[228178] in SIPB-AFS-requests
Affordable health options for you!
daemon@ATHENA.MIT.EDU (Health enrollment)
Wed Jul 23 14:21:30 2025
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Date: Wed, 23 Jul 2025 13:21:27 -0500
From: "Health enrollment" <Healthenrollment@nervefreshs.ru.com>
Reply-To: "Health enrollment" <Healthenrollment@nervefreshs.ru.com>
Subject: Affordable health options for you!
To: <sipb-afsreq-mtg@charon.mit.edu>
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Affordable health options for you!
http://nervefreshs.ru.com/fKBJL6-A3QZRIKVVbF7wQDRc20HAf7kaAROoyyEudwDsYGl8tQ
http://nervefreshs.ru.com/OxoTsHbOrpJ5_4szANDNDl_pvkdhHUzXJ1DAPOUvO3NaZQQWQw
aret Beall Lott (born 1998) is an American-British academic, activist, and model with recessive dystrophic epidermolysis bullosa (EB or RDEB).
EB is a rare terminal illness also called "butterfly skin" due to the skin fragility it causes. With it, even slight friction causes open wounds and blisters resembling severe burns, both on the outer skin and inside the throat. There is no cure, only supportive treatment.
Beall was born in Texas and raised in a small town by a single mother. She was expected to die in infancy, then by the age of 18. When she exceeded her life expectancy she moved to Britain to study medieval art history, saying that the only thing her disease could not stop her from doing was learning. She earned a joint bachelor's degree from the University of St Andrews, two master's degrees from the University of London and University of Cambridge, and is pursuing a doctorate.
Beall's EB activism began at age 17, with writing to raise awareness for her condition. As an adult, she became an ambassador for DEBRA UK, and has participated in other EB charities. She started modeling in a body positive fashion show at university, then posting photographs on her Instagram account, which led to her appearing in pictorials in Vogue Italia and Cosmopolitan UK, and walk
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<div style="color:#FFFFFF;font-size:8px;">aret Beall Lott (born 1998) is an American-British academic, activist, and model with recessive dystrophic epidermolysis bullosa (EB or RDEB). EB is a rare terminal illness also called "butterfly skin" due to the skin fragility it causes. With it, even slight friction causes open wounds and blisters resembling severe burns, both on the outer skin and inside the throat. There is no cure, only supportive treatment. Beall was born in Texas and raised in a small town by a single mother. She was expected to die in infancy, then by the age of 18. When she exceeded her life expectancy she moved to Britain to study medieval art history, saying that the only thing her disease could not stop her from doing was learning. She earned a joint bachelor's degree from the University of St Andrews, two master's degrees from the University of London and University of Cambridge, and is pursuing a doctorate. Beall's EB activism began at age 17, with writing to raise awareness for her condition. As an adult, she became an ambassador for DEBRA UK, and has participated in other EB charities. She started modeling in a body positive fashion show at university, then posting photographs on her Instagram account, which led to her appearing in pictorials in Vogue Italia and Cosmopolitan UK, and walk</div>
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