1. About dreams. For four years we have been dreaming about the recovery of the child. When we learned about Varyusha's rare genetic disease, there was no cure in the world. The doctors advised us to accept the child as he is and to put up with it.⏩ paypal.com/donate/?campai…

2. A year later, American scientists found a drug (Ravikti) that can help make my daughter an ordinary child. She will be able to talk, play with children and much more that ordinary children can do. But these options are still closed to us.⏩paypal.com/donate/?campai…

1. Every day I fight for my daughter, I fight with her against her illness. Sometimes I get very tired and I don't have enough strength. Every minute I think about how to raise money to buy her medicines. ⏩ paypal.com/donate/?campai… #VarуushaMayer #SLC6A1 #EpilepticEncephalopathy

2. Our family could always earn money for her treatment, but the war took this opportunity away from us. Please retweet this message so that more people can see it and help Varyusha. ⏩ varyushamayer.taplink.ws #VarуushaMayer #SLC6A1 #EpilepticEncephalopathy

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Now Varya has no training (they stayed in Ukraine), but we walk 2.5 km every day - this helps her to be strong and enduring. This is important for her health, because she always had weak muscles. You can learn more about Varya's disease and help her here:birdsforsofia.org/help-varvara

Varya does not speak and cannot read (illness takes away many opportunities from her), but she loves books. Her favorite books look really bad (she kisses them and crumples the pages). With your help, we can cure Varya: paypal.com/donate?campaig…

Today is World Daughter Day!!! I congratulate all parents and wish health and happiness to your daughters. I love my girls endlessly. paypal.com/donate?campaig…

Today is the day we've been waiting for. Varyusha started treatment today. Friends support us with prayers and may good luck come with us. You can help us put together the entire course of treatment here (share this information): varyushamayer.taplink.ws

👉 instagram.com/nagrada.ua?igs…

I love my daughter's smile. Every day, our family does everything possible so that there are more smiles than tears, and the disease will someday become just a memory. Your help is very important to us: PayPal: [email protected]

How to treat sadness when it's raining outside and you're in a bad mood? Mom's apple pie, of course. Quickly relieves sadness and cheers up)))

Varya began to play with toys. Before, she looked at them and did not know what to do with them. This is a new stage in development. I hope Ravikti will create the miracle we have been waiting for.

Congratulations on the Independence Day of Ukraine. I believe that everything will be fine, that our people will win this cruel war, that our children will have a childhood again. varyushamayer.taplink.ws

Friends, your help is important for Varyusha and I want you to see the result of Ravikti's rehabilitation and treatment. These videos were recorded before the treatment (three months ago).

This video was recorded after the rehabilitation and treatment of Ravikti. The result is impressive. My heart is full of hope. We continue to raise funds for treatment and rehabilitation. You can help Varyusha: varyushamayer.taplink.ws

September 1 Varyusha goes to school in Belgium, she will be there without me every day for 2 hours. I never left her alone, I hope everything goes well. In the meantime, we continue the treatment of Ravikti and enjoy the last summer days

Thanks to Ravikta's treatment, our little daughter started looking into my eyes. It is such a happiness to look into her blue eyes, to feel her spiritual presence. Thanks to everyone who helps our family and makes it possible to treat Varyusha. varyushamayer.taplink.ws

Varyushinskaya specialized school for children with special needs. Her first day of meeting teachers and children. She still doesn't know much. I hope her treatment helps her learn