Still JUMPING FOR JOY despite everything.... - Cure Parkinson's

Cure Parkinson's

25,550 members26,870 posts

Still JUMPING FOR JOY despite everything. Who else has a family history like mine?

JerriB profile image
4 Replies

My story is this; I have Parkinson's and I am the 5th person on my paternal side to have this disease. We have a familial gene of ALS on my maternal side. My mother, who passsed away in 2009 was the 5th person to have ALS, and the 6th person my only sibling, my sister just passed away from ALS in December of 2011.

It all seems like a nightmare, but this is reality our family. You know growing up as children, even in our early adulthood no one thought about our DNA, or our Genes, or the Markers that we are made up of. But we found out all to soon. I have lost my job due to my symptoms, my loss of energy, and my mental mistakes.

At this time I can no longer work due to early signs of dementia and so I have been researching products for quite some time to help with many aspects of our illness, and other illnesses like ALS and MS. I have had what I consider success which I have shared on other blogs. I am confident that in time you will see more and more things being introduced to help us combat this fight!

Thanks again for reading my blog.

JerriB

Written by
JerriB profile image
JerriB
To view profiles and participate in discussions please or .
Read more about...
4 Replies
Carrigan profile image
Carrigan

Thankyou for sharing your story with us which is very informative, you are an inspiration. Good luck and keep up your great spirit and inspiration to all who suffer from any neurological disease

NanCyclist profile image
NanCyclist

JerriB, While your story is extreme to say the least, you are not alone. My Dad died from ALS and my brother will likely die in the next few weeks, also from ALS and of course, I have PD. There is a great deal of research going on with families with multiple neurodegenerative diseases such as ALS, AD and PD. The Siddique lab at Northwestern University has a data bank of family samples, including ours. If you're interested in participating in the research, contact them, or leave a note here and I'll see that you can reach them.

I have been able to control my PD through forced pace cycling. See pedalingforparkinsons.org for more information.

JerriB profile image
JerriB in reply to NanCyclist

NancyCyclist, Thank you so much for sharing with me. Most people can not say "know what you are going through", however believe we can say that. I would love to know about the Siddique Lab and Northwestern University. I am all for anything that can help all of us who suffer from these diseases. Also, I will check out the pedalingforparkinsons, I think that will help me tremendously!

Again Thank you so much for your information. You are the first person I have found to have a the same story. Please lets keep in touch and I will keep you in my thoughts and prayers.

If you want you can messege me on here.

JerriB

NanCyclist profile image
NanCyclist

JerriB, You can reach Nailah Siddique at Nailah A Siddique <nsiddique@northwestern.edu>. She is fantastic at working with families and I'm positive she will be very interested in your story. Another world leader in familial ALS research is Dr. Eva Feldman at the University of Michigan, Eva Feldman <efeldman@med.umich.edu>. She will also be all over your story. Here is a highly recommended website for ALS: als.net/. If you send your email address, I'll forward two articles on forced pace cycling published by Dr. Jay Alberts at the Cleveland Clinic. I don't know how to attach them to this site.

You may also like...

I tried everything else...I would like to know your feelings about that one :

FB: WaterTribeTrader: Diagnosed 5 years ago, I have undergone 11 fasts of 5 to 10 days over the...

Interesting Gender Research Findings RE: Levodopa Absorption Rates

Flanagan. https://www.womensparkinsonsproject.com/our-team A recent study by Contin et al...

The 2nd FUS PTT procedure and me.

which made the whole trip too long -- to be away from our dog, Margaret, with 16 days in Solothurn...

What improvements can we anticipate within 10-15 years?

will hopefully have found at least one successful repurposed drug that helps slow our decline....

Ahlskog explains Dyskinesia

the disease our neurons are able to ‘suck’ excess Levadopa back up. So when we flood our brains,...