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Marie Jozefiak's fundraising page
by Marie Jozefiak for Association ELA
I want to help others and be a Force For Good.
I'm so proud that my company (Nu Skin) has decided to support the ELA association.
We want to be able to support the first Clinical Trial ever to help children who have a leukodystrophy and for that, ELA will need 500 000€.
I would greatly appreciate if you could help me in my fundraising efforts by making a donation to Association ELA or bringing awareness around my fundraising efforts. There are no small donations.
Donations are processed through Alvarum. It is very easy and 100% secure.
If your country allows it, you can even deduct a certain amount from your taxes !
Thank you for your help!
Marie Jozefiak
I'm so proud that my company (Nu Skin) has decided to support the ELA association.
We want to be able to support the first Clinical Trial ever to help children who have a leukodystrophy and for that, ELA will need 500 000€.
I would greatly appreciate if you could help me in my fundraising efforts by making a donation to Association ELA or bringing awareness around my fundraising efforts. There are no small donations.
Donations are processed through Alvarum. It is very easy and 100% secure.
If your country allows it, you can even deduct a certain amount from your taxes !
Thank you for your help!
Marie Jozefiak
Target
28%
So far, I've raised
€ 275
With help of people.
On my target of € 1,000
On my target of € 1,000
10 News
Hi everyone ! Great week-end "Mets tes Baskets" with more than 12 000 steps ;-)
This way I'll donnate 120€ for ELA. I'm so happy to be able to help the children.
This way I'll donnate 120€ for ELA. I'm so happy to be able to help the children.
Marie Jozefiak - 10/20/20
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We're raising funds together.
Nu Skin - Force For Good
See who's in our group
Nu Skin - Force For Good
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Partenariat Nu Skin / ELA
Partenariat Nu Skin / ELA
Association ELA
Fondée en 1992 par Guy ALBA, l'Association Européenne contre les Leucodystrophies (ELA) regroupe des familles qui se mobilisent pour vaincre ces maladies génétiques rares qui détruisent la myéline (la gaine des nerfs) du système nerveux. Chaque semaine en France, 3 à 6 enfants naissent atteints de ces pathologies qui engendrent des situations de handicap très lourd et entraînent progressivement la perte de toutes les fonctions vitales : l'ouïe, la vue, la locomotion.
