My name is Mohammad, I am a father of 2 beautiful boys age 3 and 1, my wife recently a few months back was diagnosed with a rare disease called cystic fibrosis.

Cystic fibrosis (CF) is a life-threatening genetic disease that affects the cells that produce mucus, sweat, and digestive juices. It's caused by mutations in the CFTR gene, which encodes a protein that regulates ionic exchanges. These mutations lead to the production of abnormally thick, sticky mucus that clogs organs like the lungs, pancreas, and intestines. The mucus in the lungs can block airways, making breathing difficult and causing recurring chest infections.

on the NHS there isn’t much they offer to treat this and besides the waiting time being very long it is incredibly costly. After a lot of research, I have found a place which offer the treatment for this condition with high chance of recovery but can take up to a year and the entire cost price for the treatment is 100,000.

I am a normal average working cab driver, I don’t have any saving and just about manage to pay the household bills. I did not want to resort to this but a family member suggested it.

So I ask a a helpless father and husband, please help me with whatever you can and if not money please share.