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Out of state “friends” hardly there and know everything

NMF
NMF Member Posts: 9
25 Care Reactions First Comment
Member

I am so exhausted as most here are. I need a moment to vent some frustrations. Why is it family and friends from out of state feel the need to input opinions after little to no contact except maybe a 15 minute phone conversation every 4-6 months. One has little to no knowledge of disease progression let alone what has occurred in detail for the past year and a half yet is all knowing after only 15 minutes.
here we are as caregivers spending hours dedicating time to audiobooks, online support groups, dr appointments, adjusting to altering moods from minute to hour or from day to day… being loved one minute and hated the next… endless hours spent sobbing in silence AND one person seems to want to give advice from a 15 minute phone conversation when residing in another state? It is so difficult not to want to welcome the individual into the daily happenings from day one to now and one should really reconsider such responses or do some research and act a little more concerned than a 15 minute phone conversation once in a great while.

Comments

  • Biggles
    Biggles Member Posts: 756
    1,000 Care Reactions 500 Likes 500 Comments 100 Insightfuls Reactions
    Member

    Oh yes all so knowing and knowledgeable full of what you should do, how you should do it. It does my head in and takes all of my energy to keep my south shut. I agree with Lilydaisy these people were perhaps important to your other life but are now no longer relevant. Move on and find those that really do care and understand.

  • H1235
    H1235 Member Posts: 1,786
    500 Insightfuls Reactions 500 Likes 1000 Comments 250 Care Reactions
    Member

    I’m a pretty easy going person and if someone wants to share idea with me on how I might handle a difficult situation I’m ok with that ( even if they don’t have a clue what they are talking about). I like hearing the ideas of other people (preferably the ones that have some idea what they are talking about). I see this as them just trying help. The problem I have is when I am TOLD what I should or shouldn’t do and it is presented as fact and a solution to all my problems. They know nothing about the situation but know without question how things should be handled. Grrr, these people are awful!

Commonly Used Abbreviations


DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
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