Friends.....
#1
Posted 28 April 2008 - 02:01 PM
It's a struggle for me to stay on top of all of those things needed for a good relationship. The effort of making plans, following through etc. I seem to only be able to make the time and find the energy for my boyfriend but beyond that it seems impossible.
It seems like we all somehow find a way for our partners , children, and then family, but beyond that how do you do it?
#2
Posted 28 April 2008 - 04:36 PM
I am new to my diagnosis of N, but not new to disabling illnesses (Ankylosing Spondylitis, same family of illnesses as Lupus and RA) or the symptoms of N. =) The land of disabling illnesses has been mine for at least 7 years at a consistent level, prior to that my symptoms were more sporadic, so the need to manage them didn't really exist, they were just weird things that happened.
I am a married mom of 2 boys. My hubby and I have been together for 15+ years, so he has been here for it all. One of my sons also has Ankylosing Spondylitis, so we have had to approach relationships at the adult and childhood level.
I have found that most people are just ignorant, but have good intentions. From this I mean that they still love you, want to be with you, but just cannot truly understand and are not sure how to be a part of your life. For this group of people, which for my family is close friends and family, keeping them in the loop on what is going on and when/how to interact with you is the key. If they do not feel pressure to "say something" or are worried when they can and cannot call/stop by, etc, let them know what works for you and what doesn't and that you really DO need them, including what you need (ie, just someone to be listener, someone to be your drill sargeant keeping you active, whatever fits your life). When things change, let them know that as well. Also, make sure they know how much they mean to you and that if you seem to drop off of the face of the earth at times, it is okay for them to remind you (if it is that is) to keep living and/or that you will be back in touch, you just have to have down time. For me, specifically, a lot of how to communicate w/others came from my husband and I trying to figure out how to communcate with each other and to understand that we BOTH play a role in the illness, they are just different, and to me, that is the same for all true friends and close family.
Those not in my "most people" category seem to fall into the category of "having a disability will really let you know who your TRUE friends are". This was a tough pill for me personally. I had a friend for many years that was great fun to hang out with and such, but over time, it was more and more obvious that we were not true friends. It wasn't a matter of this person just not understanding or me wanting too much, it was just that they really couldn't have a friendship with someone that had any underlying complications. Accepting that some friendships just run their course and are over was tough, but it is true and once you are battling your one health, you truly have to let go of any other relationships that are unhealthy...in the end they are unhealthy for both of you.
What I have listed is how we encourage our 9 year old son to approach his friendships, teachers, etc. We are upfront about the illness, limitations, etc, but we also make sure we focus on positive things as well. He has a core group of friends that really "get it" and he has many school friends that are fun to hang out with, but he knows who is really his buddy and who is not. At his age, we also try to make sure he stays on top of his end of being a friend, not just relying on them.
I also make lists of things like "call Jane" and try to plan things in advance, including reminders of my plans, to push myself to keep up with people. Sometimes things have to get cancelled or get off track, but with a schedule, I am able to at least remember what to do in advance.
All in all, it isn't easy, but it is possible I believe. I do speak from someone who is already married and such, so I am sure you will get feedback from others who are single and such for other ideas.
PS--I am also a pretty social person, so it was important to me to figure out how to still be alive and w/those I love and take care my health. Most days the delicate balance works, on others well, those days are gone before you know it and everyday is a new one!
#3
Posted 11 May 2008 - 01:55 PM
I am definitely lucky. I have about 6 close friends (not from the same circles) who are always there. They always invite me, even though I almost always say no. I can go months and months without speaking to them but when we do it's like no time has passed. They never have an issue with it. They never give me a hard time if I (often) have to cancel last minute. But, we don't spend enough time together. I probably see each of them only a few times a year.
I have found out about the 'others' and how true of friends they are.
#4
Posted 05 May 2009 - 07:46 PM
I can totally relate! Maybe we have the same 6 friends ?!!!! Memorial Day is coming soon and we're working on getting our yard ready for a picnic we have every year. It seems that it's the only weekend all year that all of our friends can gather at the same time. Rain or shine they never disappoint us and I suppose if I took a picture of the whole gang we'd certainly resemble the Adam's Family! Honestly I don't care what they look like because they are wonderful "true" friends who really care!
