Stephanie Evan's Medical Bills
Donation protected
Aloha! I am starting this Go Fund Me campaign for my friend Stephanie Evans who has been diagnosed with Trigeminal Neuralgia. My hope is that we can raise some money to help with the financial burden and travel costs in these tough times for her and her family.
Stephanie was diagnosed with Trigeminal Neuralgia shortly after giving birth to her second son in September 2017. TN is a neurological illness that is debilitating and also known as the suicide disease because of the extreme pain and lack of remedies for that pain. It has made this time that should be joyous for the family very difficult. Stephanie and her husband Peter are parents to two sons, a 3 ½ year old and a new 3 month old.
Stephanie has been dealing with this pain for over a year on and off and shortly after giving birth, it took a turn for the worse. After seeing over 12 different doctors, hospital visits, MRI’s and CT scans she was sent to see a neurologist and got a diagnosis.
Up to this point, she has tried anti-seizure medications, pain medications, as well as CBD pills. These medications aren't working much and she's suffering not only from the condition of TN itself but also from all the nasty side effects of the medications. Stephanie has not been able to return to work due to the fatigue from the meds and chronic pain that radiates constantly from the entire side of her face.
She is trying every natural route like supplements, vegan diet, acupuncture, upper cervical chiropractor, cranio-sacral, active release therapy, laser treatments and more. Unfortunately, majority of these treatments that are giving some slight relief are not covered under any insurance plan and are beginning to add up.
Stephanie has an upcoming appointment with the pain management clinic here on Maui to discuss possible nerve blocks and treatments. The next step she will have to undertake will be traveling to the Mainland to see specialists if she doesn’t get better soon, leading to the strong possibility of brain surgery (MVD), which in itself does not have a solid success rate. She is currently on the waiting list at the Mayo clinic and awaiting confirmation from another medical institution. This is a long and arduous journey that the family is on with no end in sight in the foreseeable future due to the nature of this chronic illness.
The medical bills are piling up, adding to the stress of being in pain. Anybody who knows Tephy knows just how BIG her own heart is, along with the amazing kindness she possesses. Let’s be kind to her!
I know the family is doing everything in their power to beat this thing, so I’m asking that we rally around the O’Riordans during these tough times. Every little bit helps.
Mahalo!
(Video explaining Trigeminal neuralgia)
Stephanie was diagnosed with Trigeminal Neuralgia shortly after giving birth to her second son in September 2017. TN is a neurological illness that is debilitating and also known as the suicide disease because of the extreme pain and lack of remedies for that pain. It has made this time that should be joyous for the family very difficult. Stephanie and her husband Peter are parents to two sons, a 3 ½ year old and a new 3 month old.
Stephanie has been dealing with this pain for over a year on and off and shortly after giving birth, it took a turn for the worse. After seeing over 12 different doctors, hospital visits, MRI’s and CT scans she was sent to see a neurologist and got a diagnosis.
Up to this point, she has tried anti-seizure medications, pain medications, as well as CBD pills. These medications aren't working much and she's suffering not only from the condition of TN itself but also from all the nasty side effects of the medications. Stephanie has not been able to return to work due to the fatigue from the meds and chronic pain that radiates constantly from the entire side of her face.
She is trying every natural route like supplements, vegan diet, acupuncture, upper cervical chiropractor, cranio-sacral, active release therapy, laser treatments and more. Unfortunately, majority of these treatments that are giving some slight relief are not covered under any insurance plan and are beginning to add up.
Stephanie has an upcoming appointment with the pain management clinic here on Maui to discuss possible nerve blocks and treatments. The next step she will have to undertake will be traveling to the Mainland to see specialists if she doesn’t get better soon, leading to the strong possibility of brain surgery (MVD), which in itself does not have a solid success rate. She is currently on the waiting list at the Mayo clinic and awaiting confirmation from another medical institution. This is a long and arduous journey that the family is on with no end in sight in the foreseeable future due to the nature of this chronic illness.
The medical bills are piling up, adding to the stress of being in pain. Anybody who knows Tephy knows just how BIG her own heart is, along with the amazing kindness she possesses. Let’s be kind to her!
I know the family is doing everything in their power to beat this thing, so I’m asking that we rally around the O’Riordans during these tough times. Every little bit helps.
Mahalo!
(Video explaining Trigeminal neuralgia)
Organizer and beneficiary
Phil Le Blanc
Organizer
Lahaina, HI
Peter O’ Riordan
Beneficiary
