Whitmore Lottie Love
Donation protected
Hi My name is Julie Whitmore, mummy to an incredibly brave little 3 year old.
In February 2018 my whole world was turned upside down when Lottie was diagnosed with Nephrotic syndrome FSGS
Lottie needs so much medication daily just to keep her alive, a very low sodium diet and can only drink 800ml of liquid a day. Doctors have advised that her kidney will most likely fail by the time she is 10, it is also likely that she won't get a kidney transplant straight away and will need dialysis until a kidney is available.
If you have never heard of Nephrotic syndrome FSGS before, it is an illness where the body leaks protein from the blood through the kidneys causing them to permanently scar.
You can learn more about Nephrotic syndrome FSGS here: Nephrotic Syndrome Awareness
And here: NEST
If you can help in any way we would be so grateful.
Thank you,
Julz
In February 2018 my whole world was turned upside down when Lottie was diagnosed with Nephrotic syndrome FSGS
Lottie needs so much medication daily just to keep her alive, a very low sodium diet and can only drink 800ml of liquid a day. Doctors have advised that her kidney will most likely fail by the time she is 10, it is also likely that she won't get a kidney transplant straight away and will need dialysis until a kidney is available.
If you have never heard of Nephrotic syndrome FSGS before, it is an illness where the body leaks protein from the blood through the kidneys causing them to permanently scar.
You can learn more about Nephrotic syndrome FSGS here: Nephrotic Syndrome Awareness
And here: NEST
If you can help in any way we would be so grateful.
Thank you,
Julz
Organizer
Julz Whitmore
Organizer