In this update, join us as we celebrate Living with Primary Sclerosing Cholangitis community’s anniversary. And check out the kind of information that we’re passing along to improve the lives of our members. We’d also like to share some updates about Patreon and our patient registry project.

Happy Anniversary, Living with Primary Sclerosing Cholangitis!

The Living with Primary Sclerosing Cholangitis community turned 11 this month!

5 tips on how to help patients better manage inclusion body myositis

Check what we’ve shared to members of our Myositis Support community to help them better cope with this condition.

Donations via Patreon

As of August 1, we have already raised 1444.63 USD from members’ contributions through Patreon. We are also working on a system for the collection of video testimonials to be included in the newsletter for patrons.

Patient Registry Project

Last year, we started experimenting on building a proof-of-concept patient registry web site for Ben’s Friends. We wanted to learn more about clinical trials and see if we have a place in it. This project has moved forward nicely. We have created a version with real functionality, and not just the prototype we initially intended to build. At present, we are beta-testing the current version.

In this update, we’re sharing some tips on how to help people living with narcolepsy and Sjogren’s Syndrome. Also, take a sneak peek at the new landing page we created for our communities. 

What is narcolepsy and how can you help someone suffering from it?

Know anyone affected by narcolepsy? Check out this blog to find out how it affects a person’s life and what you can do to help.

Ben’s Friends communities’ site visitors to be welcomed by a new landing page soon

Members and readers will soon find a new landing page when visiting each community site’s home page. Find out the details in this blog.

How to help a friend living with Sjogren’s Syndrome?

This blog includes some tips on how to help a friend living with Sjogren’s Syndrome.

Donate to Ben’s Friends everytime you shop at Amazon

We have just signed up to Amazon’s associate program. By clicking this link before shopping, you would be donating a percentage of the total amount to Ben’s Friends. Make sure you bookmark this page on your browser.

Executive Directors’ Report

Tom and Clasina’s 2nd Quarter report is now online. Check it out on this page.

PROGRESS, PLANS AND COMMENTARY FOR DISCUSSIONS

New look page design 

All of our communities received a visual redesign, which was professionally done.   Because we have a relatively large number of members with visual impairments and with brain damage, we did this redesign in consultation with an occupational therapist.  Reception has been excellent.

Improvements in SEO  

As time goes on, our communities have not grown as much as we would have liked.  We have redoubled our efforts at getting the Ben’s Friends name “out there”, in the hopes of improving our visibility on Google. To this end, we continue to add strategic, timely and topical content to both our Blog and to our Facebook pages, as well as dynamic content on our planned landing pages. 

Landing pages

Our current project is the installation of landing pages on each of our communities.  These pages introduce the community, and direct prospective members to relevant information.  The reception that we have received on the first community landing page (Livingwitheagle.org) has been very positive.  We hope to have many more communities with a similar (customized) landing page in the next couple of months.

Interns

We have fluctuating numbers of interns, varying from 3 to 15 over the course of a year.  We have seen an increasing number of interns from countries outside the US: The Philippines, Vietnam, Canada, and the UK. This past year has been particularly challenging, because many of our interns were attending colleges and universities entirely online.  The pressures and the prospect of having yet more work to do online became too much for many of them, and we experienced considerable attrition from this group.

Recruiting, involving, and uniting moderators

We have engaged one of our moderators, a retired IT professional, to unite our moderators (who have, up until now, worked in isolation) as a group.  This is proving to be a major challenge, because of the limited IT skills which many of our moderators have.

Training of Moderators and Interns

Our Interns are being trained using Google Classroom, and we are working hard to encourage Moderators to make use of their Classroom as well.  The latter is proving to be an uphill battle.

Patient Advocacy

We are moving ahead with our plans for Patient Advocacy training opportunities for our members.  As time goes on, we see more and more clearly that our 80,000 members, patients of 40+ rare diseases,  have many common needs in terms of how to become an effective patient who gets the best medical treatment that they can receive.  We visualize a central facility (site/community) where any Ben’s Friends member can learn and discuss issues such as self-advocacy, how to communicate with medical professionals, and how to manage their medical data.  We hope to include opportunities to address issues unique to some geographic populations such as health insurance and government services. This project is in its infancy, and we are starting to flesh out the conceptual framework that we have.  

