Ukungondleki kwimeko eqhelekileyo yokukhula kakubi kubantu abane-cystic fibrosis
Ukungondleki kungumqondiso oqhelekileyo we- cystic fibrosis (CF) engalawulwa okanye engalawulwa kakuhle. Ukungondleki kukukhokelela ekukhuleni okubi kunye nokulahlekelwa kwindleko, okuyiyo impawu zokuqala ezibangela ukuba oogqirha bakrokre ukuba umntwana unokuba neCF. Ukuba umntwana wakho akakhula ngenxa yokuba engenakondla, unokuva ugqirha wakho usebenzisa igama elithi "ukungaphumeleli." Oku kuthetha ukuba umntwana wakho akahlakuli kwizinga eliqhelekileyo leminyaka yabo.
Emva kokuba unyango luqalisiwe, izigulane zivame ukuphendula kakuhle kwiinguqu zokutya kwaye ziqale ukulandela amaphethini okukhula okuqhelekileyo.
Yintoni Ebangelwa Ukungondleki Kwabantu Abantu abaneCystic Fibrosis?
Impendulo elula kulo mbuzo kukuba ngaphandle kokonyango, abantu abane-cystic fibrosis basebenzisa amandla amaninzi kunokuba banako ukusebenzisa. Eyona nto ibalulekileyo, i-akhawunti yebhanki yamandla i-overdrawn. Kukho izizathu ezintathu ezibalulekileyo zokungalingani kwamandla.
Izidingo zamandla aphakamileyo. Abantu abane-cystic fibrosis kufuneka basebenze nzima ukuphefumula kwaye loo msebenzi idinga amandla. Kuqikelelwa ukuba umsebenzi wokuphefumla wedwa wandisa imfuneko yamandla ukuya kuma-9 kweepesenti ngaphezu komntu onempilo onomzimba ofanayo.
Ukungabi namandla. Ngenxa yesiphumo CF sinama-pancreas , umzimba awukwazi ukufumana amandla amaninzi ekudleni okudliwayo. Nangona umntu onesi-cystic fibrosis esidla ukutya okuninzi, amandla amaninzi asenokupheliswa, angasetyenziswa.
Abantu abane-CF banomdla wokuba ne-steatorrhea, izitulo ezihambayo kwaye zihlala ziphosa. Oku kubangelwa ixabiso elikhulu lamanqwanqwa ekugqitywa kwi-stool.
Ukungena embi. Abantu abanama-cystic fibrosis banamdla amaninzi ngenxa yokuba imizimba yabo ibatsho ukuba bayadinga amandla amaninzi, kodwa ukutya yedwa akusoloko kwaneleyo ukuqinisekisa ukutya okwaneleyo.
Ngamanye amaxesha abantu abane-CF baneminye imiba eqhubekayo eyenza kunzima ukuyidla, njenge-acid reflux, iingxaki zokuphefumla, okanye ukulwa noxinzelelo.
Ukunqongophala kokutya okunjani?
Injongo yonyango lwezondlo kubantu abano-CF kukubuyisela ibhalansi emihle kwi-akhawunti yebhanki yamandla. Imfuneko yamandla ayikwazi ukutshintshwa ukuze ugxininiso lwonyango lubhekise ekuphuculeni ukuxhamla kunye nokudla, abanye abanikelayo abanokungabikho kwemali.
Enzymes. Ngaphambi kwesidlo ngasinye kwaye ngamanye amaxesha kudla ukutya, abantu abaneCF kufuneka bathathe iipilisi ezinama-enzyme e-pancreatic ukuba imizimba yabo ayikwazi ukuyibeka. Ezi enzymes zinceda inkqubo yokugaya ukutya ukufumana izondlo kunye namandla ukusuka ekudleni okunye okuya kukhishwa.
Ukutya. Izidlo zezondlo zicwangcise izicwangciso zokutya ezizimeleyo ngabanye ukuze zihlangabezane neemfuno zesigulane ngasinye, kodwa isiseko esisisiseko sesitya sinokutya ukutya okunamafutha aphezulu anama-35 ukuya kuma-40 ekhulwini eekhalori eziphuma kwioli. I-caloric ingeniso ngokuqhelekileyo iyahlukahluka ukusuka kwi-110 ukuya kwi-150 ekhulwini kwenzelwe imihla yesibonelelo semihla yomntu onempilo ofanayo kunye nobulili. Iifayibha kufuneka idliwe ngokumodareyitha ukunqanda ukutyunjwa, kodwa ukutya okuphezulu-fiber kufanele kugwenywe ngenxa yokuba abanako ukubonelela ngeekhalori ezaneleyo kwaye ngamanye amaxesha kunokukhokelela ekukhuseleni emathunjini kubantu abane-cystic fibrosis.
Umthombo:
I-Pencharz, i-PB kunye neDurie, i-PR "I-Pathogenesis yokunqongophala kwiCystic Fibrosis kunye neNyango yayo". Isondlo seKliniki 2000 19 (6): 387-394. 20 uJuni 2008.