{"id":20695,"date":"2020-09-23T14:04:38","date_gmt":"2020-09-23T12:04:38","guid":{"rendered":"https:\/\/alan.wearequattro.com\/testimonials\/testimonials-hannah\/"},"modified":"2021-01-27T14:12:01","modified_gmt":"2021-01-27T13:12:01","slug":"temoignages-hannah","status":"publish","type":"page","link":"https:\/\/alan.lu\/fr\/temoignages\/temoignages-hannah\/","title":{"rendered":"T\u00e9moignages"},"content":{"rendered":"

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Hannah<\/h2>\n

[\/vc_column_text][vc_column_text]21 ans, vit avec Spondylolisthesis<\/strong>[\/vc_column_text][vc_empty_space height=”35px”][vc_column_text]”Je m’appelle Hannah et j’ai 21 ans. J’ai mal au dos depuis mon enfance. Aucun m\u00e9decin n’a jamais jug\u00e9 n\u00e9cessaire de me radiographier en r\u00e9ponse \u00e0 mes plaintes. J\u2019ai d\u00fb attendre 11 ans pour recevoir mon diagnostic. \u00c0 l’\u00e2ge de 15 ans, on m’a diagnostiqu\u00e9 une forme s\u00e9v\u00e8re de spondylolisth\u00e9sis, un glissement vert\u00e9bral tr\u00e8s rare pour mon \u00e2ge. Au fil des ann\u00e9es, le glissement avait tellement progress\u00e9 que j’\u00e9tais sur le point d\u2019\u00eatre paralys\u00e9. J’ai d\u00fb \u00eatre op\u00e9r\u00e9e \u00e0 l\u2019\u00e9tranger le plus rapidement possible.<\/p>\n

Cette op\u00e9ration ne marquait pas le d\u00e9but d\u2019une nouvelle phase de vie pour moi, mais plut\u00f4t le d\u00e9but d\u2019une lutte pour la survie et d\u2019une course contre la montre. Des staphylocoques s’\u00e9taient log\u00e9s dans ma colonne lombaire. Les bact\u00e9ries n’ont pas \u00e9t\u00e9 d\u00e9tect\u00e9es pendant huit longs mois. Personne n’a pris au s\u00e9rieux ma douleur infernale \u00e0 la suite de l’op\u00e9ration. \u00c0 la derni\u00e8re seconde, j’ai \u00e9t\u00e9 op\u00e9r\u00e9e. Ma colonne lombaire \u00e9tait entour\u00e9e de pus. D’autres chirurgies majeures \u00e0 l’\u00e9tranger ont suivi au fil des ann\u00e9es.<\/p>\n

La maladie a boulevers\u00e9 toute ma vie. J’ai des douleurs chroniques et les opiac\u00e9s sont devenus mon compagnon constant. Sans avertissement j’ai \u00e9t\u00e9 catapult\u00e9 de la vie d’adolescent insouciant \u00e0 un monde compl\u00e8tement diff\u00e9rent. La perte de mes amis et essentiellement mon adolescence m’a durement \u00e9branl\u00e9. La d\u00e9pression est arriv\u00e9e sans tarder. C’est ainsi que j’ai d\u00e9couvert l’art et commenc\u00e9 \u00e0 peindre. Mon art m’a aid\u00e9 \u00e0 gu\u00e9rir mes blessures \u00e9motionnelles.
\nMon histoire avec cette maladie n’est pas encore termin\u00e9e. Mais je suis reconnaissant que malgr\u00e9 la douleur, je puisse me tenir debout aujourd’hui. De l\u2019ext\u00e9rieur on ne voit pas ce que j\u2019ai v\u00e9cu, ce qui signifie que je dois me justifier dans de nombreuses situations.<\/p>\n

Je sais trop bien qu\u2019on peut se sentir tr\u00e8s seul lorsqu\u2019on vit avec une maladie rare. C\u2019est pourquoi je tends la main virtuelle \u00e0 tous ceux qui se trouvent dans une situation similaire. Nos vies avec une maladie chronique donnent malheureusement souvent l’impression de vivre dans une autre dimension.<\/p>\n

Je tiens \u00e9galement \u00e0 remercier de tout c\u0153ur l\u2019\u00e9quipe d\u2019ALAN pour leur soutien, qui a apport\u00e9 un aspect tr\u00e8s positif \u00e0 mon histoire !”
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Contactez-nous en cas de questions ou besoin d\u2019assistance<\/span><\/h2>\n\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\n\t\t\t\t\t\t\t\t\t
\n\t\t\t\t\t\t\tContact<\/span> <\/a>\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n[\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

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