Saturday, July 17, 2010

Donations for ALS- also known as Lou Gehrig's disease

Hello everyone out there in blogger world. I know I have been MIA for a very long time but I wanted to try to get this out there. Two weeks ago we had a death in the family. My brothers wife's father died of ALS. I know when I first heard of this I wasn't exactly sure what this disease was. Persons with ALS have a loss of muscle strength and coordination that eventually gets worse. This eventually makes one unable to do routine tasks such as going up steps, getting out of a chair, or swallowing. In ALS, nerve cells (neurons) waste away or die, and can no longer send messages to muscles. This eventually leads to muscle weakening, twitching, and an inability to move the arms, legs, and body. The condition slowly gets worse. When the muscles in the chest area stop working, it becomes hard or impossible to breathe on one's own. ALS affects approximately 1 out of every 100,000 people.
There is no known cure for ALS. The first drug treatment for the disease is a medicine called riluzole. Riluzole may prolong life, but does not reverse or stop the disease from getting worse. This is a horrible way to live and slowly die from. That is why I am asking for donations to help the ALS Association Greater Philadelphia Chapter. Anyone in the East Coast area can also participate in their 2010 Ocean City Board... Walk to Defeat ALS. Any donations will be grealy appreciated. As little as $5 makes a difference. Here is the link to donate or Sponsor a walker. Thanks!


  1. I'm so sorry for your loss!!!

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  3. sorry to hear about the death in your family. hope everyone is starting to feel better. ALS is so hard on its victims and their families.

  4. It seems to take a loss for us to realize when something needs more attention. Thank you for sharing this info about ALS and extend my sympathies to your family.

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  6. sorry to hear about the death in your family. hope everyone is starting to feel better.

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  8. oh...i'm so sorry. Sending prayers your way.

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  14. As a sign of gratitude for how my husband was saved from the dreaded ALS, i decided to reach out to those still suffering from this.
    My husband was diagnosed of ALS in 2013 and it was really tough and heartbreaking for me because he was my all and the symptoms were terrible, he had difficulty swallowing, all his joints were dead and that made him immobile to mention but a few. we tried various therapies prescribed by our neurologist but none could cure him. I searched for a cure and i saw a testimony by someone who was cured and he left the contact of the doctor who had the cure in 2015. I never imagined ALS has a cure not until i contacted him and he assured me my husband will be fine. I got the herbal medication he recommended and my husband used it and in three months he was fully okay even up till this moment he is so full of life. ALS has a cure and it is a herbal cure contact the doctor for more info on on how to get the medication. Thanks for reading my story.

  15. I have been following this blog for a while now and i decided to share my story on how i survived and got a cure from ALS which would have maybe by now killed me. I was diagnosed with ALS in 2013 and it came with symptoms like overall weakness and i could not swallow and i ended up in a wheelchair though my doctor tried to put me on occupational therapy and physiotherapy but none seemed to give a relief as my condition grew worse in 6 months. I was lucky to have contacted Dr. Joseph and used his herbal medicine that treated me and gave me life, just 3 months of using the medicine which spans for 6 months positive improvements were visible, like my speech, all movements. A few years have gone by and i am still very much alive and healthy. Do not give up, you too can get a cure you can contact him directly on the contact below (josephalberteo @ gmail. com) for advise and effective solution. I pray you get cured soon.