This story was written by Randi Latzman and originally appeared on The Mighty.

Parenting is the greatest responsibility I have ever had. Although it is my job to help my daughter to learn and grow, she helps me to learn and grow as well.

The truth is, the image I had of parenting is not reality. The smiling faces on Facebook and Instagram capture mere moments of real life. It is easy to look at others and think that you are the only one who struggles. That is simply not the case.

Awareness and acceptance are of paramount importance when raising a child. The road to acceptance was not an easy road for me. When I enrolled my daughter, Brielle, in a Montessori Pre-K, the teachers and director voiced a lot of concerns about my daughter’s inability to do things that other kids were doing. I believed that the large class size and lack of warmth were the cause of everything. I scoffed when they suggested she had sensory processing disorder (SPD). I was her mother, and my daughter was fine.

Related: 5 things to do when your child is diagnosed with obsessive compulsive disorder (OCD) 

When we put her into a smaller school, she adjusted well. Still, transitions were very hard for her; she would raise her hand and give answers that had nothing to do with the questions, and she often rolled around on the floor at school when asked to pick an activity at the learning stations. Brielle knew her numbers and letters, could write paragraphs, and was reading, but she couldn’t focus in large groups and was always losing her belongings.

She was well-behaved at school, but at home, she constantly threw tantrums and had no ability to self-regulate her emotions. Despite being 4, I couldn’t take her to any stores because she touched everything, and she would not sit still and follow directions. She would squeeze the cats, fall up and down stairs, and sought out constant movement. Nothing I tried seemed to calm her down.

Despite my background as a speech-language pathologist, I had blinders on when it came to my own child. I wanted desperately to believe that I could somehow make it better on my own. I thought if I tried harder or did more, I could somehow make the problems go away. There came a point when I had to admit that an assessment was needed. Her health and happiness were more important than my denial.

My daughter was diagnosed by an occupational therapist with SPD, and two years later she was diagnosed with attention deficit hyperactivity disorder (ADHD), executive functioning issues, poor working memory, and auditory processing issues.

I went from being in denial that there was anything wrong, to demanding an Individualized Education Plan (IEP) be made for my child. I learned some valuable lessons along the way, and my hope is that I can make the road less bumpy for others:

1. As parents, we must look at hard truths. It is better to err on the side of caution and get your child assessed ASAP rather than hope it will all go away. If there is a problem, the earlier the intervention, the better. You have nothing to lose by getting your child tested.

2. Labels should be used to help your child, not to define your child. Brielle has learning issues, but the labels associated with those issues do not define her. Who she is as a person is what defines her. Brielle is loving, bright, sensitive and funny.

3. You must be your child’s greatest advocate, ally and supporter. Be involved in every aspect of the assessment and intervention process. For example, I observed every occupational therapy session, and I implemented each tool at home.

At the beginning of last year, I started homeschooling my daughter. She had a psycho-educational evaluation done over the summer that determined she had ADHD.

Subsequently, I found out that I could request a meeting with the Student Support Team (SST) at the public school because we pay taxes to the county. I fought for Brielle to get a full evaluation so if she were eligible, she could have an IEP. I brought a list of my present and future concerns and was adamant that she needed testing for executive functioning and auditory processing. When they determined she indeed had weaknesses in those areas, I researched IEP goals for those delays as well as accommodations that she needed. I made sure they were all implemented into the IEP.

Related: Meet the first FDA-approved video game to treat kids’ ADHD

I planned to have Brielle virtually attend an online public school, but I insisted that she get less screen time and only go online when it would be small groups. I’ve seen her in large groups online, and she gets very frustrated and is unable to focus. They were unwilling to cooperate, so I am continuing to homeschool my daughter until we find a school that will set her up for success.

Stand up for your child and make sure they get the proper support and intervention. Don’t be afraid to stand your ground. If you do not fight for your child, then who will? Your child needs the proper support to thrive.

4. Be open and honest with your child about their struggles and their needs. Having an open line of communication is necessary so there is no shame about it.

Brielle understands that she difficulty starting and focusing on tasks, and we have discussed strategies to help her. She knows that she can ask for a break if she needs to “let her wiggles out.” I have taught her various breathing exercises to help her “calm her mind.” She will sometimes ask for a squeeze if she needs that pressure on her body (for sensory input), and she has a weighted blanket that she uses at night.

When Brielle gets exasperated because she doesn’t understand something, I encourage her to try her best and I try explaining it to her in a different way. I also try to use as many visuals and manipulatives as possible to aid in her comprehension of tasks.

Brielle’s kindergarten teachers thought she couldn’t grasp addition and subtraction number bonds; by the end of homeschool last year she was doing multiplication, division and fractions. She may have different learning needs than others, but that doesn’t mean she isn’t capable of learning. I won’t allow her to believe otherwise.

5. Make sure to emphasize your child’s strengths. Brielle struggles with her working memory, but her long-term memory is amazing. She can recall in vivid detail incidences that took place years ago. Her hyperactivity has an upside as well. She is always full of life and never gets tired. Make sure your child knows that for every challenge, there is also a strength.

6. Parenting must vary based on the child, not the other way around. In order for our children to grow up and be confident and self-sufficient, we must give our children what they need, not what we want them to need. Brielle has difficulty playing by herself and she is very accident-prone. I need to keep an eye on her because she is incredibly impulsive.

She has difficulty playing independently, so I give her options of what she can do when she has “quiet time” (time where she plays by herself), and she chooses what she’d like to do. I encourage her to be her own friend and give her lots of positive reinforcement when she keeps herself occupied and plays independently.

I believe in her fully, but I also needed to adjust my idea of how she should be. Brielle is Brielle, and I wouldn’t have her any other way.

Awareness and acceptance are the key ingredients to parent a child with disabilities. They have helped me to be the mother and person I am today. I am far from perfect, and that’s OK. I am aware of who I am, and I am aware of how special my daughter is. The sky is the limit for her, and I am honored I get to be along for the ride.

This story was written by Randi Latzman and originally appeared on The Mighty.