I find myself a little reluctant to get excited about the changes Gary is seeing taking the Reliv...we have had so many hopeful times in the last 4 1/2 year's only to become disappointed with again seeing the progression of this horrific disease squeezing ever ounce of life out of each one of us. WELL I AM HERE TO BOLDLY SHOUT OUT THE HEALING TAKING PLACE IN GARYS BODY...PRAISE THE LORD FOR THESE OPEN DOORS FOR GARY TO BE TAKING RELIV...
he is sleeping through thru the night
he is no longer sleeping 2 to 3 days in a row
his legs are stronger
his arms are stronger
his muscle movement is smoother
his digestive system is showing major improvement
his legs and feet seem to look normal no swelling or purple color
he has no muscle spasms after 3 days of use
he is able to roll over in bed
he does not get tangled in his sheets
he is not clearing his throat all the time
and gaging while eating it is amazing
he is standing with his walker for balance solely not for strength and rest.
he is picking up his feet to walk instead of dragging them
he has real shoes on
Gary was diagnosed with Als Lou Gehrigs Disease in Dec 2009 ALS is a terminal illness with no possible cure... was also told he would live 4 to 7 months Gary has not tried anything new for over 1 year we had given up hope as lack of finances to many medical cost and my crazy work schedule and the entire families health has declined over the last few years...Praising God for our new HOPE ok I am passed being a little reluctant lol :)
Needless to say :) between the Awesome Health Benefits it only made sense for myself to become a "Reliv Independent Distributor " If there is anyway I can help you or a loved one understand more about Reliv please message me or e-mail mmpeanut8229@yahoo.com
Gary thank you first off for your blog. I'll make the story of my dad short. I lost my father to ALS, he was dx on 10/2/13 and after he fought the disease with all he had lost the battle 11/13/13. The Dr's suspected he had symptoms for a while. He complained of his body hurting specifically his back but he was a truck driver his whole life plus he had been hit on his motorcycle a few times so we just thought those things contributed to his pain. When he started having breathing issues he started with Dr's appt after appt they found nothing even testing him for cancer. He went to have a sleep apnea test and it showed he had that and he got the machine and hated it, little did we know how much he would come to depend on it. On 9/9/13 he asked us to take him to the ER because his back hurt so bad, my father hated hospitals so when he asked to go we knew he was in pain. At the hospital the ER Dr made me mad he was acting like my father just wanted pain pills until he went and looked at Xrays and all my fathers medical records the hospital had due to him having tests done at this same hospital and the Dr's tone changed and my father was admitted. More tests again nothing his blood work, everything was perfect, he just retired that April at 65. The hospital finally sent him up to Shands in Gainesville more tests, nerve tests etc then a thigh muscle biopsy which confirmed what we were praying he didnt have, We asked about meds ( I work in the medical field and read up alot on ALS and meds etc) the Dr's said at the stage he was in nothing will help so he was sent home with Hospice on 10/7/13 we watched him deteriorate and his legs and arms waste away it was horrible. He refused a ventilator and feeding tube so he depended on his sleep apnea machine and wore it constantly except to eat and he ate fast he just couldn't breathe. On that cold Wed morning 11/13/13 I got the call I dreaded my father had passed, I had been praying for God to please not let my father suffer and he listened, My father only got to enjoy a few months of retirement due to the pain he was in and he was sleeping a lot, You're blog makes my heart so happy that maybe what you're doing can help someone. This disease is such a brutal one and I know how hard it is on a wife, children and grandchildren. I'm sending many prayers and blessings to you and your family. May God be with you!
ReplyDeleteI am sorry so to say just today I cam across your comment. We have been away from the blog for a while and I guess we have no alert turned on concerning comments. So please know that we so wish we had come across it sooner. On another note it is so refreshing to see your comment. So sorry about what you guys and your father had to go through. I totally understand your prayers for relief for your father. I am praying and have been praying that this blog would not only help us through sharing and telling our story but also to give hope and direction to anyone having to deal with this horrific disease. Please check out some more of the resent post as we are still seeing slowing and more reversal of some of the symptoms. Thanks again for your comments and sharing your story with us.
DeleteI come from a Pacific Island nation called Papua New Guinea. My country shares borders with Indonesia, Australia and Solomon Islands..I usual search on Youtube any interesting documentaries. Whilst looking up youtube videos I came across a documentary on people who suffer ALS and their real treatment from www.multivitamincare.org. I for had never heard of this crippling and debilitating disease affecting a lot of Americans. It is very torturous to watch and hear patients who suffer. It is more like a combination of various diseases all put into one. Like a person who has suffered a stroke, plus someone suddenly becoming paralysed, cancer etc. but I also get to know understand that there has been successful cure to this disease from multivitamin care. It is too much for a patient to endure such as they slowly begin to pass away if the right medication is not taken .Having a positive mind is a powerful tool .My prayers goes out to ALS patients and their care givers.
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