Go Back   NeuroTalk Support Groups > Health Conditions M - Z > Parkinson's Disease

Parkinson's Disease Tulip

New here --FIL w/PD and dementia?

Reply
Thread Tools Display Modes
Unread 02-12-2013, 12:46 AM   #1
anninva
New Member
 
Join Date: Feb 2013
Posts: 1
Confused New here --FIL w/PD and dementia?

Hi, hope it's okay to be here even though I'm not a person with PD. I'm not exactly a caregiver either, so not sure where I belong but I need help!

My FIL is 87, dx 10+ yrs ago. He's been home all this time with my MIL with no home help except two days of day program - thank goodness for both of them. He has been struggling with communication for a long time now, but has always been "in there", eats like a horse, relatively slow progression all things considered. Two weeks ago my partner and her sibs (they live west coast, we live 3hrs away mid-Atlantic) were home for his bday. He talked about being worn out, discouraged, depressed, and suicidal. Totally understandable to me! The he started paranoid delisional statements. By last Sunday my MIL called and told my partner: come now. She never asks for help. Long story long (sorry) he has been in hosp since last Mon, more delusions, paranoia, personality changes, etc. I need help understanding what is going in and if it means that he is going to die soon. Sorry. It's just my biggest fear. Very sad and scary. Why would it just start?

Thank you for your patience in reading this far and any help! This seems like a very loving place. Thanks! Ann
anninva is offline   Reply With Quote
Unread 02-12-2013, 01:49 AM   #2
Jo*mar
Co-Administrator
Community Support Team
 
Jo*mar's Avatar
 
Join Date: Aug 2006
Location: Pacific NW USA
Posts: 19,873
My Mood:
Default

I suppose they are checking all his medications while he is in the hospital, maybe something needs to be changed or dropped or possibly added...

His quick change in attitude/emotions would be very worrisome I'm sure.
__________________
Check the Helpful sticky threads near the top of every forum.
site FAQ's
.

Use the search tool to find information posted in other NT threads & posts
Search link -
.

NT Guidelines
.



.


.
Jo*mar is offline   Reply With Quote
Unread 02-12-2013, 07:57 AM   #3
Bob Dawson
Senior Member
 
Join Date: Dec 2008
Posts: 1,132
Default

Anninva,

I cannot answer your questions because I do not know the answers. I am taking 4 drugs and every one of them warns of hallucinations as a side effect, in addition to the disease itself. It is such a chemical soup I don't know what causes what. I know that the elderly with dementia can slip deeply into an unreal world.

It is a frightening thing to face. One way to make it less frightening is to see it. Dr. Sacks is not talking about near-death hallucinations; he is talking about people who live with hallucinations in their every day life. This does not help in dealing with the disease, but I find it helps in humanizing it, to reduce the fear of it.
Dr. Sacks latest:
http://www.oliversacks.com/books/hallucinations/
Bob Dawson is offline   Reply With Quote
Unread 02-12-2013, 10:00 AM   #4
Bob Dawson
Senior Member
 
Join Date: Dec 2008
Posts: 1,132
Default Dr Sacks on YouTube, re: hallucinations

Again, this is not an answer, but it is a humanization that allows us to see what is being said these days about hallucinations:

http://youtu.be/SgOTaXhbqPQ
Bob Dawson is offline   Reply With Quote
Unread 02-12-2013, 10:42 AM   #5
Debi Brooks
Member
 
Join Date: Feb 2009
Posts: 283
Default Insist on seeing a movement disorders specialist

I'm not sure where your FIL is being treated but there are many hospital settings where a patient would be treated by a general neurologist. In some cases, especially when complications from disease or medications arise, the neurologists are not as familiar with the nuances. Please ask the doctors if there are "movement disorder specialists" ... if not, ask them to please reach out to a specialist for consultation in his treatment.

These situations are tricky but it is critical to be proactive.

