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Try the dry free alcohol challenge for one month & learn how its good for the body.

Harvard Health Publishing states the following:

“If you’d like to cut down your alcohol consumption or start the new year with a clean slate, join in the Dry January challenge by choosing not to drink beer, wine, or spirits for one month. Dry January began in 2012 as a public health initiative from Alcohol Change UK, a British charity. Now millions take part in this health challenge every year.

While past observational studies suggested a link between drinking a moderate amount of alcohol and health benefits for some people, more recent research has questioned whether any amount of alcohol improves health outcomes. And heavier drinking or long-term drinking can increase physical and mental problems, especially among older adults. Heart and liver damage, a higher cancer risk, a weakened immune system, memory issues, and mood disorders are common issues.

Yet, cutting out alcohol for even a month can make a noticeable difference in your health. Regular drinkers who abstained from alcohol for 30 days slept better, had more energy, and lost weight, according to a study in BMJ Open. They also lowered their blood pressure and cholesterol levels and reduced cancer-related proteins in their blood.

Tips for a successful Dry January

A month may seem like a long time, but most people can be successful. Still, you may need assistance to stay dry in January. Here are some tips:

  • Find a substitute non-alcoholic drink. For social situations, or when you crave a cocktail after a long day, reach for alcohol-free beverages like sparkling water, soda, or mocktails (non-alcoholic cocktails.)
    Non-alcoholic beer or wine also is an option, but some brands still contain up to 0.5% alcohol by volume, so check the label. “Sugar is often added to these beverages to improve the taste, so try to choose ones that are low in sugar,” says Dawn Sugarman, a research psychologist at Harvard-affiliated McLean Hospital in the division of alcohol, drugs, and addiction.
  • Avoid temptations. Keep alcohol out of your house. When you are invited to someone’s home, bring your non-alcoholic drinks with you.
  • Create a support group. Let friends and family know about your intentions and encourage them to keep you accountable. Better yet, enlist someone to do the challenge with you.
  • Use the Try Dry app. This free app from the UK helps you track your drinking, set personal goals, and offers motivational information like calories and money saved from not drinking. It’s aimed at cutting back on or cutting out alcohol, depending on your choices.
  • Don’t give up. If you slip up, don’t feel guilty. Just begin again the next day.

Check your feelings

Sugarman recommends people also use Dry January to reflect on their drinking habits. It’s common for people to lose their alcohol cravings and realize drinking need not occupy such an ample space in their lives. If this is you, consider continuing for another 30 days, or just embrace your new attitude toward drinking where it’s an occasional indulgence.

If you struggle during the month, or give up after a week or so, you may need extra help cutting back. Talk to your doctor about getting the help you need.

The Rethinking Drinking site created by the National Institute on Alcohol Abuse and Alcoholism (NIAAA) is also an excellent resource. For the record, NIAAA recommends limiting alcohol to two daily drinks or less for men and no more than one drink a day for women.

Be aware of problems that might crop up

Dry January can reveal signs of potential alcohol problems, including symptoms of alcohol withdrawal ranging from mild to serious, depending on how much you usually drink.

  • Mild symptoms include anxiety, shaky hands, headache, nausea, vomiting, sweating, and insomnia.
  • Severe symptoms often kick in within two or three days after you stop drinking. They can include hallucinations, delirium, racing heart rate, and fever.

“If you suffer alcohol withdrawal symptoms at any time, you should seek immediate medical help,” says Sugarman.”

QUOTE FOR THURSDAY:

“An estimated 4.22 million U.S. adults had glaucoma in 2022, and 1.49 million had vision-affecting glaucoma, with “substantial variation” in prevalence by region and demographics, according to a research study published in JAMA Ophthalmology

“Up-to-date estimates of how many people have glaucoma in a certain area are vital for addressing the problem,” said Joshua Ehrlich, MD, MPH, lead author of the study and associate professor of ophthalmology and visual sciences at Michigan Medicine. “This kind of information is important for formulating evidence-based policy and public health solutions.”

To estimate the prevalence of glaucoma and related vison loss on a state and county level, Ehrich and colleagues conducted a meta-analysis of data from the National Health and Nutrition Examination Survey, Medicare and IBM MarketScan claims, population-based studies of eye disease and population estimates from the U.S. Census Bureau.”

Glaucoma Research Foundation (Glaucoma Study Shows Higher Prevalence Than Previous Estimates – Glaucoma Research Foundation Glaucoma.org)

QUOTE FOR WEDNESDAY:

“More than 4 million people in the United States have glaucoma and about 35% have related vision loss. Both total glaucoma and vision-affecting glaucoma vary by demographic factors.

Glaucoma is called “the sneak thief of sight” since there are no symptoms and once vision is lost, it’s permanent. As much as 40% of vision can be lost without a person noticing.”

