The Lunaboat Association (A Non-Profit Association) is and will be dedicated to Multiple Sclerosis research, sufferers, people who have family or friends who suffer.
Please show your support. I thank you all so much.
Wishing you all health, happiness and to live a great life
I am the Founder and President
Part One: September 2019
My name is Luke J. Watts and I am happy to share (now) about my experiences with Multiple Sclerosis (since 2003).
Since 2003 I hid my symptoms and my disease, only family and friends knew.
I was recently hospitalized and I had an idea about raising more AWARENESS & RESEARCH!
I started looking into the disease much closer. I saw groups and charities and was getting conflicting information.
I wanted to create this Non-Profit Association especially for:
Multiple Sclerosis – Awareness – Caring – Support – Research
Part Two: October 2019
This is also dedicated to my very beautiful sister; Venessa. She is 18 months younger than I am and since 1985, she suffers from MS (Progressive stage).
Even as her brother, I never knew what she was experiencing, going through BUT would try to support her as much as I can.
I decide to let people know what can happen (as not all forms of MS are the same).
It is all about AWARENESS!
- All donations will go to Laboratory of Neuroimmunology / Multiple Sclerosis CHUV Hospital – Lausanne, Switzerland
- Make the AWARENESS MORE TO THE PUBLIC
- To let people know, what a MS sufferer has to go through his/her life, Daily, Emotionally and Mentally
With my very best regards,
Luke J. Watts