Notes on Relationships in MS: for discussion

What might be helpful to think about if you or your partner have MS ?

MS makes it harder to understand each other.

Putting yourself in the other person’s shoes does not work in the same way

Other people react differently to illness – ‘I don’t understand why you don’t take that cure!’

Hard to touch delicate subjects – so it can be hard to find out what something means to another person

Feelings get in the way of talking:

Guilt – ‘it’s my fault, it’s my MS – what am I doing to them?’

Anger – ‘if only they would see it differently/not have MS/ behave differently’

Fear – the future can ruin the present

(But talking can help)

MS affects behaviour:

Illness behaviour


Invisible symptoms confuse the picture

Fatigue;  pain; affects on subtle emotional responses. Decision-making difficulties.

Reactions to Loss:

Adjusting your mind to any loss takes time. And it hurts.

Everyone reacts differently.

Meaning of loss different for each.  Erection problems: mobility; sensation: ‘I’m useless/impotent’;  decision-making .

Withdrawal.  Licking your wounds.  ‘DON’T TELL ANYONE’

Talking to others; telling everyone

People expect to recover more quickly than they do; it generally takes two years before a serious loss becomes incorporated into daily expectations.  (More for some losses/some situations; less for others)



How should a parent with MS behave? How should my children behave?

How do I / they  behave?  – hard even to look and find out.

Parents can help their children.  This may be a surprise.  When parents do find out what the children think or feel, they can be astonished to find how much they can help.  Children like to know their parents are concerned enough about the things that worry them.   ( eg. What would happen if mummy or daddy died?)   Such topics are hard to raise.  (Read My Mum Needs Me?).

So what can people do to maintain their relationships in the face of MS?

Assumptions and guesses can be useful, but need checking out .  Perhaps try to find out what you don’t know?  – eg what MS or a symptom means to you and to the other person? –  may be able to ask; may need help asking.

Know it is hard for everyone, you and them.   (Martyrs aren’t comfortable to live with.)

Know you will all get it wrong sometimes – and be ready to forgive.  The quality of mercy has much to recommend it.   So does a  good sense of humour.

Talking (with the right person) can help.  Partner? Counsellor?  Friends?  Other people living with MS?

Find sources of pleasure – in each other and life in general.   Most symptoms become part of normal life after two years.  MS does not have to spoil everything.

Suggested reading:

Segal, J.C. (1985)  Phantasy in Everyday Life, Pelican Books. Reprinted Karnac Books 1995, 2005 London, and Aronson USA 1996.   (Written before I knew anything about MS; based on work with Relate.)

Segal, Julia and Simkins, John. (1993)  My Mum Needs Me.  Helping children with ill or disabled parents.  Penguin Books, London.  For parents. Out of print but available on the internet.

Julia Segal and John Simkins. Helping children with ill or disabled parents; A guide for professionals.  Jessica Kingsley, London, September 1996   pb £15.95   (My Mum Needs Me re-written for professionals.)

About thetroublewithillness

I've been a counsellor for people with physical illnesses for a long time now, and learnt a lot about what it's like living with your own or someone else's illness. I want to pass some of this on.
This entry was posted in carers, children with ill parents, counselling, emotions related to illness, grieving processes, illness, talking about feelings. Bookmark the permalink.

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