This is Mia, I've known her since she was 11 when we moved in with her Mom Sarah and her brother Jacob back when we moved back to San Diego so my wife could die here.
Mia has for years now battled chronic illnesses that were a mystery, crippling migraines, fevers, sometimes multiple fevers a day that come and go, flu-like symptoms, fatigue and a host of other things off and on that no teenager typically goes through.
She's a trooper and puts on a brave face on days when she can bare the pain and fake it till she makes it, and then there are other days where crying, ER visits, medication, sleep if she can get it and whatever else is all she can do until it goes away for long enough to live like a girl her age should.
Some months she's fine and then you can count days in the month that she isn't feeling terribly. It's unpredictable.
Recently she has gotten worse, spinal and joint pain in basically every bone in her body and now numbness in both arms.
FINALLY after more trips to the ER than can be remembered over the years and too many Dr's who had no ideas or answers other than trying this drug or that drug, she has been diagnosed with Rocky Mountain Spotted Fever ( which is fatal if untreated ), Mycoplasma Pneumonia and Chronic Neurological Lyme Disease. Due to the compromised immune system and other things too complicated and unnecessary to list for the purposes here, antibiotics and such have no positive effects and actually only cause more problems and expand the compromised immune system.
There is however a treatment protocol that is quite costly and unfortunately is NOT covered by any insurance.
So here is where you can help. The 12 to 24 month treatment is $1,200 PER MONTH.
It involves regular IV treatments that can go after the issues at a cellular level. It's a painful healing process and can make you feel worse before you feel better.
I personally know this family and have known her mother for 27 years when she was younger than Mia is now and I can vouch for them. They welcomed us into their 3 bedroom home so Alicia could die here and not in Florida. Please ask yourself if you can help and even commit to a monthly contribution. Set a reminder on your phone monthly to log in a donate again.
FEEL FREE TO SHARE THIS ON A VIRAL LEVEL!! LOL
Thank you for considering this wonderful young lady who, to me, is like the daughter I never had.
Blessings!
Mia has for years now battled chronic illnesses that were a mystery, crippling migraines, fevers, sometimes multiple fevers a day that come and go, flu-like symptoms, fatigue and a host of other things off and on that no teenager typically goes through.
She's a trooper and puts on a brave face on days when she can bare the pain and fake it till she makes it, and then there are other days where crying, ER visits, medication, sleep if she can get it and whatever else is all she can do until it goes away for long enough to live like a girl her age should.
Some months she's fine and then you can count days in the month that she isn't feeling terribly. It's unpredictable.
Recently she has gotten worse, spinal and joint pain in basically every bone in her body and now numbness in both arms.
FINALLY after more trips to the ER than can be remembered over the years and too many Dr's who had no ideas or answers other than trying this drug or that drug, she has been diagnosed with Rocky Mountain Spotted Fever ( which is fatal if untreated ), Mycoplasma Pneumonia and Chronic Neurological Lyme Disease. Due to the compromised immune system and other things too complicated and unnecessary to list for the purposes here, antibiotics and such have no positive effects and actually only cause more problems and expand the compromised immune system.
There is however a treatment protocol that is quite costly and unfortunately is NOT covered by any insurance.
So here is where you can help. The 12 to 24 month treatment is $1,200 PER MONTH.
It involves regular IV treatments that can go after the issues at a cellular level. It's a painful healing process and can make you feel worse before you feel better.
I personally know this family and have known her mother for 27 years when she was younger than Mia is now and I can vouch for them. They welcomed us into their 3 bedroom home so Alicia could die here and not in Florida. Please ask yourself if you can help and even commit to a monthly contribution. Set a reminder on your phone monthly to log in a donate again.
FEEL FREE TO SHARE THIS ON A VIRAL LEVEL!! LOL
Thank you for considering this wonderful young lady who, to me, is like the daughter I never had.
Blessings!
Organizer and beneficiary
Sarah Espiritu
Beneficiary