold up to a second look, and you have every right to understand a treatment before you agree to it. That is the heart of informed consent and knowing what you are agreeing to. And remember who overturned Applegate’s diagnosis in the first place.
Doctors.
Applegate’s story is not over. She is still looking for answers, and we hope she finds them.
Frequently Asked Questions About MS Misdiagnosis
Does an MS misdiagnosis mean a doctor did something wrong?
Not necessarily. MS has no single definitive test, and many other conditions can cause similar symptoms and MRI findings. Doctors also face a real tradeoff: starting MS treatment early can help over time, but moving too fast can send someone down the wrong path. Sometimes a diagnosis simply needs a second look.
How common is MS misdiagnosis?
In a 2019 review of 241 patients referred with an MS diagnosis to clinics at Cedars-Sinai and UCLA, nearly 18% did not fully meet MS criteria and likely had another condition. The most common alternate diagnoses were migraine, radiologically isolated syndrome, spine disorders, and neuropathy. Rates may differ in other care settings.
If MS is ruled out, does that mean the symptoms were not real?
No. Ruling out MS does not make symptoms disappear. It means doctors need to keep looking for the right explanation. That can be frustrating, because it removes one answer without immediately offering a new one.
Key Takeaway
Christina Applegate’s story is a reminder that multiple sclerosis misdiagnosis is more common than many people assume, with nearly 1 in 5 referred patients in one study likely having another condition. A diagnosis is a starting point for good questions, not the end of them. Stay involved, keep records, and ask for a second look when the stakes are high.
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References
- France, L. R. (2026, October 20). Christina Applegate, a leading MS advocate, says doctors found she doesn’t have the disease after all. CNN.
- Kaisey, M., Solomon, A. J., Luu, M., Giesser, B. S., & Sicotte, N. L. (2019). Incidence of multiple sclerosis misdiagnosis in referrals to two academic centers. Multiple Sclerosis and Related Disorders, 30, 51–56. doi:10.1016/j.msard.2019.01.048.
- Neuroscience News. (2019, April 8). Study of multiple sclerosis patients shows 18 percent misdiagnosed. Neuroscience News.
- Newman-Toker, D. E., et al. (2024). Burden of serious harms from diagnostic error in the USA. BMJ Quality & Safety, 33(2), 109–120. BMJ Quality & Safety.
Disclaimer: This content is for general information only and is not medical advice. It does not replace advice from a qualified healthcare professional. Always talk with your doctor before changing your diagnosis, treatment, or medications.





