ALS: Dandy Oskey: Amazing Supplement Trial: Stay Strong, A Cure is Near

Supplement Trial: My thoughts after 90 days on the supplement
I was asked by Jason David College to share this post as a follow-up to my previous Supplement Trial post. I’ve been on my supplement for over 90 days and I want to let you know some of my thoughts.
1. Since beginning this trial, I honestly believe that my ALS symptoms have not progressed. Upon starting this trial, I stopped taking Rilutek and I take no other medication for pain or ailment.
2. I have seen positive changes in my ability to contract muscles in my legs (not done in 2 years) , as well as lift my right arm and have strength to perform simple tasks.
3. Many recent studies have been conducted on various nutritional treatments for chronic disease. This confirms what I am finding through my personal experiences within my trial. I really believe that epigenetic science and super foods are a valid treatment for disease. With the corruption of our food system, the use of pesticides, and our inability to give our bodies what they need, chronic diseases are sure to follow.
4. I have seen no ill affects from taking this supplement. I do find that I get less hungry for regular food, but I still eat regular meals. My weight seems to be staying consistent and I feel good most of the time.
5. I believe that even though I see slight improvements, most of my benefit has been from slowing the progression, if not stopping it. When saying this, it is hard to quantify it, but I know how I feel. I do know that today I am able to do things that I was unable to do 90 days ago, or were previously very difficult for me. For example:
a) When I used to eat, my wife would lift my arm up and my wrist did not have any strength to lift the food to my mouth, or even hold it up. Yesterday at the Jurassic World movie, I lifted almost an entire box of Junior Mints (one at a time) to my mouth. Boy they were good!
b) I have had multiple people visit from out of town who have told me that I am better today than the last time they saw me.
c) I was not not able to roll up my headset ear piece, or put the ear piece in since getting the headset. Lately I have had enough hand strength to do both things.
d) Since getting my iPhone 6 I have been unable to lift it. Now (as of the past month) I am able to lift it.
6. With the results that I have seen, I would be very reluctant to stop taking the supplement.
In closing, I wish that I would have known about this supplement back in 2009 when my symptoms first started. I feel that I might not even be in a wheel chair right now, had I known. If you haven’t kept up with my trial, go to my YouTube channel to see all my previous videos: https://www.youtube.com/channel/UCfawMSJWTpKxJJGE2cv973g
I started this trial because there was no other HOPE. Since starting the trial, I can honestly say I look forward to each new day. I’m looking forward to my birthday and Christmas, and being here for my wife and kids.
There are many superfoods available, if you would like more information on my particular trial, please Facebook message me. If you would like to start your own trial, we will provide you with all the information that you need to get started. Anyone that chooses to participate in their own trial will do so of their own volition and risk. Remember this is not a drug, it is nutrition that is thought to help the body heal itself. I am happy to share because I want to see all PALs healed. Stay strong, a cure is near!
https://www.youtube.com/channel/UCfawMSJWTpKxJJGE2cv973g
#als #supplements #trial#DandyOskey 

Please Help Raise Awareness of ALS

Will anyone help now that the ALS "Ice Bucket Challenges" are in the past?

Tuesday, April 28, 2015

Raising Awareness to find a cure for ALS, or the lesser known FALS...

Hihi, my name is Angela. I have what's known as FALS (Familial ALS). Most people have never hear of it. Plus, a high school friend, former NFL player Tim Shaw has regular (not that regular means better) ALS.
We're trying to raise money for the cause. Last summer a lot of money was raised, but a cure is still far off.

I'm raising money for WALK & ROLL FOR ALS TEAM MMM-SHAW... We walk to raise funds for a cure... Here's a past walk:

**ClickHereToDonate

 Only approximately 5% of people are cursed with FALS-the KNOWING, WONDERING..who'll get it next?.. When? So far we lost my great granddad & my grandma. Had I known beforehand, I may have decided to not have children lest they be stricken with this INCURABLE ATROCITY, or sort that I will..

Everyone remembers last year & all the 'Ice Bucket Challenges' but those 'fun' fundraisers have come to an end. Yet, ALS hasn't. ALS 1st touched my life in 2001 when my best friend in the world-my grandma-was diagnosed. 92-95% of ALS cases basically just happen. No rhyme or reason. That other 5%? That's the % my family belongs to. We carry familial ALS, with no way of knowing if I will get it, my mom, my Uncle, Brother, Daughter..So it's scary.

