Had it not been for the amazing people at the LFNC I may have spiraled out of control. In a period filled with panic attacks, high anxiety and multiple brain issues they kept me grounded. The support group has been an amazing resource and is inclusive of everyone, No one is ever turned away for lack of resources which puts this in the top of the Lupus Organizations. There is always a friendly face or a welcoming voice and plenty of food! A great organization to get involved with whether you are a patent or just looking for more information.
My sister contacted LFNC over 20 years ago while living and working in SF and newly diagnosed. She's has had a journey and along the way LFNC has provided support and I'm so proud of of my sister. She now lives well with Lupus. Together we support and advocate for Lupus patients and are part of the amazing and dedicated Board and staff at LFNC. LFNC, thank you and keep up the great work for the Lupus community! I can't say enough about the dedication and commitment of LFNC!
Thank you for your words and your long-time advocacy for the lupus community!
Very grateful for all the work that LFNC does for Lupus patients and their families over the years! A terrific group of dedicated, caring, committed staff and volunteers that provide education and support through their conferences, fundraisers/walk/run, and meetings. LFNC - truly provides support for patients, caregivers and the whole Lupus community. Keep up the great job! Thank you.
I have volunteered at LFNC since I retired nearly 7 years ago. It has been and continues to be an amazing trip. I have watched the organization grow and change as the world around it grows and changes. However, its mission and goals remain consistent. It continues to promote lupus awareness, to educate and provide information to patients, their families and caregivers through conferences, education classes and electronic newsletters. It also continues to support external research through fund raising activities like the 5K Run/Walk or the Gala. Volunteering 7 years ago most often meant filing, folding, stuffing, and mailings. Now, it is much more likely I will be asked to work on the computer, entering and editing data and researching. There are many fun activities to be done. In addition, I have had the opportunity to meet many wonderful people, staff, board members, lupus patients and their families, as well as other volunteers. I look forward to many more years of helping out at this great nonprofit organization.
I have volunteered at LFNC for about two years in the office and with their 5K run/walks and they were all very wonder experiences. The staff is friendly and kind to the volunteers and dedicated to Lupus patients and families. I have met many nice people and made some good friends volunteering at the organization.
I Volunteered LFNC for the 5K run/walk it was a very nice experience. All of the volunteers of this organization are so kind. Met lots of wonderful people all coming together for great cause.
I contacted LFNC many years ago when my lupus journey first began. LFNC was extremely helpful then and continues to be a strong organization that has definitely exceeded my expectations. Dedicated, caring, kind group of individuals who care deeply about helping lupus patient and their families. Can't say enough how it has helped me and continues to do so.
Lupus foundation of Northern California became a great help to me when I was first diagnosed with SLE Lupus 9 years ago. Through my rheumatologists office visits I found a flyer of the Alameda subchapter support group. I make it a priority to make all the monthly meetings, because they are encouraging and the group members have become like family. Through the years of attending this support group and going to educational class/seminars the LFNC hosts locally, I am now leading their Youth Support Groiup the Hangout once a month. Its a privilege and honor to be able to volunteer and help the foundation to continue reaching out to our community and instilling hope in the lives of those of us affected with this illness day in and day out. Their dedication and love the staff outpours to us is amazing.
Lupus Foundation of Northern California has been a great resource of information for me. They send out very informative information weekly in their news letters that are helpful and give updates on events that are coming up, giving you the opportunity to volunteer as well. When I go visit the office they always make me feel like family. They have now given me the opportunity to lead one of their Youth Support Groups and its been a great experience. The conferences that they set up for lupus patients are also very good, I have attended two of them and every time I learn something new even after having lupus for 7 years.
Review from Guidestar
I have been a volunteer for the LFNC for approximately 27 years. I first became involved when I was newly diagnosed and was seeking information and support. The organization was there to meet my educational and emotional needs. The administration is very supportive and encourages members to become involved, therefore I used my professional experience as a registered nurse to help teach classes, lead support groups and volunteer in other capacities. This nonprofit really stands out in its mission to raise awareness of lupus, support those who suffer from lupus and their families, support legislation to increase funding for research, and directly supply funding for lupus research. For this reason, LFNC should be one of the top great nonprofits in the country.
The Lupus Foundation of Northern California has been a part of my life for the past 15 years. First, as a newly diagnosed client seeking information and support. The organization provided literature, videos and classes. I also found support in one of their subchapter support groups. I met others suffering the same issues and made friends for life. As I became familiar with the chronic nature of the disease, I decided to give back by becoming a volunteer. I utilized my background as a nurse to assist as a spokesperson, teacher and coleader of a support group. During this time I earned how many people have been served by this great nonprofit.
Review from Guidestar
I have volunteered at many non-profits, but LFNC stands out among them because of the dedication of the staff and how much they care about supporting lupus patients and their families and friends. In addition to providing important information, LFNC does an incredible job advocating on their behalf, to get them the support and resources that are needed at the state and national level.
I've always been impressed with the dedication of the staff and volunteers at LFNC. They do an incredible job of educating and supporting individuals with this very severe and confusing disease, as well as helping families and friends understand and support those who have it. In addition, their advocacy work is truly admirable.
I have volunteered for LFNC for almost twenty years in Sonoma County. I love the people I've met in our support groups. We have made a queen-size butterfly quilt as a fundraiser and made more than $1,000 by selling tickets. The members of the support group are very encouraging to each other.
I started off getting involved in LFNC as a Lupus patient and soon fell in love with the organization. All the effort and these amazing people put into helping people who felt so hopeless and alone when they were first faced with their diagnosis is obvious the second you meet them. There seems to be a very warm welcoming energy about the foundation and all the people there. I felt right at home only after a few visits. Then before I knew it I was volunteering because I wanted to be a part of what they did in making a difference in people's lives. I am so grateful to have found this organization. It was a huge resource of support that helped me get back on my feet and get my life back.
I first came across LFNC when I was diagnosed with Systemic Connective Tissue disorder. I was going through a very rough time in my life and this organization became a second family. One that understands and is supportive in every way possible. They helped encourage me to never give up hope on battling this horrible and confusing disease. With the support from them and from my family and friends I have been in remission for about 6 months now. I have been volunteering at LFNC all through out my battle with SCTD/Lupus and have even spoken at a meeting regarding my remission and my journey in how I got there. LFNC has done so much for me I can't say enough. I fully support them the way they have supported me. I recommend this organization to anyone who wants to be a part of an amazing cause.
Review from Guidestar