Active Campaigns

+ Wilson Disease

+ Parkinson's Disease

+ GERD

+ Radiology

+ Chronic Fatigue Syndrome

Wilson Disease

Parkinson's Disease

Parkinsons Doctor

Find personalized resources, communities and support for PD by taking a short screener.

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Parkinsons Doctor?

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Parkinsons Family

Nobody should have to battle PD alone, so we created this screener to help people find the right resources and communities for them.

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Parkinsons Family?

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Parkinsons Tremors

Our Community is here to help connect PD patients with resources and support.

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Parkinsons Tremors?

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Parkinson's Disease

Find personalized resources, communities and support for PD by taking a short screener.

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Parkinson's Disease?

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GERD

Radiology

Kidney Disease

Kidney Help

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Kidney Help?

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Kidney disease

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Kidney disease?

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Niemann Pick Tip C

Psoriasis

Gulf War Illness

Gulf War Veterans

Our Desert Storm warriors are fighting for their health decades after the war. There are more programs than ever to support veterans with Gulf War Illness, but awareness is an issue. Check out this screener to match with a program near you.

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Gulf War Veterans?

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GWI USAF

Calling all Desert Storm Air Force veterans: 1 in 3 veterans have been fighting Gulf War Illness alone. There's finally help for Air Force veterans.

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GWI USAF?

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GWI Navy

Calling all Desert Storm Navy veterans: 1 in 3 veterans have been fighting Gulf War Illness alone. There's finally help for Navy veterans.

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GWI Navy?

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GWI Army

Gulf War Illness disproportionately affects Army veterans, but there is finally help. Check out this screener to find local resources:

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GWI Army?

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GWI USMC

Gulf War Illness disproportionately affects Marines, but there is finally help. Check out this screener to find local resources:

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GWI USMC?

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Female Gulf War Veterans

Our screener matches Gulf War veterans with local opportunities, including treatments and clinical, social, and financial support provided by organizations such as the GWIRP.

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Female Gulf War Veterans?

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GWI Ambassadors

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GWI Ambassadors?

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GWI Health

Check out this screener that matches Gulf War veterans with support and treatment programs

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GWI Health?

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GWI Family

Stop seeing your loved ones suffer. Our screener finds support and treatment programs for our Gulf War veterans based on their needs. Share this screener to a veteran that you know to connect them with help.

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GWI Family?

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GWI Help

Tired of not getting the help you deserve? Our screener will connect you to treatment and support programs based on your needs.

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GWI Help?

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GWI Caregivers

Stop seeing your loved ones suffer. There are finally programs and research going on to try to help the Gulf War veterans that we love of their pain from Gulf War Illness. Take this screener to connect your warrior to support.

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GWI Caregivers?

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GWI Soldier

There are more programs than ever to help veterans with Gulf War Illness, but awareness is an issue. Check out this adaptive screener that helps match veterans with the treatment trial or support that they need.

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GWI Soldier?

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GWI Veteran

Tired of not getting the help you deserve? Our screener will connect you to treatment and support programs based on your needs.

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GWI Veteran?

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Gulf War Illness

1 in 3 veterans have Gulf War Illness, but awareness is an issue. Check out this adaptive screener that helps match veterans with the treatment or support that they need.

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Gulf War Illness?

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GWI - New York

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GWI - New York?

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GWI COVID2

The government just approved $20B to help veterans through this pandemic. We are curating programs available to Desert Storm veterans for COVID-19 as well as Gulf War Illness.

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GWI COVID2?

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GWI COVID1

The government just approved $20B to help veterans through this pandemic. We are curating programs available to Desert Storm veterans for COVID-19 as well as Gulf War Illness.

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GWI COVID1?

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KGI Veterans

Let's raise awareness as a VFW and help our veterans fighting Gulf War Illness

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KGI Veterans?

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Desert Storm Massachusetts

Gulf War Illness has been ignored far too long. We are creating a community to help Desert Storm veterans in South Massachusetts find the local resources to help with claims, medical, and social support for GWI.

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Desert Storm Massachusetts?

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YATYAS YUT

Up to 1 in 3 Gulf War veterans have GWI, a debilitating disease that has been invisible too long. Click to help raise awareness and connect our veterans with support.

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YATYAS YUT?

