ZAKIYYAH
“Zakiyyah is a bright, inquisitive 5 year old. She loves riding her bike and playing football”.
Outwardly Zakiyyah looks like every other 5 year old and this is an issue that her family deals with constantly.
When Zakiyyah came to the studio to take part in the rare Project her parents explained a little more about her condition and the impact the diagnosis had on their lives.
“After Zakiyyah was born we instinctively felt something was not quite right and went back and forth to the doctors. Her feeding was a real issue and she was such an unsettled baby. It was not until she was three months old we found out she had this rare condition which affects approximately 1 in 100,000 people. Tyrosinaemia is one of the conditions that is tested for as part of the heel prick test that is carried out on newborn babies”.
“We had a whole weekend of not knowing how this condition would affect our baby - it was terrifying”
“The way in which we found out about her condition was really hard for us. It is never easy getting a diagnosis but we were told on a Friday afternoon and we were given very little information. The consultant and dieticians who could give us the answers we needed were not available until the Monday and so we had a weekend of not knowing how this condition would affect our baby - it was terrifying.
When we finally did see the consultant he was wonderful and explained everything clearly to us. Even though we have to carefully manage Zakiyyah's diet it is a condition that can be managed”.
“It was difficult getting used to the drugs and dietary changes to begin with. We have to monitor her intake all the time but it is surprising how much it becomes second nature. She is only allowed 5g of protein which is not very much at all - for context, there is 12.5 g in a single egg! We routinely check her tyrosine levels through blood tests and she has to take supplements and medication throughout the day”.
“The fact that Zakiyyah looks like everyone else means that her condition is very much invisible”
“We were pleased to take part in the Rare Project so that people were aware that not all rare conditions were obvious. Prior to having Zakiyyah, I wasn’t aware of metabolic conditions and the impact they can have on the body”.
FIND OUT MORE
Tyrosinaemia Type 1
Tyrosinaemia Type 1 is a rare disease where people who are affected have problems breaking down an amino acid called tyrosine from their food. In order for the body to use protein from the food we eat, it is broken down into smaller parts called amino acids. Special enzymes then make changes to the amino acids so the body can use them.
Tyrosinemia 1 occurs when an enzyme, called fumarylacetoacetase (FAH), is either missing or not working properly. When FAH is not working, it cannot break down tyrosine. Tyrosine and other harmful substances then build up in the blood. One of these substances is called succinylacetone. When it builds up in the blood, it causes serious liver and kidney damage. It may also cause episodes of weakness or pain.
If you would like more information and support on Tyrosinaemia or other inherited metabolic diseases, click here to visit the Metabolic Support UK website.
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