#GivingTuesday, Myositis Support and Understanding

GIVE TO
HELP
MYOSITIS
PATIENTS

Make a donation to Myositis Support and Understanding, #Give4Myositis

WHY GIVE
TO MSU?

When a family member, friend, or even if you are diagnosed with a rare disease, wouldn’t you like to have access to information and support programs to help you understand this disease?

We can’t do this without YOU!

Welcome to Myositis Support and Understanding Association (MSU), a patient-centered, all-volunteer 501(c)(3) nonprofit organization supporting and advocating together with and for myositis patients and caregivers by providing education, clinical trial matching, various support programs, advocacy and awareness efforts, empowering volunteer opportunities, patient-centered research, and our financial assistance program.

Your donation will allow us to continue the important patient-centered work we are doing.

Like any other nonprofit, we thrive on donations made by those like YOU. As an all-volunteer nonprofit even more of your donation goes directly to help patients. Donations made in the United States are tax-deductible.

DONATE TODAY

WHAT IS
#GIVE4MYOSITIS?

#Give4Myositis, our 2020 fundraising campaign, and support the patient-centered work we do for the myositis community.

It starts with #GivingTuesday, Nov. 30, 201, a global day of giving. Our 2021 campaign, #GIVINGISGOOD, is our year-end fundraiser and we are asking our fellow patients and care partners, along with family members, friends, and supporters to find the joy in giving for myositis, a rare, incurable disease.

Your donation, gift of time, or fundraiser are all important ways you can give.

Giving feels good. Get involved and stand with MSU as we empower the myositis community.

About #GivingTuesday

Make a $5 donation to Myositis Support and Understanding, #Give4Myositis

We are a nonprofit built with a lot of $5 and $10 donations. A five-dollar donation truly does help, so proudly make a $5 donation if that is what you are able to do.

Give of your time as a volunteer, give financially to support the work we do at MSU for myositis patients and caregivers, donate plasma, or give your time to provide support to someone newly diagnosed with myositis.

HOW CAN I GIVE?

SEE VARIOUS WAYS TO GIVE BELOW

Donate •

Volunteer •

Donate Plasma •

Text GIVINGISGOOD to 44-321
to start a mobile donation.

Say, “Alexa, make a donation to Myositis Support and Understanding Association.”

WE HAVE AWARDED OVER 200K IN FINANCIAL ASSISTANCE SINCE LATE 2016

IMPROVING THE LIVES OF THOSE LIVING WITH MYOSITIS

AND THE
PANDEMIC
STRUCK.

We pivoted, rearranged, and we have thrived thanks to your generous and caring support. When the COVID-19 pandemic hit, we immediately allocated additional resources for our patient and caregiver support programs and our myositis patient financial assistance program. We also began immediate outreach and education efforts. Drs Lisa Christopher-Stine and Christopher Mecoli joined us live on April 1, 2020, not long after the pandemic struck, and took questions from patients about COVID-19.

And it doesn’t, and can’t, stop there. COVID-19 is likely going to have a severe impact on our lives for a long time. We can’t do this without you! It is only through your generous giving that we work to succeed together as a community.

Give Today!

COVID-19's impact is real.

We can’t do this without YOU!

MSU IS EMPOWERING THE MYOSITIS COMMUNITY

I want to say that this program is a gift sent from heaven. With rare diseases, life is a struggle with our health and financial stress, causing us more harm. If not for the help of the Myositis Support and Understanding Financial Assistance Program, I would have lost my home. This program has helped to lift a huge burden of financial distress, and I pray the program will be able to continue. From the bottom of my heart, Thank you! Patty T

Burden of financial distress lifted Patty T., financial assistance program
I want to say a huge THANK YOU for the help of the MSU Myositis Financial Assistance program. This disease is horrible and it is a daily struggle because of the pain. We know that stress triggers flares and I have been in a terrible flare due to the stress of my house possible going into foreclosure, and the medical bills piling up. Due to the illness, my hours were cut at work and I was struggling. I am doing my best to work while I still can. No bank would help, so every day I worried what am I going to do? Then through MSU, I came across the financial assistance program info, applied, and was approved! What a huge relief! I am already coming out of this nasty flare because now I will not lose my home! You have no idea how much this means to me to have a program like this to help us while struggling with the disease. Thank you from the bottom of my heart! — Financial Assistance Recipient

Not losing my home , Financial Assistance Recipient
I am so filled with joy and gratefulness! Not just for the help but how the help has been given with so much support, timeliness, and understanding! I can’t express how much this will help me to become stable in my home! God Bless you all!

Stable in my home , Financial Assistance Recipient
As a myositis researcher, I support MSU’s mission and their excellent work!!!

