Child care muscle shoals al: THE Top 10 Daycares in Muscle Shoals, AL
THE Top 10 Daycares in Muscle Shoals, AL
Daycares in Muscle Shoals, AL
Recent review:
My 2 boys went here. My oldest started at age 3 1/2 & youngest was age 2, both went until they started Kindergarten. They both LOVE Ms. Betty, the owner; Ms. Aday, the oldest class teacher. They helped pottytrain my youngest and got them ready for Kindergarten. My boys both excel in school and I feel it’s a big thanks to these ladies I mentioned and the other workers….
Reviewed by Stephani W
Jane’s Home Daycare
409 W Richton Ave, Muscle Shoals, AL 35661
Costimate: $100/wk
Description:
Jane’s Home Daycare is a local child care provider that offers daycare and early education services designed for preschool children. Located at 409 W Richton Avenue, the company serves the residents of theMuscle Shoals, AL community. Jane’s Home Daycare has been in business since 2010….
JOHNSON DAY CARE
500 W State St, Muscle Shoals, AL 35661
Costimate: $100/wk
Description:
JOHNSON DAY CARE in Muscle Shoals, AL offers a caring staff with activities that stimulate the body and mind of the students. They provide age-appropriate curriculum and ensure that the children have aneducationally enriching and fantastic time. This child care organization accepts children of all ages and is available for part-time or full-time care….
Description:
All of God’s Children Child Development Center is a ministry of Greater Fellowship MB Church and located at 138 2nd Street, Muscle Shoals, Alabama. The center serves children ages six week to twelve years old,providing them a safe and nurturing Christian environment that supports spiritual growth and physical, social and intellectual development. It is open from Mondays through Fridays, 6:00 AM to 6:00 PM….
Description:
Sheffield Head Start Center is an early childhood education facility that offers child care, head start, and school readiness programs for preschool children. Located in Sheffield, Alabama, the company enrollsand handles children ages three weeks to five years old. The company also provides services geared for pregnant women.
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FAQs for finding daycares near you in Muscle Shoals, AL
What are the benefits of daycare near me in Muscle Shoals, AL?
Daycare centers near you in Muscle Shoals, AL offer a number of benefits to both children and their parents or guardians. For the kids, daycare is an opportunity to learn coping and social skills, explore the world, and form relationships with other children – all while staying active and stimulating their minds with educational activities. For parents and guardians, daycare often provides peace of mind that their children are supervised in a safe and nurturing environment with skilled professionals on board to tackle responsibilities such as discipline, problem solving strategies, and nutrition.
All in all, daycare is a valuable resource for families by providing quality childcare and early childhood education services.
What services do daycare centers offer near me in Muscle Shoals, AL?
Daycares near you in Muscle Shoals, AL provide a range of services that allow children to grow and develop in safe, secure environments. Daycare centers are staffed by qualified professionals who create a caring atmosphere that teach kids lessons fundamental to their well-being, and typically include activities such as playtime, meals, and learning opportunities designed to prepare young minds for the world ahead.
What should I look for in a daycare center near me in Muscle Shoals, AL?
Finding the right daycare center near you in Muscle Shoals, AL for your child can be an overwhelming experience, but the process can be streamlined with a clear understanding of what to look for. It’s important to consider factors such as certification and accreditation, as well as any health and safety protocols that are in place.
Factors such as cost, accessibility, and the quality of care provided are sure to be top of mind as well, and ultimately, selecting the best daycare center will depend on finding one that meets your expectations and your child’s specific needs.
What questions should I ask when looking for a daycare for my child near me in Muscle Shoals, AL?
Some questions you might consider asking daycare centers near you in Muscle Shoals, AL include: What are the teacher-to-child ratios? What types of activities do you plan as part of the daily program? Is there an outdoor play area and what safety regulations are in place regarding that space? How often is communication provided to parents regarding their child’s progress or issues that arise? Be sure to ask specifics about any policies related to enrollment fees, tuition payments, health and vaccination requirements and anything else that is important to you and your family as well.
