Post-Traumatic Stress Disorder (PTSD) Support Group
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Husband has Vascular Dementia

We finally got a diagnosis a few weeks ago, after months and months of tests. My husband has dementia. I haven't been here at DS much. I have been really depressed trying to cope and finish up an online class. He is so different from the person I knew. I have to watch him because he forgets what he is doing. He has flooded the kitchen twice leaving the faucet running, gotten lost at our movie theatre, and his coordination is really bad.
i don't like to be touched much and he constantly has a hand touching me which is very triggering. I think it must be a security thing. I know he must be really scared. I can't sleep until he rolls over and stops touching my back. I have tried to explain my PTSD symptoms to him, but because his short term memory is gone, he dosent remember an hour or so later. I am really scared. My anxiety and depression are at an all time high. My husband does not have any family that is close by so his care is totally up to me. My Pdoc is really concerned and has increased my meds again. I feel very sedated right now. I could use some support and ideas on how to help my husband.
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Has anyone here diagnosed with ME/CFS been prescribed Repatha?If you tried it, did you have any reactions that 'normal' doctors didn't consider? Or, pain more severe, fatigue increased.I had a very bad reaction to statins decades ago so I've snarled at any doctor in regard to my cholesterol levels. My new doctor is more patient and homeo/holistic minded, but she's still pushing.I have an Rx for a...
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I have 3 kids. 24. 17. 15. My 17 yr old has become super defiant. He and his 15 yr old sister have on their own decision stopped going to their dads because he and his household is so toxic.My 15 yr old and myself feel like we have to tip toe around my son who is 17. And physically towers over us and out weighs us. He has become emotionally abusive and on the verge of becoming physically...

First, all the comments have had excellent suggestions. From music therapy, to "loving lies" (meeting them where they are at, not trying to correct them, redirecting them instead).
When you see the neurologist, is it at a hospital office? Whatever the case, check with your insurance and see if Palliative Care is included. Palliative begins at time of diagnosis and is NOT the same as hospice. Palliative provides a support service team as the diagnosis progresses. If the neuro's office is in a hospital setting, the hospital may have social/caseworkers who can help.
Also check with the disability lawyer and see if their office has a case or social worker who can direct you to any programs that might be available.
Your county or state Department of Aging may also be able to help.
Tam Cummings and Teepa Snow have videos online about how to handle dementia. Tam Cummings' book, UNTANGLING ALZHEIMER'S is excellent, and the information can be applied or adapted to most forms of dementia.
In our area a company called "Visiting Angels" has a program called "Angel Visits". They are short visits to help with some of the ADLs, and last I heard a contract didn't need signed. (That may have changed with COVID.)
I hope this helps. Everyone is correct, this should not be handled by one person. And you have enough to shoulder.
Your support and suggestions have really helped me so much. Thank you all!
Sending some more support your way. Remember self-care, it will help.
Peace and blessings.
How are you doing?
Sending you lots of support & many prayers
Gentlest of hugs <3