DISCLAIMER
The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.message sent
email sent successfully
rareLife solutions 606 Post Road East #397 Westport, CT 06880 |
||
You are receiving this because you have an account on www.oneMPSvoice.com | ||
To unsubscribe from these emails, click here |
Trusted Resources: News & Meetings
Latest announcements and gatherings
Believe in G Golf Tournament
Gianna, was diagnosed with Sanfilippo Syndrome in June 2021. Her family is heartbroken, but is “fighting the big fight.”
In a message her family posted to Facebook: [Sanfilippo Syndrome is] one of the ????? childhood diseases out there, and currently there is no cure. Gianna is one of 70,000 children diagnosed with this devastating disease. We need funding. We need more research. We have partnered with the Cure Sanfilippo Foundation to help raise money for treatment, for research, and so much more to help Gianna and all these children fighting the fight against this disease.
Date & Time:
Friday, May 20, 2022
8:00 AM – 5:00 PM
Venue:
Pevely Farm Golf Club
400 Lewis Rd
Eureka, Missouri, United States
This event has ended.
Related Content
-
educationA Guide to Understanding MPS III (Sanfilippo Syndrome)MPS III belongs to a group of inherited ...
-
people & placesGlenn O’NeillSince its creation, the Foundation has g...
-
educationGlobal Epidemiology of Mucopolysaccharidosis Type III (Sanfilippo Syndrome): An Updated Systematic Review and Meta-A...Mucopolysaccharidosis III, an autosomal ...
-
news & meetingsNew Type A ERT Candidate on Track for Clinical TrialJapanese company, JCR Pharmaceuticals, h...
-
educationChallenges of Enzyme Replacement Therapy for Sanfilippo SyndromeWhat Is Enzyme Replacement Therapy?Enzym...
-
educationMucopolysaccharidosis III: Molecular Basis and TreatmentMucopolysaccharidoses (MPSs) are known a...
-
Community CenterSanfilippo Children’s Foundation – LinkedInSanfilippo Children's Foundation is a no...
send a message
Reset password
password changed successfully!
please log in with your email address and new password.
your activation key expired
this confirmation key has expired. please try to log in again or resend confirmation email.
confirmation email sent
a confirmation email has been sent to your inbox. click the link in the email to activate your account.
can't find the email? be sure to check your spam folder.
password reset email sent
an email has been sent to you with a link to reset your password.
can't find the email? be sure to check your spam folder.
If you are a doctor or other qualified health care professional, you should not offer any medical advice or treatment on our Sites, nor should you allow the content of our Sites to substitute for your own medical judgment. Please thoroughly review the information provided on our Sites before deciding whether any of the products, services, or treatments therein are right for you or others.
your account is now activated!
Log in
This feature is only available to members.
you haven't confirmed your email address yet. resend confirmation email
Want to find the info you need faster?
The symptoms of Mucopolysaccharidosis and the treatments that are available vary depending on which type of Mucopolysaccharidosis a patient has been diagnosed with. Select which type you want to learn more about, and can highlight the resources that are most relevant to your MPS/ML type.
Not now