A simple two-step plan
Reader Bill Williams responded almost immediately to yesterday’s blog post about yet another bill being introduced to limit, and eventually end, public access to the Social Security Death Index (SSDI).
“And what is the thing that is appropriate to do with our congressman?” he asks. “I may not have magic wand, but there is email and the magical device called a phone. I would like to help on my end.”
Good for you, Bill. We’re all going to need to get involved in this fight… and we need to do so wisely. Here’s a simple two-step plan.
1. Learn about the issues
The first step is to make sure we understand the issues involved in the SSDI fight. We have to have our facts straight and not sink access to one type of record in order to save access to another. It might sound easy to argue “it’s birth certificates, not Social Security numbers, that cause problems!” Right. And you know what would happen next, right? Right. We’d lose even more access to birth certificates.
So… don’t wing it! There are a lot of good resources out there to really understand the issues involved in records access, from organizations like the Records Preservation & Access Committee (a joint committee of the Federation of Genealogical Societies, the National Genealogical Society, and the International Association of Jewish Genealogical Societies) and the Massachusetts Genealogical Council. We can all start with these:
From the Records Preservation & Access Committee:
• Video: “Got Records? Threats to Genealogy Records Access,” featuring RPAC member Jan Meisels Allen, a good overview of RPAC and the issues confronting access to the SSDI and other records.
From the Massachusetts Genealogical Council:
And if you want to read through everything The Legal Genealogist has written on this subject since January 2012, this link will take you to those older posts. In particular, posts that may help include:
• SSDI hearing: “no silver bullet”, 21 March 2012
• SSDI: The art of the possible, 4 April 2012
• Fraud prevention firm: keep SSDI public, 25 April 2012
• SSDI still at risk, 9 May 2012
2. Teach our Congress member the facts
Once we’re sure we understand the ins and outs of the issue, the next step is to communicate what we know to our own individual member of Congress.
The simple truth is, members of Congress respond best to the people who are in a position to vote in their districts. Yes, we’ll all need to contact members of key committees when the anti-SSDI bills start coming up for hearings and action later this year, but right now we can all take time to educate our own representative.
The bottom line here is that nobody can get the ear of my Congressman here in the 7th District of New Jersey better than I can. And nobody can get the ear of your Congressman in your district in your state better than you can. Why? Because nobody else can look that member of Congress in the eye the way we can and say, simply and flatly, “Look, pal, I’m a genealogist and I vote. In your district.” We can all pick up the phone. We can all write letters. We can all let our own representatives know — we’re genealogists and we vote.
We can all find out who our representative is by simply entering a zip code into the Find Your Representative box at the House of Representatives website. And then, either one by one or joining with other genealogists and our local genealogical societies, we need to teach them the facts.
Members of Congress are home in the summers and on weekends. They are accessible at town meetings and local gatherings. We need to make appointments. Meet with them. At a minimum, send letters and emails. Educate them — teach them — about genealogy, genealogists and records access.
Bottom line: this fight is for all of us. And all of us can join in.