Jump to content
The MS PEOPLE UK Forum
Support, help, advice and information for Multiple Sclerosis. Ask questions and share experiences with people affected by MS.
Marina

Stress - How does it affect your MS?

How does Stress affect your MS?  

91 members have voted

You do not have permission to vote in this poll, or see the poll results. Please sign in or register to vote in this poll.

33 posts in this topic Last Reply

Recommended Posts

Sluggish
Marina

Comments allowed.


Marina

(belated DX in June '05, SPMS)

Share this post


Link to post
Heste

Before I was diagnosed with MS I was diagnosed with Stress. It was not until my leg and eye stopped working that they had to come up with a better answer. The other symptoms could be put down to stress.

So I can not really answer your poll properly as for me stress and MS are have been blended in together.

If my stress symptoms were really MS then did I really have stress symptoms? Perhaps I actually cope with stress really well but have MS. Perhaps MS is really just super-stress?

 

I have been in extremely stressful situations. They gave me counseling sessions in which they identified 8 major causes of stress all happening at once. (For the nosier reader - my mother died just after her divorce, my horse died from colic, my horse's insurers didn

Share this post


Link to post
scubachick

I am unsure whether stress was the trigger for my current attack.

 

Previous ones have been "virus" induced usually after a bad cold or the flu.

 

This one the cold came after the attack and I am currently under a lot of stress.

 

So I not sure if stress was one of the factors this time.


Tracy

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

There is a fine line between hobby and mental illness!

Share this post


Link to post
mayb

I am very aware that stress is my worst enemy - every time I have had a bad session it has been during a stressful time. I don't mean the daily ups and downs but when life is putting the pressure on and you can't just do something about it.

 

This time it was caused by a call back to the hospital after a routine mamogram showed a possible problem. I knew I shouldn't get worked up about it - these things happen to lots of people - most times it turns out to be nothing. The wait for the return appointment and the subsequent tests were very stressful and although I got the all clear, within days I lost the use of one leg and was in an awful lot of pain. Things are slowly improving but this is one of the worst set backs I have had for years and there was no way of seeing it coming.

 

Funny thing though Scubachick - I very rarely catch the colds etc that go around, I sometimes feel I am about to get the bug but it never develops. At those times I nearly always suffer some sort of ms symptoms instead. I can't remember the last time I had a cold and everyone in the office envies me my health!! Its a strange world. (I am touching wood as I speak). I suppose fighting off the germs is another type of stress - bodywise anyway.


Mayb

Share this post


Link to post
Hils

During the busy summer at work we have a student in our office to 'help out'. The student we had last year caused so many problems for us that in the end I had my doctor sign me off with 'work related stress'. I had head pains that I'd never had before, not just what I would descibe as normal headaches, but real pains that I am sure were ms related and I felt generally unwell.

 

The pains went after a couple of weeks off work and, fortunately, the student had been removed from the office by the time I returned to work.

 

Hils :hairraising:


If you can meet with triumph and disaster...and treat those two imposters just the same...

Share this post


Link to post
Lauri04

I think mostly it makes my symptoms worse but this last time I think it definitely brought on a relapse.


NEW Awareness Jewelry on my homepage!

Share this post


Link to post
RedSonja

I can handle a bit of stress, but falling off the motorbike gave me my second relapse. Since then I take my medication like a good girl and have avoided kissing the asphalt. I have had no more knockout, dead-to-the-world, stay in bed relapses since then.

Since MS came to stay I have tried avoiding stress as best I can, makes life much simpler.


Bibo ergo sum

Share this post


Link to post
smiffy

The way stressful situations affect me was one of the first symptoms of my MS. It made me feel as if I had been stuffed full of cotton wool. There must have been a lot of it 'cos it made it difficult for me to walk, talk and write/type. People at work thought I was a bit odd when this happened but that's the way it goes eh.

 

Happy Midwinter to you all. I lit my candle on the evening of the 21st to light my way through the longest night. Postponed my feast day until 25th due to family work commitments, otherwise we would have been together on the evening of 21st.

 

:shakehead3:

Share this post


Link to post
marcia

It is only extreme stress which affects me, it causes symptoms I have not had before but they eventually disappear, I have ppms


ppms, diagnosed 1992

Share this post


Link to post
mayb

Two days after I was suspended from work the worst session I had ever had kicked in - it took that long for the shock to wear off I think. Funnily enough though, and I have everything spare touching wood at the moment, I have not had one cold or upset stomach or all of the other ailments that have been around me since then. I have just read an interesting article on the connection between stress and lower back pain. It is all down to the stress reducing your ability to protect yourself from anything else happening to your body. I think my body bypases every other ailment and goes for this every time!!


Mayb

Share this post


Link to post
angela

Hi Mary

Have you got a link to that article about stress and its connection with lower back pain? just over a month ago we had to forcibly, for reasons I won't go into,throw our 19 year old son out (third time), I thought I was coping pretty well but the last couple of weeks I've had lower back pain and now reading your post I wonder if it's connected!

 

Angela


Give a woman the right shoes and she can conquer the world! Bette Midler.

 

 

Share this post


Link to post
Sluggish
Marina

Oh Angela, I'm terribly sorry to hear that...

 

Re back pain and stress - also, any stress will cause muscles to go into a certain amount of spasm through tension. In a way, it's similar to a tension headache.

 

Having said that, if anybody's going to discuss a topic of back pain and stress, please start a new thread in the MS Discussion area, as this is topic is purely related to the poll. Thanks! :shakehead3:


Marina

(belated DX in June '05, SPMS)

Share this post


Link to post
angela

Thank you Marina, it was hard but had to happen!

 

Angela


Give a woman the right shoes and she can conquer the world! Bette Midler.

