mai 31, 2025
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Dress from Azalia – Kommersant

Dress from Azalia – Kommersant

The first eight years of life, Azalia Gabbasova from Ufa practically did not hurt. At nine moms began to notice that her daughter would be a little stooping. At eleven, doctors revealed the 2nd degree of scoliosis, at the age of 12 severe back pain began, Gorb grew on the right, and 3 diagnosed 3rd degree scoliosis. A year later, the 4th, the most severe degree and permanent painkillers. A healthy girl became disabled. But you can still return everything back. To do this, you need an operation in Moscow using the new VBT technology (Vertebral Body Tethering) and then a couple of months of rehabilitation.

Azalia returns home from school and lies in lessons. And how else? It is impossible to sit again after a few hours at the desk – the back hurts. It hurts too. Nevertheless, even in such an unusual position, Azalia does not relax: after forty minutes he puts his notebooks and gets a little, leaning on his elbows-everything is ready. She was always an excellent student, although she did not make special efforts to this. Now the first annual four appeared in the diary – in algebra. An unloved object was the first to suffer from scoliosis. Well, let. It is much worse that I have long moved to the closet and there is an sewing machine idle.

“Azalea from the fifth grade went to a circle, where the girls came up with clothes of clothes, painted patterns and sewed themselves,” says Mom Lilia, another “flower” in the family Gabbasovs. – Classes were built very interestingly – entire collections sewed. For example, « Africa »: bright colors, full of scope for imagination. Or “London”-there, on the contrary, dark green, restrained, well, in extreme cases, into the cell. And our Bashkir outfits, of course. My daughter had a favorite dress with a beautiful gray apron with embroidery, she came up with everything herself.

The girls were lucky with the leader of the circle – she also drove them to contests. For example, on the famous « Golden I needle » in the Moscow Fashion House Vyacheslav Zaitsev, where the children gathered from all over the country. It was especially great that the participants of the circle there themselves showed their clothes – they went out to the podium.

First of all, I had to part with the catwalk. Azalia, previously so slender, was terribly shy. The back could be hidden under long loose hair, but it is impossible on the stage. The dress went to the closet, the girl began to wear oversize. She even came up with such styles, because they sew clothes not only for slender long -legged beauties, everyone wants to look good. But she has grown from those models, but it is not possible to sew new ones: working after a sewing machine is certainly not for scoliosis of the 4th degree. Yasmin’s best girlfriend still goes to the circle, but Azalia is not.

Then school events left. Together with Yasmina, Azalia arranged contests of crafts, picturesque work. And the girls asked for labor lessons from first -graders – they taught them from simple things to create all kinds of beauty. But during such a lesson you have to stand a lot – soon it became impossible.

How to live on? In the first scolious years, doctors recommended Azalia therapeutic gymnastics, sports. She carefully did everything, but in vain.

“We and we took my daughter to the osteopats, kinesiologists,” Mom says. “This is all some kind of deception: one trick-3 thousand rubles, you need ten tricks, and then they say: wait, soon everything itself will fall into place. And nothing changes.

The operation loomed on the horizon. “It is required to install a rigid fixing structure on the spine. But not now, but at 18 years old, when the growth will end, ”the doctors said. To suffer another four years? Lilia learned from acquaintances about VBT technology: instead of a hard design, flexible cords-cords are used-they gently pull the vertebrae in the right direction, while without depriving them of mobility. We went to the Moscow clinic, consulted with a doctor who does such operations – and, as Lilia says, “confidence immediately appeared.” The doctor considers the operation necessary.

“It would be nice to make it this summer in order to have time to undergo rehabilitation in the fall, then finish the ninth grade and enter our Ufa State College of Technology and Design: there is a specialty“ Clothing Designer, ”Mom makes plans.

And Azalia now has geometric models of youth clothing on his mind – she cannot think about anything else.

VBT technology operations are not yet paid by state insurance medicine. Only with your help can Azalia be cured.

To save Azalia, Gabbasova lacks 727 243 rubles.




Head of the Center for Pathology of the spine “Clinical Hospital on Yauz” Andrei Baklanov (Moscow): “Azalia has a darkest clap of the 4th degree. Spine deformation is rapidly progressing, pain, squeezing of internal organs, respiratory and cardiovascular failure increase. The girl needs an operation using the new VBT technology, which will adjust the deformation, preserving the mobility of the spine. After the operation, the spine will straighten as much as possible, the pain syndrome will leave, and a full breathing will restore. Azalia will be able to live a full life. ”

The cost of the operation is 2 158 243 rubles. LLC Institute of Source Code contributed 300 thousand rubles. Companies that wished to remain unnamed are another 1,100,000 rubles. The viewers of the GTRK « Bashkortostan » will collect 31 thousand rubles. Not enough 727 243 rubles.

Dear friends! If you decide to save Azalia Gabbasov, even if you are not embarrassed by the price of salvation. Any of your donation will be gratefully accepted. Money can be transferred to the Rusfond or to the bank account of the mother of Azalia – Lilia Akhmadeevna Gabbasova. All the necessary details are in the Rusfond. You can use our electronic payments system by making a donation from a bank card, mobile phone or electronic cash, including from abroad (Details on rusfond.ru).

Alexey Kamensky, Bashkortostan

About Rusfond




Rusfond (Russian Assistance Fund) was created in the fall of 1996 to help the authors of desperate letters in Kommersant. Having checked the letters, we post them in “Kommersant”, on rusfond.ru sites, kommersant.ru, on the TV channel “Russia 1” and radio “Vera”, on social networks, as well as in 132 printing, television and Internet media. Translations from bank cards, electronic cash and SMS publication are possible, including from abroad (details on rusfond.ru). We just help you help. In total, more than 22.578 billion rubles were collected. In 2025 (on May 29), 683 527 553 rubles were collected, 1044 children received assistance. Rusfond – Laureate of the Silver Architect National Prize for 2000, since September 2017 is a member of the register of NPOs – performers of socially useful services. In June 2024, the Presidential Grant won the project of the National RDKM « Consulting Service for the Donesty of the Bone Marrow » Landmark « . In January 2025, the Presidential Grant won the Rus Funde project “PROGRASTRAL. Continuation ». President of Rus Funda Lev Amber – laureate of the State Prize of the Russian Federation.

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