[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"article-5d9acd66-db96-49d6-b05b-b143045e54be--":3,"related-articles-undefined-undefined-45feec94-9167-4a5f-9873-8afced2a21c7-true":54},{"id":4,"type":5,"title":6,"pubDate":7,"logoUrl":8,"anpFeedCategory":9,"organisationTitle":10,"thirdParty":11,"body":12,"note":13,"videoUrl":14,"city":15,"website":16,"orgId":17,"branches":18,"description":53},"5d9acd66-db96-49d6-b05b-b143045e54be","PRESSRELEASE","Nationaal MS Fonds start indringende collectecampagne","2018-09-18T10:08:05.171+02:00","https:\u002F\u002Fwww.persberichten.nl\u002Ffile\u002Flogos\u002F45feec94-9167-4a5f-9873-8afced2a21c7\u002F67a2a626-bc88-487d-8d3b-8fae11b2803c.jpg","Binnenland","Nationaal MS Fonds",false,"\u003Cp>\u003Cstrong>PERSBERICHT \u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong> \u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong>Nationaal MS Fonds start collectecampagne: Laat mensen met MS niet aan hun lot over\u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong>\u003Cem> \u003C\u002Fem>\u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong>\u003Cem> \u003C\u002Fem>\u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong>Het Nationaal MS Fonds lanceert deze week de campagne voor de MS Collecteweek 19 tot en met 24 november 2018. Uniek aan deze campagne is dat échte mensen met multiple sclerose (MS) hun verhaal met de buitenwereld delen.\u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong> \u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>De campagne bestaat uit een televisie- en radiocommercial en drie authentieke portretten van mensen met MS. Wat de uitingen met elkaar verbindt, is de angst en onzekerheid die de ziekte MS met zich meebrengt. \u003C\u002Fp>\n\u003Cp>\u003Cstrong>Ambassadeurs\u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>In de drie portretten delen Anouk, Edo-Jan en Janneke hun persoonlijke verhalen en onzekerheden over hun ziekte MS. Zo vertelt Anouk over haar kinderwens, die zij vlak na het krijgen van de diagnose MS tijdelijk losliet vanwege de bevalling die MS-klachten kan verergeren. Inmiddels leert ze omgaan met haar angst. Edo-Jan deelt zijn allergrootste nachtmerrie: zien dat zijn dochtertje van 2,5 jaar wordt aangereden door een auto en haar niet kunnen redden ómdat hij MS heeft. De 23-jarige Janneke moest door de MS stoppen met haar studie. Ze besloot te gaan solliciteren en vertelt in het interview dat zij door haar ziekte regelmatig werd afgewezen. \u003C\u002Fp>\n\u003Cp>\u003Cstrong>Laat mensen met MS niet aan hun lot over\u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>Met de televisie- en radiocommercial en de drie persoonlijke interviews vraagt het Nationaal MS Fonds aandacht voor de ziekte MS. Multiple sclerose is een chronische ziekte van het centrale zenuwstelsel. In Nederland hebben meer dan 17.000 mensen MS en jaarlijks krijgen 800 mensen de diagnose. De eerste ziekteverschijnselen openbaren zich meestal tussen het 20e en 40e levensjaar en het is de meest invaliderende ziekte onder jonge mensen in Nederland. Er is nog weinig over de ziekte bekend; een oplossing is er niet. Daarom zamelt het Nationaal MS Fonds onder andere geld in voor onderzoek naar de ziekte.