Lets Help Stuey & Shelley V

Stuey Vieyra & his wife Shelley are facing some difficult times ahead. They are not asking for any handouts whatsoever, but i have made a decision to donate my show payments for the next 6 mths to this great & beautiful couple and build this Go Fund Me Page. As an ETA we are ALL one big family. It's not much, but im sure any $$$ may help with some relief as Stuey is a fulltime provider, husband, father and a well respected ETA and most importantly person. Stuey is always willing to help others and give advice when required. You have been inspirational in me following my ETA dream, and i feel you and your family deserve a break. I would like to at this stage ask if any ETA'S are willing, lets dedicate a day to Shelly and have a benefit show for her. Im sure ongoing medical bills will be coming in for this family. Any interested ETA'S want to come onboard inbox or ring me. This Go Fund Me page is for help now for this beautiful couple. FROM SHELLEY'S PAGE: Awareness is the key..... for those that dont know I'm struggling with Functional Neurological Disorder (FND). This is a brain disorder that is not allowing my nervous system to function correctly. This means I'm having issues with co-ordination and walking as well as nerve pain, confusion, headaches and so much more. I can not move around very much. I spent weeks on the mobility walker and it became more intense and extremely tiring. I'm now using the wheelchair to move around as i can't even walk to the toilet. On Sunday this shaking started and is progressively getting worse. The hardest thing is, this disorder, is not a recognized disability so there is no government help and all comes out of our pocket. Stuart has been amazing, he pushes me around to make it easier for me and less tiring, he has moved the bedroom around to make it more wheelchair accessible and won't let me do anything strenuous. In spite of all this I still smile and try to keep normal routine although getting harder, I'm positive and won't let this take over. It is basically like having MS with out having any damage to my brain. It is debilitating and I can't work. But I'm blessed to still wake up every day despite the struggle. I'm grateful for the friends and family that I have looking after me and keeping in touch with me. Some have been super understanding. And a special thanks to my mother in law Eunice, who takes me shopping and drives to my specialist appts even though she has her own health issues. I'm eternally grateful. The positive news is it will get better in time but never go away as I will always have it. Treatment starts soon and should make a big difference. Looking forward to getting my legs back. So many people have contacted me and sent well wishes and I thank you all. Your positivity keeps me pushing through.