Dear Whitney family and friends,I’m a family friend, and I volunteered to write this email, and then to post regular (hopefully weekly) updates on the whitneywellness.org website to keep people informed in the future. We’ll address more specific details on the website as we respond to any questions you add there.
The family wanted me to express their gratitude. Oh how they wish they could write to each person who has strengthened them or lifted them through countless acts of kindness. As I sat with them this week, I was struck by the sincerity of their desire, their need, to communicate how much they love you for your kindness.
They also wanted people to know that they recognize the fact that not everyone agrees with or understands the various paths they’ve taken to care for and treat Whitney. Many of you have offered ideas, direction, and input on what you feel might be best for Whitney. ALL those suggestions and leanings have been prayerfully weighed, and then, using the resources at their disposal, the family has made the best choices they could for and with Whitney. This has sometimes been an agonizing process. Sometimes there were differences of opinion even within the family. Sometimes it seemed impossible to sort through all the options. Other times the options became very limited and less than promising. But, Whitney and her family feel very peaceful and comfortable with the paths they’ve chosen and the path they’re on. They hope that you can find the same resolve.
Whitney is now under hospice care. Just the word hospice when connected with a loved one can elicit all sorts of emotion, depending on your experience with it. But Whitney and her family are moving into this phase of life from a place of peace and power. There are many changes that necessitated this step, but mainly, when the doctors said there was nothing more they had to offer, and when healing treatments were not working, it made sense to engage the expertise of hospice workers. They feel this is a positive move forward.
Whitney’s tumors are still growing and multiplying. Sometimes her breathing is difficult so she takes oxygen for parts of most days. The itching, which has plagued her for some time, is worse and has been little effected by medication. In fact Whitney does not respond typically to almost any medication, including the initial chemo, which normally cures Hodgkin’s lymphoma but did not work for Whitney. She takes several medications every day, many of which are intended to calm and relieve, and yet rather than settling down, she becomes almost manic and cannot sleep at night. In the last few days the newer regimen seems to have kicked in and she has rested more peacefully and seems to be more alert in the daytime, but she still has difficulty with her memory and her focus, losing words and ideas. And the itching, though sometimes abated, never quite goes away. Her appetitive also comes and goes resulting in a significant weight loss since last spring. On Dec. 23 Whitney experienced seizures in the night. No one seems to know the actual cause-maybe the tumors, maybe the medications, but since then it feels right to always have someone with her.
She is working on documenting the important aspects of her life, her photos, her music, and her writing. She wants to write an ethical will, something of value that she can leave behind for others. These endeavors require reflection and stretches of time without distraction (as welcome as those distractions might normally be). Just when Whitney’s energy began ebbing and her focus began turning rather inward, people understandably felt the need to find out more and re-connect with her. It’s been a struggle for the family to find a balance between protecting their limited and waning energy while accepting the love of those they care about. They feel so grateful, both in a general way, and in many specific ways for the care and love they receive. And at the same time they are feeling a need to set some parameters that will allow them to experience this new phase with some kind of order and decorum.
So visiting times will be limited, and the family asks that you arrange a visit in advance. Call Ami on her cell and she will try to return your call to set up a time when and if it’s possible. Please be patient: it may not happen in a timely way, and perhaps not at all. Family members are working to help Whitney in her hospice journey, and they need time to do that.
Rather than phone calls or visits, the family is hoping that people will use the website as a way to keep informed, stay connected, and wish Whitney well. Whitney has committed to posting some of her journaling there. I’ll be adding details weekly. You can post comments at the bottom of any posting, and ask questions in those comments. We’ll try to answer questions as they come up. Whitney seldom returns phone calls because she finds it very difficult to talk personally on the phone, so she very much encourages people to move from leaving phone messages to posting comments on the website. She said the website will be her new voice, her link to you.
If you would like to help in any way, please email Polly Farrimond who is helping to schedule assistance things like meals, laundry, repairs, groceries, etc. PollyAF@aol.com
Please continue in your prayers and positive energy, and please feel free to visit the website and stay engaged.
Love and peace to all those who are connected to each other through our love for Whitney,
Mary Anne Cropper