Funding

Here you can see the sources from which the financing of our association is composed. The two most important pillars are the GKV-Gemeinschaftsförderung and donations. In addition, we receive membership fees and project-related funding.

Donations for research funding since 2014

We use 100% of donations for Research funding. Dank des großen Engagementes einzelner NBIA-Familien (siehe auch Fundraising) ist unser Spendenaufkommen in den Jahren 2019 und 2020 besonders hoch gewesen. Die Spenden sind meist zweckgebunden für die gezielte Förderung der Erforschung einer NBIA-Erkrankung.

  • 2023: 36.924 €
  • 2022: €25,011
  • 2021: €42,681
  • 2020: €74,391
  • 2019: 150.899 €
  • 2018: €30,099
  • 2017: 12.715 €
  • 2016: 11.233 €
  • 2015: 6.545 €
  • 2014: 6.635 €

We would like to take this opportunity to thank all donors and the fundraising NBIA families!

GKV-Gemeinschaftsförderung for costs of the association's work since 2015

Den Grundstock zur Finanzierung unserer Selbsthilfeorganisation bildet die pauschale Selbsthilfeförderung durch die GKV-Gemeinschaftsförderung Selbsthilfe auf Bundesebene. With these annual grants, we cover a large part of the costs for our daily association work, which would otherwise not be possible. In recent years, Hoffnungsbaum e.V. the following sums:

  • 2023: 17.600 €
  • 2022: 17.146 €
  • 2021: 16.000 €
  • 2020: 16.000 €
  • 2019: 15.000 €
  • 2018: 13.000 €
  • 2017: 12.000 €
  • 2016: 11.000 €
  • 2015: 8.000 €

We would like to take this opportunity to thank the members of the "GKV-Gemeinschaftsförderung Self-help at the federal level":

Further Funding

These organizations supported our association's work with grants – lump sum or project-related.

DAK Health

We would like to thank you for your support of the strategy meetings of the Hoffnungsbaum-Board.

Technician Health Insurance

We would like to thank you for the financial support of our 8th NBIA Family Conference in Germany.

Kindness for Kids

We would like to thank you for the financial support of our 8th NBIA Family Conference in Germany.

European Commission

The project work of Hoffnungsbaum e.V. within the framework of TIRCON (Work Area 7: Dissemination) funded by the European Commission (FP7/2007–2013, HEALTH-F2–2011, grant agreement 277984, TIRCON)

Appeals for donations, the proceeds of which go to Hoffnungsbaum goes

Most of the time, it is dedicated NBIA parents who launch appeals for donations or even collect donations non-stop.

Aus einer Geschenkspende werden zwei

Aus einer Geschenkspende werden zwei

Seit einiger Zeit gibt es auf unserer Website die Möglichkeit, mit dem Spendenformular eine Geschenkspende zu generieren. Man spendet ganz normal, kann aber zusätzlich eine Urkunde mit verschiedenen Motiven generieren und einen Absender und Empfänger der Spende...

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NBIA-Gentherapie Updates

NBIA-Gentherapie Updates

Historische Spende von 1,2 Millionen Dollar gibt Treibstoff für PKAN-Gentherapie Eine beeindruckende Spende in Höhe von 1,2 Millionen Dollar hat es der PKAN-Gentherapie (Pantothenat-Kinase-assoziierten Neurodegeneration) ermöglicht, einen großen Schritt nach vorn zu...

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Cycling for BPAN – Million Dollar Bike Ride 2021

Cycling for BPAN – Million Dollar Bike Ride 2021

It's that time of year again: The Million Dollar Bike Ride (MDBR) of the University of Pennsylvania in Philadelphia will take place for the 8th time until June 12, 2021. Due to the pandemic, this charity bike race will again take place not only in the USA, but virtually all over the...

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PKAN family launches another fundraising campaign

PKAN family launches another fundraising campaign

As at the beginning of the year, the Bianchi family is once again actively collecting donations for PKAN research during Advent, as their 3-year-old son Giulio suffers from this form of NBIA. In their home town of Kronau, parents Melanie and Tony have set up a stand with...

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Half marathon becomes BPAN charity run

Half marathon becomes BPAN charity run

Participants of the MPIA at this year's SAS half marathon in Heidelberg, Image: MPIA/J. Henshaw On April 7, 2019, 14 colleagues of our board member Markus Nielbock from the Max Planck Institute for Astronomy (MPIA) took part in the...

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Rhein-Neckar-Zeitung reports on Milly's mission

Rhein-Neckar-Zeitung reports on Milly's mission

February 28 is International Rare Disease Day. Numerous events have been taking place around the world for days now to mark the occasion. Media interest is also high. The aim of Rare Disease Day is to...

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News from Maya and the MPAN fundraising campaign

News from Maya and the MPAN fundraising campaign

In December, we presented the Matthiesen family's fundraising campaign for MPAN research. Maya herself actively supports this crowdfunding campaign, which was launched by her parents shortly after her diagnosis. Together with her older brother, she...

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Matthiesen family launches fundraising campaign for MPAN research

Matthiesen family launches fundraising campaign for MPAN research

Saarländischer Rundfunk (SR) drew attention to the family's situation and their fundraising campaign in a sensitive television report on November 29 as part of its "Wir im Saarland" magazine program. It was only in September that the Matthiesen family had been diagnosed with...

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News from Milly and her mission

News from Milly and her mission

On 22.12.2017, Rhein-Neckar-Fernsehen (RNF) presented Milly and her family in the program RNFlife: http://www.rnf.de/mediathek/video/heidelberg-wie-die-kleine-emilia-gegen-ihre-gen-krankheit-ankaempft/ Emilia has BPAN. About a year ago, her parents...

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