An Urgent Call for Integrative Neuroimmune Clinics
404 Comments
B
Blair Bock
9 months ago
For the Nolan Boys and all others that need thr additional support
D
David E Clabeaux
9 months ago
PLEASE PROVIDE YOUR SUPPORT AS SOON AS POSSI LE.
J
Jeffrey Kney
9 months ago
This is so scary & serious !
K
Kerri Eldredge
9 months ago
These kids and families are suffering for years, Please make the needed changes.
J
Jennifer Danielsen
9 months ago
We have struggled with my daughter and almost lost her several times to mental health issues related to PANS. We have spent close to $100k out of pocket for treatments that have brought her back. It is unimaginable what families have to go through in order to get our children better. Please make necessary changes to help those dealing with watching their child decline sometimes overnight.
R
Roberta Kledas
9 months ago
My niece's son is afflicted by this terrible disorder and has suffered enormously. He is an extremely intelligent and remarkable child, and is struggling to be his normal self once again.
H
Heather Ellis
9 months ago
Please help these patients and families. I too am willing to share my son’s story. His story is still a road to healing with a new request for IVIG pre authorization required in January. It’s a frightening time due to a required change in insurance carrier.
K
Kristin Donahue
9 months ago
Seeing what this has done to a child is heartbreaking, and made so much worse when insurance won’t cover treatment. PANS/ PANDA needs to be recognized as a disease that can be covered under insurance and the families struggling this unfortunate diagnosis need to be better supported.
P
Patrick Hayden
9 months ago
Please help the children
M
Mercedes Cecala
9 months ago
My granddaughter suffers PANS this horrible disease that is so terrible for children and the families
V
Vicki Eisen
9 months ago
My son has autism and PANS. The autism is not nearly as devastating and horrific as trying to treat this immune system disorder! Please help!
P
Patrick Cullinan
9 months ago
Very important cause, please help
R
Regina Nischan
9 months ago
Please give this serious consideration.
D
Donna Russell
9 months ago
Please help these children & their families!
J
Jamie Beishuizen
9 months ago
My 12 year old son has been diagnosed with Pandas since July 2024 with onset being August 2023. It has been the darkest season we have ever walked through as a family and is eating us up financially. Please help spread the word!
M
Michael Sweeney
9 months ago
M
Mary Jamerson
9 months ago
My 25-year-old daughter has pandas and she has sorely missed out on treatment because she was already handicapped. Doctors was just dismissed, but our entire family has altered their life and as I grow old constantly concerned about how my children will manage her there’s so many families that are hurting and this is so important.
L
Lynda Heilman
9 months ago
My 14 year old son was diagnosed PANDAS in 2023. He’s severely affected because he was misdiagnosed with psychiatric illness for years. He’s still extremely ill because we have to fight and appeal insurance for every treatment. And we live in a state where IVIG is mandated! His has no quality of life and his childhood has been stolen. We are in trauma.
R
Rachael Dioguardi
9 months ago
It is important to note that the public school system also fails to support these children and their families and these children not only suffer medically,, mentally, physically and emotionally but socially and academically. We need support AND remediation for the children that have lost their childhoods due to the lack of medical and educational resources and support
For the Nolan Boys and all others that need thr additional support
PLEASE PROVIDE YOUR SUPPORT AS SOON AS POSSI LE.
This is so scary & serious !
These kids and families are suffering for years, Please make the needed changes.
We have struggled with my daughter and almost lost her several times to mental health issues related to PANS. We have spent close to $100k out of pocket for treatments that have brought her back. It is unimaginable what families have to go through in order to get our children better. Please make necessary changes to help those dealing with watching their child decline sometimes overnight.
My niece's son is afflicted by this terrible disorder and has suffered enormously. He is an extremely intelligent and remarkable child, and is struggling to be his normal self once again.
Please help these patients and families. I too am willing to share my son’s story. His story is still a road to healing with a new request for IVIG pre authorization required in January. It’s a frightening time due to a required change in insurance carrier.
Seeing what this has done to a child is heartbreaking, and made so much worse when insurance won’t cover treatment. PANS/ PANDA needs to be recognized as a disease that can be covered under insurance and the families struggling this unfortunate diagnosis need to be better supported.
Please help the children
My granddaughter suffers PANS this horrible disease that is so terrible for children and the families
My son has autism and PANS. The autism is not nearly as devastating and horrific as trying to treat this immune system disorder! Please help!
Very important cause, please help
Please give this serious consideration.
Please help these children & their families!
My 12 year old son has been diagnosed with Pandas since July 2024 with onset being August 2023. It has been the darkest season we have ever walked through as a family and is eating us up financially. Please help spread the word!
My 25-year-old daughter has pandas and she has sorely missed out on treatment because she was already handicapped. Doctors was just dismissed, but our entire family has altered their life and as I grow old constantly concerned about how my children will manage her there’s so many families that are hurting and this is so important.
My 14 year old son was diagnosed PANDAS in 2023. He’s severely affected because he was misdiagnosed with psychiatric illness for years. He’s still extremely ill because we have to fight and appeal insurance for every treatment. And we live in a state where IVIG is mandated! His has no quality of life and his childhood has been stolen. We are in trauma.
It is important to note that the public school system also fails to support these children and their families and these children not only suffer medically,, mentally, physically and emotionally but socially and academically. We need support AND remediation for the children that have lost their childhoods due to the lack of medical and educational resources and support
Find the cure!