Jump to content
RemedySpot.com

Re: Re: explaining RA to my family?

Rate this topic


Guest guest

Recommended Posts

Guest guest

This is a very insightful response, Jennie. I hope these ideas help you,

Sharon.

I used to do a lot of entertaining, but I wouldn't consider hosting 30

people for 4 days for the 4th of July unless I were the president

herself!

I'll tell you where to go!

Mayo Clinic in Rochester

http://www.mayoclinic.org/rochester

s Hopkins Medicine

http://www.hopkinsmedicine.org

[ ] Re: explaining RA to my family?

> Go to this site and click on the spoon theory.

> http://www.butyoudontlooksick.com/

>

> I recently went to Boston to visit my friend. I go up there about 3

> times per year with my daughter (she turned 4 on the 4th). The

> drive is 5.5 to 6 hours long. I make it because I rest before and

> after, and really, the trip is all about hanging out with my

> friend. My daughter plays with her daughters and it's usually very

> restful. This trip a few weeks ago was to celebrate her and her

> friends 40th birthday. They had dozens of people over, weeks of

> preparation, days of errand running, etc. All I did was helped the

> morning of the party by washing dishes, setting things out on the

> table, putting some food in the proper dishes, etc. It involved

> maybe 2 hours of standing and walking. By the time the party

> started I was wiped out. The next day I told my friend, " Do you

> realize I could never throw a party like you just threw. " She asked

> why and I tried to explain that with the RA I would not have the

> stamina. I don't think I got my point across well. I didn't go

> through the whole spoon theory, I think, because I was just to

> darned tired to explain.

>

> It's hard to make someone understand when they have never

> experienced anything like this. It takes time, patience and

> perseverance. I have no idea how you could manage to host 30 people

> for four days! Of course you are having a flare. I am going to

> have a flare just THINKING about it!

>

> One way I have described RA to others is that it's like being 9

> months pregnant without the baby. People get why pregnant women

> need rest, they understand the lack of energy. It's easy when you

> see that huge belly. People don't get it about RA because they

> don't see anything. But to me it feels just like when I was

> pregnant, and people seem to understand the analogy. Show your

> husband your ankles. Explain to him that throwing such a party

> means you are going to be in bed for days. Take him to the doctor

> and show him some pictures of people with severe joint damage. Keep

> doing it until he see's that not understanding your limitations is

> going to cause you harm each and every time you over do it, and the

> harm can be permenant.

>

> Then try to UNDERestimate what you think you can handle. It's easy

> to think that " oh, next week I'll be able to do that. " But the more

> you understand your limitations the better able you will be to

> predict what you can and can't do. Part of this is about setting

> your husband's expectations that you can't do what you used to be

> able to do. Part of it is about your own expectations of yourself.

>

> Now, my mom is disabled from RA and when I told her about the Boston

> trip and that I'd never be able to throw a party like that, her

> response was, " yes you could, you'd just have to pay someone to do

> the work. " And she's right. I'm moving in a few days and I'm

> paying someone to move me. If I understood my own limitations

> better, I'd have realized I needed help packing too. Oh well, I'll

> remember for next time.

>

> Jennie

>

>

> > Hi. I am a new member to this site and joined to ask for help on

> how to explain to my husband how it feels to have RA. He is very

> intense, active and likes to entertain, travel, socialize and have

> family over a LOT! I can't keep up with his needs. We also have a

> six year old daughter and I am getting totally worn out by the both

> of them. It is so difficult to set limits with my husband even

> though he tells me to say no when I don't think I can do something.

> Sometimes I think I will be able to entertain family or travel in

> the future, and when the time comes I may be too tired. He then

> feels let down and doesn't understand why I can't just take a nap

> and push through to the next event. We just finished entertaining

> 30 of his family members for a four day fourth of July celebration

> and now I feel like I am having a flare. My feet and ankles are so

> stiff and I am so exhausted, I have little left to offer our six

> year old. If anyone has any advice on how to explain the severity

> and unpredictability of my symptoms, please let me know. Thank you

> so much - Sharon

Link to comment
Share on other sites

Guest guest

Thank you so much for all of your replies. The spoon theory is very powerful!

