Pregnancy is a life-transforming journey and while there is so much changes that happens during this time, you cannot always be prepared for everything. Here are 10 surprising facts that you did not know were true during pregnancy.

The Nesting Instinct

If you have seen animals look for paper scraps, or take fur out of their own body or collect small twigs and stem to build a nest for their upcoming babies, even if the animals are domesticated, humans do the name. Humans do not take fur or hair out of their body, but we too experience a powerful urge to prepare our home for the baby. We clean it, decorate it and thanks to modern homes, we can now baby proof it do!

Mommy Brain

This happens in the first trimester, when tiredness, morning sickness and other symptoms can make the mother feel worn out and mentally fuzzy, often called the mommy brain. The National Institutes of Health also notes that cognitive function decline in the third trimester of pregnancy, leading to memory problems.

Mood Swings

Premenstrual syndrome (PMS) and pregnancy share several symptoms, such as breast swelling and tenderness, hormonal fluctuations, and mood swings. If you’ve experienced severe mood swings due to PMS, you may notice an intensification of these emotions during pregnancy. It's common to feel joyful one moment and tearful the next as your body adjusts to hormonal changes.

Breast Growth

An increase in breast size is one of the earliest signs of pregnancy apart from your missed period. It happens in the first trimester due to the higher levels of hormones like estrogen and progesterone. The growth continues throughout pregnancy.

Skin Changes

Have you heard about pregnancy glow? This happens because pregnancy women have an increased blood volume, this happens to provide extra blood flow to the uterus and other organs, especially the kidneys. This greater volume brings more blood to the vessels and increases oil gland secretion.

Hair and Nails

During pregnancy, many women notice changes in their hair texture and growth. Hormonal shifts can make hair grow faster and reduce hair loss. However, these changes are typically temporary, and many women experience some hair loss during the postpartum period or after they stop breastfeeding. In some cases, hair growth may also occur in unexpected areas like the face, belly, or around the nipples. Additionally, hair texture can shift, becoming drier or oilier, and some women even notice a change in hair color.

Nails can also undergo changes during pregnancy. Increased hormone levels may cause nails to grow faster and become stronger, but for some women, nails may become more brittle, splitting and breaking more easily. Like hair changes, these nail changes are usually temporary. If your nails are more prone to splitting or tearing, it’s helpful to keep them trimmed and avoid exposure to chemicals in nail polish and nail polish remover.

Your Feet Grow

If you have heard about it, then you already know that it is not just the clothes that do not fit you, it is your shoes too. Extra fluid in the pregnant body also leads to swollen feet. The joints also tend to be looser during pregnancy.

Joint Mobility

Your body also releases hormones like relaxin that prepares your body, especially the cervix for the birth. This loosens the ligament in your body, which may make you less stable .

Varicose veins, constipation, and hemorrhoids

Varicose veins, common in the legs and genital area during pregnancy, result from blood pooling in veins enlarged by pregnancy hormones. They often disappear after delivery. To prevent them, avoid prolonged sitting or standing, wear loose clothing and support hose, and elevate your feet when seated.

Hemorrhoids, which are varicose veins in the rectum, may develop due to increased blood volume and uterine pressure. They can cause pain, itching, bleeding, or stinging, especially during bowel movements. Constipation, caused by hormonal changes and uterine pressure on the large intestine, can worsen hemorrhoids by straining during bowel movements.

Prevent constipation and hemorrhoids by eating a fiber-rich diet, staying hydrated, and exercising regularly. If needed, consult your doctor about stool softeners, laxatives, or creams for relief.

Labor and what goes out of your body

When you are in labor, your amniotic sac, that has fluid that surrounds the baby, breaks or ruptures, which is what is also known as water breaking. For most women contractions start before their water breaks, if not, then the doctor may have to rupture the amniotic sac, in case the cervix is already dilated. Some women may feel the urge to pee, while for some it may feel a trickling their leg.

Many people carry the thalassemia gene without knowing it because they may not have any symptoms. A simple carrier screening test before pregnancy can help couples understand risks and make informed decisions while planning parenthood.

Importance of Genetic Screening

Parenthood planning today is not only about financial preparation or healthy lifestyle changes, but also about understanding genetic health risks that can impact the child’s future. And one such condition that tends to go unnoticed is thalassemia carrier status.

Did you know? Many individuals discover they are carriers only after facing difficulties during pregnancy or after the birth of a child with thalassemia major.

What Is Thalassemia?

Thalassemia is an inherited blood disorder that affects the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. People who are carriers usually live normal and healthy lives and may not experience major symptoms. Because of this, many remain unaware of their carrier status for years.

However, it becomes a matter of concern when both partners are carriers of the thalassemia gene. In such cases, there is a huge risk that the child may inherit thalassemia major, a severe condition that may require lifelong blood transfusions, regular hospital visits, medications, and continuous medical care.

Why Thalassemia Often Goes Undetected

These are some of the challenges faced by families: So, challenges are that the thalassemia carrier status is often detected very late. Mild tiredness or anemia may be ignored or mistaken for iron deficiency, and many will not seek help.

So, couples do not consider genetic testing before marriage or pregnancy because they feel healthy and have no family history of the disease. When a child is born with thalassemia major, families may face stress, anxiety, repeated hospital visits, financial burden, and long-term treatment responsibilities. The condition can also affect the child’s growth, immunity, and overall quality of life.