Glaucoma Research Foundation (January Is Glaucoma Awareness Month – Glaucoma Research Foundation)

QUOTE FOR TUESDAY:

“Some types of glaucoma are caused by other medical conditions — but for other people, the doctor doesn’t find another condition that causes it. When the doctor doesn’t find another cause, it’s called primary glaucoma.

Sometimes glaucoma is caused by another medical condition — this is called secondary glaucoma.”

National Eye Institute – NIH (Types of Glaucoma | National Eye Institute)

QUOTE FOR MONDAY:

“In most children, the cause of tetralogy of Fallot isn’t known. It’s a common type of heart defect. It may be seen more commonly in children with Down syndrome or DiGeorge syndrome. Some children can have other heart defects along with tetralogy of Fallot.  Infants and young children with unrepaired tetralogy of Fallot are often blue (cyanotic-not enough oxygen getting to their tissues).”

AHA American Heart Association (www.heart.org/en/health-topics/congenital-heart-defects/about-congenital-heart-defects)

QUOTE FOR THE WEEKEND:

“The ductus arteriosus is a normal fetal artery connecting the aorta and the main lung artery (pulmonary artery). The ductus allows blood to detour away from the lungs before birth.

Every baby is born with a ductus arteriosus. After birth, the opening is no longer needed and it usually narrows and closes within the first few days.

Sometimes, the ductus doesn’t close after birth. Failure of the ductus to close is common in premature infants but rare in full-term babies. In most children, the cause of Patent Ductus Arteriosus-PDA isn’t known. Some children can have other heart defects along with the PDA.

Truncus arteriosus occurs when the two large arteries carrying blood away from the heart don’t form properly and one large artery is present instead. This artery (the truncus) sits over a large opening or hole in the wall between the two pumping chambers (ventricular septal defect). With only one artery, there is no specific path to the lungs for oxygen before returning to the heart to deliver oxygen to the body.”

American Heart Association-AHA   (www.heart.org/en/health-topics/congenital-heart-defects/about-congenital-heart-defects)

QUOTE FOR FRIDAY:

“Every 4.5 minutes a baby is born with a condition that affects the structure or function of their body. Collectively, these conditions are referred to as birth defects. They can vary widely in how and where they affect the body and include things from cleft lip to heart problems. While medical advancements have greatly improved health and survival, many of these conditions are lifelong and require lifelong care.

Achieving the best possible health will look different for different people. No two people living with these conditions are exactly alike. Everyone’s journey is unique, shaped by their specific condition, individual strengths, and the support system in place. However, a community of support can help people with these conditions no matter what health experiences they are navigating.”

Centers for Disease Control and Prevention – CDC

(Birth Defects Awareness Month | Birth Defects | CDC)

QUOTE FOR THURSDAY:

“Congenital heart disease is a heart problem that a person is born with. It means that the heart’s structure — for example, its walls or valves — did not develop properly before birth. More than a million American adults live with congenital heart disease. Many were diagnosed as infants and had surgery or other treatment as a child. Others don’t know they have congenital heart disease until they develop symptoms as adults, like shortness of breath or an abnormal heartbeat.

No matter the cause or the age of diagnosis, people with congenital heart disease need continued care and treatment throughout their lives. It can be difficult for adults to find heart specialists familiar with their particular anatomy and problems–NewYork-Presbyterian has one of the few programs in the country with the depth and breadth of expertise to address the complexity of congenital heart disease in adults.

Our highly trained heart specialists understand congenital heart disease’s unique physiological, anatomical, and clinical features at all ages. Your care team includes physicians, surgeons, and genetic experts specializing in adult congenital heart disease. They’re experts in echocardiography, interventional cardiac catheterization, interventional electrophysiology, complex congenital heart surgery, and heart transplantation.

With this team approach, we address the complex needs of people with adult congenital heart disease at three centers where you can receive treatment in a hospital setting designed for adults without having to stay in a children’s hospital:

  • Schneeweiss Adult Congenital Heart Center at New York-Presbyterian/Columbia University Irving Medical Center is one of the nation’s oldest, largest, and most experienced adult congenital heart disease programs.
  • Cornell Center for Adult Congenital Heart Disease at New York-Presbyterian Weill Cornell Medical Center
  • Ronald O. Perelman Heart Institute, NYP/Weill Cornell”

New York Presbyterian Hospital

(Congenital Heart Disease | NewYork-Presbyterian)

What to know in Prevention for Congenital Defects.

Though not all birth defects can be avoided, prenatal care and awareness of past or current conditions can help with prevention.

  • Prenatal care. Taking a daily prenatal vitamin that includes at least 400 micrograms of folic acid can help prevent a variety of birth defects. You should be taking prenatal vitamins if you’re of reproductive age, when you’re actively trying to conceive and/or as soon as you find out you are pregnant. In addition to taking your prenatal vitamin, avoiding alcohol, tobacco and illegal drugs can significantly help prevent birth defects and pregnancy complications.
  • Awareness of past or current conditions. If you previously had a pregnancy with a birth defect, it’s important to find out the most likely causes because it can help your physician plan preventive measures for your next pregnancy. For example, spina bifida is caused by a deficiency in folate, so if your previous pregnancy had spina bifida, you can take a high dose of folate to help prevent future spina bifida diagnoses.

