Zinthu zomwe muyenera kuziganizira ngati muli ndi cystic fibrosis
Cystic fibrosis sichitha matenda okhaokha. Anthu ambiri omwe ali ndi cystic fibrosis amachititsa moyo wawo kukhala wopindulitsa kukhala wamkulu, ndipo ena mwa iwo ali ndi ana awoawo. Amuna ambiri omwe ali ndi cystic fibrosis nthawi zambiri amakhala osabala. Pafupifupi 95 peresenti ya amuna omwe ali ndi CF akusowa vuto lawo, chubu yomwe imagwirizanitsa ma testes ku urethra.
Mosiyana ndi amuna omwe ali ndi CF, amayi ambiri amatha kutenga pakati.
Amayi ambiri omwe ali ndi cystic fibrosis amene amatenga mimba amatha kunyamula mimba mpaka nthawi. Pali zinthu zambiri zoti muganizire za anthu omwe akukonzekera kukhala ndi ana. Komabe, pamene makolo omwe angathe kukhala ndi cystic fibrosis, pali zinthu zina zofunika kuziganizira. Nazi zinthu zingapo zomwe mukufuna kudziwa pamene mukukonzekera banja lanu
Kumvetsa Kuopsa kwa Mwana Wanu Wachibadwa Cystic Fibrosis
Ngati muli ndi cystic fibrosis, zikutanthauza kuti muli ndi makope awiri ofooka a jini la CFTR . Mudzadutsa mmodzi mwa iwo kupita kwa mwana wanu. Mwana wanu angakhale wonyamulira kapena ali ndi matenda a cystic fibrosis, malingana ndi jini lomwe amapeza kuchokera kwa mnzanuyo.
- Ngati mnzanuyo ali ndi majini awiri achilendo a CFTR, mwana wanu adzakhala ndi jini imodzi yolakwika kuchokera kwa inu ndi jini imodzi yochokera kwa mnzanuyo. Mwana uyu adzakhala chithunzithunzi cha cystic fibrosis.
Ngati mnzanuyo ali ndi kachilombo koyipa komanso kamodzi kake, ndiye wothandizira. Mwana wanu adzakhala ndi mwayi wokhala ndi matenda a cystic fibrosis ndi 50 peresenti yokhala ndi chonyamulira, malingana ndi jini lomwe mwanayo amachokera kwa mnzanuyo.
Kuyezetsa magazi kuti mudziwe ngati mnzanuyo ndi wothandizira alipo ndipo angakuthandizeni kupanga zisankho zodziwa za kukhala ndi ana pamodzi. Palinso zina zomwe mungachite pokhapokha mutakhala ndi pakati pa omwe akuyang'ana kufalitsa mabanja awo. Kugwiritsira ntchito dzira kapena wopereka umuna kapena kulandira akhoza kuthetsa banja lanu.
Mavuto Okhudzana ndi Matenda a Matenda a Chibwana
Kuvuta kwa mimba kungapangitse cystic fibrosis. Mavuto omwe amapezeka mwa amayi apakati omwe ali ndi CF ndi awa:
Kuonjezera kupuma kovuta. Kuchepetsa mapapu ntchito kungathe kupha anthu omwe ali ndi cystic fibrosis. Ichi ndi chiopsezo chachikulu kwambiri cha mimba kwa amayi omwe ali ndi CF.
Kuchulukitsa matenda opatsirana. Kuchepetsa mapaipi ntchito kungayambitse matenda opuma, zomwe zimapangitsa kukhala kovuta kupuma.
Matenda a shuga . Thupi limasintha pamene ali ndi mimba lingayambitse amayi odwala kukhala ndi shuga. Vutoli ndi lalikulu kwambiri kwa amayi omwe ali ndi cystic fibrosis chifukwa cha kuwonongeka kwa CF kumene kumayambitsa makoswe.
Kusadya zakudya m'thupi. Mimba ikuwonjezera kuwonjezera mphamvu za thupi, kupanga zakudya zokwanira zovuta kwambiri.
Azimayi omwe ali ndi CF nthawi zambiri amakhala ndi pathupi pamene akukonzekera chifukwa amalandira mosamala kuyambira pachiyambi. Othandizira anu a cystic fibrosis ndi akatswiri pa matenda anu ndipo muyenera kulankhula nawo kuti mudziwe ngati muli ndi thanzi labwino lolimbana ndi vutoli.
Ngati muli ndi pakati, muyenera kusiya kumwa mavitamini A, D, E, kapena K omwe mungakhale nawo. M'malo mwake, sungani mavitamini opititsa patsogolo ndi Vitamini E.
Maantibayotiki monga fluoroquinolones ndi tetracyclines ayenera kuimitsidwa.
Chitsime:
Edenborough, F., et al. (2008). Malangizo othandizira kusamalira mimba mwa amayi omwe ali ndi cystic fibrosis. Journal of Cystic Fibrosis. (7) S2-S32.