73 Alternatives to gaucherdisease.org

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gaucherdiseasenews.com

jewishgeneticdiseases.org

cerdelga.com

osmifw.com

healthybonesaustralia.org.au

Osteoporosis is a chronic disease affecting over 1.2 million Australians and leading to over 173,000 broken bones each year.

jscreen.org

Home - JScreen

momentmag.com

Covers Jewish politics, religion and culture. Moment provides a unique lens on the issues that trouble, concern, and inspire American Jews. Subscribe here.

ewggd.com

sanofigenzyme.com

Global pharmaceutical and healthcare company Sanofi's specialty care & general medicines focus areas.

gaucher.org.uk

Information for patients, relatives, doctors and researchers from an independent charity. Over two hundred pages for use by patients and doctors.

cerezyme.com

Learn about Gaucher disease, its causes and symptoms, treatment of Type 1 Gaucher disease with Cerezyme therapy, and ways to cope with the disease.

geneticdiseasefoundation.org

The Genetic Disease Foundation (GDF) was established in 1997 to support research, education and the prevention of genetic diseases.

ntsad.org

An organization offering support and programs geared to families affected by Tay-Sachs Disease and over 40 other fatal degenerative genetic disorders.

gauchercare.com

Find information about gaucher disease for people living with it, their friends and families, and health care professionals.

jewishgenetics.org

neuropathology-web.org

Neuropathology

tay-sachs.org

childrensgaucher.org

gaucher-disease.eu

gaucherdisease.info

Learn about the rare genetic disorder, Gaucher disease (or Gaucher's). Symptoms include enlarged liver and spleen, bleeding and bruising, and joint pain.

ldnz.org.nz

Information, support and advocacy for families affected by Lysosomal Storage Diseases, a group of rare genetic diseases.

mgmjournal.com

doryeshorim.org

Jewish Genetic Screening - Dor Yeshorim

avrobio.com

jnetics.org

knowyourgenes.org

cats-foundation.org

canavanfoundation.org

Not-for-profit foundation providing information about Canavan disease, prenatal screening, support, and research.

aldurazyme.com

mpssociety.org.uk

lysosomaldiseasenetwork.org

curetay-sachs.org

modernlab.org

lysogene.com

liferaftgroup.org

Support group for patients with gastrointestinal stroma tumor. Located in Wayne, New Jersey.

theopavlidis.com

jobsatgenzyme.com

panfoundation.org

Patient Access Network Foundation is helping underinsured patients get the medication they need.

raredr.com

lateonsettay-sachs.org

genome.gov

Leads the Human Genome Project for the National Institutes of Health, conducts cutting edge research in its laboratories and supports genomic science worldwide.

rxassist.org

RxAssist - Patient Assistance Programs

jewishmag.com

Since 1997, this magazine has offered a monthly independent Jewish resource guide with articles on Israel, Zionism and religion.

neuroundiagnosed.com

pparx.org

worldsymposia.org

Lysosomal diseases conference, WORLDSymposium 2022, on the latest research to be held February 7 - 11, 2021 in San Diego, CA and online.

doryes.com

script-design.com

akimusa.org

artyourworld.com

thegeneticscenter.com

givf.com

Provider of infertility treatment and genetics services. Locations in Fairfax, Virginia and Gaithersburg, Maryland.

gaucherwest.com

pompediseasenews.com

gtmb.org

ancestralfindings.com

Free genealogy research of birth, census, death, land, marriage, military and state records indexes. A must see for those conducting family genealogical research.

sanoficareassist.com

Info for patients on CareASSIST by Sanofi Genzyme, including financial assistance, enrollment & forms & resources.

lefthandcitizen.net

biomarin.com

Researches and develops therapies for debilitating, fatal, chronic genetic disorders causing enzyme deficiency of carbohydrate metabolism, such as phenylketonuria. Headquarters in Novato, California. (Nasdaq: BMRN).

aboutgeneticcounselors.com

littlemisshannah.com

Hannah Ostrea's journey and fight against neuronopathic Gaucher's disease, an extremely rare and fatal life-limiting genetic metabolic disease. As a result of raising a medically fragile child with this rare disease diagnosis, I have become a mom on a mission for rare disease awareness, pediatric hospice and palliative care, and forever the fighter for a cure for Neuronopathic Gaucher's disease. Hoping to connect all families of children with Gaucher's type 2 and type 3 together.

lumizyme.com

victorcenter.org

sanofigenzyme.in

mpssociety.org

sanofigenzyme.com.au

pompe.com

For individuals and families who are living with Pompe disease, and for the health care professionals who treat them. From Genzyme Corporation.

canavan.org

palawards.com

andilab.com

projectshui.com

A Bar Mitzvah boy's web-based project to raise funds for a gene therapy cure for Tay-Sachs disease.

dartmedicallab.com

modernlab.net