Search for:
Search Button
Contact Us
Donate
Prayer
Hunter’s Day of Hope & Prayer for Children
About Us
Mission
Hunter
Hunter Kelly Legacy Endowment
Kelly Family Story
Hunter’s Hope Team
Annual Reports & Financials
Newsletters
Hope ~ Life
Hunter’s Gifts of Love
Legacy Collection
Books to Inspire
Podcast
Podcast Family Stories
Podcast Mental Health
HH x MH Collection
Families
Leukodystrophy Family Registration
Living with Leukodystrophy
Leukodystrophy Care Network
Family Programs
Wall of Fame
Hunter’s Wish Gift
Morgan’s Legacy Gift
Equipment & Supply Exchange
Resource Library
Symposium
Family Stories
LCN Family Collection
LCN Family Collection – Family Challenge
LCN
Leukodystrophies
Leukodystrophy Types
ALD
Alexander Disease
Krabbe Disease
Metachromatic Leukodystrophy
Unspecified Leukodystrophy
Leukodystrophy Care Network
LCN Organization
LCN Coordinating Center
LCN Leadership
LCN Care Centers
LCN Clinical Care Coordinators
LCN Clinical Practice Guidelines
LCN Membership
Family Stories
LCN Videos
LCN Funding Support
Leukodystrophy Publications and Videos
Clinical Trials and New Treatments
Symposium
NBS
What is Newborn Screening?
NBS Federal Advisory Committee
Krabbe NBS
Krabbe NBS Council
Krabbe NBS Publications
ALD NBS
Supplemental NBS
Take Action
Partners
Katelynn’s Butterfly Kisses
Morgan’s Legacy Gift
Help
Hunter’s Hero
Ways to Give
LCN Funding Support
Special Fundraisers
Volunteer
Please Donate
Donate Monthly
Shop
Legacy Collection
Cards
No Matter What… Collection
HH x MH Collection
JK12 Collection
LCN Family Collection
Supplemental NBS
Books
Kelly Family Books
Bears – Collectible, Limited Edition
My Account
My Shopping Cart
Search for a Product
Menu
Donate
Prayer
Hunter’s Day of Hope & Prayer for Children
About Us
Mission
Hunter
Hunter Kelly Legacy Endowment
Kelly Family Story
Hunter’s Hope Team
Annual Reports & Financials
Newsletters
Hope ~ Life
Hunter’s Gifts of Love
Legacy Collection
Books to Inspire
Podcast
Podcast Family Stories
Podcast Mental Health
HH x MH Collection
Families
Leukodystrophy Family Registration
Living with Leukodystrophy
Leukodystrophy Care Network
Family Programs
Wall of Fame
Hunter’s Wish Gift
Morgan’s Legacy Gift
Equipment & Supply Exchange
Resource Library
Symposium
Family Stories
LCN Family Collection
LCN Family Collection – Family Challenge
LCN
Leukodystrophies
Leukodystrophy Types
ALD
Alexander Disease
Krabbe Disease
Metachromatic Leukodystrophy
Unspecified Leukodystrophy
Leukodystrophy Care Network
LCN Organization
LCN Coordinating Center
LCN Leadership
LCN Care Centers
LCN Clinical Care Coordinators
LCN Clinical Practice Guidelines
LCN Membership
Family Stories
LCN Videos
LCN Funding Support
Leukodystrophy Publications and Videos
Clinical Trials and New Treatments
Symposium
NBS
What is Newborn Screening?
NBS Federal Advisory Committee
Krabbe NBS
Krabbe NBS Council
Krabbe NBS Publications
ALD NBS
Supplemental NBS
Take Action
Partners
Katelynn’s Butterfly Kisses
Morgan’s Legacy Gift
Help
Hunter’s Hero
Ways to Give
LCN Funding Support
Special Fundraisers
Volunteer
Please Donate
Donate Monthly
Shop
Legacy Collection
Cards
No Matter What… Collection
HH x MH Collection
JK12 Collection
LCN Family Collection
Supplemental NBS
Books
Kelly Family Books
Bears – Collectible, Limited Edition
My Account
My Shopping Cart
Search for a Product
Resources
Home
Resources
Palamaro Family
Posted
January 11th, 2016
Jack Palamaro
Alexander Disease
Concord, CA
Born: 8/14/01
Post navigation
Previous Post:
Paquette Family
Next Post:
Osman Family Child 2
Please Donate