Best, Debi
Debi Brooks is offline   Reply With Quote
"Thanks for this!" says:
Brain patch (02-15-2013), Thelma (02-12-2013)
Unread 02-15-2013, 04:30 PM   #6
aj04
Junior Member
 
Join Date: Aug 2006
Posts: 49
Default

Quote:
Originally Posted by anninva View Post
Why would it just start?

This is the million dollar question. Unfortunately, there is no million dollar answer. Everyone's PD manifests itself differently and the drugs that we take affect each one differently. And it all can change seemingly for no reason at all. But, advanced age plus length of disease may increase the risk for dementia.

I hear the frustration of your simple question. Believe me, after 18 years of this disease, I ask it myself along with its corollary: Why would "it" just stop?. But, my better angel reminds me that we have come as far as we have in our understanding and knowledge of PD because we continue to ask these seemingly simple questions in the face of our personal struggles. Thank you and I wish the best for your family.

(And my better editorial angel makes me realize that I turned this answer to your post into my own soliloquy on my own simple questions. I am sorry. This is not a simple thing that you are dealing with, not at all. I do not have an answer for you except to say that it sounds like your FIL is a fortunate man to have such a caring family.)

Last edited by aj04; 02-15-2013 at 04:57 PM.
aj04 is offline   Reply With Quote
"Thanks for this!" says:
Bob Dawson (02-15-2013), Brain patch (02-15-2013)
Unread 02-15-2013, 07:57 PM   #7
Brain patch
Member
 
Brain patch's Avatar
 
Join Date: Feb 2013
Location: Salt Lake City, Utah
Posts: 516
My Mood:
Default Love and prayers are with you

My father has Parkinson's with dementia. He has had some days where he had total delusions and then the next day he was ok again. This disease has a lot of good and bad days. I don't have the answer to your question either but just wanted to tell you I will pray for your family. Make sure you call the neurologist/movement disorder specialist That has been treating him to come to the hospital. We just got a bunch of literature from the parkinsons foundation and they say this is crucial as the hospital doctors are not specialized in this area and could make things worse or ruin progress with medication that took months/years to achieve. God bless. Love to you.
__________________
Brain patch.
.


Had MVA in 2006 resulting in post concussive syndrome manifested by cognitive impairment, chronic pain/ fatigue. Chronic pain of head, neck, back, left leg.
Other problems include REM sleep behavior disorder, nocturnal frontal lobe epilepsy, chronic migraines associated with nausea/vertigo, episodes of passing out, hypoglycemia, liver dysfunction (had accidental overdose of acetaminophen in 2009) had liver and kidney failure, hernia, degenerative disc disease with compression of nerve root, PTSD, and other problems associated with functioning problems from traumatic brain injury (light, sound sensitive, easily overloaded, easily distracted, cannot focus, anxiety problems etc.)
Brain patch is offline   Reply With Quote
Reply

Thread Tools
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
Dementia Care In Hospitals: Findings From National Audit Of Dementia Interim Report, NewsBot Health News Headlines 0 12-27-2010 11:20 AM
Your Dementia Risk Rises if Spouse Has Dementia NewsBot Health News Headlines 0 05-06-2010 02:00 PM
What is Dementia? imark3000 Parkinson's Disease 1 10-14-2009 06:37 PM
What is Dementia? What Causes Dementia? Symptoms of Dementia (Topix) NewsBot Health News Headlines 0 03-13-2009 07:30 PM
dementia.. and PD yiannakas Parkinson's Disease 0 05-29-2008 01:20 AM


All times are GMT -5. The time now is 10:46 PM.
Brought to you by the fine folks who publish mental health and psychology information at Psych Central Mental Health Forums

The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider. Always consult your doctor before trying anything you read here.


Powered by vBulletin • Copyright ©2000 - 2014, Jelsoft Enterprises Ltd.


All posts copyright their original authors Community Guidelines Terms of Use Privacy Policy
NeuroTalk Archives