Ben’s Friends’ Patient Registry

A companion project to our Patient Advocacy Initiative, our registry will help match patients to research, trials and expertise,  and help researchers and expertise to find patients.  The key difference in our registry is that Ben’s Friends members will maintain control of their data at all times, which is not universal in other medical and rare disease registries.

Community Expansion and Support Enhancement Support

We have applied to the Chan-Zuckerberg foundation for a grant to enable our implementation of the Patient Advocacy and Registry projects.

Future plans and directions

  • Establishment of Ben’s Friends Moderators as a cohesive community of their own
  • Continued recruitment and involvement of patient advocacy interns
  • Increased use of volunteers from within our communities
  • Improved SEO
  • Improved visibility of our communities in the Rare Disease world
  • Introduction of Patient Advocacy training and awareness for all our members

Conference, Boston October 2021

We will be attending the Orphan Drugs and Rare Diseases conference in Boston, where both of us will be featured as speakers.

We look forward to the exciting prospects that the next year brings.

Tom and Clasina

TJ Lambdin and CE Field

In this newsletter, we’re sharing some tips on preparing for a surgery and improving mental and emotional health. 

Also check out some of the things that patients with chronic illnesses like trigeminal neuralgia and systemic lupus erythematosus might be experiencing and how friends and family can help. 

We are also introducing our volunteers, DickD of AVMSurvivors.org and Mark of the Living with PSC community. And please join us in celebrating Living with Erythromelalgia community’s anniversary. 

1. How to prepare for a surgery

In this blog, learn some tips on how to prepare for a surgery.

2. Some tips on how to improve your mental and emotional health 

Having a rare or chronic illness can be a source of stress. Check out some tips on how to improve mental and emotional health in this blog.

3. An Unspoken Conversation between a TN patient and Her Son

Chronic illnesses can affect a patient’s relationship with a loved one, but it doesn’t have to be a negative effect. What could be a good conversation between a patient and a family? 

4. Some things to understand about systemic lupus erythematosus (SLE)

Know anyone living with SLE? Check this blog and find out some of the ways you can help.

5. Spotlight on our Moderator: DickD of AVMSurvivors.org

Get to know one of our awesome moderators, DickD of AVMSurvivors.org, and find out what Ben’s Friends means to him.

6. Spotlight on our volunteer: Mark of Living with PSC community 

Meet one of our amazing volunteers, Mark, who generously helps us out with so many things at Ben’s Friends.

7. Happy Anniversary Living with Erythromelalgia Community!!

Living with Erythromelalgia is turning 10 this year! 

In this update, we’re sharing some tips on preparing for a surgery and improving mental and emotional health. We are also introducing DickD, one of our AVMSurvivors.org moderators. Also, we included below a quick update on our Patreon project.

1. How to prepare for a surgery

In this blog, learn some tips on how to prepare for a surgery.

2. Spotlight on our Moderator: DickD of AVMSurvivors.org

Get to know one of our awesome moderators, DickD of AVMSurvivors.org, and find out what Ben’s Friends means to him.

3. Donations via Patreon

Just a quick update that as of May 1, we have already raised 1,093.12 USD from members’ contributions through Patreon. We are also working on a newsletter that we can send to patrons on a regular basis. The newsletter will contain information about developments in the Ben’s Friends communities as well as thank you messages from members. 

In this update, we’re sharing some information about Fabry that you can forward to friends to help raise awareness this month. 

Also check out some of the things that patients with chronic illnesses like trigeminal neuralgia and systemic lupus erythematosus might be experiencing and how friends and family can possibly help. 

1. April is Fabry Awareness Month

This month, help spread awareness about Fabry so that more people could be diagnosed earlier and receive appropriate treatment. 

2. An Unspoken Conversation between a TN patient and Her Son

Chronic illnesses can affect a patient’s relationship with a loved one, but it doesn’t have to be a negative effect. What could be a good conversation between a patient and a family? 

3. Some things to understand about systemic lupus erythematosus (SLE)

Know anyone living with SLE? Check this blog and find out some of the ways you can help.

4. Chan-Zuckerberg Rare as One project EDs Tom and Clasina are preparing a grant application to the Chan-Zuckerberg Rare as One project. They would appreciate hearing from you if you have any insights, “ins” or advice on this. 