#5
Posted 06 May 2009 - 01:08 AM
this is the place that i notice it the most.
but i'm me. i hate life. i hate n. wtf ever. i can't keep up with my kids. my marriage? it sux. friends? energy that should be spent on kids. my whole life is controlled by N. I can't stay coherent in discussions with people if i'm on meds, but without them, I'm sleep deprived and insane. damned if i do. damned if i don't.
if it weren't for my kids... geez, but if i didn't have this disease i would be a better person. too much energy to have friends. isolating and -
sleep deprivation is getting too strong. starting meds again soon. It's been a month and a half? two? since i stopped taking them, but it's too much. I'll come back and answer again when my brain is sane. hopefully. i'll try my damndest to be coherent when i do.
#6
Posted 06 May 2009 - 01:38 AM
ssssssssssuperfreaky
#7
Posted 06 May 2009 - 01:40 AM
ha.
on facebook there is this guy that doesn't have n that i'm friends with. uh oh. he made the mistake of discussing dreams, etc.
ha.
yeah, i scared him away.
#8
Posted 06 May 2009 - 12:54 PM
ha.
on facebook there is this guy that doesn't have n that i'm friends with. uh oh. he made the mistake of discussing dreams, etc.
ha.
yeah, i scared him away.
hahaha yea our dreams will do that to people!
#9
Posted 07 May 2009 - 11:19 AM
#10
Posted 07 May 2009 - 01:24 PM
not just our dreams..our lives scare people away
#11
Posted 07 May 2009 - 05:33 PM
If my life scares someone away, then GOOD! I'm probably better off without them in it.
My friends are great. They've been with me since before my N diagnosis, so they've seen the bad, the really bad, and the awful days, and now I'm doing better so they can see my good days. It's always difficult to try to communicate what you're going through to someone else, when they just can't relate, because they don't have N. My friends that I've kept through this all are wonderful to me, and they wanted to understand as best they could about N. That desire to learn more about it really showed me who cared tons about me. I'm lucky to have them in my life.
It is still difficult though. My being late bothers some, but they do know I'm not trying to be late all the time. They also don't always understand why I can't go out partying 2 nights in a row. If I could... trust me, I would!
My very favorite friends that actually "get it" and totally understand if I go MIA are you guys! All of you have touched my life in a wonderful way on here.
#12
Posted 07 May 2009 - 11:17 PM
That is a-okey dokey. I began replying to this one statement of yours about an hour ago.
#13
Posted 08 May 2009 - 04:19 AM
His name is Rupert
Rupert the Bear.
#14
Posted 08 May 2009 - 01:37 PM
HI, HENRY!
#15
Posted 08 May 2009 - 01:49 PM
HI, HENRY!
HellooOOooo
#16
Posted 08 May 2009 - 08:30 PM
as for every one else... haha well sleepless i think *BEEP*es like us would scare lots of them off with or without N LOL j/k. what i mean is, with us you get what you see... lots of friendships out there are based on people pretending to build up the other so they in turn get built up themselves. i irritate the crap out of lots of people. but my close friends know that when i say somethign i mean it, and i would do anythign for any of them - not just SAY i would.
anwyas it's my bed time night night
#17
Posted 09 May 2009 - 12:15 AM
So this is where u'v been? Ah HA! You should try giving your dear old NN friend a call (or msg) sometime. You were here a LOT and then GONE. I was worried that your N dreams gobbled you up. I was trying to set up conference hallucinations, but it seems that your dream peeps and my dream peeps had continuous scheduling conflicts. I hate when they do that.
GLAD TO C U AGAIN. Dammit. I don't like missing people. NN does NOT accept MIAs. Well, I guess it's ok this time. You had good reason. Friends, family... yeah, ok.
#18
Posted 04 June 2009 - 04:04 PM
so, i don't have much energy for a long post, but im still alive. i dropped my one job and am just part time at the clinic now, plus "extra" shifts while people take vacation time, so im doing a bit better.
med situation not great, but i have an appt later this month
AND i finally got in to see the new obgyn, and he's pretty sure it is PCOS i have, so im going later this month for another appt with him
when i can think of something to add or even something at all to write i will. my shifts at the clinic aren't until one usually, so i'll be on more often before i go to work again
hope everyone is well, and those who aren't are hanging in there
#19
Posted 05 June 2009 - 03:59 AM
that usually helps
also, i love being with my friends...id go crazy without em, but if they want my company so much, then they have to put up with my sleep just as much
you either accept me and facilitate for my naps, or you *BEEP* off - its as simple as that
one thing that does piss me off though is when people get pissed off at you becuase they say u make no effort, and then when ur there, they get pissed off at you for being sleepy and tell you that you shouldve stayed home.
people like that get discarded pretty soon