What we're looking for us simple: a TINY amount of help. Help us find a cure: Everyone 'knows' cancer-when someone wears pink, people KNOW WHY-there's literally a billion dollar industry just in pink cancer flair products & advertising, along with the what? $3300 you have to raise JUST FOR THE STATUS OF A Susan Colman WALKER!!! We do it out of LOVE.
 Lou Gehrig's Disease (ALS) isn't like that. Not a bit. For instance, if I were to wear turquoise for ALS? No one would know why! But we still struggle with it & walk..& walk..& do our best to raise the little money we can.
The ICE BUCKET CHALLENGE of last summer REALLY HELPED, but that's all over now & people are still dying. My school friend Tim? Had to retire from the NFL-due to ALS. He didn't know that's what it was then, but it didn't take long..long

**We're all walking for someone. My Team Triple MMM? My grandmother: For (M)arjorie (M)arie (M)cDonald...I hope you never have to walk for anyone.

Beginning with this year's walk, (Which I'm looking forward to several more walking with our team this year, the more walkers, the more donations, the closer the cute! So I pray daily that I have a larger than life team!) is now.....
              **Team Triple MMM-Shaw**

**ClickHereToDonate

**It has changed for the beloved Clarenceville High School & Penn State Alumni, former Carolina Panther, Chicago Bear, & most recently, Tennessee Titan. He also is a very religious man who did absolutely AMAZING

missionary work, even AFTER diagnosis, he simply did what came natural to him-helping others!!

My grandmother was diagnosed at 79, Tim at 29. ALS as I'll explain below, doesn't discriminate...

Last year, when I found out Tim had contracted ALS, I knew we'd do things a little differently. This year, I would like to walk & raise money not only in my grandma's honor, but his as well.

ALS is similar to Cancer in some ways: it doesn't discriminate-gender, age, race, class, fitness, health, wealth, it has no preference, but UNLIKE Cancer, it doesn't matter WHEN you catch it.

(Side Note: There IS 1-yes, ONE, INCREDIBLY EXPENSIVE medication you can take [They even got the name correct on the bottle Lucious Lyon held on the show 'Empire'] It's called Rilutek (Riluzole). Honestly?? IDK how much it is now, I heard they've FINALLY made a generic, but still...We paid $957 PER MONTH for this medication running up credit cards, selling my grandmother's belonged vacation home... but we'd have done anything, & I mean ANYTHING. PROBLEM IS, it has HORRIFYING side effects, & WORST OF ALL???
It gives the average user an extended 3-6 mo. MONTHS. Let THAT sink in!!

**There are close to 1,000 pALS (people with ALS) in Michigan battling ALS everyday, and another 200 are diagnosed every year.

**ALS of Michigan provides critically needed, community based services to Michigan pALS and their families. From respite care to speech services to equipment loans to support groups, seminars, and workshops, we are there every step of the way to make living with ALS a little bit easier.

But, we need your help!

**I HAD to walk for someone, HAVE to.  Scratch that. I CHOOSE to walk for someone. Someone I loved dearly. Please PLEASE won't you help & donate?
**Every cent is a chance to make it so that NO ONE ever has to walk in someone's memory again! If it were ME reading another's plight, it wouldn't even be a matter of question, even if I could only afford $5!

**You know you can! Do it to feel good, do it for me, my grandmother, or another pALS angel. Or do it for Tim, for his team, or the NFL. Do it for Stephen Hawking, do it for the thousands of unknown victims who feel they have no hope because their disease just isn't "POPULAR ENOUGH" Do it because you beat cancer, or know someone who didn't.
Do it for a tax break, do it to pay it forward, to feel happy, helpful or accomplished, do it to warm your soul...
Whatever your reason, I DO know ONE THING & I ABSOLUTELY PROMISE: **There is not a SINGLE REASON NOT TO!!

**We ALL walk for someone..see:

**I pray with all my heart and soul that NO ONE who reads this will EVER have to walk for anyone, but the more we can raise, the less likely our future generations will have to...

**ClickHereToDonate

If you've gotten this far, i wasn't too thank you.
 **Thank You, from the impossible depths of my soul, Team Triple MMM-Shaw team leader, & unfortunate carrier of the FALS gene, Angela Galvin (amgalvin3@gmailDOTcom... Hopefully, with enough donations for the suprising amount of diligent doctors and scientists, one day the daily worry that one of my daughters will contact ALS will slip easily and happily from my mind...

**Please support our walk team so we can continue to provide the services that our pALS community has come to depend on. REMEMBER-there may not be an I in 'team' but there also isn't a 'cure' without U!

About Me

Angela Galvin

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#AngelaGalvin #ALS #support #awareness #fundraising #donate #MMMShaw #FALS