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Victor nimmt die Gesichter von Menschen plötzlich als verzerrte Fratzen wahr. Grund ist eine seltene Krankheit.
Seltene Krankheit

Plötzlich sehen alle wie Dämonen aus

Besser Leben
Macy Williams hat seit einem Jahr nichts mehr gegessen, weil ihr der Gedanke zu viel Angst macht. Sie leidet an der seltenen Krankheit "Arfid", einer Lebensmittelphobie.
Seltene Erkrankung Arfid

Macy (18) hat große Panik vor Essen

Besser Leben
Die kleine Olivia hat Kinderdemenz. Liv, wie ihre Eltern sie nennen ist gerade einmal vier Jahre alt. Ihre Eltern waren von der Diagnose geschockt. Aber sie wollen für ihre Liv kämpfen. Was die Krankheit bedeutet und wie auch ihr helfen könnt, seht ihr im Video.
Seltene Kinderdemenz

Liv (4) wird nie erwachsen werden

Besser Leben
Auf den Aufnahmen des Gehirns konnten die Ärzte den Bandwurm erkennen.
Schuld war der Frühstücksspeck

Mann hat Bandwurm-Larven im Gehirn

Besser Leben
Anelize Koster
Was steckt dahinter?

Anelize hat das Katzenaugensyndrom

Besser Leben
Mutter und Sohn Sebastian im Krankenhaus
Fatale Fehldiagnose!

Junge (6) stirbt nach „Ohren-Infekt“

Besser Leben
Poppy Massey
Poppy stirbt mit 15 Monaten

Kleines Mädchen wird zu Steinen

Besser Leben
HANDOUT - 20.11.2023, Sachsen-Anhalt, Magdeburg: Ein 32 Kilogramm schwerer Tumor. der einer jungen Frau entfernt wurde, liegt in einem Raum der Universitätsklinik. Die gutartige Geschwulst, ein sogenanntes Zystadenom, hatte sich nach Klinikangaben über längere Zeit unbemerkt entwickelt. (Zu dpa: «32 Kilogramm schwerer Tumor bei Frau in Magdeburg entfernt») Foto: -/Universitätsfrauenklinik Magdeburg/dpa - ACHTUNG: Nur zur redaktionellen Verwendung im Zusammenhang mit der aktuellen Berichterstattung und nur mit vollständiger Nennung des vorstehenden Credits +++ dpa-Bildfunk +++
Mega-Geschwulst!

Frau (24) hat Tumor in Kindes-Größe

Besser Leben
Jennifer Saro ist alleinerziehende Mama.
Prader-Willi-Syndrom

Diese Auswirkungen hat der Gendefekt

Besser Leben
Julius sucht dringend einen passenden Stammzellenspender.
RTL Hessen

Julius (1) sucht seinen Lebensretter

RTL
Elowen im Krankenhaus
Rattenlungenwurm-Infektion!

Mädchen schwebte in Lebensgefahr

Besser Leben
PIC FROM KENNEDY NEWS AND MEDIA (PICTURED: BETH TSANGARIDES, 20, AFTER A SKIN FLARE-UP) This young woman is so 'allergic to HERSELF' that even laughter can leave her looking like 'an acid attack victim' - but has finally worn makeup for the first time in years. Beth Tsangarides says her skin and body react to 'everything' she does, flaring up when she laughs or cries 'too much' and even going into anaphylaxis from many foods, herbs and spices. Horrifying photos show the 20-year-old's scorched, weeping and scabby skin that baffled docs claim is a 'medical mystery'. DISCLAIMER: While Kennedy News and Media uses its best endeavours to establish the copyright and authenticity of all pictures supplied, it accepts no liability for any damage, loss or legal action caused by the use of images supplied and the publication of images is solely at your discretion. SEE KENNEDY NEWS COPY - 0161 697 4266
Mysteriöse Hautkrankheit!

Was Beth (20) jetzt noch Mut macht

Besser Leben
Story from Jam Press (Traumatic Skin Condition) Pictured: Assya Shabir. ‘I have rare butterfly skin condition – trolls say I look like Freddy Krueger’ A woman who suffers from an incurable condition says her skin is as “fragile as butterfly wings”. Assya Shabir, from Birmingham, was born with junctional epidermolysis bullosa (JEB) – a form of EB that describes a group of genetic conditions that affect a person’s skin. The 36-year-old often has to deal with blistering, open wounds, skin loss, friction and irritation – heavily impacting her day-to-day life. She is often “judged or ignored” by strangers and is in and out of the hospital for treatment. “My skin is as fragile as a butterfly’s wings,” Assya, who shared her journey on Instagram with her 10,900 followers (@assyaebqueeen), told NeedToKnow.co.uk. “The slightest grip or even a bump can blister and graze my skin. “It’s not just external; I get blistering in my oesophageal system, eyes, mouth, gums and other areas too. “Living with JEB is complicated at the best of times, it doesn’t just affect me physically but mentally and emotionally too. “It is hard to find genuine friendships and relationships. “Some people don’t acknowledge me – they’ll judge or ignore me.” Sadly Assya also has to put up people staring or making faces. She said: “Most of the time I try not to react or even respond. “But when I’m going through a flare-up and I’m already feeling worse because the pain is unbearable and I’m already feeling useless as it is, their looks hit hard and just make me feel like s**t. “I’m sure you can imagine the kinds of comments I get too. “Ironically it’s from adults more than kids – yes of course kids comment but they’re not aware of why I look different, I always say kids are very innocent. “One of the worst ones I’ve had face to face is ‘you look like Freddie Kruger’ and ‘your mum should have aborted you’. �
Jede Berührung ist eine Qual!

Assya hat die Schmetterlingskrankheit

Besser Leben
Sisco als Harry Potter verkleidet
Mutter kämpft für Sisco (7)

Kasse verweigert Tumorbehandlung

Besser Leben
Story from Jam Press (Brain Eating Bug) Pictured: Stefanía Villamizar González. Girl, 10, dies after contracting brain-eating bug from swimming pool A 10-year-old girl died after allegedly contracting a brain-eating bug from a swimming pool. Stefanía Villamizar González developed ear pain and a fever and began vomiting two days into her family holiday. She was treated for a suspected ear infection before returning home, where her discomfort eased off. But a fortnight after her initial symptoms, she struggled to get out of bed and began convulsing. She was taken to a hospital, where she remained under strict medical care until her death over three weeks later. After a weeks-long investigation, experts gave her cause of death as amoebic encephalitis. It is a rare central nervous system infection with a 95 per cent chance of death. They believe it was caused by Naegleria fowleri, often dubbed the “brain-eating amoeba”, which is often found in badly managed pools or stagnant water. Devastated Tatiana González believes her daughter contracted it through her nose as she played in the water in Santa Marta, Colombia, in June. Stefanía, from Bucaramanga, was a keen tennis player, skater, and ballet dancer who dreamed of becoming a gymnast. A close relative told local media: “We share our story so that other children and families do not suffer what we are going through. “We are destroyed, devastated.” The operations manager of the hotel where Stefanía is believed to have contracted the amoeba has pledged to reinforce safety standards. Local media made no mention of any criminal charges. ENDS EDITOR’S NOTE: Quotations have been translated to English.
Junge Sportlerin (10) stirbt

Tod durch „hirnfressende Amöbe"

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