`` Teen idol of the 90s says it was his first symptom of the sep

Emma Caulfield details the frightening feeling that led to her diagnosis.


Since its broadcast in 1997, the supernatural aficionados have lovedBuffy against vampires, a show originally based on the 1992 film of the same name. The crew ofBuffy Finally built seven seasons, an empire of novels, comics and video games, the continuous turn on streaming platforms, and of course an unconditional fans base. A beloved character in the later seasons of the series is Anya Jenkins, a former student who has become a school who joined Buffy and the "gang scooby" of adolescents fighting against the dark forces in Sunnydale. NowEmma Caulfield, the actress who gave life to the socially clumsy and endearing Anya, reveals a long kept secret to her health to her family, friends and fans.

You will not only recognize Caulfield of herBuffy years. She portrayed the intelligent and ambitious Susan Keats in season six ofBeverly Hills 90210, as well as Enchanted WestView Reside Dottie Jones in Marvel's Streaming SensationRodvision. Caulfield has decades of films and television on her name, and hopes to have years to act before her too, but all of this was questioned when she received a shocking health diagnosis in 2010, after having experienced frightening symptoms. Read the rest for the first Caulfield index that something is wrong.

Read this then:If you notice it with your hands, it could be an early sign of MS.

Caulfield now reveals its 2010 diagnosis.

Emma Caulfield at the Los Angeles Gay And Lesbian Center Homeless Youth Services Benefit held at the Sunset Tower in West Hollywood on January 23, 2012.
Tinseltown / Shutterstock

Like other actorsSelma Blair,,Christina Applegate, andJamie-Lynn Sign, Caulfield is in publicHave a multiple sclerosis (MS), a disease that affects the brain and the nervous system, and can bedeactivation for some. According toMayo clinic, there is currently no remedy for MS, although the treatment can be very effective in managing symptoms and accelerating the recovery of thrusts.

For many years, his own father, who has died since, has had trouble with MS, Caulfield recentlyToldVanity- Explain that hearing her doctor that she also had the condition looked like "an out of the body". Despite herselfannoying and mysterious symptoms, it took him a while to shake the shock of the diagnosis. Her initial response, she says, was an understandable, "no, this is not possible."

A frightening symptom prompted her to get an MRI.

Gilbert Carrasquillo / Getty Images

The first Caulfield index that did not go with his body? "I woke up one morning and the left side of my face felt that there were a million ants that crawl on it," she saidVanity, explaining that it was similar to the feeling of pins and needles that can occur when you sit in a position for too long. "I could still scratch myself [my face] and feel my nails," she recalls, adding that the feeling was extremely dull. She knew something was going, so she visited an acupuncturist, who seemed confused, but suggested that she could haveBell paralysis, which can cause a sudden (generally temporary) weakness of the muscles on one side of your face.

However, she could still move all her muscles, which would be strange for the diagnosis of a bell paralysis. "It was just constantly itching," she said. An MRI confirmed that it was the MS, which can present itself in several ways,disgraient, electrical sensations ofPain by nodding, eye pain, and eventemporary vision loss.

Your health history can also play a huge factor to find out if you are likely to develop MS. A story with the Epstein-Barr virus lands you to32 times more likely To develop the disease, according to leading experts. And according to theUK National Health Service, although the MS is not directly inherited from parents or grandparents, "people related to a person with a condition are more likely to develop it; the chance of a brother or child of someone With a SEP which also developed approximately 2 to 3 in 100. "This means that the six -year -old girl from Emma Caulfield is more at risk than the average child. "It made me think about her and how much she is full of joy and active," thinks about Caulfield, "and she is just a little creature so remarkable."

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She feared that the diagnosis affects her career.

LOS ANGELES - SEP 24: Emma Caulfield at the 5th Annual Red Carpet Safety Awareness Event at the Sony Picture Studios on September 24, 2016 in Culver City, CA
Kathy Hutchins / Shutterstock

"I'm so tired of not being honest," said CaulfieldVanity, explaining that she was terrified that if she spoke to her colleagues and her friends of the diagnosis, it would be a death of death for her career on the screen. "I did not want to give anyone the opportunity not to get involved," she said, explaining how easy it is to raft an actor who seems to even need a hint of special treatment.

"There are already many reasons not to hire people, reasons why most actors do not even know." You look like my ex-girlfriend ... You are too short. You are too big. You look mean. You look too nice. You don't have the right color eyes. "" She knew in her bones, she shares, that "if you talk about it, you just will stop working. That's all."

Caulfield does not let it slow it down.

Emma Caulfield attends the Black Widow World Premiere Fan Event at Dolby Theatre on June 29, 2021 in Los Angeles, California
Alberto E. Rodriguez / Getty Images for Disney

Despite everything risk for future roles, Caulfield is ready to stop hiding, and it is clear that it has no intention of slowing down. "I go back to work!" She shares with enthusiasm. "Everyone has been informed who must be informed."AE0FCC31AE342FD3A1346EBB1F342FCB

His next project will be to resume his role as a dottie for the newRodvision spin-offAgatha: Coven of Chaos. But this time, she will proceed more intelligently, and with more precautions, because she no longer hides her condition. During the shooting forRodvision, who had to shoot in the stifling heat of August because of the delays COVID-19, the heat of Atlanta was "unbearable" for her (the sensitivity to heat and rinsing are a common struggle for those who suffer from ,,According to the National Multiple Sclerosis Society). "If people knew" on her condition, she thinks, "I could have had a small cooling costume under my top and kept my heart cool."

In the future, Caulfield insists: "If I have a platform, I should use it." Now that she has shared her story with the world, she intends to publicly promote the work that theMS company fact, in addition to giving financial donations. "I will continue to talk about it. It's not a unique thing."


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