Daycare in Muscle Shoals, AL
A Nurturing Environment to Learn & Grow
Johnson’s Day Care & Cradle Care considers the individual developmental needs of each child and which classroom will suit them best.
Our philosophy is that for a child to develop a positive self-image and appropriate social skills, they need to be grouped with peers whose developmental age is similar to their own.
Explore our programs below!
Our Philosophy
We are based on the belief that children of all abilities benefit from an inclusive environment, emphasizing acceptance of individual differences and ability levels. Inclusion allows all children to relate and interact with peers in play and daily routines, engaging in experiences that promote independence skills, self-control, and an understanding that others have different backgrounds and perspectives other than themselves.
For children with special needs, inclusion facilitates developmental progress by exposure to role modeling of social, language, and physical skills through interactions with typically developing peers. We also believe that the typically developing children gain solid interpersonal skills, including self-confidence, acceptance, empathy, and communication.
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Why Choose Us?
Small Classroom Sizes
Talented & Dedicated Staff
Over 40 Years of Experience
After-School Transportation to Our Center
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Parent Reviews
“My children have been coming to your daycare for several years. Having foster children who sometimes have behaviors, finding a daycare willing to go the extra mile for my kids was challenging. Over 23 kids have felt welcome at Johnson’s Day Care & Cradle Care. Many of my kids have exhibited undesired behavior, but you and your staff handle them with love and understanding. As I leave my children, I feel confident they will be loved and safe each day. mile” to my kids.”
Teresa S.
“All of my three children attended Johnson’s Day Care & Cradle Care. The decision to move our children from their babysitter to daycare was a tough one to make. That decision was made so much easier after seeing the teachers with our children! It was obvious they were loved and cared for.
Sheila, thank you and your staff for caring for my children and helping us raise them into the wonderful people they are today!”
Dwight & Shea P.
“All three of our children attended Johnson’s Day Care & Cradle Care. They were part of the first pre-kindergarten classes offered by certified teachers at the center. I do no doubt that the early learning opportunity was vital to their success in being ready to go into kindergarten and beyond. I have never worried about leaving my children because we knew they would be well fed and cared for while there. They made lifelong friendships as many of their classmates also learned at Johnson’s.”
Stormy P.
“I cannot say enough about our experience at Johnson’s Day Care & Cradle Care! This momma (and her baby) had major separation anxiety starting in Pre-K. Ms. Jennifer and Ms. Kelly made sure we were fine. They never got upset if I called once or 100 times and loved my child as their own!”
Felicia & Lexie T.
Parent Information
Johnsons Day Care & Cradle Care
500 W State Ave
Muscle Shoals, AL, 35661
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Business Hours
Monday-Friday: 5:30 AM- 6 PM
Saturday-Sunday: Closed
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90,000 Life with SMA. What should families do? Psychologist and Parent Experience
Based on Life After Diagnosis: What SMA Learned in 25 Years with Albert Friedman, PhD, Psychologist, Practicing Psychologist and Father of a Child with Spinal Muscular Atrophy, a story about the life of a family with a child with SMA, as well as ways of self-support and support of all family members in such a situation.
About the author
Albert Friedman, PhD, practicing psychologist and father of a child with spinal muscular atrophy. Albert lives and works in Philadelphia, Pennsylvania, USA. For twenty years he has been advising children, teenagers and their parents. 25 years ago, Albert had a child with SMA, and the psychologist began to speak frequently at international conferences, talking about the problems faced by families with children with this diagnosis.
He also advises many organizations that fight for the rights of patients with rare diseases, pharmaceutical companies and healthcare organizations.
What changed the lives of people with SMA in 1995?
