One of the toughest things for my husband, diagnosed four years ago, is the frustration with the loss of function and communication. He recently told me "you don't understand". I responded, "you are right,I do not....But I am trying with everything I have". It is that gap between being a Caretaker and significant other. we started ALS/MND programme from vine health centre . c om 5 months ago, he has regain some functionalities, we noticed his speaking has gotten better since we started on this treatment programme, it didn't make the ALS go away but it gave him a better quality of life. I also understand that God does not give us more than we can handle...

Last year, my 68-year-old partner was diagnosed with Lou Gehrig's disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither the riluzole nor the medical staff did much to aid him. He would not have survived if our primary care physician hadn't given him attentive care and attention, as the hospital center didn't provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms. This year our family physician suggested using vine healthcentre. com ALS/MND treatment, which my husband has been receiving for a few months now. I'm delighted to say that the treatment greatly reduced and reversed his symptoms of ALS, he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband's tale; in the end, you have to do what suits you the best.