Pregnancy is a very important and crucial moment in the life of a woman and family. This is not only pleasant chores, but also a serious psychological test. It is very important that during the gestation period the expectant mother is healthy, calm and happy, since her condition is transmitted to the fetus.
In addition to the psychological stress, the body of a pregnant woman is subjected to physiological tests. If he is weakened by chronic diseases, bad habits and an unhealthy lifestyle, the chances of bearing and giving birth to a healthy child are significantly reduced.
Women who are mentally and physically ready for the birth of a child can tolerate pregnancy much easier. Therefore, careful preparation will not only preserve the health of the mother and child, but also enjoy the process. 10 important things to do before pregnancy
Naturally, the first thing to do is to see a doctor and get tested. On the basis of this, treatment or simply corrective therapy is prescribed. I know women mostly take folic acid, but SpermaPlant helps men well in this regard. Improves spermatogenesis and reduces the risk of developing fetal pathologies.
As soon as a couple has decided to prepare for the birth of a child, doctors recommend checking their health. At a minimum, undergo a general medical examination or check-up to identify those deviations in health that need to be compensated before conception or be kept in mind when managing a pregnancy and in deciding how best for you to give birth (for example, often eye or heart problems are indications for a caesarean section).
A responsible approach to family planning today also means genetic testing. It includes a study of chromosomes (karyotype) for both spouses and allows you to identify such abnormalities in parents that can cause the birth of a child with a severe syndrome or miscarriage. These are quite rare cases, but when chromosomal features are identified, they allow a couple to give birth to their first child healthy.
The second step in genetic testing is to identify the carrier status of hereditary diseases, such as cystic fibrosis or phenylketonuria, for which neonatal screening is performed in our country in the first days of a child's life. This information will allow you to assess the risk of having a sick child in a single family. And if both parents have a mutation in the same gene or some chromosomal rearrangements, it will help to form a package of examinations necessary during pregnancy, or to choose the use of IVF with the study of embryos before transplantation into the uterus (preimplantation genetic diagnosis) to minimize the risk of birth a sick child.
The third stage includes a genetic study of frequent changes in the genes of the coagulation system, folate cycle, female hormones and receptors, the peculiarities of the exchange of these hormones - all this is important for the normal course of the processes of fixing a fertilized egg in the uterus, the development of pregnancy and reducing the risk of birth defects and fetal growth retardation. If necessary (for example, in the absence of the desired pregnancy after 2 years of sexual activity), a geneticist can send both a man and a woman for additional research, since some genetic changes can affect fertility.
Also, patients can undergo a comprehensive genetic test, which reveals the status of carriage of rare diseases, changes in genes that affect the course of pregnancy, genetic characteristics of vitamin metabolism, intolerance to certain foods, which will form the basis of dietary recommendations for future parents. Now medicine has great potential to ensure that the pregnancy period proceeds without complications, and healthy children are born in the family.