In 1995, scientists discovered the gene responsible for the development and course of spinal muscular atrophy. This event led to the results that can be observed now. First of all, this is the emergence of drug therapy, which radically changed the prognosis of life and condition in children and adults with SMA. The situation has changed completely, but it is very valuable to know the opinion of the father of a child with SMA, who has been watching his son grow and develop for 25 years.
Albert understands that a diagnosis is not a death sentence, but there are a huge number of medical, economic, social and psychological problems facing every family where a baby is born with a diagnosis of spinal muscular atrophy.
But SMA is not only difficulties and problems, it is also a very important experience with a positive effect that can be seen only at a great distance.
Over the course of 25 years, the family of a child with SMA has certainly learned to overcome difficulties and find ways to cope with them, and therefore the experience of Albert Friedman is valuable to many people.
What can you learn in 25 years of living with a child with SMA?
As the father of a young man with SMA and a highly experienced family psychologist, I have learned a lot in 25 years. I help people, I work with requests on social, behavioral and partly medical issues. In the fall of 2020, in the era of the pandemic, I cannot personally share my life experience with you, but I can tell you about my experience online with the help of modern technology.
How to accept a serious diagnosis in your own child?
I will never forget the day I was told that my son had SMA. It was in the hospital, the doctors thought that the child would live no more than a year.
This was very traumatic news for our whole family, in which we needed psychological help.
Even two weeks after I found out about my son’s diagnosis, I was very exhausted: I didn’t eat well, I didn’t sleep well, and I was scared.
Many families with sick children have asked me, as a psychologist, “Dr. Al, is it normal for me to cry, get upset, scared, and sleep badly?” Based on my experience, I answered: “This is normal, this is an adequate response to a frightening and traumatic situation.”
Personally, it was his smile that helped me accept my son’s diagnosis. I was afraid of losing Jack, and I began to learn how to be a really good father. It was a very difficult time, but it taught me a lot.
In 1995, families with children with SMA had little to hope for. Before the advent of effective drug therapy, there were still 20 years left (then we did not know about it). The only thing that gave us a chance to continue life and gave us strength to fight the disease was communication with other families that also had children with SMA. We tried to maintain closeness and a positive attitude, we exchanged experiences, got a lot of useful things from meeting each other.
The doctors told us that Jack was going to have a lot of problems in life, they told me what my boy would never be able to do, and I met a woman from Wisconsin who also had SMA.
We began to correspond, and she gave us hope, saying that her parents supported her when she was a child. True, they still expected their daughter to die soon.
“Fortunately, they were wrong,” she said, and added, “Don’t give up. Live your child every day. Don’t wait for your child to die. You know, my father waited for me to die. Now he has been dead for 25 years, but I live, and I have a partner, my own apartment, work, and I am a happy person. I am an accomplished happy woman”
Then my son and I went to visit her, and she showed us her house. Now she is over fifty years old, and Jack and I are very grateful to her.
My own family also helped me a lot. My father, my adopted daughter Kara, my brother and my mother. Luckily my parents are alive. My father is now 91 and doing well.
Recently I called him and told him that I would perform for Russian families who have children with spinal muscular atrophy. In response, I heard that my dad was proud of me, because my great-grandfather and great-grandmother came to the USA from Russia a hundred years ago. My father told me that it is very important to remember your roots and your past.
So a kind loving strong family helps a lot to survive the news of a difficult diagnosis of a child and find the strength and opportunity to live on. And this was the first important lesson for me that I learned in 25 years of living with Jack’s SMA diagnosis.
Why is it important to communicate with other families who have children with SMA?
In addition to family support, the support of a wider circle of people is very important. Work, friends and community of families with SMA children. In the US, SMA families don’t often ask for help.
The second important lesson that I have learned in 25 years of living in a new situation is the ability to accept help from the community and from those people who care about you, because all these people are sincerely ready to help you.
In the photo you see me and my daughter, who volunteers at one of the SMA conferences. On the right you see Angela – she has SMA, but she works as a school teacher, and there is a group of children with the same diagnosis nearby.
