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The journey begins.
My name is Abe. I just read your post. I dont have MS. I am a diabetic though.
We are working on a project to fund medical researchers directly. Cutting out the middleman, therefore cutting out waste and corruption.
If any of you are willing, I would appreciate it if you could make a short video stating why being sick sucks, and why its so important that we fund and work on a cure. Why waiting one more day is too much. Why management isn’t enough.
You can do it on your webcam or your phone. Then email it to our youtube address :
We will be featuring your video on the CUREALL website to be launched at the end of the month.
This video explains my project. I am happy to answer any questions.
My dad first presented symptoms on Feb. 10, 2014, and we thought at the beginning he had a sleeping disorder. He was tired all the time and acted confused while doing everyday tasks. Two weeks later he lost coordination on the left side of his body, which is when we found the glioblastoma. The next day, he had a seizure, and he passed away Feb. 28. The whole thing lasted only a few weeks, and he was only 56 and healthy, enjoying life. Thanks for creating this group.
We will keep her and your family in our prayers. Keep us posted. Add her to one of our albums if you would like to also. Hang in there.
Hi all, I am here for my SIL. Dx Jan '11 after seizure. Resection within four days, then tx 6wks later. Another resection in Oct '11 not bad until about Feb '12. Then the downhill slide begun. Now bedridden, not eating, drinking or using bowels. Just hoping and praying now
You are very welcome. Thank you for joining!
Thank you for creating this site!