Alright, I've never dealt with a proton like this before, and I'm not sure I have the answer. My solution has the hydrogen cation in solution deprotonating the "tent-post" methyl group (this is the step I'm uncertain of, I've never seen that before), producing a carbocation which undergoes a 1,2-methyl shift to produce a resonance stabilized cation. From there I just need to protonate the cation, I'm not sure if there would be any issue of using the hydrogen gas I generated earlier.
Thanks again for your guys' help so far!