Mothers of Special Needs Children

If you're looking for support while raising special needs children, you're in the right place. Feel free to ask questions or give other moms advice. We all know that sometimes parenting can be a struggle so take comfort in knowing we are here to support you!

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Can anybody help

Hello everyone, I'm at my last resorts at the moment, my eldest son is 10 years old he has bilateral tailpipes, hydrocephalus, global development delay, learning difficulties...

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I was wondering if

I'm the grandmother of a child with executive function disorder ADHD separation anxiety sensory deception disorder child does anybody out there have one just like me

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I was wondering if

I'm the grandmother ivy executive function disorder ADHD separation anxiety sensory deception disorder child does anybody out there have one just like me

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Soto Syndrome Mom's **

My name is Jenny and I have an 8 year daughter named Mackenzie who has Sotos Syndrome. I would love to hear from other mom's who have children with Soto's. It has been a long...

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Traumatic Brain Injury

My 18yr old has a tbi that he acquired at age 15. He's VERY immature...I don't know how much discipline is the right amount! I don't want to jump on him for something beyond...

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16p12.2 microdeletion

Hi, may daughter was diagnosed with a chromosome defect yesterday 16p12.2 microdeletion but I can't find any information I was given a print off but it's very long doctor...

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Encropresis

My son is 12 years old and been dealing with encropresis for 1.5 years now .last year we found out he has Celiac disease on top of encropresis. . We have done everything, seen...

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Encropresis

My son is 12 years old and been dealing with encropresis for 1.5 years now .last year we found out he has Celiac disease on top of encropresis. . We have done everything, seen...

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Encropresis

My son is 12 years old and been dealing with encropresis for 1.5 years now .last year we found out he has Celiac disease on top of encropresis. . We have done everything, seen...

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Breast feeding problem

I have given birth my first child through cesarean section. For first 2-3 days i couldnt able to nurse my child and doctor advised him bottle milk. He has become so used to...

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Autism - 12 year girl

My daughter suffers from speech & language ,social skills , she makes friends easily but keeping them not good , and mad about boys , thinks she can have a few at the same...

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Polymicogyria

I would love to have someone to talk to. My son nicholas was giagnosed at seven weeks. He couldn't eat at 11 months. He was having seizures 200 times a day. He was the most...

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Polymicogyria

I would love to have someone to talk to. My son nicholas was giagnosed at seven weeks. He couldn't eat at 11 months. He was having seizures 200 times a day. He was the most...

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My son nicholas

My son was polymicrogyria. Diagnosed at seven weeks. My heart broke . Had no idea what was in store for me and him. He was on a peg , multiple seizures, shunt, blind,severe...

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My son nicholas

My son was polymicrogyria. Diagnosed at seven weeks. My heart broke . Had no idea what was in store for me and him. He was on a peg , multiple seizures, shunt, blind,severe...

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Polymicogyria

I would love to have someone to talk to. My son nicholas was giagnosed at seven weeks. He couldn't eat at 11 months. He was having seizures 200 times a day. He was the most...

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Sotos syndrone

Hello Moms! I am not a mom, but someone I love dearly has a daughter that was just diagnosed with Sotos syndrome. I want to be supportive but am afraid of saying the wrong...

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Sotos syndrone

Hello Moms! I am not a mom, but someone I love dearly has a daughter that was just diagnosed with Sotos syndrome. I want to be supportive but am afraid of saying the wrong...

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Sotos syndrone

Hello Moms! I am not a mom, but someone I love dearly has a daughter that was just diagnosed with Sotos syndrome. I want to be supportive but am afraid of saying the wrong...

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Cp

Hi I was always wondering wen my daughter will walk she's 3 in April and still not walking only wiv a walking frame she can't walk unaided

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My son nicholas

My son was polymicrogyria. Diagnosed at seven weeks. My heart broke . Had no idea what was in store for me and him. He was on a peg , multiple seizures, shunt, blind,severe...

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My son nicholas

My son was polymicrogyria. Diagnosed at seven weeks. My heart broke . Had no idea what was in store for me and him. He was on a peg , multiple seizures, shunt, blind,severe...

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Polymicogyria

I would love to have someone to talk to. My son nicholas was giagnosed at seven weeks. He couldn't eat at 11 months. He was having seizures 200 times a day. He was the most...

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Cp

Hi I was always wondering wen my daughter will walk she's 3 in April and still not walking only wiv a walking frame she can't walk unaided

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Ughh!

1. I said that Savannah has mild spina bifida, but I noticed she wasn't walking and she couldn't sit straight. Turns out she has normal spina bifida. I am so angry at the...

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Is this an issue....?

My friends 10 year old has walked on her tip toes since she was 2. She actually is almost 11. She has never had castings or AFOs. Is this a problem? She has not been diagnosed...

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Introduction and summary of DS

Hi all! I'm Christina and new to the group. the journey we are on with our son is quite lonely at times and I felt it was time to reach out to others for more support. Here's...

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my son's needs

My 6 yr old son has been presented with a number of issues. He doesn't olways answer questions that he knows the answer to he' spends most of his time away with the fares he He...

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Cerebral Palsy baby

Good day All My son was diagnosed by a Neurologist at 8 months with C.P.. I think from the shock and knowing that this is a problem, I did not manage to hear if it is severe or...

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Hi, mom of 7 girls here!

4 of them have special needs and 1 is on the way that has a possibility of special needs. Met them all! Cecilia is 10 and healthy Sienna is 9 and has asperger syndrome...

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Sotos Syndrome???

Are there any mothers out there who have a child with Sotos Syndrome? My daughter may have this condition, but it is very rare so I have not met any other children that are...