Help Faye fight ALS

Hello! Most of you know that our beautiful friend Faye has been diagnosed with ALS.

ALS is a devastating motor neuron disease which results in the gradual deterioration of nerve cells in the brain and spinal cord, impacting voluntary muscle control and respiratory function.

It has been almost a year now since this devastating diagnosis and the courage and strength that not only Faye but the Murphy family has displayed has been nothing short of inspiring. She is strong, fierce and she will fight this but she can't do it alone. If you know Faye, you know she reluctant to ask for assistance, so rather, the people that love her are asking instead.

While the ALS society generously covers some medical expenses, we have been learning it will not cover all and there will be many! The progressive nature of the illness underscores the importance of the Murphy family creating lasting memories together.

We are thankful that so far the progression has been slow, but the disease is progressing and life is expected to present more and more challenges along the way.

If you wish to contribute to a fund to support the Murphy family in creating memories, overcoming obstacles, and alleviating some financial strain, your generosity would be greatly appreciated.