My name is Katrine, and I am the mother of 3 boys - the youngest, Theo, has C3G.
I work as a doctor in Child Psychiatry, and am currently doing MRI research fulltime. My son Theo has been ill for 3 years. When he first was diagnosed I really needed to connect with other families going through the same thing, and am so happy that our community has a new platform where we can meet and talk about C3G.
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KatrineM
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I too am so excited about the community platform! I think it is going to be great for patients and caregivers to connect and learn about C3G. I'm so glad you are here and sharing
HI Katrine, thank you for your post and welcome to the site! Your expertise will be extremely valuable for your young patients. We're looking forward to hearing more from you!
How is you son Theo doing? I too am grateful we have a way to connect with others who have C3g or family members who have it. We can all help each other while we wait for a cure.
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