This is the 4th post by Anna on being a caregiver. Earlier posts are The Depression Dialog, Know the Enemy and Trigger Unhappy.
I’ve been asking James to take our old mattress to the waste dump for about 4 months. Today, I decided enough was enough. I asked an understanding friend (whose husband also has depression) to help me transport it. She has a car with roof racks. It took a while but we got it onto the roof, and tied it down with baling twine. It was not exactly satisfactory, but James had taken the rope to work and left it there.
So we drove that way and the mattress stayed on for about a mile before sliding. We checked it, and checked it again, and continued like this until we were nearly there, when a truck passed us with speed and the mattress flew off altogether. (Queen size by the way.) The twine was still intact, but the mattress handles were shredded. So we eventually limped in to the dump, mattress carefully balanced on top and hazard lights on. It was a funny experience and we had a lot of laughs.
I’ve written about this because it says a couple of things about how I handle my role as a caregiver.
Know the limits of what your partner or friend can do
Removing a mattress was overwhelming for James. He put it off, and ignored it, and put it off some more. The reason was that the task – mental as much as physical – was insurmountable to him. It’s quite different from laziness, as anyone with depression will know. But the mattress was stopping me from getting to my wardrobe and it had to go. My frustration was building up, despite knowing what was going on in James’ mind. I decided to just do it myself rather than let it become a big issue. That’s not to say I’m being a doormat. When I stop and think about it I recognize what’s happening under the surface and take a practical approach.
My support network is crucial
I have a small network of friends who will help me in this sort of situation. Through bitter experience, I know that some people are understanding about mental illness and others are not. My close friends are. I also know not to wear them out, so I share my problems around. They give the emotional support I need when I’m not getting it at home. They let me vent, they help me in practical ways, and they still share good times with me. They also think highly of James even though they know how awful he can be. That’s very important to me. I’m very fortunate as a caregiver to have supportive people around me. I know that many people are struggling along without much help. I can’t emphasize enough how important it is to develop those supportive relationships, for friendship, for emotional support and for practical help for things like moving mattresses.
My mental health is crucial
I have to be proactive about having time out, having a break from the intense times, and even some fun. I used to feel guilty about this, but it’s actually wise to keep looking after your own health. My family are good with giving me practical help, like taking the kids, when I need to do something on my own.
Learn to forgive and grieve
It’s easy to feel sorry for myself, but I’ve learned to forgive and move on. James forgives me for a lot of things too; it’s not a one way street. I’ve had to mourn the life that I thought James and I were going to enjoy together. He is not at all like he was when we married. But I always remind myself that I should be thankful for what we have, and what I have, and not dwell on what we don’t have, and to pray on all occasions.
Click here for the fifth and final post in this series, Loving the Person You Care For.

Trigger Unhappy 21 Oct 2007 @ 8:04 am
[...] Click here for the fourth post in this series, Keeping Your Mind Together. [...]
Wanda M. Adams 31 Dec 2007 @ 8:28 pm
Hallelujah! Finally some one that gets it! I cannot thank you enough for informing society on the trials and tribulations people who love bi-polar people experience! Happy Holidays!!! and keep up the great work!
christine r. tinkey 9 May 2008 @ 6:22 am
this site is the best info and insite to bipolar. i have done a good bit of research about my illness and have learned my triggers. i have shared these with my children. my friends also know my signs and triggers. ithink this illness was a part of my failed marriage. some ppl dont accept things and wont look it up to find out more. i have ppl tell me its in my head and i dont need meds and i tell them you have no idea. i hope to someday find that special someone to share my life with. i know its possible after reading these stories and they have given me hope for a happy semi-normal life. i dont think there is ever a normal for ppl with this disease or their families. i just wanted to let all of you who share your stories definately help others out there
thank you!!!
STEPHANIE BOSTON 26 May 2008 @ 7:00 pm
I have grown up with bipolar. My mom was diagnosed with it as well as both of my younger sisters. My mother in the last year has had a complete break due to the stress caused by the death of her mother and careing for one of my sisters who had cancer. Your tips on how to cope and help her is greatly appreciated! I thank God that I received this today!
Jenna Gibson 27 May 2008 @ 8:37 am
I really enjoyed the mattress story, simply because I have lived it and still am. I am living with a husband who is bipolar. We go through these problems alot. I really am interested in these stories.
anna 1 Jun 2008 @ 5:55 pm
Hi Stephanie,
It’s really hard to comment on your situation as I am not sure how you or your mum are placed. However, it is really important that there is a team approach to caring for your mum and you. That team will need to include your treating health professionals, your friends and relatives and maybe social services as well. Make time for your self so that you have the emotional energy to help others. Learn as much as you can about stay well strategies and what resources your community has in place for your situation. Then start knocking on the doors!
Hope that gives you a few ideas
Anna