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Junior Member
Posted
This is my first time on. The neurologist has diagnosed my husband, age 43, with dementia, probably frontal lobe dementia. My husband has had all the tests - mri, bloodwork, lumbar puncture, etc. They tried him on an anti-depressant for six weeks which only made him worse. My husband and I are convinced he's not depressed. The neurologist sent us to a memory disorders clinic at a respected university. The dr. there said he wasn't ready to concur with the neurologist here bcs. he said he needs more information. But yet he didn't really get our whole story. I'm starting to see how frustrating all this can be - to get a diagnosis. Now my husband will get neuropsych testing. I don't know how helpful that will be, but we are jumping through the hoops.

My questions are - has anyone heard of someone getting eoa at the age of 43? Most people posting seem to have loved ones who are at least in there late 40s when diagnosed.

My husband does have both memory and personality changes, but he is responding well to razadyne. It seems like he could have either ad or fld. Does the fact that he is so young make it more likely that he has fld? Also, he has no relatives that had/have eoa. Does that mean that more likely he has fld than eoa?

I am thankful for any information......
 
Posts: 2 | Registered: February 19, 2006Reply With QuoteEdit or Delete MessageReport This Post
Senior Member
Picture of angel0704
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Question: I may be wrong so anyone jump in and correct me. I thought that there is no "real" test for AD....just the symptoms and the real diagnosis cant be made until the person dies and an autopsy is done.? How do they know a person has AD??? I know it may sound like i'm just stressing but since my granny has it and her aunt had it and i seem to be losing my mind sometimes i wonder if i have EOAD?? When/if i ever get insurance again I want themt to test me immediately!


"Procrastinate now!! Don't put it off!---- Ellen Degeneres
 
Posts: 584 | Location: winter haven | Registered: January 15, 2006Reply With QuoteEdit or Delete MessageReport This Post
Junior Member
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Hi Janie,
My name is Tracy and I was diagnosed at the age of 38 in 2002 with EOAD. I am now 41 and my neurologist is now pointing towards FTD I think. Ihave done well on Namenda and Exelon. I wrote a book that chronicles our journey to getting adiagnosis at a young age and how it affects the family. It is called Young Hope. I would like to invite you to my support group as well: www.health.groups.yahoo.com/group/dementiarescue

I hope that knowing you are not alone helps. Feel free to join us!

Tracy


Tracy
Author Young Hope & I Remember When
 
Posts: 3 | Location: Midwest | Registered: September 25, 2005Reply With QuoteEdit or Delete MessageReport This Post
<May>
Posted
I read an article that the youngest to be diagnosed was 23.
 
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Senior Member
Picture of SnowyLynne
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I was dx with AD at age 57.


Lynne
 
Posts: 713 | Location: Iowa Park,Tx | Registered: March 08, 2003Reply With QuoteEdit or Delete MessageReport This Post
Senior Member
Picture of Kittycat
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Welcome to the board....I am a newbie myself.

My Mom was diagnosed at 55, although she exhibited signs several years before then. Yes, it's definitely possible that, even at that young age, it could be EOAD. I have someone in my Yahoo support group, and he is 31 and just diagnosed. Breaks my heart!

Again, welcome!


Cat

Early-Onset_Alzheimers_Caregivers_Group-subscribe@yahoogroups.com

Visit my website: www.geocities.com/kittycat13132004

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Proud member of Alzheimer's Art Quilt Initiative - www.AlzQuilts.org
 
Posts: 199 | Location: Kansas City | Registered: February 06, 2006Reply With QuoteEdit or Delete MessageReport This Post
Senior Member
Picture of Janie
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Birdie, how's it going? Any further testing yet for your husband? I hope the two of you are doing ok. Please let us know when you can. Smile


~ Janie ~

 
Posts: 5199 | Location: NC - USA | Registered: September 14, 2000Reply With QuoteEdit or Delete MessageReport This Post
Senior Member
Picture of Janie
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quote:
Originally posted by birdie:
Thank you guys for your words. Janie, I would love to know of the websites you mention re EOAD for someone as young as my husband. Thank you so much for your kind words.


Hey again, Birdie! I searched on this very site and found quite a remarkable amount of posts. We "used" to have an extremely active group of EOAD caregivers. If you click on the link below, and follow down and read through all the topics, you'll see so many of the postings from spouses who were cg's to their affected loved ones.

http://eldercare.infopop.cc/eve/forums/a/frm/f/8306025151

(This, actually, is where YOU posted your topic as well, so you "may" have already read them.) If so, I apoloize. Just scroll on down; there are three pages of posts.