Are all birth defects discovered before a baby is born?

It’s not always possible to detect all birth defects in utero. However, high-resolution ultrasounds done by certified prenatal ultrasound groups make it possible to diagnose defects that will cause a significant impact before birth.

Baschat says: “At the Center for Fetal Therapy, we recommend that pregnant women have the first-trimester nuchal translucency scan between 11 and 14 weeks and the anatomy scan between 18 and 20 weeks. These two ultrasounds provide us with the best opportunity for detecting birth defects.”

In recent years, some pregnant women have turned down the first-trimester ultrasound because a maternal screening blood test now exists for Down syndrome. The ultrasound is still strongly recommended, though, because there are many other serious birth defects that can be detected this early in pregnancy.

Is it possible to treat birth defects while a baby is in utero?

Absolutely. While there are many different types of birth defects, it’s extremely important to try to correct those that damage vital organs before the baby is born. The Center for Fetal Therapy specializes in treating several of these defects in utero, including:

  • Congenital diaphragmatic hernia. This condition, in which a hole in the diaphragm allows abdominal content to enter the chest and restrict lung development, can be significantly helped in utero through fetoscopic endotracheal occlusion, a surgery that improves lung function and significantly increases survival rates.
  • Lower urinary tract obstruction. This occurs when the flow of urine is blocked from exiting the fetus’ body, leading to permanent kidney damage. Relieving this obstruction before birth protects the kidneys.

Fetal treatments also exist for conditions that make the baby unhealthy, even if they are not considered to be birth defects. For example, if a fetus has an irregular heartbeat, you can give the mother medication that will cross the placenta and treat the fetus.

How successful are in utero treatments for fetal conditions?

By treating fetal conditions in utero rather than waiting until after birth, fetuses are given significantly better chances of survival and a reduced need for major surgery after birth. For example, with a condition like twin-to-twin transfusion syndrome, in which identical twins develop a blood volume imbalance, both babies could die without any intervention. By performing laser surgery in utero, there is approximately a 95 percent chance that at least one baby will survive.

Explains Baschat, “Success rates vary depending on the condition, available treatments and the individual patient, but overall, where fetal interventions are available, we see a much higher rate of survival for affected fetuses.”

If a baby has fetal surgery, will he/she need different care after birth?

This will depend on the individual condition and type of surgery performed. For all fetal surgeries, your baby needs to be delivered at a hospital where pediatric subspecialties are in-house so the baby’s care can be managed after birth. Baschat says: “Many of the treatments we perform require patients to deliver at the highest-level multispecialty hospital, like The Johns Hopkins Hospital. This way, all prenatal and postnatal care is available to you in one location.”

If you have one child affected by a birth defect, will all of your future children have that same condition?

All future children will not definitively be affected by the same birth defect, but it will depend on what the cause was. If the birth defect was caused by a genetic mutation, there may be a higher likelihood of recurrence, but if you seek care from a specialized center, maternal-fetal medicine specialists and genetic counselors can work with you to assess future risk.

The risk of some conditions can be determined before you become pregnant through genetic testing. If that doesn’t exist for the condition in question, maternal-fetal medicine specialists and genetic counselors can genetically test your fetus during pregnancy to see if she or he exhibits the mutation that affected your previous child.

Are there communities in which you can speak with other families who have had children affected by birth defects?

There are many forums online, whether on the web or social media platforms, in which parents come together. “At our center, we reach out to previous patients to see if they are interested in communicating with new patients affected by the same condition,” Baschat explains. “They can empathize about the specific birth defect, but they can also provide guidance and advice about the experience of working with our center throughout the pregnancy and after the baby is born.”

In the future, what advances will take place in treating disease before birth?

Through prenatal diagnosis and understanding fetal disease better, physicians are learning more about what harms the fetus and what may be of benefit before birth. Additionally, new uses for minimally invasive surgical equipment are regularly being discovered.

There are also stem cell therapies, genomic medicine and a whole host of related treatments that are currently used for children and adults. One day, these may also apply to the fetus. “While it’s hard to predict the future, we’re currently doing things we couldn’t have foreseen 10 years ago, so we’re very hopeful for continued advancements in fetal care,” says Baschat.

QUOTE FOR WEDNESDAY:

“Vitiligo is a skin condition that has impacted millions of people worldwide. It affects people of all ages and genders. Vitiligo is a chronic skin condition that causes loss of natural pigment of the skin and results in the appearance of light-colored or white spots on arms, legs, and other parts of the body. Although it is not a life-threatening condition, vitiligo can significantly impact a person’s self-esteem, clothing choices, and quality of life.”

PERFECTFAQS (PerfectFaqs.com | Perfectly Curated, Fact-checked Blogs For You)