Shalom!~Hey~Greetings!~Good morning~
I decided to post an update to my personal search for help with this disease...
I had scheduled an appointment with the Mayo in Rochester for the end of March as my Neurologist sent a referral to them for me to go since no specialist in MO that my insurance will allow can help me.
Plus, Mayo will have the most up-to-date technologies and solutions for this neuropathy.
But, they told me to prepare to stay for at least 7-10 bus days. Well, we live on a fixed income of my husband's pension and SS and I do not work. So to go and stay there in Rochester for extended stay isn't going to happen for us until we can save for it.
So, I'm looking at moving it far out probably into the Fall!.
This question is for the moderator or mentor... Do you know of a way through Mayo to get donations to come for a visit? Is there any suggestion on how raising the funds for this? Thanks.
Darlia

Jump to this post