My mom has Multiple Myeloma and I am her primary caregiver. The AZ Myeloma Network provides programs, information and access to professional we would not have otherwise.
Thanks so much to this great team of people that make a difference in the lives of those who need it most!
I met Barbara and Jack after I was diagnosed with Multiple Myeloma 6 years ago. They have become like family to me and my family. We have attended the AzMN annual conference for the past 6 years. It is always excellent!!! Outstanding medical professionals present information in a manner that is easy to understand for those of us who are not in the medical field. What a wonderful opportunity it has been to personally meet and visit with doctors from various parts of the country who are top-notch in researching and treating those of us with this incurable form of cancer. I've also attended their excellent Roundtable a few times. Information presented at the Roundtable is of a more technical nature geared more toward medical professionals. It is a fantastic opportunity for medical professionals to earn continuing education units in a very positive environment. The Cancer Caregiver Seminars that AzMN began hosting about 3 years ago have been an amazing source of support for my family members who are my steadfast companions on this journey of cancer survivorship. They have found these seminars to be a great source of strength and a wonderful way to "recharge" themselves in their roles as cancer caregivers. One of the most special aspects of AzMN is the message of hope that is evident at every event. It is very encouraging for me and my family to know we are not alone in this journey with cancer. We now have a wonderful extended family which includes Barbara and Jack along with many wonderful volunteers and others who are also traveling the path of multiple myeloma themselves or with a loved one or friend. Congratulations, Jack, on being a 25-year multiple myeloma survivor! Congratulations, too, to you and Barbara as you celebrate 25 years of marriage! You are both a great source of inspiration to all of us. It is through the efforts of people like you and the collaboration AzMN is fostering among everyone involved in treating multiple myeloma that hopefully in the not-too-distant future, multiple myeloma will become a CURABLE form of cancer. Thank you for all you do to improve the quality of life for so many of us. For anyone considering making a donation, rest assured your contribution is going to a very worthwhile cause. I think you would be hard pressed to find any charity that makes better use of funds in providing a greatly-needed service to many people. When anyone is diagnosed with multiple myeloma, it obviously has a huge impact on family finances. The fact that all AzMN events are provided free of charge to cancer patients along with their family members and friends makes it possible for many people to benefit from these events when they might otherwise not be able to participate. Thank you, thank you, thank you, Barbara and Jack, for founding and energetically continuing this terrific organization!!!!!
My husband was diagnosed with multiple myeloma three years ago. We were told about the Arizona Myeloma Network by my father-in-law who saw an article about the yearly conference. We have attended the yearly conference three years in a row and each time we learn something new. I have also attended a seminar for care givers and found it to be very helpful. The experts they bring to their conferences and seminars are leaders in this type of cancer. The Arizona Myeloma Network has made a positive difference in our lives.
I can't say enough about the Arizona Myeloma Network! They are always there with information on my illness. One of the most honest organizations I have had the pleasure to be associated with...
God bless Them!
The Arizona Myeloma Network means a great deal to me and my family. They provide a great deal of support to caregivers and valuable resources for patients. The connections that we have made through the Arizona Myeloma Network have made a huge difference in my Mom's battle with Multiple Myeloma. I cannot imagine Arizona Myeloma Network not being a part of my family!!!
At every program I see the direct positive and immediate impact Barbara and her team has on the cancer patient, family and friends that care for them. Attendees come to learn something new that they can put into action now. I compile the program evaluations and it is statements like this that make me proud to support AzMN: "I now understand the difference between my oncologist and the Myeloma specialists here" and "as a cancer caregiver, I learned to care for myself first. It is like the flight safety announcement 'put your own mask on first, before helping others' I get it now!".
The 1st time I met Barbara was when I was an "event planner" for a small cancer education non-profit. I asked Barbara to exhibit at our health fair. That was 5 years ago! Arizona Myeloma Network is a small but mighty non-profit. I have witnessed how relevant programming literally saves lives. The people at AzMN not only connect patients to local Myeloma (and other cancer) resources they also educate patients, caregivers and their families on obtaining the best quality of life. Barbara has my support, always.
I recently attended the Cancer Caregivers seminar in Scottsdale. What an amazing & helpful seminar. the best of its kind.
The Arizona Myeloma Network is a quality organization, locally founded by a very determined, resourceful woman who is passionate about getting help and information to Myeloma patients in my state. I myself am a Myeloma patient and help facilitate a Myeloma support group that she joined (her husband has Myeloma) and can tell you first hand that she gets things done for patients in our state like no one else. Her organization networks with all the other organizations that help Myeloma patients and she made it her job to get to know all the Myeloma specialists in our area. Her organization was instrumental in bring some of the best doctors in the field to speak to our support group and in so doing opened up a whole new level of care and information to patients in Arizona. The next best thing the organization did was start a yearly Myeloma conference that is free of charge and brings in top quality Myeloma experts as speakers. It is one of the best places to get information for the newly diagnosed patients as well as seasoned ones. People come from all over the state and it fills a very important function of providing a truly quality program close to home. This is a wonderful service, especially for those who aren’t well enough to travel great distances for help and information. This organization has been life enhancing on many levels for Myeloma patients. Thank you AZMN!
Arizona Myeloma Network (AzMN) has been a godsend for my husband and I. My husband has multiple myeloma. When he was diagnosed nearly 5 years ago, it was staggering. We started looking online to get information. He found information about AzMN and contacted them. We met with Barbara and heard about Jack's journey and it was very encouraging since he proved there was a chance of continuing to have a good quality of life. We quickly became involved with AzMN when we realized this was an organization that had ties to the top doctors and researchers in the field. We both have learned a tremendous amount and it has been the best source of information on a current basis with the annual Living with Myeloma Conference. We have been very actively involved in the promotion and activities that are a part of AzMN and believe our lives have become more positive with the knowledge we are gaining.