Is there anyone here diagnosed with MCNS/ MPGN?

If anyone here is suffering from MCNS/MPGN we have a great support group on Facebook with 50 members now. All of which have the disease or their children do, And we are posting many helpful links and will eventually have our own web site to raise money and awareness. Follow the link below and ask to join this private group. We all know theres not a lot of support out there, were hoping to change that. Thanks Tara https://www.facebook.com/groups/mcgn.mpgn.type.1/286080701440022/?notif_... if this link does not work, you can locate me on Facebook: kids with MPGN kids with nephrotic syndrome Parents of children with nephrotic syndrome

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