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Worlds In Need

OurĀ Friends who Need Help

Find a Cure for FSGS for Matthew!

https://www.youtube.com/watch?v=5EWBXDOhkaw&feature=youtu.be

It's every mother's worst nightmare, to hear your child, has an incurable disease. That's what Dana Levine's family was told when her son, Matthew was diagnosed with FSGS. FSGS is a kidney disease that currently has no cure. When you have FSGS, the filtering units in the kidneys do not work, the proteins in the blood and body leave the body, go through the kidneys and cause the kidneys to scar and fail. Hear Dana's struggle (click above) and be part of the solution.  Nephcure.org has the best and the brightest searching to find a cure, so no child or audlt should have to die from this devestating disease. Learn more and then make a difference http://nephcure.org/. Save 1 Person. Save The World.
 

Are You a Mom's Miracle Match?

 
Imagine going in for a routine doctor's visit and then hearing from your physician you have a deadly disease.  It's everyone's worst nightmare. And that is what Adriana Vidals, a mom of three from Arkansas heard from her health care provider. Doctors diagnosed Adriana with Leukemia and she has been fighting an uphill battle ever since.  Adriana needs a bone marrow transplant to survive. Will you get tested, the test if fast, easy and painless? Click here to save a mom of three: https://bethematch.org/ And if you'd like to support her during these trying times and help with medical bills,  click here:  https://www.gofundme.com/6p3buwpp3bSave 1 Person. Save The World.
 

Can You Help This Baby with CHD?

View image on Twitter
 
Save 1 Baby. Save The World.  1-Year-Old  Paloma Bartocci, was born prematurely at 26-weeks.  This little soldier, needs life-saving surgery for congenital heart defects (CHD)  as well as other health related issues due to her premature birth. The family needs your help? To find how you can make a difference and save Paloma click here  https://www.giveforward.com/fundraiser/xpjb    Save 1 Child. Save The World.
 

Save This Angel!

 
 
Alara needs to find a blood stem cell donor to help beat her leukaemia.
 
Save 1 Child. Save The World. Alara Basturk, a young Irish girl is fighting a devastating battle, at such a young age.  This princess has Leukemia and needs a blood cell donor. This six year old  girl needs to find a donor and – as her mom is Irish and her father is Turkish – white, Middle Eastern and Turkish people are particularly needed. Will you get tested and see if you can save this angel? Go to http://www.deletebloodcancer.org.uk/en and save a life. Save 1 Child . Save The World.
 
 

Amanda has ALS, Can You Help Her?

http://email.change.org/mpss/c/ggA/3CE/t.1r9/R6Sx9HMyTPKuB_wPwXfyLA/h1/KLcqj6mm2DNwtPZFTP391mh-2FulOQ2SQ5OWii6lSgf4STScMluh6-2BMNnnDW-2FvMgsOFtVpPGprDU56hWm6L-2BVNcFItkSimM59jb7aql9qLRaBPug6mGVM6-2FqajsvIi-2Bx-2FSsbVz1UpmYF8cDGE85TOxr4o4OzXye1yWEiHPE9vNiHexPnh-2BNcmvlJs9DQbRbKAXldoyjq6lXfNv8YNHxgyxmkFFtIdlA-2FYocA3-2FcjlWYvZrDvHtuG3MTaPzfyUO2zmCzq5t-2FZgRESyXL5kkvEr5qIBeFQRgbI1hyKn04aCMRrk-3D
 
This is a Save 1 Person Alert. Save 1 Person. Save The World. Amanda Bernier may only have months to live. When Amanda was a couple of months pregnant she was diagnosed with ALS. Amanda and her family need your help in overcoming this huge obstacle. This family needs the FDA to apply Accelerated Approvals (AAP) - an expedited approval process to treat fatal diseases, to promising ALS treatments.The FDA has refused to apply any ALS medications to AAP because the FDA says ALS kills people too quickly. We have to change that thinking. Will you sign a petition and give Amanda a chance?