Nëse ti ose të afërmit e tu jeni prekur nga kanceri i trashëguar, mund të pyesni veten se si mund ta përdorni këto njohuri në të ardhmen dhe të jeni proaktiv kur bëhet fjalë për parandalimin. Ja diçka që do të të ndihmojë të bëhesh më aktiv në parandalimin e kancerit. Pothuajse çdo familje në botë është prekur nga kanceri dhe shumë prej tyre mund të kurohen dhe trajtohen efektivisht nëse zbulohen herët. Në këtë artikull, do të sqarojmë kancerin e trashëguar dhe do të ju tregojmë se ka një mënyrë të mençur dhe të fuqishme për ta trajtuar atë – dhe kjo lidhet me ADN-në tuaj.
Mbroni veten dhe familjen tuaj me depistimin gjenetik
Në një epokë ku përparimet mjekësore vazhdojnë të ndryshojnë peizazhin e kujdesit shëndetësor, një e vërtetë themelore mbetet e pandryshuar: parandalimi është pa dyshim arma më e fuqishme kundër kancerit. Testi ynë i Cancer Screen ne nivel ADN-je është një shembull i shkëlqyer i këtyre përparimeve mjekësore – teknologjia e fundit e sekuencimit (NGS) na lejon të zbulojmë rrezikun tuaj për kancerin e trashëguar përmes një testi të thjeshtë me pështymë. Duke ekzaminuar deri në 90 gjenet, testi mund të vlerësojë rrezikun për 25 lloje të kancerit të trashëguar, përfshirë atë të gjirit, ovarian, prostatës, kolorektal dhe të tjerë.
Identifikimi i rrezikut të kancerit në familjen tuaj
Testi Cancer Screen nuk parashikojn nëse ju ose familja juaj do të zhvillojë kancer, por zbulon mutacionet gjenetike që rrisin rrezikun, duke ju dhënë mundësinë për parandalim. Ato zbulojnë praninë e variantëve patogjenë, të cilët rrisin rrezikun e zhvillimit të kancerit deri në 99%. Për shembull, një variant patogjen në gjenin BRCA1 mund të rrisë rrezikun e kancerit të gjirit deri në 85%, krahasuar me rrezikun mesatar prej 13%. Nëse kjo ju ngjan e njohur, mund të keni dëgjuar historinë e Angelina Jolies. Kur nëna e saj vdiq nga kanceri i gjirit, ajo bëri një test ADN që tregoi se ajo mbante variantin patogjen të gjenit BRCA1 dhe kishte një shans 87% më të lartë për të zhvilluar vetë kancerin e gjirit. Angelina mori masat parandaluese të nevojshme në formën e një mastektomie të dyfishtë. Ajo siguroi që fëmijët e saj të mos kalonin përmes përvojës së njëjtë si ajo, duke humbur nënën e saj. Kryerja e testit Cancer Screen është veçanërisht e këshillueshme nëse keni një prind që mbart një variant patogjen, pasi kjo rrit shanset tuaja për ta pasur atë me 50%. Por aspekti më kritik është që ju mund të mos e dini që një variant patogjen ekziston në familjen tuaj, pasi një person që e trashëgon variantin patogjen nuk zhvillon gjithmonë kancer. Prandaj testi është i vlefshëm për këdo që dëshiron të zbulojë rrezikun e tyre për kancer.
Nëse doni të dini rrezikun tuaj të kancerit trashëgimor, klikoni këtu për ta llogaritur!
Interpretimi i rezultateve tuaja me udhëzim ekspert
Nëse statistikat më lartë mund të duken të frikshme, është esenciale të mbani mend se dija është fuqi, dhe testi Cancer Screen është këtu për të ofruar mbështetje dhe ndërgjegjësim. Testi gjithashtu përfshin informacion specifik mbi çdo variant patogjen të zbuluar dhe ndikimin e tij të mundshëm mbi rrezikun e zhvillimit të kancerit. Por nuk keni pse të shqetësoheni për të interpretuar rezultatet tuaja vetëm. Mjeku do t’ju ndihmojë në këtë. Nëse ndonjë rezultat kthehet pozitiv, një gjenetist klinik ose onkolog do tju ofroj informacion shtesë. Së bashku, mund të përcaktoni hapat tuaj të ardhshëm.
Fuqia e ndërgjegjësimit
Pas ndërgjegjësimit për rrezikun ndaj kancerit trashëgimor, mund të merrni hapa proaktivë drejt parandalimit dhe zbulimit të hershëm. Parandalimi mund të përfshijë ndryshime në mënyrën e jetesës dhe vendime që mund të ulin rrezikun e zhvillimit të kancerit. Këto ndryshime në mënyrën e jetesës mund të përfshijnë:
- ushqim më të shëndetshëm,
- ushtim të rregullt fizik,
- reduktim të duhanit dhe alkoolit,
- menaxhim stresi,
- dhe mbi të gjitha – monitorim i rregullt për zbulim të hershëm.
Rezultatet gjithashtu ju tregojnë se si këto variante mund të ndikojnë në familjen tuaj. Ky informacion është i çmuar nëse një anëtar i familjes suaj ose ju vetë jeni diagnostikuar tashmë me kancer. Kjo do të thotë që ju mund të ndihmoni të dashurit tuaj të bëhen më të ndërgjegjshëm për predispozitën tuaj gjenetike të përbashkët dhe për pasojë t’i ndihmoni ata të shmangin kalimin përmes të njëjtës përvojë.
Rezultate të besueshme
Ne e kuptojmë rëndësinë e rezultateve të sakta dhe të besueshme në marrjen e vendimeve rreth shëndetit tuaj, sidomos në parandalimin e kancerit. Prandaj testi ynë Cancer Screen përdor teknologjinë e sekuencimit (NGS) për të analizuar mostrën tuaj për variantet gjenetike të lidhura me rrezikun e kancerit. Metoda është shumë e besueshme në zbulimin e varianteve tuaja gjenetike (me saktësi 99.4%). Më tej, nëse rezultatet tuaja zbulojnë ndonjë variant patogjen, ato verifikohen në vazhdimësi me sekuenca të Sangerit ose metodën qPCR. Kjo garanton që të gjitha informacionet që merrni rreth rrezikut tuaj të kancerit janë mbështetur nga prova shkencore solide.
Një e ardhme më e sigurt për familjen tuaj
Kanceri mund të ketë një ndikim të thellë në familjet. Për fat të mirë, teknologjitë e avancuara, si testi ynë Cancer Screen ju nxit të merrni hapa drejt parandalimit dhe zbulimit të hershëm. Nuk keni pse të pyesni për rrezikun tuaj dhe të familjes suaj, sepse me testin tonë, mund ta zbuloni me një mostrë të thjeshtë pështyme. Informacioni që merrni jo vetëm që do të jetë i dobishëm për ju por është edhe një investim në të ardhmen e të gjithë familjes suaj. Të armatosur me dituri dhe informimin mbi riskun tuaj të përbashkët ju mund të qëndroni më të fortë së bashku.
Nëse doni të dini rrezikun tuaj të kancerit trashëgimor, klikoni këtu për ta llogaritur!
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