My Story - Ted Hunter




I was diagnosed with ALS on February 11, 2021. The onset happened slowly; first in my legs and feet, and then about six months later my tongue and speech were affected. My upper body is still strong. 

Over the past three years I have been in and out of physical and occupational therapy. I started with in-home health care until I could no longer manage 24/hour personal care at home. I moved into Assisted Living on March 7, 2023. I needed help with taking medications, meals, dressing, showering, and other day to day activities.


I have a great care team of doctors at Duke University’s ALS clinic. I like the fact that they are open to complimentary and alternative modalities, as well as traditional medicine. I feel empowered to explore as many options as possible under their care.


I am fortunate that my condition is on the side of the spectrum that progresses very slowly. This gives me the opportunity to try to optimize and improve my overall health as much as possible. On this website, I have included all the protocols I currently use. I pray that my website will also be a valuable resource for others living with ALS and their caregivers.

In the past I have been on two FDA drugs to slow down the progression of ALS. I used them for a brief period of time and had very bad reactions and had to discontinue taking them. 



Dr. Bedlack who heads the Duke University ALS Clinic has documented 62 ALS reversals from all over the worldI believe it’s possible that I could be the next ALS reversal using many of the protocols I have gathered on my website. I cover topics related to Mind Set, Prayer, Spirituality, Music Therapy & Sound Healing, OTC Supplements, Physical & Occupational Therapy, Meditation, Energy Healing and multiple links to online ALS resources.

Since starting the LifeWave X39® Patches, I have had significant improvement in my speech, additional muscle strength, better finger dexterity & coordination, better sleep, and an increase in my lung breathing capacity by 2%, as verified by my doctors at the Duke University ALS Clinic..

Comments


  1. My husband was diagnosed with MND ALS (amyotrophic lateral sclerosis) when he was 69 years old, 6 years ago. The Rilutek (riluzole) did very little to help him. The medical team did even less. His decline was rapid and devastating. The psychological support from the medical center was nonexistent,t and if it were not for www. madibaherbalcenter. com and the sensitive cure of their herbal formula he would have not been alive today, there was a significant improvement in the first 4 weeks of usage that gave us hope that he will be alive, His doctor put him on riluzole, letting us know there was no cure until we gave try on total cure herbal supplement that cure him totally form this disease after 13 weeks of his usage.There is nothing positive about the cure for ALS condition except for their herbal treatment ( www. madibaherbalcenter. com )

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  2. I was living a peaceful life with my family when I started noticing muscle stiffness and twitching. After seeing a neurologist, I was diagnosed with ALS. The news was overwhelming, and as the disease progressed, I lost the ability to walk and became dependent on a wheelchair.
    A friend recommended the ALS/MND protocol at DR AZIEGBE HERBS CURE. Skeptical but hopeful, I gave it a try. After three months, I noticed significant improvements—less stiffness, fewer twitches, and I could even walk short distances again, to reach out to him contact: DRAZIEGBE1SPELLHOME@GMAIL.COM
    It was a life-changing experience that brought back hope I thought I'd lost. This journey reminded me that healing can sometimes come from the most unexpected places.

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