Ellen Martin, 25, from Surrey, said her life changed in a split second when she was diagnosed with “the suicide disease” which is so painful people often turn to suicide. The disease, which affects the central nervous system, causes indescribable pain and is usually brought on through trauma or injury.
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Ex-Aston Villa player dealing with excruciating pain after a footballing injury developed into a condition known as Suicide Disease.
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Hayley Wright is 20 years old and a Junior at the University of Mobile. She has suffered from Complex Regional Pain Syndrome (CRPS) for the past 4 years.
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Royse City, Texas. Two years ago, Meagan Alford was diagnosed with complex regional pain syndrome (CRPS)– also referred to as “suicide disease.”
Now, the wife and mother of three has launched a GoFundMe to share her story and ask for financial support in her CRPS battle.
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A teenager suffering from a ‘debilitating’ disease that makes it feel like his limbs are submerged in boiling water has launched a GoFundMe campaign to help raise money for ‘life-changing treatment’.
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When asked how she feels about her new pain-free life, Heather said that she feels amazing and super excited to go to school next year and experience everything again.
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When 15-year-old Heather Botha arrived at the airport in Gqeberha this week after spending nearly a year undergoing treatment in the US, she did a cartwheel for her loved ones who had gathered to welcome her home.
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SALISBURY — From the age of 4, Emma Myers had never been without extensive nerve pain. Diagnosed with a condition called Complex Regional Pain Syndrome, Emma has spent the previous 38 weeks at the Spero Clinic in Fayetteville, Arkansas.
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Dr. Katinka to speak at the 2021 Master Circle SuperConference that gathers the highest-rated professionals in the industry to share their thoughts and to help others advance their practices.
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SALISBURY — Emma Myers has some things on her bucket list. She wants to go bear hunting and offshore fishing. Most aren’t typical for a 16-year-old girl, but then Emma’s journey over the last 12 years isn’t typical either. In fact, most medical professionals haven’t even heard of Emma’s disease.
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