Are There Resources For Children With Cystic Fibrosis In New Jersey?
Are There Resources For Children With Cystic Fibrosis In New Jersey?
If you are the parent of a child with cystic fibrosis, you know that it can be difficult to find resources and information about this condition. That is why we have put together a list of resources for children with cystic fibrosis in New Jersey. This list includes both online and offline resources, so you will be able to find what you need no matter where you live. We hope that this list will be helpful to you!
Resources For Cystic Fibrosis
There are many resources for children with cystic fibrosis in New Jersey. Although some may not be local, there are still resources that they can benefit from reading.
Some of the resources for cystic fibrosis include the following.
Local And Non-Local Resources For Children With Cystic Fibrosis
New Jersey State Organization Of Cystic Fibrosis (NJSOCF): NJSOCF is an organization that provides resources to those suffering with cystic fibrosis. You can take a look on this page here to learn more about their mission and how they’ve been helping cystic fibrosis sufferers since 1977. In addition, NJSOCF provides pharmaceutical services for adults with cystic fibrosis. Their program provides state funded financial assistance for those who need help with medication, nutrition and appointment costs in New Jersey. You can fill out an application on this page here.
The Cystic Fibrosis Foundation is a national nonprofit organization that provides resources and information to people with cystic fibrosis and their families. The website includes a variety of resources, such as an online health library, fact sheets about CF, and a directory of local support groups.
CF Roundtable is a national nonprofit organization that provides support to people with cystic fibrosis and their families. The website includes a forum where parents can share information and advice, as well as a directory of local support groups.
KidsHealth is an online resource for parents that covers a wide range of topics related to children’s health. The website has articles about cystic fibrosis, as well as videos, quizzes, and other interactive tools.
The National Jewish Health website provides information about cystic fibrosis and other respiratory conditions. The website includes an online health library, news updates, and a directory of local support groups.
The Cystic Fibrosis Association of Ontario is a nonprofit organization that provides resources and information to people with cystic fibrosis and their families in Ontario, Canada. The website includes an online health library, fact sheets about CF, and a directory of local support groups.
The Cystic Fibrosis Trust is a national nonprofit organization that provides resources and information to people with cystic fibrosis and their families in the United Kingdom. The website includes an online health library, fact sheets about CF, and a directory of local support groups.
Cystic Fibrosis Caregiver Resources is a helpful website that provides information and support for caregivers of children with cystic fibrosis.
Families Living With Cystic Fibrosis is another website that provides information and support for families living with cystic fibrosis.
The Irish Cystic Fibrosis Association is a national nonprofit organization that provides resources and information to people with cystic fibrosis and their families in Ireland. The website includes an online health library, fact sheets about CF, and a directory of local support groups.
The Queensland Cystic Fibrosis Society is a nonprofit organization that provides resources and information to people with cystic fibrosis and their families in Queensland, Australia. The website includes an online health library, fact sheets about CF, and a directory of local support groups.
The Cystic Fibrosis Association of South Africa is a national nonprofit organization that provides resources and information to people with cystic fibrosis and their families in South Africa. The website includes an online health library, fact sheets about CF, and a directory of local support groups.
We hope that this list of online resources will be helpful to you as you navigate the challenges of having a child who is diagnosed and living with cystic fibrosis.
Hospitals In And Close To New Jersey That Provide Resources For Children With Cystic Fibrosis
Along with online resources, there are several hospitals in and close to New Jersey that specialize in treating children with cystic fibrosis. These hospitals offer comprehensive care for patients with the condition, including respiratory therapy, nutritional counseling, and social work services.
Some of these local hospitals include:
The Children’s Hospital of Philadelphia (CHOP)
The Children’s Hospital of Philadelphia (CHOP) is a national pediatric hospital that specializes in the care of children with cystic fibrosis and other respiratory conditions. This hospital is located in Philadelphia, Pennsylvania, but it accepts patients from New Jersey. The CHOP website includes information about CF, as well as videos, quizzes, and other interactive tools. It offers a range of services for children with cystic fibrosis, including respiratory therapy, pulmonary rehabilitation, and genetic counseling.
Hackensack University Medical Center
This medical center is located in Hackensack, New Jersey. It offers a variety of services for children with cystic fibrosis, including nutritional counseling and social work services.
Saint Barnabas Medical Center
This medical center is located in Livingston, New Jersey. It offers a number of services for children with cystic fibrosis, including respiratory therapy and pediatric gastroenterology care.
These hospitals/medical centers can become valuable sources of information for children diagnosed with cystic fibrosis. Since there are hospitals available and online resources, there seems to be no shortage of resources for children in New Jersey with cystic fibrosis.
Conclusion: Resources For Children With Cystic Fibrosis In New Jersey
Even though there are many resources available, Your child’s doctor is the best source of information about cystic fibrosis. Your doctor can tell you about your child’s specific condition and recommend treatment options. You can also find helpful information on the National Institutes of Health website.
If you want to make a donation to someone living with cystic fibrosis, that would be an excellent thing to do. We hope you now have a better understanding of your question are there resources for children with cystic fibrosis in New Jersey?
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