Nephrotic Syndrome App

Nephrotic Syndrome is a kidney disease, patients of nephrotic syndrome have to keep track of data about their protein, illnesses, dosage and weight on daily basis for many years.
My daughter has Nephrotic syndrome, so I have first hand experience of the struggle of such patients and their carers. I have filled stack of diaries, at times you could also miss it. My cause is to get mobile app developed for patients/carers to track this data on daily basis. A mobile app is handy and great way to keep track of your personal protein level, which than can be shared with the doctor for medical analysis. Patients can also generate pdf/graphical reports using the mobile app.
My ambition is to develop this app as free app for patients across the world, who are already going through a lot. This app can make keeping daily records a lot easier for such patient who are already going through a lot of suffering. However, app development has costs associated with it, it is even more expensive to develop an app when your ambition is to develop app which is available free of cost to patients/carers across the world. There are costs associated with development, release and even more costs associated with getting the word to the patients across the world (multi-lingual development/marketing costs).
Please donate generously for this humble cause, which I envision can help alleviate suffering/pain of nephrotic syndrome patients across the world. 2 to 4 out of every 100,000 children are diagnosed with primary nephrotic syndrome each year.