Help Mitchell pay medical bills etc
Donation protected
Accessibility for Mitchell
Hello, I am Mitchell, a prisoner in my own body! However, my Spirit is not!
As I digress, momentarily, from the following story,
I have been very much involved
with BVT, bee venom therapy, 4000 live bee stings to date,
and still counting https://www.facebook.com/groups/398477540313310/
https://www.facebook.com/mitchell.waxman.5
I am also in need of funding for BVT.
I have been researching stem cell implant brain surgery.
I have gotten together a team of professionals to gather
all the necessary information to make this possible.
Stem cell research is past the developmental stage onto actual successful implementation.
Won’t you please donate to my gofundme drive
to help make this a reality?!
Thank you! <3
After a plethora of negative physical tests and six "negative" Lyme Complex tests, (false negative, an all too common problem in the Lyme Disease world). I was finally diagnosed by a proper LLDr, Lyme Literate Doctor in 1999 with Lyme Disease, an umbrella term covering multiple pathogens including bacteria, parsites, viruses, thus weakening the immune system as further strategy for attack of the body from head to toenail!
https://www.facebook.com/groups/398477540313310/
Having come and gone through over 100 symptoms, which has affected every and any system and nook and cranny of my entire body, I have been left a quadriplegic, though fully tactile. (yes, Lyme Disease can do that)! I am cognitively intact, but confined to my bed. I am verbal (try me!), and I am able to use a computer through speech recognition software, which is how I am dictating this.
I am trying to raise enough money to pay medical bills etc, appropriate physical therapy, and whatever additional funds obtained would be used for an electric wheelchair, replace outdated laptop/speech recognition, medical bills loan, household bills/repairs, food, etc ...
My story includes a constant struggle with insurance companies refusal to cover my further needs, and Medicaid, forcing me to spend my life's savings/assets in order to "cover" me, thus leaving nothing for other neccessities with which to cover my paralyzed life!
Having neccessities, such as a powered wheelchair, updated laptop/speech recognition, paid medical bills/medical loan, physical therapy, home repairs/maintainance, food, etc, would allow me the independence for which I struggle. We all believe I should be able to negotiate myself around my own home and town, involve myself with the community, and touch life and lives as I did before my illness. I have left my bed very few times since returning to my home in 2015, after two years in nursing hospitals.
With your outreach I will have so many more means with which to find some semblance of "normalcy"! I have tried the conventional means for obtaining the neccesseties needed for greater accessibility, only to be given unreasonable and frustrating and time delayed resistance.
Please extend your aid to assist in making my life more managable and bearable, more purposeful and meaningful.
And so please "gofundme"!
~ That's my story ... SHORT!
Thank you!
amazing grace
all you givers
give me the shivers
through the rivers
of life
cheers!
~ from my straight jacket ~ out on a limb ~ lookin like a cocoon ~ hangin by a thread ~ waitin for a butterfly ~ under the moon ~ Lovey-Dovey ~ Mitchell!
Hello, I am Mitchell, a prisoner in my own body! However, my Spirit is not!
As I digress, momentarily, from the following story,
I have been very much involved
with BVT, bee venom therapy, 4000 live bee stings to date,
and still counting https://www.facebook.com/groups/398477540313310/
https://www.facebook.com/mitchell.waxman.5
I am also in need of funding for BVT.
I have been researching stem cell implant brain surgery.
I have gotten together a team of professionals to gather
all the necessary information to make this possible.
Stem cell research is past the developmental stage onto actual successful implementation.
Won’t you please donate to my gofundme drive
to help make this a reality?!
Thank you! <3
After a plethora of negative physical tests and six "negative" Lyme Complex tests, (false negative, an all too common problem in the Lyme Disease world). I was finally diagnosed by a proper LLDr, Lyme Literate Doctor in 1999 with Lyme Disease, an umbrella term covering multiple pathogens including bacteria, parsites, viruses, thus weakening the immune system as further strategy for attack of the body from head to toenail!
https://www.facebook.com/groups/398477540313310/
Having come and gone through over 100 symptoms, which has affected every and any system and nook and cranny of my entire body, I have been left a quadriplegic, though fully tactile. (yes, Lyme Disease can do that)! I am cognitively intact, but confined to my bed. I am verbal (try me!), and I am able to use a computer through speech recognition software, which is how I am dictating this.
I am trying to raise enough money to pay medical bills etc, appropriate physical therapy, and whatever additional funds obtained would be used for an electric wheelchair, replace outdated laptop/speech recognition, medical bills loan, household bills/repairs, food, etc ...
My story includes a constant struggle with insurance companies refusal to cover my further needs, and Medicaid, forcing me to spend my life's savings/assets in order to "cover" me, thus leaving nothing for other neccessities with which to cover my paralyzed life!
Having neccessities, such as a powered wheelchair, updated laptop/speech recognition, paid medical bills/medical loan, physical therapy, home repairs/maintainance, food, etc, would allow me the independence for which I struggle. We all believe I should be able to negotiate myself around my own home and town, involve myself with the community, and touch life and lives as I did before my illness. I have left my bed very few times since returning to my home in 2015, after two years in nursing hospitals.
With your outreach I will have so many more means with which to find some semblance of "normalcy"! I have tried the conventional means for obtaining the neccesseties needed for greater accessibility, only to be given unreasonable and frustrating and time delayed resistance.
Please extend your aid to assist in making my life more managable and bearable, more purposeful and meaningful.
And so please "gofundme"!
~ That's my story ... SHORT!
Thank you!
amazing grace
all you givers
give me the shivers
through the rivers
of life
cheers!
~ from my straight jacket ~ out on a limb ~ lookin like a cocoon ~ hangin by a thread ~ waitin for a butterfly ~ under the moon ~ Lovey-Dovey ~ Mitchell!
Organizer and beneficiary
Mitchell Waxman
Organizer
Wilmington, DE
Thornton Carroll
Beneficiary