Such meetings allow one to share experiences and communicate. This is my favorite thing from professional experience. Every year I organize several groups for such meetings. During the pandemic, these groups are also held remotely. Therefore, the community of people with SMA is very important. This is a place where people are ready to help and accept each other’s support.
And that was another important lesson I learned.
Why is it important for families with SMA to communicate with doctors?
My son Jack had to stay in the hospital a lot and we talked a lot with the doctors. Doctors are ready to help, they know a lot, but they don’t know everything. Each doctor has his own style of communication, his own approach to the patient and his own individual characteristics.
Sometimes it seems to us that one doctor is more suitable for us, and the other is less suitable. In these conditions, it is important to remember that doctors are not us and we cannot objectively assess our situation.
The main problem of the SMA family in communicating with doctors is the state of uncertainty. Each parent asks himself the question: “How long will my son live, what will he be like?”. But no one can give a real answer to it. The future is hidden from us.
I always have a bag with things and a spare brush in the trunk of my car, because at any moment my child and I can end up in the hospital, in intensive care. You have to be ready for this. I have a T-shirt that says “SMA families never give up.” We were lucky. Jack grew up, and we thank the staff of children’s hospitals for their help and support, but we have had to live in conditions of uncertainty for a very long time.
Not only doctors and hospitals. How to save yourself?
In addition to addressing medical issues, it is important to maintain good emotional health for both children with SMA and other family members.
Parents and relatives of patients with SMA should monitor their health and psychological state so that additional problems do not appear. Children with SMA can strongly support parents, relatives, and other families with SMA by sharing their experiences. When speaking, it is important to remember that the voice of a person with SMA may be quiet, so it is important that they speak into a microphone.
Another way to get support is to talk to friends. People with SMA talk about children and friends who help the child. Starting with the simplest things, a child with SMA dropped a toy and your friend picked it up and returned it so that the child could continue playing. Friends do their best to include children and adults with our diagnosis in a normal communication environment. Friends and girlfriends of my son, my friends make our life so much better.
Be prepared for change
One of the most important skills for all SMA families is readiness for change.
It is difficult for any person to live in an era of constant change. It is difficult for us when a child goes to school, it is difficult when he is in the hospital, it is difficult when he is transferred from one wheelchair to another.
Each birthday of a person with SMA is a certain stage of life and a certain search associated with a constant change in the situation.
When Jack moved from middle school to high school, we had to build an elevator and develop a personalized learning program. We were supported by teachers, but every step related to the education of our son is the need to answer new questions that life has posed and solve new problems. It was a very difficult time, but we got through it.
Why the life of an SMA family is a constant window of opportunity
In 1995 there was no effective treatment for SMA, now there is. What seemed like science fiction 25 years ago is now a reality. This means that everything is possible for SMA families now.
Look at this photo. Jack is 22 years old and this is his first job. He became a teacher at the same school and at the same age as me. He graduated from college and teaches children. Jack cannot use a computer mouse, but uses special devices that allow him to control the computer with his eyes. During the pandemic, he can work remotely. As a result, my son is alive, working and in a community of people who accept and care for him. This means that under certain conditions, the possibilities of a person with such a diagnosis become almost limitless.
Thanks to Jack, our family got into the “Group with children of the SMA family”. There we were told that a child with SMA is a gift. It was very difficult to accept it, but then we realized that it was true. Our children are constantly working, developing, learning despite all physical limitations. A child with a nasal probe and in a wheelchair can enthusiastically build a tower of blocks, although he does not immediately succeed.
Children with SMA are able to attract people who are capable of compassion, as a result, our families communicate and make friends with the best people in the world. There are a lot of them in our SMA community.
Another unique gift of a child with SMA is the ability to be a pioneer. He often does things that no one else has done before him. My son Jack, at a summer camp in Pennsylvania, was the first to use a portable ventilator and a video conferencing system to communicate. Every parent of children with this diagnosis can recall similar stories.
