Pagan Parenting of Special Needs Kids Blogroll
(last updated June 25, 2009)
(last updated June 25, 2009)
- Mrs. B. at Confessions of a Pagan Soccer Mom: My 12 year old son has PDD-NOS, a mild form of autism and is hearing impairment.
- Sabrina at Goddessaday : My kids are both profoundly deaf and hear with cochlear implants.
- Sage Moonstone: My son has autism.
- E from Only a Movie: Special needs teacher and single parent of a thirteen year old son who has various mental health concerns.
- Apryl at Caustically Charming has an 11 year old son who is diagnosed as “high functioning autistic / aspergers”
- MarZel from The Play of Light and Shadow has a 20 year old son with Aspergers and a 14 year old who has mental retardation.
- Fallyn WynterMist at Intrinsically Beautiful: We’re a Pagan family with a 5-yr old son with mild autism. (This blog has not been updated since Oct. 2008)
- Shaylawolf at Has Broom Will Travel has an 8 yr old with mild aspergers and is looking to meet other pagans with special needs kids in the Nashville, Tn area. (Blog is inactive)
- Bridget has a daughter who is deaf. Learn about her story here.
- Fae from The Soccer Moms’ Guide to Wicca has a 9 year old daughter who has Celiac Disease. (Blog has not been updated since April 2009)
- Ant from AntB Pottery says: I have several special needs kids. Williams Syndrome, bipolar, NF type 1, and FAS/FAE are on my list.
- Luna from Consonants and Vowels has a 12 year old son with PDD-NOS.
If you’d like to be added to the blog roll, please leave a comment, or contact Mrs. B.!
Hi, So glad I’m not alone out here!!If any of you are in the Nashville Tn area let me know please.I have an 8 yr old with mild aspergers. Yeah this is quite a ride but he is so loving I feel very blessd. We found a wonderfull counceler who helps Ian bridge gaps and helps us make better bridges for him.Thanks for being here and posting this!!!!BB Shaylawolf
Hey Mrs. B,Gillian is about to turn 9, and has Celiac Disease. We’d love to be added to your list.Also, just FYI, Alumah has an H on the end.:)FaeWiccamoms.com
I have several special needs kids. Williams Syndrome, bipolar, NF type 1, and FAS/FAE are on my list. I would love to be added to yours!
Hi Ya Kris ~Ok.. I started a new Blog all about Special Needs stuff.. thought I’d share with ya:http://evil-mommy.blogspot.com/Hugs~ Sage
Hello! I have a 12 year old son with PDD-NOS. I really do feel alone sometimes in this mess. It is nice to know I am not…
Hi Ya Mrs. B ~You can actually change #1 Sons diagnosis to autism… we got a new evaluation done and they switched it from PDD-NOS to autism. At least we’re getting more info, and will hopefully get more help as well now too! Hugs~ Sage
My son has a gross motor delay and several sensory processing disorders. My youngest I believe also has sensory issues (almost everyone in my family/extended family seems to-genetic?). Good-in a way-to know I'm not alone!
Hello,I came by this blog as I was surfing. I, too, am a mom to a wonderful little boy who has moderate to high functioning Autism.Would love to be added to your list.BB )O(Rowan Silverstar
Love your blog! My son got a kick out of your homepage graphics. I have a 7yo daughter with autism, and my son has ADHD/Asperger's. Can you please add me to your directory next time you update it?BB Alisonhttp://whateveritneedstobe.blogspot.com/
Hi,I just found your blog through a link from another one, and I was excited to find another pagan parent! Then I saw the section for Pagan Parents with Special Needs and I'm ever so grateful. My son has Septo Optic Dysplasia, which means he has no pituitary gland (and therefore no hormones), is missing part of his brain, and is legally blind. I would love to be added to your blog roll if you'll have me.
I somehow missed this! Anyway, I'm mom to an almost 3-year-old former preemie – he came home with a trach and a ventilator, for BPD though we're hoping to have his trach out this spring. He has very very mild CP which may yet get diagnosed as something else, a severe speech delay due to the trach, several heart defects, pulmonary hypertension (resolved), formerly 100% tube fed (hoping to have that out this summer now that he's 100% oral), and severe medical anxiety (still debating w/ the doc whether it's at a point of calling it PTSD or not).