Caregiver Support Resources


Download the Fact Sheet HereThe following resources are provided for those caring for someone with MPS. Many of the websites listed have online support groups you can join to get immediate advice, support, or understanding. Some of the sites have great advice for taking care of the caregiver. All of the resources listed can help you if you are feeling alone on your journey.

Garden of Eagan

Leah Spring’s blog documents her life with 11 children – biological and adopted – six of whom live with Down Syndrome. Leah’s photo-laden blog, which she has faithfully written since 2005, is a quite remarkable account of her family as it has developed and grown over the years. A fascinating aspect of Leah’s blog is the insight into international adoption, and the significant obstacles she has had to overcome to bring some of her children home.

gardenofeagan.blogspot.com

The Caregiver Network

The Caregiver Network of Canada offers free educational events to help caregivers, and their blog features a melting pot of authors, sharing their personal experiences and tips for others within the community.

thecaregivernetwork.ca

Rx for Caregivers

Caregiving is, by nature, an emotional and often difficult topic to write about. Sometimes, a dose of humor and whimsy can help provide a level of comic relief, which is where Rx for Caregivers steps in. Whilst still very much in its infancy, the daily posts have thus far suggested that the blog, scribed by auntdeev, whose mother lives with Alzheimer’s, is one to bookmark in 2018.

rx4caregivers.wordpress.com

Family Caregiver Alliance

Founded in 1977, Family Caregiver Alliance was the first community-based nonprofit organization in the country to address the needs of families and friends providing long-term care at home. FCA now offers programs at national, state and local levels to support and sustain caregivers.

www.caregiver.org

National Family Caregivers Association

The National Family Caregivers Association (NFCA) supports, empowers, educates, and speaks up for the more than 50 million Americans who care for a chronically ill, aged, or disabled loved one. NFCA reaches across the boundaries of different diagnoses, different relationships and different life stages to address the common needs and concerns of all family caregivers.

www.nfcacares.org

The Courageous Parents Network

CPN is a destination created by parents, for parents, to support, guide and strengthen families as they care for a seriously ill child. Here you will find wisdom from fellow parents and pediatric care providers to help you be the best parent you can be to your child and children—and get through each moment.

courageousparentsnetwork.org/

Caregiver Warrior

Caregiver warrior Susanne White, set up her website having cared for both of her parents. Along with guest bloggers, Susanne shares her tips to help caregivers take care of themselves, in order to be better prepared to care for their loved ones.

caregiverwarrior.com

The Mighty

The mighty is a digital health community created to empower and connect people facing health challenges and disabilities. There are over 2 million registered users. This site has articles written by patients and caregivers and is organized by topic. Try visiting the rare disease category.

themighty.com

Facebook Group Pages

There are several group Facebook pages which are disease group specific. To find these online support groups, go to the Facebook search line and enter your child’s syndrome. The following are examples of Facebook groups, search their exact name to find them on Facebook or click the links below:

mps-1 hurler’s syndrome

hunter syndrome (mps II)

Mps Maoteaux Lamy

Sanfilippo syndrome/MPS III

Morquio Syndrome

If you’d like to download this fact sheet, click below.

Download the Fact Sheet Here

Our Mission

The National MPS Society exists to cure, support and advocate for MPS and ML.

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