Look at artwork, find and connect with a group, get connected to podcasts, and more. Also the main thing is find and become part of a dementia family💜💜💜
No longer able to live the life I had, due to Lewy Body Dementia. I now do artwork and raise awareness with others of my Lewy Family
Helping raise awareness for Lewy Body Dementia patients and their carers.
Also offer a list of group sites, that are very beneficial to people, whose lives have been touched by dementia.
There are only benefits of joining a support group, and zoom meetings when dealing with dementia. You do not need to be diagnosed to join many of these wonderful support groups.
Thank you 💜💜💜
Artwork done by myself and recommendation of groups, other sites I belong to. Also YouTube, TikTok and other informative sites of others raising awareness in the area of dementias.
Thank you💜💜💜
Artwork to help raise awareness of Lewy Body Dementia💜💜💜
Art is wonderful therapy for everyone
Curry Whisenthunt a warrior living with Lewy Body Dementia, and a magnificent advocate of Lewy Body Dementia, shares his journey and knowledge of this not so well known disease. He is very open about every aspect of living with LBD and the symptoms he has experienced. He manages two extremely wonderful FaceBook support groups for Lewy Body Dementia. (1) Our Journey With Lewy Body Dementia which he and his very beautiful supportive wife Linda manage together https://www.Facebook.com/groups/1782340522035405/?ref=share
And (2)Lewy Body Roller Coaster Podcast Group, which he and a very caring and loving women,Linda Ashcom Szypula, whose husband is living with Lewy Body Dementia manage this group. https://www.facebook.com/groups/4916902618334775/?ref=share
Curry is also co-host of Lewy Body Roller Coaster with Host Linda Ashcom Szypula- a podcast for Lewy Body Dementia patients and their families, presented by Lewy Body Dementia Patients and their families.
https://lewybodyrollercoasterpodcast.buzzsprout.com/
Curry is a very inspiring person, who truly cares about his Lewy Family he has created and wholeheartedly conveys, that with early diagnosis, proper treatment and meds, there is still plenty of life to live with this disease, you just have to live it differently. It is not an easy task, but he has taught me and many others it is possible. A major tool in making this happen is joining a support group like ours, where you are with people dealing with the same illness. Each person’s symptoms with Lewy vary greatly, some may have had symptoms that other have not and may never get, but when you speak of your symptoms you are never doubted or judged. Every Lewy family member listens very intently, cause we never know when or if that symptom is going to happen to us.
The carers in our group are so understanding, patient and open minded. They teach us many things and they also get to learn from us that what their loved one does or says , may be something that we also may do. Also a major benefit for carers or patients with Lewy, is joint in on our zoom meetings. The wonderful thing of the zoom meetings is, there is no pressure for you to talk if you do not want to. You may just come and listen, you do not need to have your camera on if you wish not to. Just for you to be there and listen is extremely beneficial. I can guarantee, if you attend our zoom meetings, you most likely will end up participating. Cause everyone is treated like family sitting around the dinner table and just talking about everything. Curry’s groups have 5 zoom meetings a week.
Monday and Friday is for everyone 10:30am central time. Thursday is for those living with Lewy/Parkinson’s or seeking a diagnosis 3:30pm central time
Saturday Only for spouses 10:30central time
Saturday Cargivers only (sons,daughters,etc.) 6:00pm central time.
Curry and the entire Lewy Family welcome y’all to join us on this journey that truly needs to be traveled with the support of others living with this disease.
Thank you 💜💜💜
Dementiafied Christian
Baylen Dupree TikTok about living with Tourettes
A Brother that is a wonderful, live acoustic guitar
New owners Nick Hoffman and wife Melissa Long-Hoffman are the best. Come and visit for Great Food, Drinks and Entertainment. The cooks are awesome and the servers and bar staff are second to none. And all are my Friends and Family 🤗🤗🤗💜💜💜
Former owners Jack and Anita were wonderful owners. Jack has recently lost his loving wife Anita to Dementia. Please come out and have a Drink with Jack when he is there. He loves shots of Windsor☺️☺️☺️ Love ya Brother 💜💜💜
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