Amy’s Story

Site created on May 13, 2020

Welcome to Amy's Warrior Wall for well wishes, where family and friends can all come together in one place to support and empower Amy and her family, as well as find peace in answers and updates about her well being throughout her journey with her new diagnosis. We're excited to share the page with her once we get it up and running and know she will love and appreciate all of the love and prayers sent her way, as do we very much.

Her most recent hospital stay began on Wednesday, March 22, 2020 when doctors wanted to safely monitor her after her in-home IVIG treatment caused her blood pressure to drop.  Unfortunately, due to COVID19, we were not able to be with Amy, adding stress to an already frustrating time, searching for answers as her rare Progressive MS condition was declining.

After new symptoms arose and she underwent many tests to search for definitive results, our new battle to fight CNS Lymphoma together began on May 7th. While all of us, including Amy, can find a somber comfort in having answers (although it will be time until we find out if the MS is still there), Amy's journey and our family's is a long road ahead with many unknowns and variables.

Positivity, prayers, hope, and awareness are what will keep us all strong, as well as showing Amy she is not alone at this very lonely time in the hospital. We facetime with her daily as well as deliver care packages several times a week to lift her spirits. We are also working on devices to help her ability to communicate, as her speech has been affected by the disease(s), so that she can regain control in her life 1 step at a time.

We don't have many answers and nothing is definite as Amy's chemo journey can have several different outcomes and we must all pray for the best. We also won't know when we will have updates and we will do our best to post everything here from the family vs. Facebook and messages.

Please also know that while you may not hear back from each message you leave, they will all be read and shared with Amy and we so appreciate your support.

We understand this time has been difficult for many friends to see Amy in this state and to accept her new normal. From training for her first Marathon to not being able to walk, we are all faced with changes in her abilities, including herself which is very hard for anyone to do. Many of you expressed not knowing what you say or do, and some just couldn't find the words, and that's ok. We know everyone deals with health changes and grief in many different ways. I've asked in the past to send texts saying hello and photos of dogs, which Amy really enjoyed. At this time, she can't use her phone or facebook, so we hope this page will be a great venue for those messages of love that we can share with her on a regular basis, all in 1 place. 

We encourage and ask you to leave positive messages, letters, photos, to Amy that we will share, as well as the great memories that you shared with her for all to see into her life and friendships!


Thank you all from the bottom of our hearts, as we take so much joy in knowing that Amy is loved very much by you all!


With Love, Laura, Bob, Melissa, Billy and Bagel (woof woof!)

Newest Update

Journal entry by Melissa Miller

It's a NEW MONTH, a new "HOME." On Tues, Jan. 19th, Amy left Penn State Hershey Rehabilitation Hospital and moved back to Harrisburg.  She is now residing at The Homeland Center.   Amy completed nine chemotherapy treatments and her MRIs show NO EVIDENCE of a tumor.  Amy continues to work hard in therapy every day.

We are excited for the new month to begin and Amy's new chapter ahead as well. We wanted to update everyone that she is already showing improvements there!

As her quarantine period comes to an end this week, we are excited to share we will be able to go inside to see her.  This is a long time coming...since November!

Currently, we have scheduled window visits and Facetime calls (not as much as we could at the Rehab Hospital) and along with your support and love posting photos and encouraging words to help us be cheerleaders with Amy, we'll be sharing a lot more improvements.

Thank you!

Patients and caregivers love hearing from you; add a comment to show your support.
Help Amy Stay Connected to Family and Friends

A $25 donation to CaringBridge powers a site like Amy's for two weeks. Will you make a gift to help ensure that this site stays online for them and for you?

Comments Hide comments

Show Your Support

See the Ways to Help page to get even more involved.

SVG_Icons_Back_To_Top
Top