Interview with Georgie Maxfield

In the November issue of AOLM we interviewed Georgie Maxfield, Georgie left us on December 29 and will be sadly missed by all that knew her. Our feelings go to her family especially husband Don. What Georgie accomplished in support of amputees is a goal we all hope to meet one day.

 

 

 

 

For more information on the book check this page

 

For more information on the Northern Nevada Amputee Support Group - check out their web site

What inspired you to start the NNASG ?

A desperate need to find fellow amputees to learn from. I seemed to be all alone in a new universe, with no instruction manual, talking to all two legged individuals.

 

What was the most difficult aspect of starting a support group at that time ?

Finding other amputees, no one could or would give me names or contact numbers due to the privacy act. My first contact with another amp was arrange through a friend who knew someone who knew and amputee who agreed to talk with me. It just shouldn't be this difficult, but 14 years ago it was.

 

What is the most rewarding part of running a support group?

Meeting heroes almost everyday, helping someone else through those terrible first few months, learning from everyone I encountered, and having people to share with that actually understood what the problems were.

 

The NNASG has used the internet significantly - how has the advent of the net changed the way you do things (if at all)?

Fourteen years ago I was making hand made flyers to hang up in hospitals, then I discovered the world of computers and a million doors opened. NNASG is relatively new to the internet. We find it a fantastic tool, filled with precious information that it used to take years of time to accumulate and disperse. It has greatly enhanced our power to reach people and have them reach us. Web sites are available asset to support groups.

 

Can you tell us about your book?

The book was written because establishing and maintaining relationships, and the problems of sexuality & disability were certainly among the prime concerns of myself and all the amputees I walked with. Nothing written I found seemed to be of much help and the subject needed to be brought out into the open. This is not a dry, how to book, but a very human and often humorous approach to the fact that amputees still are interested in sex and have sex lives.

 

What kind of responses do you get to the book ?

So far very positive response, most people seem to find it entertaining and informative and rather like sitting down to have coffee with and old friend. The book is in it's second edition now and still selling well. I have had more than my share of contacts from devotees perhaps because of the book and the fact that the subject is mentioned in it. Some feel I dealt with the subject fairly others don't.

 

You have been heavily involved with the ACA over the years, it has seen some changes over the last few months - what do you see in the future for the ACA ?

I was an ACA Board member from the time of it's inception until 1997 when I accepted a position as the ACA's outreach coordinator. ACA is very close to my heart. Change is always hard to absorb, but ACA has a strong board of directors who will be improved by the selection of several new members shortly. I think ACA's future is filled with new possibilities and we will become stronger than ever with fresh outlooks on the problems that are part of our growing process. ACA is only 10 years old, I'm very proud of what we have accomplished in that time.

Remmeber we were only a handful of volunteers working with no staff or real office until late fall of 1997. In three years we've come a very long way, watch us grow in the next three, or better yet get involved and help.

 

What have been the biggest changes for amputees that you have seen in your time as an amputee ?

Technological progress, informed consumers, national communication, and the creation of new support groups almost weekly. We were the only group in the state of Nevada, many state had none. Now there are people to reach out to and share with even prior to amputation. The ACA, The internet, web sites, list serves no one has to stumble along alone any more help is easily available.



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