In this update, we’re sharing information about ADHD and endometriosis, two of the 40+ conditions in Ben’s Friends communities. Also, find out what I shared in the Two Disabled Dudes podcast episode that was posted online recently.

1. He’s not a bad kid. He’s living with ADHD 

What is it like to live with ADHD and what can people around them do to help? 

2. March is Endometriosis Awareness Month

Learn what endometriosis is and share information to increase the chances of sufferers getting an early diagnosis and receiving appropriate treatment. 

3. Two Disabled Dudes Podcast features Ben Munoz

In this podcast episode, I shared inspiring lessons I learned from having an AVM stroke, coping with the loneliness and fear during recovery, and making the most out of life.

In this update, find out what Ben shared in the podcasts Once Upon a Gene and Nonprofit SnapCast and learn what makes Chiari Support a wonderful community all these years. 

We are also about to conclude our World Rare Disease Day fundraiser and we’re sharing with you some of the details here.

1. Once Upon a Gene podcast Features Ben’s Friends 

This blog highlights what Ben and Effie Parks talked about in the podcast which includes the story behind the founding of Ben’s Friends and what ripple effect the community has on the people that found help on the sites.

2. Nonprofit SnapCast Features Ben Munoz

This blog shares some of the things Ben and Mickey Desai covered in the Nonprofit SnapCast episode which revolves around how the organization is able to do more with less resources.

3. Happy 11th Anniversary, Chiari Support Community!

What makes Chiari Support a great community? Find out in this blog.

4. Ben’s Friends World Rare Disease Day Fundraiser

Just a quick update on our World Rare Disease Day fundraiser. We launched our GoFundMe fundraiser earlier this month and promoted it through an email series sent to Ben’s Friends past donors, friends and family.  

Twenty four individuals have already extended their support either directly through GoFundMe or other methods such as via Paypal or check. We have so far received $19,450 in donations. Thank you for your support.

In this update, you’ll meet our Lead Interns Danielle Havord-Wier and Arjuna Srikrishnaraj, learn about the different ways to help OPMD patients, and find out the benefits patients receive from online support groups.

1. Some of the Things You Can Do to Help Patients with OPMD

This article discusses some of the things other people should know and can do to help their friend or relative living with OPMD

2. Spotlight: Ben’s Friends Lead Interns

Meet Danielle and Arjuna and find out what being a Ben’s Friends Intern means to them.

3. Benefits of Having a Rare Disease and Chronic Illness Support Group

This blog post highlights some of the ways a patient benefits from an online rare disease and chronic illness support group.

4. Patreon Project

Last year, we launched a number of experiments to find the best fundraising design using the Patreon platform. We have created Patreon pages for our Living with PSA, AVM Survivors, and Living with Fibromyalgia communities. Everything we have learned from previous iterations was applied to the Ben’s Friends Patreon page. 

While all of these pages are active and generating donations, it is the Ben’s Friends Patreon page that we are actively promoting. 

At present, we receive a net monthly donation of USD 119.69 from all our Patreon pages.

In this update, find out what Scott shared on What’s Your And?, a podcast that focuses on what the guests love to do outside of their job. And our Living with PsA community is now 10 years old! 

Also, learn about vaccine protocols and COVID-19 in Tom’s informative article, and get updated on recent studies about depression and chronic illnesses.

1. What’s Your And? Podcast features Scott Orn

In the What’s Your And? podcast episode, Scott talked about his volunteer work at Ben’s Friends. He recalled how Ben’s Friends has empowered patients and shares how it feels to be able to change people’s lives. 

2. Happy 10th Anniversary, Living with PsA!! 

In this blog, our moderators shared some trivia as well as some of their unforgettable experiences in the community through the years.

3. Vaccine protocols and COVID

In this article, Tom gives a brief overview of the vaccine trial process, what they look like in the case of COVID, and what we can expect in the near future.

4. Effects of eculizumab use shows promise for patients with myasthenia gravis 

Recent studies show encouraging results of the use of eculizumab in treating myasthenia gravis.

5. Depression and Autoimmune and Chronic Illnesses

This blog presents findings from recent studies regarding the relationship between depression and autoimmune and chronic diseases.