When I don't know what to do, I defer to people with greater knowledge, greater wisdom, greater experience, and greater perspective.
And Marshall's health is no exception.
The difference between life and death for hundreds of babies, like Marshall, born with special hearts, comes down to a lot of things. But in the process of securing the help Marshall needed, I found it often came down to knowledge, money, resources, and access to information.
We're working as hard as we can to gather all of the above. And sometimes that just isn't enough.
You may check out the fundraising website some truly incredible people set up for our family by going
here
Any donations we receive will be designated solely for the purpose of ensuring Marshall gets the best care we can offer during our time with him. Though I hope that time is long, there are no guarantees. But one thing is certain: every dollar we raise (beyond covering Marshall's medical and travel expenses) will be used to establish a foundation dedicated to helping other families as they manage their child's congenital heart disease and congenital heart defects.
An anonymous donor once offered to match every dollar in donations up to $10,000. For his or her support, help, and prayers there are not words enough to ever repay our debt.
Think of the number of lives we could help if we could.
Please help if you can.
themiracleofmarshall 
It is really great to see Marsh running. I was not sure he could do this any more. Good news! Good work Marsh and Moml
—————————————–From: “themiracleofmarshall”
To: blmaltz@charter.net Cc: Sent: Monday September 28 2020 5:01:24PM Subject: [New post] Follow up with Super Smith
WordPress.com
mamawillloveyouforever posted: ” Hi everyone.. Marsh had a follow up with Dr. Super Smith in Syracuse today. The appt went ok. X-ray looks better than when we were here last. Dr. Smith suspects the blood flow will return to the lower left lobe (hard to visualize in echo because of al”