«Jag var dålig, utan styrka, och doktorn berättade att jag var en svag person»

Hur ett liv i en minut kan förändra oss vet mycket en 42-årig från Sevilla som heter  Teresa García García . Idag är hon glad eftersom domstolen, inte staten, har erkänt henne “att jag inte kan dra min kropp”; för att han har två barn som hjälper honom, en exemplarisk man och en stor familj. Men han har ingen styrka, ingen behandling som ger honom energi och tar bort smärtan. Han tar bara antidepressiva medel för att klara sig bättre än hans kropp motsvarar inte hans ålder, “men med en 80-årig kvinna” och att “jag vill bara ligga ner med mina ögon stängda”.

Teresa García García med meningen som ger henne anledning

Bara ta antidepressiva  eftersom det också har att smälta vad händer om från början hade han diagnosen sin sjukdom, om han hade citerade fem år före det domstolsbeslut som gav i juni förra året , den totala bestående invaliditet, och i stället för en ersättning på 640 euro skulle ha varit en av 1300.

Han var 33 år gammal år 2009 ett bra jobb på ett kontor, bra betalt och ett perfekt liv  med sin man och två barn i åldern 5 år och 6 månader.

Men en morgon han fick upp att gå till jobbet och  kändes som jag hade i influensa. Efter ett par dagar och efter att ha sett det värre gjorde ett möte med sin läkare i öppenvården La Plata.

“När jag kommenterade att jag ont överallt, hade jag ingen kraft att stå eller skriva på datorn sa att det var stress. Jag lämnade kontoret och visste att det inte var sant. Några veckor senare återvände jag till den ihållande symptom dag och natt och jag återigen säga att det var stress. Och så i 8 månader. En dag prata med en vän, berättade han att han hade samma symptom som hans fru och hade fibromyalgi. Så återigen jag frågade min läkare utnämning och frågade om jag kunde vara att sjukdomen. Han svarade att det var en sjukdom som uppfanns av någon som skulle bli uttråkad. “

Allvarlig fibromyalgi

Teresa bytte läkare och hon fick en ny läkare. Vid första besöket, efter att förklara dina symptom, sade han att han visste redan vad som hände, men jag var tvungen att skicka till den ortoped och reumatolog för att vara säker. Efter testerna bekräftade diagnosen:  svår fibromyalgi, kronisk ländryggssmärta cervicodorsalgia och mekanik.  Sedan gick till en invärtes som också bekräftade ‘efter fler tester, eftersom det är en sjukdom kasse eftersom det inte finns någon biologisk markör som säger att det just nu. ” Så småningom de kom flera sjukdomar förknippade hur Raynauds syndrom, artrit, ångest, depression … .. “Hur att undvika att falla in i en depression när du ser du har fastnat i en kropp av en kvinna på 80 år. När du inte kan hämta dina barn, när den minsta ansträngningen lämnar dig i sängen tre dagar. När din man måste agera som pappa, mamma, hemmafru … “, säger han.

Så han arbetade ytterligare två år där hans liv gick mellan arbete och säng eller soffa. Fram till en dag berättade hans chef för honom att han inte kunde fortsätta så här, att han skulle släppas ut. Jag hade förlorat 10 kilo. Han stannade i 43  och under “mina advokaters felaktiga råd” bad han att han skulle överlämna medicinska domstolen.

Han fick inte handikapp och gick till rättegång. Han förlorade det för att han inte hade “uttömt alla terapeutiska vägar” och hade inte “rapporter som  indikerar min oförmåga att arbeta eller mitt dagliga liv”.

“Vid första jag sjönk -mer- men till slut var det fick mig att fortsätta kämpa för mina rättigheter kronisk hur sjuk, även om frågan var nästan omöjligt. För tre år sedan diagnostiserades jag med kronisk trötthetssyndrom och efter flera resor av olika specialister hänvisade hon mig en dag till en internist på en dag i akuten. Detta i sin tur till en pulmonologist som var den som gjorde alla nödvändiga tester och mer, för att veta vilken grad han hade av sjukdom.  Jag har det syndromet i grad IV och svår handikapp . Det är jag säker på att jag har haft från början, men hur att tvätta händerna och när du går till den akuten de skickar dig att ta dina barn till den parken, att träffa människor som är riktigt sjuk, jag fick höra ordagrant … ” säger han.

Han lyckades få bra rapporter och rådde av en vän, anställde en av de bästa juristerna i dessa sjukdomar:  Javier León Iglesias, från Zaragoza . Efter mer än ungefär ett och ett halvt år väntade, kom rättegången för rättegången mot Socialstyrelsen och Socialstyrelsen

“Många månader senare,” tillade hon, “domaren gav mig absolut permanent funktionsnedsättning. Det var en väldigt konstig känsla. Jag var väldigt glad för att de till slut hade insett att jag var väldigt sjuk och inte kunde arbeta på någonting, men samtidigt var jag djupt ledsen att inse det. Så ung, 42 år gammal. Hela livet framåt, men vilken typ av liv. Jag har haft två försök på autolys och när jag tittar på framtiden ser jag bara smärta, extrem trötthet och mer smärta ».

«De berättade för mig att jag inte ville arbeta»

Han minns när läkarna sa till honom att “allt var i mitt huvud att jag inte ville var att arbeta, det var en lös och ta hand om mina barn” . Nu kommer han att begära hjälp omfattad av beroende lagen och han har också hävdat 33% funktionshinder som har erkänts av Junta de Andalucía. Men han vill framför allt att de människor som återspeglas i sin situation “kämpa och inte kasta i handduken” för att åtminstone uppnå att deras funktionshinder är erkända “.

«Mitt liv går trött, jag sover men jag går upp som om jag inte hade sovit. Men jag har min familj, mina 13 och 9-åriga barn som jag hjälper till att studera även om jag ligger i sängen . Jag kan inte göra motion, bara gå 15 minuter om dagen och långsamt, eller husarbete eller något. Havet slappnar av mig, även om jag inte kan bada för att jag inte kan hålla temperaturen förändras, men det slappnar av mig, “avslutar Teresa.

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