Ukungahlambuluki kwe-urinary, noma ukuvuza okungavumelekile komchamo, kuyinkinga evamile kwabesifazane abane- cystic fibrosis . Ukuxhuma phakathi kweCF nokungahlambuluki kuye kwabonakala kuphela kusukela ngasekupheleni kwawo-1990, kanti izifundo zisenziwa ukuze ziqonde imbangela.
Ubani Othola Ukungena Kwe-Urinary?
Ucwaningo luye lwabonisa ukuthi inkinga ayijwayelekile kakhulu ngaphambi kweminyaka engama-20, kodwa emva kwalokho, abaningi abangama-68% wabesifazane abane-cystic fibrosis bane-urine ukuvuza okungenani.
Amadoda ngokuvamile abhekana nokungahambisani namagciwane njenge-symptom ye-CF.
Yini Eyibangela?
Ijaji lisekhona esiyimbangela esiyimbangela yokungahlambuluki kwamagciwane kwabesifazane abane- cystic fibrosis . Incazelo ejwayelekile kunazo zonke ukuthi yindlela yokucindezeleka ukungalawuleki okubangelwa ukukhwehlela okwesikhashana, okuvamile okudambisa imisipha yomzimba. Le ncazelo ingachaza ukuthi kungani inkinga ingathinti abantu, inikezwe ukuhlukahluka kwezinto eziphilayo. Abesifazane bane-urethra emifushane, ngakho-ke umchamo awudingi ukuhamba kude ukuze ufike kusuka kwesishayi kuya ngaphandle komzimba. Amadoda ane-urethra ende futhi umchamo kwakufanele athathe uhambo olunzulu ukuze athole indlela yokuphuma.
Ukwelapha
Ngenkathi kukhona imithi emakethe ukusiza ukumisa ukuvuza kwesisu, izifundo zibonise ukuthi indlela engcono kakhulu yokwelapha ukungathembeki kwabesifazane abane-CF ukuqinisa imisipha ye-pelvic ngezivivinyo. Abesifazane abangenakho ukukhubazeka bangaphinda benze ukuzivivinya kokuqina kwe-pelvic ukusiza ukuvimbela inkinga ukuthi ingabikho.
Ukuzivocavoca kwama-pelvic floor, okubizwa nangokuthi umzimba we-Kegel, kwenziwa ngokucindezela nokuphumula imisipha efanayo oyisebenzisayo ukulawula ukugeleza komchamo. Lezi zivivinyo zikhulu ngoba zingenziwa noma kuphi, ngisho nalapho uhlezi edeskini yakho emsebenzini noma embhedeni ubuka ithelevishini.
Umthombo:
McVean, RJ, Orr, A., Webb, AK, Bradbury, A., Kay, L., Philips, E., noDodd, ME "Ukwelashwa kwe-Urinary Incontinence ku-Cystic Fibrosis". Journal of Cystic Fibrosis 2003 2: 171-176. 20 Juni 2008.