Help-Jackae's Lyme Disease Treatment

      Hello, my name is Jackae. I'm 35 years young and I have chronic Lyme disease. 
            I acquired Lyme disease in 2013 and I was misdiagnosed for 9 years with a multitude of conditions such as  perigo nodularus, shingles, and more than often "unknown." I usually look pretty OK, but inside my body is extreme debilitating pain that I've learned to live with and endure. In my head, a mind nearing Alzheimer's. Behind my smile, I am hurting.
           The disease is progressing. I experience neurological symptoms similar to an MS patient. Lyme has caused me brain & nerve damage, I have motor issues, sensory ataxia, severe cognitive issues such as memory loss, chronic fatigue, and arthritis & neuropathy pain.
Daily tasks are challenging and exhausting. Not to mention the psychological ramifications of having an "invisible" chronic illness and the experience of invalidation from friends, family, and the medical community for almost a decade.
     Although Lyme disease has robbed me of much, I am staying positive and optimistic about the future.
My amazing Son (Thats him below) is 16 years old. More than half of his life, I have been ill. I am determined to recover and to see him into adulthood, have grandchildren, and great grandchildren! Maybe I'll even be able to keep up with him in the gym one day!

      I am in need so much right now. I do not have a significant other, so I am taking care of myself the best I am able. Being ill, and alone is the most difficult challenge I've faced in life, and I humbly ask for support and assistance from my family and community. 
                                                                                       Any size donation is greatly appreciated.
       
                   Donation funds will be used for medical treatment expenses, (Doctor visits, medication, treatment protocol supplements, and all thing related to my treatment and recovery.) Sadly, my insurance won't cover any of the expenses.
I have chosen Stem Cell therapy as my primary treatment for my disease. As it is the most promising for a full recovery.
For more information on Stem Cell therapy, and what my goal$ is exactly for visit http://www.stemaidinstitute.com 

         I have found a local Lyme specialist and started treatment (May 13,2022) until the goal is reached for stem cell therapy.
 Conventional Treatment for chronic Lyme is extremely complexed, strenuous, and usually helps only some symptoms temporarily. It does not cure chronic Lyme or heal any damage done to the nervous system and organs. Stem cell therapy will heal the damage.

         

I appreciate you taking the time to read this, Thank You! Please visit the links below to learn more about Lyme disease and how it is affecting myself and so many others, unbeknownst for far too long.
 
Please share this post and my story with everyone you'd like. Your support is appreciated. 

Much Love and Peace❤️

Learn more about Lyme now 

https://www.lymedisease.org/ 

https://www.lymedisease.org/anthropologist-lyme-suicide/ 

https://www.google.com/amp/s/www.yahoo.com/amphtml/lifestyle/reality-lyme-disease-talk-190046483.html 

https://www.lymedisease.org/touched-lyme-threading-path-morgellons-disease/