I support the MSU Mission , Rohit Aggarwal, MD, MS
I have only recently been diagnosed with Myositis. This organization has helped me more than I could have imagined. The information on the website is fantastic, the stories from people, etc, Before I found this group I was looking at my life as pretty much over, now I see hope and have learned many ways to help myself. GREAT ORGANIZATION

Now I see hope , Louise D. , Member and Donor
I just wanted to tell you how important your work has been for me. I have been struggling with DM. Your live chat with Dr Chung from Johns Hopkins has been a major factor in my muscle recovery and everyday well-being. Thank you!

Important Work , Donor and Member, Fiona
This organization has become an important part of my life since I was diagnosed with a disease I never heard of, Dermatomyositis. My Johns Hopkins Rheumatologist told me about it.

Important part of my life , Donor and Member, R. Thompson
This group has been a lifeline to me in the midst of so much uncertainty. I spent months muddling through with numerous doctors, stumbling toward a diagnosis. It’s only been in connecting with this group that I’ve felt a sense of hope. These are my mentors, the people who have walked the path before me and walk with me. I can receive and give encouragement and learn so much more than my doctors can tell me. With this group I have a place where I can complain, ask questions and be understood, and know that I am not alone.

Not alone anymore Facebook group member
It is so comforting to hear stories of others who were stuck… And overcame! The stories of others who are in the same boat now, of fighting to reduce [prednisone], are strength to me. This group and the people in it… Hero’s to me and my lifeline to deal with something no one gets … But us. Thank you all for making me feel “normal”!

Comfort Melony Righter

LIVING WITH
A RARE DISEASE
IS EXPENSIVE.

Myositis affects every aspect of a person’s life; physical, mental, emotional, financial, spiritual, and relationships. As myositis patient’s ourselves, we know firsthand the battles patients face with off-label use of expensive medications, the need for costly mobility and assistive devices, travel expenses to see one of few myositis specialists, and exorbitant medical bills.

Our financial assistance program helps provide much needed financial relief for patients, whose lives are already stressed due to illness, allowing them to more fully concentrate on their health. Donate today to help improve the lives of myositis patients.

We have awarded over 200K in patient financial assistance since 2016

MAKE A DIFFERENCE & #GIVE4MYOSITIS TO HELP MYOSITIS PATIENTS

Your donation will help fund our crucial myositis patient financial assistance program so patients can stress less about finances and focus more on their health.

Whether it’s providing support and assistance to parents of children with juvenile myositis or adult patients with myositis, we help patients and caregivers live their best possible lives despite the challenges and limitations they face.

Make a one-time donation or set up a recurring monthly donation to give all year long!

Give Today!

DONATE TODAY

#GIVINGISGOOD

Will you select MONTHLY to setup a recurring donation?

Make your secure online donation using a bank account, credit card, PayPal, or Apple Pay; or text GIVINGISGOOD to 44-321 to start your donation via text message.

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Donate here.

Donations in the U.S. are tax-deductible in accordance with IRS code 501(c)(3).

#Give4Myositis before the end of 2021 . . .

2021/12/31 23:59:59

GIVE TO HELP MYOSITIS PATIENTS

WHY GIVE TO MSU?

When a family member, friend, or even if you are diagnosed with a rare disease, wouldn’t you like to have access to information and support programs to help you understand this disease?

WHAT IS #GIVE4MYOSITIS?

#Give4Myositis, our 2020 fundraising campaign, and support the patient-centered work we do for the myositis community.

HOW CAN I GIVE?

SEE VARIOUS WAYS TO GIVE BELOW

WE HAVE AWARDED OVER 200K IN FINANCIAL ASSISTANCE SINCE LATE 2016

IMPROVING THE LIVES OF THOSE LIVING WITH MYOSITIS

AND THE PANDEMIC STRUCK.

COVID-19's impact is real.

MSU IS EMPOWERING THE MYOSITIS COMMUNITY

LIVING WITH A RARE DISEASE IS EXPENSIVE.

We have awarded over 200K in patient financial assistance since 2016

MAKE A DIFFERENCE & #GIVE4MYOSITIS TO HELP MYOSITIS PATIENTS

DONATE TODAY

#GIVINGISGOOD

Other Ways to Give

Mail your check payable to MSU to:

Rather give using another platform?

#Give4Myositis before the end of 2021 . . .

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GIVE TO
HELP
MYOSITIS
PATIENTS

WHY GIVE
TO MSU?

WHAT IS
#GIVE4MYOSITIS?

AND THE
PANDEMIC
STRUCK.

LIVING WITH
A RARE DISEASE
IS EXPENSIVE.