Helping is easy! Charity fundraising for the treatment of little Amelia
Information about all kinds of fees flashes before your eyes every day. But today we want to tell you the story of one little man who needs our attention.
We are not magicians, but we want to be involved in this. This is not the first gathering and we hope it will not be the last, which, we believe, will end well. Violity launches a limited edition of the rare Violity Magazine. All proceeds from sales will be directly transferred to the card of the baby's parents.
We assure that all data for authenticity is verified personally by the Violiti administration. Also, if you wish, you can get all the information of interest yourself. Thanks to social networks, it is easy to find it in the public domain on the Internet. The forum Violity has also created a theme to cover the story of little Amelia.
A few months ago, the girl was diagnosed with type I SMA. It is a genetic disorder that causes muscle weakness due to neurotrophy. Without treatment, the child cannot continue to exist.
The child needs urgent treatment to help. It can block further development of the disease and restore Amelia's physical abilities.
Helping is easy! It is enough just to want and make a minimum of effort.
Any ideas and opportunities to join? We are pleased to welcome you to our ranks! After all, help can be very diverse: starting with the purchase of a magazine in support of the collection, ending with the placement of information on your website, or even just a kind word and support for the girl's parents.
Let's act together! We believe in success, and you believe too!
We are not magicians, but we want to be involved in this. This is not the first gathering and we hope it will not be the last, which, we believe, will end well. Violity launches a limited edition of the rare Violity Magazine. All proceeds from sales will be directly transferred to the card of the baby's parents.
We assure that all data for authenticity is verified personally by the Violiti administration. Also, if you wish, you can get all the information of interest yourself. Thanks to social networks, it is easy to find it in the public domain on the Internet. The forum Violity has also created a theme to cover the story of little Amelia.
A few months ago, the girl was diagnosed with type I SMA. It is a genetic disorder that causes muscle weakness due to neurotrophy. Without treatment, the child cannot continue to exist.
The child needs urgent treatment to help. It can block further development of the disease and restore Amelia's physical abilities.
Helping is easy! It is enough just to want and make a minimum of effort.
Any ideas and opportunities to join? We are pleased to welcome you to our ranks! After all, help can be very diverse: starting with the purchase of a magazine in support of the collection, ending with the placement of information on your website, or even just a kind word and support for the girl's parents.
Let's act together! We believe in success, and you believe too!
