Seltene Krankheiten: Alle News & Infos - Seite 26

Deutschland am Morgen

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Das Familiengericht

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Das Böse im Blick - Augenzeuge Kamera

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Wasserallergie

Abbie verträgt kein Wasser

Allergie gegen Schweiß, Tränen & Co.

CONTENT WARNING: GRAPHIC PICTURES

Story from Jam Press (Swallowed Cup)

Pictured: An x-ray shows the glass inside the man's stomach.

Doctors remove WHOLE GLASS from man’s STOMACH who ‘swallowed cup while drinking tea’.

Doctors have been left mystified after removing a whole glass from the stomach of a 55-year-old man – who claims he swallowed the cup while drinking tea.

A surgical team operated on the man at a private hospital in Madipur in Bihar, India.

The patient, from Vaishali, was admitted to the hospital with constipation and severe abdominal pain.

He underwent an ultrasound and X-ray, where doctors found a “serious disturbance” in his intestines – which turned out to be a glass.

Doctors struggled to remove the glass from the rectum with an endoscopic procedure, and later had to operate to remove it.

The embarrassed patient claims he swallowed the glass while drinking tea – although doctors said this does not hold up due to the food pipe being too narrow for the object.

Dr Mahmudul Hasan, who headed the team of doctors operating on the patient, said: “How the glass got inside the body of the said patient, it is still a mystery.”

The patient is currently stable.

ENDS

Inder hat Trinkglas im Darm

Die Erklärung blüfft die Ärzte!

Mit Freunden um die Häuser ziehen, Fußball spielen, auf Partys gehen – für den 20-jährigen Can Yetimoglu aus Lüdenscheid kaum möglich. Seit seiner Geburt leidet er an der Schmetterlingskrankheit. Seine Haut ist so empfindlich wie der Flügel eines Schmetterlings. Dadurch ist sein Leben stark eingeschränkt. Doch aufgeben kommt für ihn nicht in Frage.

Jede Berührung kann verletzen

Can hat die Schmetterlingskrankheit

Claire Muffett-Reece während ihrer Enzephalitis-Erkrankung im Krankenbett

Zwanzig Jahre wie ausgelöscht

Frau verliert nach Infekt Gedächtnis

Bild zu: "Die kleinste Stripperin der Welt"

Cassee (32) ist 86 cm groß!

Die kleinste Stripperin der Welt

Bild zu: "So lebt Janina (26) mit Hemiparese"

Schlaganfall noch VOR Geburt

So lebt Janina (26) mit Hemiparese

Child, son, toddler, baby. (CTK Photo/Martin Sterba, Josef Horazny) MODEL RELEASED, MR

Krankheit der lachenden Kinder

Was ist das Angelman-Syndrom?

Mama Melanie Bähr mit der lungenkranken Tochter Merle und ihrem Sohn Lennart.

Ärzte gaben Merle nur ein Jahr

Für ihre Mama "stand die Welt still"

Der achtjährige Stanley Barnes leidet am Sanfilippo-Syndrom und verliert seine Fähigkeiten. Auf dem Bild sieht man ihn mit seinen zwei Geschwistern und seinem Papa Ross.

Grausame Krankheit

Junge erkennt seine Mutter nicht mehr

Allesha Barnfield

Seltene Krankheit

Allesha droht "innere Enthauptung"

Doris leidet an einer seltenen Krankheit, weswegen sich ihre Mutter Alexandra nun geschworen hat ihr zu helfen.

Sie wird nie sprechen können

Mutter will Doris eine Stimme schenken

Story from Jam Press (Cannot Smile)

Pictured: Taylor Clement at school aged 17 (L) and now (R).

Woman born with extremely rare condition that means she can't SMILE becomes Instagram star

Meet the woman born with a one in four million condition which means she can't smile.

Tayla Clement, 24, from Christchurch, New Zealand, has spent her entire life unable to move her eyes from left to right, raise her eyebrows or her upper lip due to Moebius syndrome.

She was born with the condition, which is characterised by weakening or paralysis of muscles in the face used to control expression and eye movements.

The neurological disorder has no cure but the symptoms can be treated.

"It’s not always been easy," Tayla, who has 18,400 followers on Instagram, told Jam Press.

"I’ve spent many years hating my smile, wishing I had a 'normal' smile, wishing I just didn’t exist because that seemed easier than being alive, but by some miracle, I’m still here.

"I now know I was born to stand out.

"I was born to make a difference in this world and I know that whole-heartedly.

"My syndrome and not being able to smile is the greatest gift I could have ever been given, it has allowed me to already help and inspire so many people."

Tayla underwent facial reanimation surgery aged 12 in the hope of restoring voluntary movement in her face.

The corrective procedure – often referred to as a 'smile operation' – saw doctors transplant soft tissue from her thigh to both sides of her face, in a bid to grant her the ability to clench her mouth to mimic a smile.

But the eight-hour procedure was unsuccessful and left devastated Tayla with a completely swollen and bruised face.

Her condition saw her bullied throughout her time at school – where she was called "ugly" on a daily basis and claims to have had sheep poo thrown at her.

The experiences saw her diagnosed with severe clinical depression and anxiety with PTSD and dissociative attacks at the age of 18.

Tayla said:

Seltenes Möbius-Syndrom

Tayla kann nicht lächeln

Baby hat seltenen Gendefekt

Organe liegen außerhalb des Körpers

"Myles ist voller Entschlossenheit und hat immer ein Lächeln im Gesicht", beschreibt seine Mutter ihren kleinen Jungen.

Kleinem Junge (3) fehlen Zähne

Myles kämpft mit dem 4H-Syndrom

Dylan Lombard / CATERS NEWS - (PICTURED Dylan ) A Scottish teenager has opened up about his life with an ultra rare condition - which affects just 13 people worldwide - as his body is unable to store fat. Dylan Lombard, 18, from Glasgow, Scotland, was diagnosed with MDP - Mandibular Hypoplasia, with Deafness and Progeroid Features - when he was 18 months old. The condition - which affects just one in six-hundred-million people worldwide - prevents fatty tissue from being stored underneath the skin, and results in a small lower jaw, ears, deafness and tightening of the skin. Dylan said: "I was born with this condition, but it did not become visible until I was 18 months old.SEE CATERS COPY

Extrem seltenes Syndrom

Dylan: Kein Gramm Fett unter der Haut

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