Children with SMA are able to awaken the best qualities in a person, allow them to look at the situation from a different angle and become an object for imitation. I am grateful to my son for the fact that for all 25 years he has been helping our family to become better.
How to prepare a child with SMA for school?
First of all, you need to take into account the situation of a pandemic, in which there may be special conditions.
To resolve the issue of teaching a child at school, you must first consult with a doctor who can tell you what conditions your son or daughter needs at school. After that, you should talk to the teachers. They may not know about SMA, so it’s best to tell them about your child in advance. It is also worth talking with future classmates and their parents.
When Jack began to study, some of his classmates had never seen a person in a wheelchair before, did not understand how to communicate with him. My son went to school with a nurse and that also raised questions. Therefore, we gathered the class and teachers and answered all the questions about SMA and our son.
It is very important to explain to teachers and classmates that protection from infectious diseases is important for a child with SMA, especially during a pandemic.
How to talk to a child about his illness?
It all depends on the age of the child. For example, small children could come up to my son, point a finger at him and ask: “What happened to him?”.
Parents are usually embarrassed, and I answer that a question from their child can help Jack and become more confident and stronger. After that, I ask the kid to show his muscles, then I say that my son’s muscles are weak and he cannot walk with his feet, so he moves with the help of a chair. It is clear that an older child can be given more information. But this is not an easy topic, even for adults, so I would focus on comparing muscle strength in a person with and without SMA.
If a child with SMA asks a question, hold him. Even a preschooler quickly realizes that he cannot do some of the things that his siblings, friends or peers do. Therefore, first you need to say that he is not alone, that he will be helped, and then tell about the medicines that have now appeared and that give hope.
A very subtle point is the conversation about the limits of hope. Some adults tell a child with SMA, “If you work hard, you will walk.” Others think it’s better to say “no, you won’t be able to walk, but you’ll have a cool wheelchair that you can move around with quickly.
” Which of them is right?
From my point of view, the main principle is this. No one, not even the child’s doctor, knows the future, so you should only make promises that you can keep. A good answer might be something like this: “I don’t know, and no one knows what the future holds for us. But we will do everything on our part so that you can walk. And maybe in the future you will be able to walk. Scientists are already working in this direction. But none of us knows what the future holds for us.”
Another important issue for everyone is related to the ability of a person with SMA to live independently.
Much depends on the country and the severity of the disease. In the US, there are people who are 50 years old, they have SMA and they live on their own and start a family. My son Jack has severe SMA and is unlikely to be able to live on his own.
Much depends on the quality and accessibility of health care and the availability of an accessible environment. For example, the state pays for Jack’s services as a nurse, but he does not live separately from us.
Societies in the US are not yet ready for people with severe forms of SMA to live separately. Previously, many patients died young, and now life expectancy, fortunately, is growing, but this raises new questions for society, and time is needed to resolve them. But at the same time, in the US, many people with SMA live on their own, although this is not easy.
What to do when a child with SMA enters adolescence?
As a psychologist, I would say that parents of teenagers with SMA should be patient and supportive of their child.
Adolescents change a lot, whether they have SMA or not. It is very important that the child has friends, because in adolescence, attitudes towards disability and physical limitations change.
In any case, adolescence is a difficult time. This is short, because a detailed answer can take another hour.
Does a teenager with SMA need an assistant dog?
Whether or not to get a dog depends on the situation of the particular family.
The dog is a good companion and can be specially trained to help people with physical disabilities. If the child wants a dog, and the family does not mind, then you can get one.
How can parents “let go” of an adult child with SMA?
This is a difficult question. Family members with SMA require a lot of attention, physical care, and care. Parents get used to constantly taking care of the child and it is difficult for them to survive this moment of separation. Parents of children with SMA must be sure that their grown son or daughter is safe, if they believe that independence can be dangerous for a person, they are not ready to let him go.
