TO ATTENTION of visitors!

About changes in surrogate motherhood in Ukraine:

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In connection with frequently asked questions from our clients we inform you
Currently in Ukraine:

The activities of official surrogate motherhood clinics are approved and welcomed by the Ministry of Health of Ukraine. We are such a clinic.

Our prof. Feskov A.M. clinic has the highest reliability and enjoys trust precisely among foreign citizens.
All children born as a result of surrogate motherhood programs went home with their genetic parents without hindrance.

The standard practice of leaving Ukraine with a baby is to visit the consulate to obtain a travel document or passport. In addition to the standard practice of leaving Ukraine, we successfully carry out repeatedly tested methods:


If you have any questions about participating in surrogate motherhood programs, you can ask your questions to our lawyers, in the contact form, or by contacting directly.
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Ideal genetics for your child!

What is Human genomics services?

Genomics is the science of the human genetic apparatus, which studies the structure of the genes of their functions and participation in the formation of the characteristics of the organism. It allows us to understand in detail how genes work, how they affect the functioning of the organism and interact with each other. This makes it possible to predict and influence the variability of generations of a species (in our case, a human).

Everyone has genetic mutations in their genome that do not manifest themselves and do not have a negative impact on health. This is completely normal. But when a child receives from father and mother two identical "sleeping" mutations - their "activation" takes place, which leads to the development of hereditary diseases.

How exactly are the diseases activated?

The cells of the human body contain chromosomes, the chromosomes are made up of genes. Genes produce proteins that regulate the work of cells, and accordingly of  the whole body. Mutations in the genes lead to the fact that the proper production of proteins is disturbed and this causes the occurrence of various pathologies.

Human genomics services offers future parents to protect their child from this and to avoid the occurrence of genetically determined diseases.

In order to create a genetically ideal person, we conduct a study of the genome (of all genes) of the biological father and the biological mother of a child (or of the donor of the oocytes, the sperm donor) on all genetic mutations known to date in the genes that have a clinical manifestation or carry a risk for the quality of the child's life.

Then, based on the mutations found, we make pre-implantation genetic diagnosis (PGD), which allows us to detect and examine mutations directly in the embryo. This makes it possible to get an absolutely healthy embryo, which will then be transferred to the uterine cavity. From this embryo carefully checked and selected, the perfect human is born - a genetically perfect healthy child!

Who needs the service Human genomics services?

Who can use the service of Human genomics services and choose the birth of a genetically healthy child?

  • Healthy couples, single men or women - all who want to have a baby, avoiding any possible risks associated with genetic problems.
  • People with hereditary pathology of monogenic diseases (cystic fibrosis, hemophilia, spinal muscular atrophy and others, total about 400 diseases).
  • People who have had oncological diseases. Including those who have family forms of cancer.
  • People who have multifactorial diseases (hypertension, thrombophilia, autoimmune diseases and other common diseases in which hereditary predisposition plays a role).

How does it work?

Human genomics services includes the following stages:

  1. Blood test of a man and a woman - the biological parents of a future child. It can be partners from a married couple, or a sperm donor, an oocyte donor. A blood test of other relatives may also be performed, depending on the method of examination and the disease sought.
  2. The IVF program + preimplantation genetic diagnosis with the genetic testing + chromosomes on the embryo. Selecting a healthy embryo.
  3. Transfer of a healthy embryo (you choose the sex of the embryo) into the uterine cavity. The onset of pregnancy.
  4. The birth of a genetically perfect child Perfect human.

What programs Human genomics services are used for?

Human genomics services can be used if you choose the following programs:

  • surrogate motherhood Guarantee,
  • IVF Guarantee,
  • egg donation Guarantee,
  • embryo adoption guarantee.

Why do we offer these services only for guarantee packages? The fact is that the creation of a perfect human is a complex process. In order for you to have a healthy child with ideal genetics, our specialists need to put a lot of effort and perhaps it will take many attempts to achieve the desired result. Feskov human reproduction group takes all responsibility for the result, which is prescribed in the contracts of guarantee packages.

