Situs Foundation

Partners & Collaborators

Partners

StickyJ Medical ID is a reputable provider of personalized medical identification jewelry, with a focus on quality, safety, and customization, serving individuals with critical medical conditions or specific legal directives.

Collaborations

Genome Medical is a medical practice specializing in genetics. Through its telehealth genetic counseling and genetic test ordering services, Genome Medical provides expert guidance, accelerates diagnoses and helps to improve care for individuals with rare conditions.

Genome Medical makes it easy to talk with a genetic expert from home. Their friendly, board-certified genetic counselors can help you understand whether there is a genetic cause to your or your child’s symptoms, order testing if needed, and explain your results. Appointments are done over the phone, usually within a week. You can schedule an appointment here.

RARE Revolution is a FREE, quarterly digital magazine for the Rare disease community. It seeks to give RARE patients and the charities that represent them a voice to be heard on their terms, while providing useful tips, guidance, features and current news.

The Starlight Children’s Foundation’s mission is to deliver happiness to seriously ill children and their families. The organization strives to ensure that children’s hospitals are easier places for kids to be by providing vital programs that ease fear, distract from pain, and spark joy.

What Families Are Saying

Emily R.

When our daughter was diagnosed with Situs Inversus, we felt overwhelmed and lost. The Situs Foundation gave us the information we needed and reminded us we weren’t alone.

James and Maria L.

Thanks to the resources and support we received, we were able to understand our son’s condition and speak confidently with his doctors. This foundation truly makes a difference.

Joby M.

Thank You SITUS Foundation Inc & Dana. Received mine day before yesterday.

Emma B.

Just received my little ones medical band, absolutely perfect, thank you so much

Emma J.

Thank you so much for this bracelet, it will give me piece of mind when she’s at nursery and school that she has something on her which identifies her condition xx

Katelin M.

Ours is the Minecraft one thank you so much.

SandrayJ.

Gracias!!mi bebe a recibido la suya y es chulísima

Ana W.

We’ve recently been introduced to this foundation who graciously donated a new medical ID bracelet to our little dude with this condition! It’s not a very well known condition (I mean how many people do you know with their organs and heart on the opposite side of their body?) but I wanted to share because the mama who started it has a child with it also. She’s done some amazing work trying to get more research done so that medical professionals know more about this unique medical phenomena. #situsinversus #dextrocardia #righthearted #unique

Ruth K.

A great foundation and support group for us with rare condition.

Sandra

Muchas gracias!que tengas buena semana tú también

Emily R.

When our daughter was diagnosed with Situs Inversus, we felt overwhelmed and lost. The Situs Foundation gave us the information we needed and reminded us we weren’t alone.

James and Maria L.

Thanks to the resources and support we received, we were able to understand our son’s condition and speak confidently with his doctors. This foundation truly makes a difference.

Joby M.

Thank You SITUS Foundation Inc & Dana. Received mine day before yesterday.

Emma B.

Just received my little ones medical band, absolutely perfect, thank you so much

Emma J.

Thank you so much for this bracelet, it will give me piece of mind when she’s at nursery and school that she has something on her which identifies her condition xx

Katelin M.

Ours is the Minecraft one thank you so much.

SandrayJ.

Gracias!!mi bebe a recibido la suya y es chulísima

Ana W.

We’ve recently been introduced to this foundation who graciously donated a new medical ID bracelet to our little dude with this condition! It’s not a very well known condition (I mean how many people do you know with their organs and heart on the opposite side of their body?) but I wanted to share because the mama who started it has a child with it also. She’s done some amazing work trying to get more research done so that medical professionals know more about this unique medical phenomena. #situsinversus #dextrocardia #righthearted #unique

Ruth K.

A great foundation and support group for us with rare condition.

Sandra

Muchas gracias!que tengas buena semana tú también

Charleigh B.

Thank You so much for your kind donation of the bracelet

Shelby W.

We would love to highlight the SITUS Foundation Inc They are newly founded and an incredible resource for families who face this rare disease and I’m so so happy they are shining a light on the unknown.

Scroll to Top