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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
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Fall Family Fundraising
Last year, we initiated our annual Fall Families Fundraising asking you to reach out to your families and friends to donate to the ML4 Foundation to support the research we conduct. MLIV research is a multimillion-dollar enterprise, and we cannot do this work without your help. We run this campaign from October 15-November 30 each year. In our first year, participating families collectively raised $60,850 for the ML4 Foundation which went to support gene therapy research at Massachusetts General Hospital. This was terrific and inspiring to us and to the researchers!
It’s time again for Fall Family Fundraising and we are excited for more families to join and for more giving. Again, here is what we know from donation research:
• People want to give to organizations engaged in purposeful work;
• People want to give to support your situation;
• People will give when asked for specific reasons.
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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.
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