Fight for a cure for childhood ALD

Recently, my son Peyton has been diagnosed with an medical diease called ALD (adrenoleukodystrophy.) Currently, ALD is not curable, and in many cases is fatal. It effects 1 in every 17,900 boys, and because it is genetic, there is no way to prevent it.  Because it is a rare condition, Doctors are continuing to do as much research as possible. We have a long road ahead of us, and we are unsure what types of costs we are looking at. Because this will effect my sweet boy for the rest of his life, I will do everything I can to raise awarness and raise money for research. If you know Peyton, you know how smart and energetic he is. He will fight his best, I know it ❤️

Please, if you have any fundraising ideas I'd love to know and use them!