Necessary conditions for the program

  1. There are age restrictions for this service.
  2. Human genomics services is used only for guarantee packages of services. In the confines of Advanced VIP Guarantee packages (IVF program, donation of oocytes, surrogate motherhood).
  3. Before the beginning of the program, a preliminary examination is carried out, according to which a decision is made about the possibility of creating a healthy genetically ideal child.

What is Human genomics services?

Genomics is the science of the human genetic apparatus, which studies the structure of the genes of their functions and participation in the formation of the characteristics of the organism. It allows us to understand in detail how genes work, how they affect the functioning of the organism and interact with each other. This makes it possible to predict and influence the variability of generations of a species (in our case, a human).

Everyone has genetic mutations in their genome that do not manifest themselves and do not have a negative impact on health. This is completely normal. But when a child receives from father and mother two identical "sleeping" mutations - their "activation" takes place, which leads to the development of hereditary diseases.

How exactly are the diseases activated?

The cells of the human body contain chromosomes, the chromosomes are made up of genes. Genes produce proteins that regulate the work of cells, and accordingly of  the whole body. Mutations in the genes lead to the fact that the proper production of proteins is disturbed and this causes the occurrence of various pathologies.

Human genomics services offers future parents to protect their child from this and to avoid the occurrence of genetically determined diseases.

In order to create a genetically ideal person, we conduct a study of the genome (of all genes) of the biological father and the biological mother of a child (or of the donor of the oocytes, the sperm donor) on all genetic mutations known to date in the genes that have a clinical manifestation or carry a risk for the quality of the child's life.

Then, based on the mutations found, we make pre-implantation genetic diagnosis (PGD), which allows us to detect and examine mutations directly in the embryo. This makes it possible to get an absolutely healthy embryo, which will then be transferred to the uterine cavity. From this embryo carefully checked and selected, the perfect human is born - a genetically perfect healthy child!

Who needs the service Human genomics services?

Who can use the service of Human genomics services and choose the birth of a genetically healthy child?

·         Healthy couples, single men or women - all who want to have a baby, avoiding any possible risks associated with genetic problems.

·         People with hereditary pathology of monogenic diseases (cystic fibrosis, hemophilia, spinal muscular atrophy and others, total about 400 diseases).

·         People who have had oncological diseases. Including those who have family forms of cancer.

·         People who have multifactorial diseases (hypertension, thrombophilia, autoimmune diseases and other common diseases in which hereditary predisposition plays a role).

How does it work?

Human genomics services includes the following stages:

1.      Blood test of a man and a woman - the biological parents of a future child. It can be partners from a married couple, or a sperm donor, an oocyte donor. A blood test of other relatives may also be performed, depending on the method of examination and the disease sought.

2.      The IVF program + preimplantation genetic diagnosis with the genetic testing + chromosomes on the embryo. Selecting a healthy embryo.

3.      Transfer of a healthy embryo (you choose the sex of the embryo) into the uterine cavity. The onset of pregnancy.

4.      The birth of a genetically perfect child Perfect human.

What programs Human genomics services are used for?

Human genomics services can be used if you choose the following programs:

• surrogate motherhood Guarantee,

• IVF Guarantee,

• egg donation Guarantee,

• embryo adoption guarantee.

Why do we offer these services only for guarantee packages? The fact is that the creation of a perfect human is a complex process. In order for you to have a healthy child with ideal genetics, our specialists need to put a lot of effort and perhaps it will take many attempts to achieve the desired result. Feskov human reproduction group takes all responsibility for the result, which is prescribed in the contracts of guarantee packages.

Necessary conditions for the program

1. There are age restrictions for this service.

2. Human genomics services is used only for guarantee packages of services. In the confines of Advanced VIP Guarantee packages (IVF program, donation of oocytes, surrogate motherhood).

3. Before the beginning of the program, a preliminary examination is carried out, according to which a decision is made about the possibility of creating a healthy genetically ideal child.