\u003Cbr>\u003Cbr>\u003Cstrong>The making of\u003C\u002Fstrong>\u003Cbr>Edgar Wurfbain van Starsound Productions heeft de regie gedaan voor deze campagne. \u003Cem>“\u003C\u002Fem>\u003Cem>Het is een heel bijzondere campagne geweest waarbij we vooral hebben ingestoken op de angst en onzekerheid van de ziekte. Tegelijkertijd zegt dit niet alleen iets over hoe mensen met MS de ziekte ervaren maar ook wat de ziekte letterlijk is: zenuwslopend. Dit in tegenstelling tot wat veel mensen denken, dat het een spierziekte is. Ik vond het bijzonder om met 'echte' mensen met MS te werken en om hen, met hun authentieke portretten, een podium te geven.\u003C\u002Fem>”\u003C\u002Fp>\n\u003Cp>\u003Cstrong>Laat mensen met MS niet aan hun lot over. Word collectant. Meld je aan: \u003C\u002Fstrong>\u003Cstrong>www.mscollecte.nl\u002Fms-collecte\u002Fword-collectant\u003C\u002Fstrong>\u003Cstrong>   \u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong>Voor de redactie:\u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cem>Contact Nationaal MS Fonds:\u003C\u002Fem>\u003Cbr>Leontine Heisen\u003Cbr>(010) 591 98 39\u003Cbr>pers@nationaalmsfonds.nl \u003C\u002Fp>\n\u003Cp>\u003Cem> \u003C\u002Fem>\u003C\u002Fp>\n\u003Cp>\u003Cem>Meer informatie:\u003C\u002Fem>\u003C\u002Fp>\n\u003Cp>Bekijk de commercial: www.mscollecte.nl\u002Fms-collecte\u003Cbr>Bekijk alle andere persmaterialen: www.mscollecte.nl\u002Fpers \u003Cbr>\u003Cbr>\u003Cstrong>\u003Cem>Over Nationaal MS Fonds\u003C\u002Fem>\u003C\u002Fstrong>\u003Cbr>\u003Cbr>Het Nationaal MS Fonds strijdt voor een beter leven voor mensen met MS. Het fonds initieert en financiert innovatief wetenschappelijk onderzoek naar betere behandelmethoden én naar uiteindelijke genezing van MS. Het fonds heeft sinds de oprichting in 1993 een nationale functie als MS-expert en is uitgegroeid tot dé organisatie die voorlichting geeft over en onderzoek doet naar MS in Nederland.\u003C\u002Fp>\n\u003Cp>www.nationaalmsfonds.nl\u003C\u002Fp>\n\u003Cp>\u003Cstrong> \u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong> \u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong> \u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong> \u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>\u003Cstrong> \u003C\u002Fstrong>\u003C\u002Fp>\n\u003Cp>  \u003C\u002Fp>","Deze campagne gaat over de onzekerheid en angst die het hebben van MS met zich meebrengt; Het wachten op een volgende symptoom van je ziekte voelt als het wachten op een onheilspellend lot; en dat is zenuwslopend.