How it works
Our daughter Ruby was diagnosed with Zellweger’s Spectrum Disorder in November. We had always known she likely suffered from some form of genetic disorder but were told we would probably never get a diagnosis. Furthermore, we were informed that a diagnosis likely wouldn’t change much for her as she was already receiving all the requisite care. While continuing to push for more testing, what we had not prepared ourselves for was an incredibly rare diagnosis that would shorten her life expectancy greatly. Most kiddo’s with this disorder don’t make it past 1 year of life, so in a sense, we do consider ourselves lucky as Ruby has just surpassed 4 years this past June!
Over the past year, we have been forced to pivot from making Ruby “better” and focus on her quality of life and comfort. Today, Ruby relies upon a G-Tube for feeding, a Tracheostomy + oxygen, and is completely immobile. With Ruby spending all of her time in a wheelchair or bed, we are trying to find ways to reduce pressure on her body and just make her more comfortable overall. Insurance, as I’m sure most of you know, tends not to help with anything that is not a “medical necessity” (and even then, who knows!). The items we are looking to get for Ruby we do view as a necessity as they both, help us provide proper care for her, as well as make her comfortable and content.
So many of our friends and family have reached out recently to offer help and support, often asking if you can buy her a gift. Given she has lost all of her strength and ability to play with toys, this felt like a great way to let you contribute toward something that will go to great use.
We greatly appreciate any/all donations to help us achieve this goal, as I am sure Ruby does also!
Contributors (0)
contributed
$150
Anna Taylor
1 month agocontributed
$300
Anonymous
1 month agocontributed
$10
Anna Taylor
1 month ago
contributed
$1050