I can give a couple of tips from personal experience:
- Your control should not interfere with the independence of the person.
- If a person with SMA has a partner, we must trust him and understand that he is able to take care of our adult child with SMA.
Should a child with SMA limit their time on the computer or smartphone?
On the one hand, gadgets help people with SMA communicate.
My son has 2000 Facebook friends. He meets new friends. Social networks level the playing field for people with disabilities. It is easier for them to find interlocutors and friends, they can find remote work, help develop educational games for children with SMA.
My son Jack can’t play football in the yard, so I need to take this into account.
On the other hand, you don’t have to sit at your computer for hours on end. It is necessary to set some kind of time frame, realizing that for a child with SMA a computer or smartphone plays a greater role than for his peers without a diagnosis.
How to maintain a balance between rehabilitation and normal life?
It is important that even a child with severe SMA has a balance between medical procedures and normal life. A person’s day cannot consist only of a set of medical procedures. My son Jack has a tracheostomy and a ventilator, he has a lot of medical manipulations. We try to simplify all medical procedures, making them simple and effective.
If you have consumables, equipment and a relative, a health worker or a nurse, a person with SMA, even on a ventilator, can walk in the park and meet friends.
Of course, this is easier said than done. Every time I, like other parents of children with SMA, worry about my child on a walk, my anxiety does not decrease over the years, but at the same time I understand that Jack, despite his limitations, should have the brightest and most interesting life. You should not lock a person with SMA within four walls.
How to keep calm in the era of a pandemic and other cataclysms?
If we talk about a pandemic, then SMA families are more prepared for them. We are used to washing our hands, protecting ourselves from infections, taking care of children. Emotionally, our families are also more stable – for many years they have been living in a situation of an unpredictable future and have accumulated a lot of internal strength to overcome such situations. We are already doing our best.
The main thing in a pandemic is for doctors to save their lives and strength in order to help people, and my general advice would be this. Control only what you can. Don’t worry about what you can’t change.
This is the best approach for maintaining emotional and mental health in such situations.
Unfortunately, shortly after this conversation, Albert’s son Jack passed away. We express our condolences to Albert and his entire family.
Coping with stress: a psychologist told how to maintain brain health after 50 years
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Sometimes internal contradictions reach such a peak that they result in specific diseases.
Photo: freepik.com
After 50 years, it is very important to monitor your health. Taking care of your body is the key to maintaining physical independence and psychological awareness. About how to maintain brain health in adulthood, the editors of “MK in St. Petersburg” decided to ask the psychologist Inessa Spinka.
According to the specialist, she often encounters a situation where an aged client undergoes a complete examination of his body, and it turns out that he is constantly under stress. Preventive measures in such a situation are very important. Sometimes internal contradictions reach such a peak that they result in specific diseases.
“And if many people come to the idea that they need to maintain their physical health by undergoing annual examinations – this way there is a higher chance of detecting any disease in the early stages, then internal health is usually forgotten,” shared Back.
According to the expert, inner balance is as important as physical well-being. Psychotherapy corrects childhood traumas and removes unnecessary internal blocks. Feelings have serious power and influence, so you need to be able to redirect them in a creative, rather than destructive direction.
“There is no doubt about the thesis that regular dental check-ups, clean from plaque and calculus, early relief of carious processes – prolong the life of teeth? They stay healthy, strong and beautiful longer,” Spinka explained.
That is why, according to her, it is very important to visit a psychologist at least once a year. Emotional problems are not always obvious, and it is dangerous to engage in self-diagnosis, but visits to a specialist definitely support a long stay “in a sober mind and sound memory.”
The close relationship between internal and external health is indicated by the fact that sometimes the ways of maintaining them are exactly the same, the psychologist believes.
So, regular workouts can not only make muscles stronger, but at the same time they can effectively relieve the load on the brain and reduce stress levels. The choice of a specific direction will depend only on the person. The main thing is that the chosen sport brings pleasure.
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