I'll look again for some more of those sites I mentioned.


~ Janie ~

 
Posts: 5199 | Location: NC - USA | Registered: September 14, 2000Reply With QuoteEdit or Delete MessageReport This Post
Experienced Member
Picture of path2others
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Hi birdie, About 5 years ago my wife was dx as dementia most likely EOAD. She was 51 but started having problems years before I got her to see a doctor. While it is important to get the best diagnosis so your husband is getting the proper treatment - it takes a lot of time. My wife's diagnosis has changed several times. Your doctor has done you a favor by sending him to the specialist. In our case my wife had some medical problems which lead us to the Cleveland Clinic. We found out she has a form of Lupus causing her blood to be too thick. She had many small strokes which caused her dementia. I guess all I am trying to say is that you are on the right track. People don't always fit the "slots" that the doctors try to place them in. I am beginning to think there is no 100% diagnosis of EOAD except in hindsight. Try to hang in there - a lot of adjustments will have to be made but there is still a life after your LO is diagnosis with this disease.
Don
 
Posts: 54 | Location: Cleveland, Ohio | Registered: January 09, 2005Reply With QuoteEdit or Delete MessageReport This Post
Junior Member
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Thank you guys for your words. Janie, I would love to know of the websites you mention re EOAD for someone as young as my husband. Thank you so much for your kind words.
 
Posts: 2 | Registered: February 19, 2006Reply With QuoteEdit or Delete MessageReport This Post
Senior Member
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Birdie, hi and welcome to the forum. Actually, just a few days ago I was doing some research on EOAD. I found a LOT of sites and one of them was being run by a young woman who was diagnosed at the age of 30! Very, very sad.

Gwen, it is wonderful to see you posting again. I think you made a valid point when you said your husband had been injured and THAT is what started the onset. I had no idea of all the trials the two of you have been faced with. My sympathies, Gwen.

Thank you very much for posting. That is what makes this family so wonderful. We all support one another.


~ Janie ~

 
Posts: 5199 | Location: NC - USA | Registered: September 14, 2000Reply With QuoteEdit or Delete MessageReport This Post
<gwen>
Posted
Dear Lynne, There is a strong possibility that he does have eoad; has he had a truma to his head ie car accident? My husband was diagnosised with complex siezure disorder and that caused his brain cell to die when he was in a siezure. Then he was diagnosised with vascular dementia. The beginning is so very hard and I developed a support system right away including the doctors, lawyers, my church, and friends. However, he is only 57 and we have been into this for 2 years now. He had to retire from the school system after 27 years and he was a principal of an elementary school. He also has 3 college degrees and 12 hours away from his doctorate when this happened. Now it's like living with a teenager. Lossing the ability to drive and work is very hard on him and I have had to retire also as a social worker. I can pick up contract work to supplement our income. Everything is a shock for a long time and still it amazes me how "friends" do not like to deal with you because they do not know what to do or say. So they don't. It took us 2 years to find the right doctor to do testing after we went to the Mayo clinic in Rochester, Mn. My husband was on too many medications and he slept most of the time. We also have a 17 year old Downs daughter; so the responsibility can be very heavy at times. I wish you well in your endeavors to find out what is wrong and how to fix it.
 
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<gwen>
Posted
quote:
Originally posted by birdie:
This is my first time on. The neurologist has diagnosed my husband, age 43, with dementia, probably frontal lobe dementia. My husband has had all the tests - mri, bloodwork, lumbar puncture, etc. They tried him on an anti-depressant for six weeks which only made him worse. My husband and I are convinced he's not depressed. The neurologist sent us to a memory disorders clinic at a respected university. The dr. there said he wasn't ready to concur with the neurologist here bcs. he said he needs more information. But yet he didn't really get our whole story. I'm starting to see how frustrating all this can be - to get a diagnosis. Now my husband will get neuropsych testing. I don't know how helpful that will be, but we are jumping through the hoops.

My questions are - has anyone heard of someone getting eoa at the age of 43? Most people posting seem to have loved ones who are at least in there late 40s when diagnosed.

My husband does have both memory and personality changes, but he is responding well to razadyne. It seems like he could have either ad or fld. Does the fact that he is so young make it more likely that he has fld? Also, he has no relatives that had/have eoa. Does that mean that more likely he has fld than eoa?

I am thankful for any information......
 
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Senior Member
Picture of SnowyLynne
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EOAD happens below the age of 65 to anyone.


Lynne
 
Posts: 713 | Location: Iowa Park,Tx | Registered: March 08, 2003Reply With QuoteEdit or Delete MessageReport This Post
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