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Užasna sudbina
ŽENA SE PRETVARA U KAMEN!
Sreda, 6. April, 2011.| Autor:
LONDON - Britanka Rejčel Vinard (26) pretvara se u kamen!
Nesrećna Rejčel jedna je od stotinak ljudi na celom svetu koji imaju progresivnu koštanu fibrodisplaziju, neizlečivu bolest zbog koje se mišići, ligamenti i vezivno tkivo pretvaraju u kost.
Bolest je kod Rejčel već uznapredovala, a uskoro je očekuje i užasan životni izbor: moraće da odluči u kakvom položaju želi da provede ostatak života. Jer, kad joj jednom okošta trup, promene položaja više nema. Moraće da bira hoće li da stoji, sedi ili leži.
http://www.kurir-info.rs/planeta/zen...amen-83944.php
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---Chelsea Fc---
sumporna ki$elina umije da omechi kosti, ili ono bjeshe neka druga, bem ti hemiju sad zaboravio sam...
SO MANY WOMEN ... SO LITTLE TIME
ne znam sto da ti kazem.
Prosto nevirovatno sta sve postoji. Katastrofa.
"Ostavite mi to mastanje, ono mi dodje kao melem, ono mi moze obezbediti vecnost u vama i sa vama."
e zaisto ne znam kolko je grdno kad dodjete u prekretnicu zivota da birate u kojem polozaju cete biti kad postanete prakticno biljka, koja tu zelja za zivotom vas mora ocuvati da ne izaberete eutanaziju, i slucajevi covjeka drvo zatim one animalije elefantis ili kako se to sve vec zove, stravicno
Risk , is what makes life worth living
Never a failure, always a lesson!
Fibrodysplasia ossificans progressiva (FOP) is a very rare inherited connective tissue disorder characterized by the abnormal development of bone in areas of the body where bone is not normally present (heterotopic ossification), such as the ligaments, tendons, and muscles. Specifically, this disorder causes the body's skeletal muscles and soft connective tissue to undergo a metamorphosis, essentially a transformation into bone, progressively locking joints in place and making movement difficult or impossible. FOP is characterized by malformation of the big toe that is present at birth (congenital). As the disease progresses, there may be other skeletal malformations and the abnormal development of bone may lead to stiffness in affected areas and limited movement in affected joints (e.g.,knees, wrists, shoulders, spine, and/or neck).
Fibrodysplasia ossificans progressiva usually begins during early childhood and progresses throughout life. Most cases of FOP occur as the result of a sporadic new mutation. The genetic mutation that results in this disorder has been identified. FOP is caused by the mutation of a gene in the "BMP pathway", which is associated with the formation of the skeleton in the embryo and the repair of the skeleton following birth.
Last edited by yyy; 13-04-11 at 10:23.
ja bi sjeo, a ona sto se mene tice moze i lec i stojat..
Sacuvaj Bože.
There are so many dawns that have yet to shine!
vala baš sačuvaj bože.
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