I will try it on my husband when he gets home from his work trip. Maybe I will

wait and do it next time he is sick with the flu or something. Anyway, I do

appreciate all of the encouraging and kind words and I hope I can help someone

in the same way. - Sharon

[ ] Re: explaining RA to my family?

Go to this site and click on the spoon theory.

http://www.butyoudontlooksick.com/

I recently went to Boston to visit my friend. I go up there about 3

times per year with my daughter (she turned 4 on the 4th). The

drive is 5.5 to 6 hours long. I make it because I rest before and

after, and really, the trip is all about hanging out with my

friend. My daughter plays with her daughters and it's usually very

restful. This trip a few weeks ago was to celebrate her and her

friends 40th birthday. They had dozens of people over, weeks of

preparation, days of errand running, etc. All I did was helped the

morning of the party by washing dishes, setting things out on the

table, putting some food in the proper dishes, etc. It involved

maybe 2 hours of standing and walking. By the time the party

started I was wiped out. The next day I told my friend, " Do you

realize I could never throw a party like you just threw. " She asked

why and I tried to explain that with the RA I would not have the

stamina. I don't think I got my point across well. I didn't go

through the whole spoon theory, I think, because I was just to

darned tired to explain.

It's hard to make someone understand when they have never

experienced anything like this. It takes time, patience and

perseverance. I have no idea how you could manage to host 30 people

for four days! Of course you are having a flare. I am going to

have a flare just THINKING about it!

One way I have described RA to others is that it's like being 9

months pregnant without the baby. People get why pregnant women

need rest, they understand the lack of energy. It's easy when you

see that huge belly. People don't get it about RA because they

don't see anything. But to me it feels just like when I was

pregnant, and people seem to understand the analogy. Show your

husband your ankles. Explain to him that throwing such a party

means you are going to be in bed for days. Take him to the doctor

and show him some pictures of people with severe joint damage. Keep

doing it until he see's that not understanding your limitations is

going to cause you harm each and every time you over do it, and the

harm can be permenant.

Then try to UNDERestimate what you think you can handle. It's easy

to think that " oh, next week I'll be able to do that. " But the more

you understand your limitations the better able you will be to

predict what you can and can't do. Part of this is about setting

your husband's expectations that you can't do what you used to be

able to do. Part of it is about your own expectations of yourself.

Now, my mom is disabled from RA and when I told her about the Boston

trip and that I'd never be able to throw a party like that, her

response was, " yes you could, you'd just have to pay someone to do

the work. " And she's right. I'm moving in a few days and I'm

paying someone to move me. If I understood my own limitations

better, I'd have realized I needed help packing too. Oh well, I'll

remember for next time.

Jennie

> Hi. I am a new member to this site and joined to ask for help on

how to explain to my husband how it feels to have RA. He is very

intense, active and likes to entertain, travel, socialize and have

family over a LOT! I can't keep up with his needs. We also have a

six year old daughter and I am getting totally worn out by the both

of them. It is so difficult to set limits with my husband even

though he tells me to say no when I don't think I can do something.

Sometimes I think I will be able to entertain family or travel in

the future, and when the time comes I may be too tired. He then

feels let down and doesn't understand why I can't just take a nap

and push through to the next event. We just finished entertaining

30 of his family members for a four day fourth of July celebration

and now I feel like I am having a flare. My feet and ankles are so

stiff and I am so exhausted, I have little left to offer our six

year old. If anyone has any advice on how to explain the severity

and unpredictability of my symptoms, please let me know. Thank you

so much - Sharon

>

>

Link to comment
Share on other sites

Guest guest

In a message dated 07/07/2004 07:25:58 Central Standard Time,

sharongra@... writes:

>

> Thank you so much for all of your replies. The spoon theory is very

> powerful! I will try it on my husband when he gets home from his work trip.

Maybe

> I will wait and do it next time he is sick with the flu or something.

> Anyway, I do appreciate all of the encouraging and kind words and I hope I can

help

> someone in the same way. - Sharon

>

The spoon thing is what finally got thru to my boyfriend. Cary

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...