Is this site providing medial advice ?

No

WE ARE NOT DOCS!

 

We share our first hand personal experience and journey in hopes it can help others.

Info posted here should not be considered medical advice; it's not intended to replace consultation with physicians or other health care providers. 

Every parent or adult with 22q needs to find their own path for achieving optimal wellness. While we do tons to help guide you, it’s up to each of you to make well-informed choices and live with the consequences. mommiesquietplace.com assumes no liability or responsibility for stuff that goes wrong.

Links to other web sites are provided as a service, but do not constitute endorsement of those sites by mommiesquietplace.com; we are not responsible for their content. We do our best to find the most resources but .

Take what you likeand leave the rest. Use what you learn to make your life better. Be responsible for your own choices.

Do you offer one on one phone calls/coaching?

No, we no longer do that but if you are in Michigan you can contact Parent to Parent and ask for a mentor. If you are local in Kalamazoo, Mi contact http://www.p2pswmi.org/

is this the same blog of mommies quiet place that started in 2014? where are all past posts?

This is the same blog and founder only we changed from a blog to a website to meet readers wishes and suggestions. You can subscribe at the top and never miss any future blog post. My blog post is saved and I am ading new post frequently. I will even take some older post and jazz the older post up such as the meet and greets which can be found on home page menu bar under meet and greets.

Love Amanda and Adam

 

 

Is this site an awareness site ?

No,

we do promote events such as 22q at the zoo.  there are other sites that are out there promoting only 22q awareness. If you would like us to help please use the contact me form

 

 

 

What is mommies quiet Place mission ?

MQP.jpg

Dedicated to sharing hope,compassion and balance while living with 22q11.2 deletion syndrome.

To bring awareness of 22q11.2 deletion syndrome though my stories and other peoples stories. Providing information from first hand personal experience.


Who in my family has 22q that makes me experienced with living with 22q?

My father has 22q, a half sister has 22q, two half brothers have 22q, one half sibling passed away age age 6. I myself have 22q.  daughter Bella has 22q