\r\nDe campagne wordt ondersteund door 3 verhalen van jonge mensen met MS (http:\u002F\u002Fwww.mscollecte.nl\u002Fwerving-collectanten\u002F )\r\nverhaal Anouk: https:\u002F\u002Fwww.youtube.com\u002Fwatch?v=3GTZqzgUkKk&t=14s ","https:\u002F\u002Fwww.youtube.com\u002Fwatch?v=jzM9Vbz6hjE ","Rotterdam","http:\u002F\u002Fmscollecte.nl","45feec94-9167-4a5f-9873-8afced2a21c7",[19,23,26,29,33,36,39,42,45,48,51],{"id":20,"title":21,"parentId":22},"12102","Beheer van verenigingen en liefdadigheidsinstellingen","94942",{"id":24,"title":25,"parentId":22},"34138","Derde wereld",{"id":27,"title":28,"parentId":22},"41001","Dierenrechten",{"id":30,"title":31,"parentId":32},"93272","Diversiteit","34119",{"id":34,"title":35,"parentId":22},"34110","Kinderwelzijn",{"id":37,"title":38,"parentId":22},"34108","Liefdadigheidsorganisaties",{"id":40,"title":41,"parentId":22},"93992","Maatschappelijk verantwoord ondernemen",{"id":43,"title":44,"parentId":22},"34143","Niet-gouvernementele organisaties",{"id":46,"title":47,"parentId":22},"11020","Sponsoring",{"id":49,"title":50,"parentId":22},"12115","Werkgelegenheid voor invaliden",{"id":22,"title":52},"Ngo - goede doelen","PERSBERICHT Nationaal MS Fonds start collectecampagne: Laat mensen met MS niet aan hun lot over Het Nationaal MS Fonds lanceert deze week de campagne voor de MS",[55,68,108,116,124,132,471],{"id":4,"title":6,"pubDate":7,"logoUrl":8,"thirdParty":11,"orgId":17,"branches":56,"description":53},[57,58,59,60,61,62,63,64,65,66,67],{"id":20,"title":21,"parentId":22},{"id":24,"title":25,"parentId":22},{"id":27,"title":28,"parentId":22},{"id":30,"title":31,"parentId":32},{"id":34,"title":35,"parentId":22},{"id":37,"title":38,"parentId":22},{"id":40,"title":41,"parentId":22},{"id":43,"title":44,"parentId":22},{"id":46,"title":47,"parentId":22},{"id":49,"title":50,"parentId":22},{"id":22,"title":52},{"id":69,"title":70,"pubDate":71,"logoUrl":72,"thirdParty":11,"orgId":17,"branches":73,"description":107},"6310ccb9-ecb8-4a24-9bdc-441827d9f27e","Sponsorevenement MS Motion Utrecht haalt € 160.010,- op","2018-09-10T12:03:32.628+02:00","https:\u002F\u002Fwww.persberichten.nl\u002Ffile\u002Flogos\u002F45feec94-9167-4a5f-9873-8afced2a21c7\u002Ff0b78f1e-2deb-49f0-9266-23425cc8abda.jpg",[74,78,81,84,87,90,93,96,99,102,105],{"id":75,"title":76,"parentId":77},"38101","Internationaal nieuws","38100",{"id":79,"title":80,"parentId":77},"38102","Lokaal nieuws",{"id":82,"title":83,"parentId":77},"38103","Nationaal nieuws",{"id":85,"title":86,"parentId":77},"594aba81-f219-42c2-8dd7-9d3cd0547682","Dagbladen",{"id":88,"title":89,"parentId":77},"0ab0e99b-345d-43b7-95ce-a4268e20a02c","Online",{"id":91,"title":92,"parentId":77},"90528a49-b59e-4a39-8a47-2f77067c302f","Nationaal nieuws - radio",{"id":94,"title":95,"parentId":77},"69d90a55-c180-4ff9-9da2-4c276aefadf5","Nationaal nieuws TV",{"id":97,"title":98,"parentId":77},"38105","Nieuws - andere",{"id":100,"title":101,"parentId":77},"38104","Regionaal nieuws",{"id":103,"title":104,"parentId":77},"35d5c089-fb24-460e-801f-5d0d0f434723","Regionale nieuwsomroep",{"id":77,"title":106},"Algemeen nieuws","PERSBERICHT Utrecht, 10 september 2018 Sponsorevenement MS Motion Utrecht haalt € 160.010,- op voor het Nationaal MS Fonds