The Need For Awareness And Early Action

This is why screening is important for couples: Carrier screening is a simple blood test that helps identify whether a person carries the thalassemia gene. If one partner tests positive, the other partner is advised to get tested as well.

Early screening before pregnancy helps couples understand their risks and explore available options with proper guidance. Thalassemia carrier screening is a small step that can make a major difference in parenthood planning.

Increasing awareness and encouraging timely testing can help families make informed decisions and reduce the burden of severe thalassemia in future generations. So, it is imperative to go for timely screening as advised by the expert and improve the quality of life.

Preeclampsia is usually discussed as a pregnancy complication, but the risk does not end automatically after childbirth. Delivery is an important part of treatment, but it is not an instant cure. A woman can still develop postpartum preeclampsia in the days or weeks after delivery, even if her blood pressure was normal during pregnancy.

The risk is highest soon after childbirth, but it can remain for up to six weeks. This period needs close attention because the mother is recovering, sleep-deprived, caring for a newborn, and may mistake warning signs for normal post-delivery discomfort. This is when the condition can become dangerous if symptoms are missed.

The warning signs of postpartum preeclampsia should be taken seriously. A severe headache, blurred vision, seeing spots, swelling of the face or hands, pain below the ribs, nausea, vomiting, breathlessness, chest pain, reduced urination, sudden weight gain, or very high blood pressure should be checked urgently.

If postpartum preeclampsia is not treated in time, it can lead to seizures, known as eclampsia, and may also cause stroke, fluid in the lungs, acute liver or kidney injury, and, in rare severe cases, hepatic subcapsular hematoma, which is bleeding beneath the capsule of the liver, or intracranial bleeding, also called brain hemorrhage. In the most severe cases, it can be fatal.

The reassuring part is that the condition is treatable when identified early. Treatment may include blood pressure medicines such as labetalol, nifedipine, or amlodipine, magnesium sulphate if there is a risk of seizures, and diuretics in selected cases where there is fluid overload. Many of these decisions can be safely planned even if the mother is breastfeeding, but treatment should always be guided by her treating doctor.

The responsibility should not fall only on the mother. Families need to watch her health with the same seriousness with which they attend to the newborn. As a precaution, blood pressure checks should continue at home or during scheduled visits, especially in the first few weeks after delivery. Postpartum follow-ups should not be missed, prescribed medicines should be taken properly, and self-medication should be avoided, particularly painkillers or over-the-counter drugs unless approved by the doctor. If symptoms worsen, or if there is headache, breathlessness, chest pain, visual disturbance, or swelling, she should be taken back to the hospital without delay.

A history of preeclampsia also remains important after recovery because it can increase the woman’s future risk of chronic hypertension, heart disease, stroke, and kidney disease. Postpartum care should never be treated as a formality. It is an essential part of protecting the mother’s recovery, her future pregnancies, and her long-term health.

Bone marrow transplant (BMT), also known as hematopoietic stem cell transplant, is regarded as a lifesaving and even curative therapy. It is important to note that no surgery is required; rather, stem cells are transfused from a bag, like a blood transfusion.

BMT has revolutionized the treatment of several severe pediatric disorders, including thalassemia major, severe aplastic anemia, immunodeficiency disorders, high-risk blood cancers, and certain neurological and metabolic disorders such as metachromatic leukodystrophy and mucopolysaccharidoses (MPS). Despite major progress in transplant science, many still see BMT as a last resort. This can have a high effect on the survival rate, recovery process, and overall quality of life.

Why Are Bone Marrow Transplants Delayed?

One big reason for postponing transplant decisions is the belief that BMT should only be considered after all standard therapies have failed. There is also limited awareness about the excellent outcomes and curative potential of BMT in many benign pediatric disorders when performed early.

Children often go through repeated chemotherapy cycles, frequent blood transfusions, or long-term supportive care before anyone seriously discusses transplant. While this therapy may help in stabilizing the condition temporarily, it can cause lasting damage to the organs, increase the risk of infections, and affect the immune system, making transplant surgeries risky and less successful.

Delays Can Reduce Success Of Transplant

For instance, in children with thalassemia major, years of blood transfusions can lead to iron overload, which harms the heart and liver, reducing their ability to handle intense transplant conditioning. Likewise, in diseases like MPS, metachromatic leukodystrophy, where the disease has progressed, role of BMT becomes guarded.

Why Early Referral And Timely Treatment Matters

In addition to medical hesitation, systemic and emotional barriers also cause delays. The long-standing belief that a fully matched donor is essential has also changed significantly, with recent years witnessing remarkable growth and success in haploidentical (half-matched) donor BMTs. There are challenges related to awareness and affordability in India. The fear of risks such as graft-versus-host disease, infection, or death from transplant surgery results in parents adopting a "wait and see" attitude until their child’s health deteriorates further.

It is ironic that lack of awareness and accessibility to pediatric bone marrow transplant specialists are also among the factors that can cause delay in proper diagnosis and referral. Yet, the wait could put the children’s lives at greater risk due to the damage caused by chemotherapy and other forms of treatment.

Modern medical professionals emphasize that BMT does not have to be used only as a “last resort” treatment but can be administered in a timely manner to provide a cure for the patient.