Cure JM Foundation
At the Southern California Walk Strong to Cure JM® Saturday, February 23rd at Griffith Park, YOU have a chance to help accelerate JM research.
Working with top genetic researchers at the Children's Hospital of Philadelphia (CHOP), Cure JM is seeking to better understand the genetic causes of JM. This research is important to help find better treatments and a cure.
Who: All Cure JM families and extended families. Families can participate even if the JM patient is not present.
When: Saturday, February 23rd, 2019. The Walk is from 10:00am - Noon and research samples will be collected before, during, and after the event.
Where: Griffith Park
Pettigrew area of Crystal Springs Picnic Area
4730 Crystal Springs Drive
Los Angeles, CA 90027
What: Sign up here for your family to take part by providing a genetic sample. A genetic researcher and phlebotomist from CHoP will be collecting blood or saliva samples.
Ideally, blood samples will be collected from each JM patient, parent(s), and sibling(s) in attendance, but saliva samples would also be helpful if the participant prefers to give saliva instead of blood. Grandparents in attendance will also be asked to either provide a blood or saliva sample.
You must sign up in advance to participate. Each family will sign up for a 30 minute time block, though in many cases the collection will not take the full time allotted.
Contact Shannon Malloy, [email protected], with any questions. If the time slots are full please email to be added to the waiting list.
*This is the same research study you may have participated in at the Cure JM National Conference in Austin last year. Please do not sign up if you participated in this CHOP Research Study at the National Conference in Austin, TX or the National Conference in Washington, D.C. Email [email protected] if you have any questions.
More information on the research:
Center for Applied Genomics (CAG) at Children's Hospital of Philadelphia (CHoP), Hakon Hakonarson, PhD, MD and Charlly Kao, PhD. Cure JM has invested in a genetic discovery program at the Center for Applied Genomics (CAG) at Children's Hospital of Philadelphia (CHoP). With their state-of-the-art facility and biobank, the Center for Applied Genomics aims to identify the genetics that play a part in Juvenile Dermatomyositis. The goal is as we find specific genes that regulate autoimmunity in JM and better understand what genetic mutations are at work in those genes, we can find drug interventions to modify genetic behavior.
Frequently Asked Questions:
- How do I prepare for the blood draw? Please review the consent form that will be provided to you in advance. Families should be well-hydrated. If you have numbing cream, you may apply it before your scheduled time slot (please apply to both inner arms).
- The healthy siblings in our family are too young or unable to give a blood sample. Can we still participate? Yes. Please sign up for a time slot. Although blood samples are preferred, siblings can give saliva samples.
- The siblings and grandparents are not attending. Can we still participate? Yes. Please sign up for a time slot for the parent(s) and JM child to give their sample. We will then provide you with instructions for additional samples (such as siblings, additional parents, or grandparents) to be collected locally.
- Additional family such as aunts, uncles, cousins, etc. are attending. Should they participate? If any of the cousins or aunts/uncles have an autoimmune condition, then it is best to get a blood sample. We would want to collect saliva from 1st degree cousins/aunts/uncles even if unaffected by autoimmune disease. More distant relatives who are unaffected by autoimmune disease do not need to give a sample. Come to the collection room to learn more.
- My child has a port-a-cath. Can they still participate? Yes. Please sign up and come to the collection site. Samples will be collected from the family members. For the patient with the port-a-cath a saliva sample will be collected. In addition, a patient could give a blood sample by vein or take instructions on how to collect a blood sample at the patient's next blood draw by their local healthcare provider. Please sign up and come to discuss all of these options with the CHOP research team to find the best fit for your family.
- I prefer that my JM child give the sample at their next scheduled blood draw. Can we still participate? Yes. Although please keep in mind it is much preferred to collect the samples at the conference when possible. However, please do sign up for a time-slot and we will collect the samples from the parent(s), sibling(s), and grandparent(s) and will collect saliva from the JM child if they cannot give a blood sample now. We are setting up the process to enable giving samples from home and we will provide you instructions.
- There are no open times/no times that work for me left on the sign up, how do we participate? Please email [email protected] for more information and to join the waiting list.
|| Cure JM Foundation