Ruim duizend deelnemers hebben op zon",{"id":109,"title":110,"pubDate":111,"logoUrl":8,"thirdParty":11,"imageUrls":112,"orgId":17,"description":115},"c3b0e384-2b3b-4414-9639-8816d789537f","MS Motion Rotterdam haalt € 102.697,- op!","2018-06-04T15:53:46.766+02:00",[113,114],"https:\u002F\u002Flh3.googleusercontent.com\u002FsUGrTuQqE8ehCfxWOojSX4UP8QLDgdQgrgRAfQcmiRL5dGSCXWegtUStKa3oLVpYqBeZfcalEdZo1yujjt4p8qzCzJbUnDukJQ","https:\u002F\u002Flh3.googleusercontent.com\u002F8Mk6nOyu5N9q8iOsXU3QLRyyGt5YjyzjdG2o9OgXhgIBFla-5sCI9l0MWWu58MBfIPai617jSn99PF_TOytz5aHF9-MBqbbfKw","Op zondag 3 juni hebben 605 deelnemers hun steentje bijgedragen aan een wereld zonder MS. Zij liepen mee in het hardloop- en wandelevenement MS Motion Rotterdam",{"id":117,"title":118,"pubDate":119,"logoUrl":120,"thirdParty":11,"imageUrls":121,"orgId":17,"description":123},"246f94c3-f372-465b-84ae-1192add4d8f7","Nationaal MS Fonds lanceert animatie op Wereld MS dag","2018-05-30T08:15:41.139+02:00","https:\u002F\u002Fwww.persberichten.nl\u002Ffile\u002Flogos\u002F45feec94-9167-4a5f-9873-8afced2a21c7\u002F3cf60dad-54d2-417d-ae67-f3fe6ad308a9.jpg",[122],"https:\u002F\u002Flh3.googleusercontent.com\u002F8kZagkojveZJpi_w-DyWHuNr9Ct6BXceXrPEi6tZ2Yf3QK99OU8y0SjRkC8FGD-C3F2hzSRYr50XZFdVVK4ot3LgY-EEXgAKVw","Nationaal MS Fonds lanceert animatie op Wereld MS dag Op Wereld MS dag, woensdag 30 mei, lanceert het Nationaal MS Fonds de animatie ‘Wat is MS’. Deze video leg",{"id":125,"title":126,"pubDate":127,"logoUrl":120,"thirdParty":11,"imageUrls":128,"orgId":17,"description":131},"ed9b8115-c9a2-4c77-a11c-1419a4bb13e4","Maak je sterk tegen MS: MS Collecteweek 20 t\u002Fm 25 november","2017-11-15T08:00:00.502+01:00",[129,130],"https:\u002F\u002Flh3.googleusercontent.com\u002FtHeTCVif_gXvSWD_50gpgoGqj0cZ7AOZsbKEjWysLtehYALDmZ9acf2lhgvWEfx0BBlBmDeUnNnPCxIpSr_fHJVgy6SrURHvaw","https:\u002F\u002Flh3.googleusercontent.com\u002F_D1NzzYKsX9_VjB9tcKkoOpYuIErUmjN_yY0WzT3JD95eKb4NRtod4U-iMG9ZD5LEakJ1DpXZRrEzHQXKWskFXvPcT21_qXYiw","Van 20 t\u002Fm 25 november organiseert het Nationaal MS Fonds de landelijke huis-aan-huiscollecte om geld in te zamelen voor onderzoek naar de ziekte Multiple Scler",{"id":133,"title":134,"pubDate":135,"logoUrl":136,"thirdParty":11,"orgId":17,"branches":137,"description":470},"848017ce-cdb3-411b-8975-a6c4476565ac","Mensen met MS bewandelen de Mont 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Als team doen zij mee met het eve",{"id":472,"title":473,"pubDate":474,"logoUrl":136,"thirdParty":11,"imageUrls":475,"orgId":17,"description":477},"3f934aab-68ab-4d88-9a48-1041d6473278","Kraantje Pappie en Tony Scott maken zich sterk tegen MS","2017-05-10T10:52:30.821+02:00",[476],"https:\u002F\u002Flh3.googleusercontent.com\u002FawVuX7HwsfS-7TFSx2NLShQqbXiRhYdLT64DFjjpiUQFecU5PiQhz4gXRm_9xoaYusqSq221N2BITr5UwZZXSwAZuqIIaMrR","Zaterdag 13 mei 2017 staan 1.000 deelnemers aan de start van het sponsorevenement MS Motion dat voor de vierde keer door het Nationaal MS Fonds georganiseerd wo"]