Case update - Help Baby Sabri! His Rare Hereditary Disease (PKU) Prevents Him from Eating Regular Foods
Sabri Started Receiving His Alternative Special Food!

19 - 05 - 2022

Thanks to the donations we have raised so far by Tadamon’s generous donors, Sabri received his weekly special dietary needs, which are crucial to maintaining his health and fixing the protein levels in his body. 

 

Sabri, 1 year and 2 months old, will always be unable to digest the regular food we eat on a daily basis, due to a hereditary disease which left him unable to digest a certain type of amino acid found in protein. As a consequence, Sabri’s daily diet must provide expensive alternatives and be calculated to a great degree of precision so as not to worsen his condition. 



A CHANGE IN THE AMOUNT RAISED

In the past two years during COVID, and due to various logistical obstacles, Sabri wasn't receiving the needed amount of special milk required to complete his dietary needs. Therefore, Tadamon stepped in and started raising funds to cover this amount. Yet, thankfully since the pandemic restrictions have eased, he is now being provided with the complete supply of milk. As a result, Tadamon will now focus on raising funds for his special foods as well as fruits and vegetables for 6 months. 

 

Tadamon lowered the amount to 660 JOD (after eliminating the special milk) as shown below: 

 

  • Special food alternatives (special wafers, biscuit, pudding etc): 70 JOD/month, 420 JOD for 6 months
  • Fruits and vegetables: 40 JOD/month, 240 JOD for 6 months 

 

Totaling 660 JOD.