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Re: Family support?

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I am the queen of rejection from family and friends from not only my illness but

also from my marital abuse and pending divorce. I am all alone. No compassion

for illness or abuse.

God Bless

Bonnie

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Yes, monica, I have gone through this. I am here for you as a support

as I am still going through it so I do not have much to offer in the

way of advice. My in-laws are the worst and done everything they can

to destroy my marriage and my life. Cassy

>

> I'm having trouble with getting emotional support from my family. I

was wondering if

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Sorry to hear you have family trouble .

Mine don't live close but they aren't too compassionate towards me

either. Maybe we need to educate them more. Try print some of the

great articles posts here for your family to read. Does your

rheum have pamphlets on it? Mine does and I have one for RA even

though I don't have it. I think my sister does believe me to the

extent that she thinks her 15yo daughter has fibro now.

Sorry can't give any better advice.

Debbie L

>

> I'm having trouble with getting emotional support from my family.

I was wondering if

> anyone else has had problems with friends or family members who

won't believe that

> there is really something wrong with you. My family if sure that

if I just put a little effort

> into it got up off the couch stopped whining and made some goal I

could stick to I'd be

> better instantantly. Because of course my problems are all in my

head. If any one has

> gone though this and has any advice about how to reach my

relatives, and how to teach

> them more about RA I would be most greatful.

>

>

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Family support? What is that? Yes, I am bitter that my family and my in-laws are

not supportive, including my husband. Autoimmune diseases are very isolating

and I feel like a hypochondriac most of the time. We may look " normal and

healthy " but we are not. , I feel for you and have no answers, but pray we

all find peace, as we cannot become bitter because of what others think. I sent

everyone in my family a " letter to normals " re: my autoimmune problems and they

all told my husband I needed psychiatric help.

Hugs,

Kim

monica_p4 <monica_p4@...> wrote:

I'm having trouble with getting emotional support from my family. I

was wondering if

anyone else has had problems with friends or family members who won't believe

that

there is really something wrong with you. My family if sure that if I just put a

little effort

into it got up off the couch stopped whining and made some goal I could stick to

I'd be

better instantantly. Because of course my problems are all in my head. If any

one has

gone though this and has any advice about how to reach my relatives, and how to

teach

them more about RA I would be most greatful.

---------------------------------

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,

I am sorry for your diagnosis and obvious pain. I pray you have a

therapy that is working for you. There is an analogy here about a

number spoons given to us in a day and how we ration them out to have

enough energy to last the whole day. Maybe someone here can give

more detail about the analogy. Some give that to their family

members.

Sorry to sound so pessimistic but in my opinion you did the best

thing you could have when you joined a support group for RA. Some

also seek counselors to help them through which is not a bad idea,

some seek spiritual guidance is what I do, some have wonderful family

members who stick by them through it all..

I lost my mom last year and I don't think she ever understood the

condition regarding the condition. My grandmother still lives,

healthier than I am and don't know what I am talking about. My

siblings are in their own world. The only reason I ever mentioned

the RA is because my daughter was disabled and I wanted my family to

understand I may need help with her physical care down the road. I no

longer have my daughter so as one family member told me, " you don't

to have to wonder who will care for your daughter anymore… " and

something else I drowned out from the shock of that statement. My

mother-in-law (MIL) told me " it's just arthritis. It may cripple you

but you won't die from it and I believe people should care for their

own children. "

So, it was me and my kid completely on our own and me flaring on a

daily basis sometimes for 6 weeks at a time.

I finally decided to stop trying to convince others I was sick and

place all of that energy into getting better. If my child had a

chance, it would be because I got better in order to be here for

her. Even though I no longer have my baby, I still feel that way.

Do all that you can on your own without their support just as if you

were living on your own. Everyone is not a caregiver and not able to

feel that sort of empathy. Join whatever group that helps you, pray

whatever prayer that helps you, see whatever counselor who helps you

because if your family wanted to support you, you wouldn't have to

convince them for the support. They would be online researching this

condition and offering you the support you need.

Besides, what are we here at the support group -- chopped liver?

(smile) We understand and I pray your family will eventually come

around too but know we are here for you and don't forget to live your

life regardless who understands.

peace and healing.

Ebony

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,

I am sorry you are going through this but i think I have met through here goes

through the same thing, either family doesn't even know the difference between

osteo or rheumatoid or just gives you the sympathetic nod like " OH OK, your not

feeling good. It is unfortunately a very frustrating situation with family and

friends and it has been continuously with me. I am having problems with friends

also, they say " U have to be on ALL that medicine, I mean you can't live without

all that stuff? " They have no comphrension and some try, I am not trying to be

negative because there will be people in your life who have someone who has

suffered through it and understands (it is your light at the end of the tunnel

or you will meet someone through here that will be a very good support system

for you). I have met a few. I wish you luck and I would be happy to talk to you

individually if you would like, i have been just recently been diagnosed. I wish

you well, bless you and wish you a

painless day!

---------------------------------

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