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GWI COVID3

The government just approved $20B to help veterans through this pandemic. We are curating programs available to Desert Storm veterans for COVID-19 as well as Gulf War Illness.

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GWI COVID3?

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Gulf War Illness

We are creating a community to help Desert Storm veterans find resources to help with claims, medical, and social support for GWI.

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Gulf War Illness?

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Lipodystrophy

Team Ashley

I am helping raise awareness for people with unique fat distribution, who might have FPL like me. There are very clear features to look for - please click my link to help connect them with help.

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Team Ashley?

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FPL Patient

You may be in danger of heart and liver failure, but there’s help. Take this screener to find out if you have FPL and connect with support.

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FPL Patient?

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Team Andra

I am a mother, a patient and the co-founder and President of Lipodystrophy United. My story is only one of hundreds living with Lipodystrophy (LD), each varying by subtype or severity.

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Team Andra?

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Team P.L.

When I was a little girl I was fairly healthy, but I was very skinny and had a big appetite. When I reached puberty I developed a muscular look, my veins started popping out, and I got a double chin.

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Team P.L.?

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Team Rhonda

My FPLD was diagnosed when I was 27 years old after a routine yearly physical from my primary care physician. I had elevated levels of proteins in my urine and because of that he sent me to see an endocrinologist.

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Team Rhonda?

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Team WeHealth

WeHealth uses social media to locate patients and connect them with advocacy groups and clinical support.

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Team WeHealth?

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Team Ian

I was misdiagnosed for many years, from age 11, when fat wasting developed. My hopes for being an advocate are to raise awareness and help others with a similar situation to myself, as living with a rare disease is not easy.

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Team Ian?

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Team Afnan

A long time ago when I was born, I wasn’t like normal babies… I hope that by sharing my personal diagnosis journey I can raise awareness and help inspire and connect other Lipodystrophy patients to support and available treatments.

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Team Afnan?

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FPL

FPL all too often goes undiagnosed. We can help by spreading this message and connecting Lipodystrophy patients with help. Please click my link to help out.

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FPL?

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FPL Pro

FPL all too often goes undiagnosed. We can help by spreading this message and connecting Lipodystrophy patients with help. Please click my link to help out.

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FPL Pro?

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Team Linda

I developed a very muscular, somewhat masculine physique, with small hips and a disproportionately chubby face. I was diagnosed with FPL years later and am raising awareness to help others like me.

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Team Linda?

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Cindy

I wasn't diagnosed until I was 38, though symptoms started at 15. This is too long to wait for a diagnosis! I am elated to be working with Lipodystrophy United and WeHealth to spread awareness and help patients get the answers that they deserve.

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Cindy?

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Team Kayce

I was diagnosed at the age of 27, after nearly 10 years of untreatable diabetes and a number of other things. I was treated with the wrong medications and fought for doctors to look for the answers. My husband was completing his nursing degree and came across a description of the different forms of Lipodystrophy in one of his books.

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Team Kayce?

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Team Marilyn

I always knew that there was something wrong. Complications during simple surgeries, cholesterol sky rocketing along with BP in my 40's should have been enough for my doctors to look for an answer and help.

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Team Marilyn?

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Team Cassandra

I found out in 2017 that I have FPL. I want to help get the word out and be an advocate to help people that may have this disorder find the help they need.

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Team Cassandra?

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Deafness

Parents of Deaf Children

We started a movement to connect parents of deaf children with resources. Take the screener to find the right resource for your family.

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Parents of Deaf Children?

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Deaf Children

We started a movement to connect parents of deaf children with resources. Take the screener to find the right resource for your family.

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Deaf Children?

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Chronic Fatigue Syndrome

CFS

90% of people with Chronic Fatigue Syndrome have not been diagnosed and are not receiving appropriate treatments or healthcare advice. Check out this screener for local help.

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CFS?

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CFS New York

90% of people with Chronic Fatigue Syndrome have not been diagnosed and are not receiving appropriate treatments or healthcare advice. Check out this screener for local help.

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CFS New York?

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ME/CFS

90% of people with Chronic Fatigue Syndrome have not been diagnosed and are not receiving appropriate treatments or healthcare advice. Check out this screener for local help.

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ME/CFS?

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CFS Dog

90% of people with Chronic Fatigue Syndrome have not been diagnosed and are not receiving appropriate treatments or healthcare advice. Check out this screener for local help.

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CFS Dog?

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