 

 

Share this post


Link to post
liddy

Im abit of an authority on stress at the moment still having to share a home with my ex husband who refuses to leave (and a very upset 13yr old!).

When things get really bad (constant visits to solicitor/threatening letters etc) I can feel my smptoms getting worse. Usually starting with the feelings of desperation, then the headaches and eye pain, lack of sleep, stomach upsets, strange metallic taste in mouth... all leading to more general unwellness.

I found out that yesterday he went and had the house valued behind my back as he is taking me to court to make me sell it.

I now have to trawl through estate agents to provide lists of suitable properties for myself and my daughter that we probably cant afford PLUS I have to see a mortgage advisor and show what sort of mortgage I could take on.

My solicitor feels once the judge looks at the case (including a letter from my GP regarding MS dx and the stress I have been under for over a year) he will very likely decide to let me and my child stay in the house and that the ex will have to rent somewhere until I am ready to sell.

Incidentally the house was valued at

Share this post


Link to post
fiddlestix

It depends on the severity & the duration of the stress as to whether it causes a full-blown relapse or 'just' makes most symptoms worse.

'Scuse me for being picky here, but by 'stress', d'you mean simply the emotional kind Marina, or were you including stuff like bugs - which the body sees as forms of stress.

 

My daughter has just decided on the theme of her dissertation for her BSc in Herbal Medicine: it's 'The role of stress as a precipitating factor in the onset of MS' ..... perhaps I should give her the link to this site? :nuts:


I used to have a handle on life, but it broke

Share this post


Link to post
gordon

yeah stress affects me bad , i recently got married and i think all the stress of that made me relapse so i have an mri booking which i hate :cheerleader3:


i LOVE CHOCOLATE HEE HEE

Share this post


Link to post
Sluggish
Marina
by 'stress', d'you mean simply the emotional kind Marina, or were you including stuff like bugs - which the body sees as forms of stress.

Sorry, I've only just seen this. I mean the emotional kind of stress, due to circumstances and which can be accompanied by anxiety. Stuff like bugs would be in a separate category of infection, which is also known to affect MS.


Marina

(belated DX in June '05, SPMS)

Share this post


Link to post
SkattyBell

Prolonged physical stress can sometimes make things worse, due to back problems, perhaps? so I have to try to find a happy medium when it comes to physical activity. Most flare-ups have happened regardless of wether or not I've been physically or mentally stressed. Never a good idea to push yourself when feeling tired or to get overly stressed in any walk of life. Pacing oneself and knowing your limitations does help.

Funnily I never suffer too badly with cold symptoms, although when I get slight colds MS like symptoms increase during & after.

Share this post


Link to post
mayb

Like you skatty I rarely pick up other people's bugs. I was quite amazed when I went down with a sore throat a while back as I can't remember the last time I had a 'normal' illness. I find when other people are fighting bugs I may get a feeling I am about to succumb but then it goes away. I think my immune system goes into overdrive normally at the slightest sign of a bug and I suffer a relapse of symptoms instead. In some ways this makes sense but doesn't explain why so many people with ms do get these bugs and their exacerbations as well. It is all a puzzle I don't ever expect to understand.


Mayb

Share this post


Link to post
SkattyBell

Starting a new topic in connection with this thread.

 

Sorry, all!

Oooops! forgot to say where! New topic in MS Tips -

Share this post


Link to post
sylvia

Hi,

 

Stress definitely makes my symptoms worse, of course it depends on the severity of the stress and symptoms, but even the smallest stress gives me pins & needles, burning & aches straight away atleast into my face and head.

Share this post


Link to post
Hezza

Having just been through a year which included an MS diagnosis in January, a few relapses in-between and redundancy as the climax just before Christmas I know for definite that stress affects my MS.

I didn't have a full relapse but did suffer an exacerbation of symptoms, old and new, for around 4 weeks after I finished work.

 

Rested up, let it run its course, and now I'm fine - well as fine as I get :hearts:


Life is short. Eat dessert first. Jacques Torres

Share this post


Link to post
mayb

I sometimes think that if I could take out the stress in my life I could recover almost totally from my current problems. This is not an option with a Tribunal pending and the money worries that come with losing my job. This has been going on for over a year now and I think some of the damage is permanent. What can you do? Stress is something we have little control over as it comes from outside sources working on our bodies in ways we cannot control either. Once things start going wrong we worry about that and stress is exacerbated too and round we go. :hearts:

 

Thankfully God invented chocolate!!


Mayb

Share this post


Link to post
vix

Last year when I was dx I was at the time studying for my medical exams (which I passed) I was so stressed out that I would not pass I was studying and re-studying everything 6 times over. I was unable to stand up straight or even sit straight and when it came to walking it was as if I had too much to drink!!!! I was slurring my words and couldnt move my left arm where it was suppose to go!!!!

I was actually dx with having a stroke, but a student doctor asked if she could do an MRI and lumber punch so I said yes and it all came back with MS x


vix.jpg

Share this post


Link to post
mayb

Funny Vix I thought I had a stroke when everything went wrong at once the first time. It was all left sided so that was the first thing I thought of. I was referred by my gp to a neurologist straight away and told not to panic I would be seen in about 3 weeks. How do you not panic when someone tells you not to?? I think I saw a neurologist about 10 months later and I still have no diagnosis 14 years down the line.

 

It must have been a shock to you finding out this way. Do you think it would have happened if you weren't so stressed out by the exams? How have you been since that time and did you know much about MS from your training as a doctor?


Mayb

Share this post


Link to post

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Similar Topics

    • Stress levels

      Is it normal for MS to make usually unflappable people into screaming panickers? Five years ago I was a professional person juggling all sorts of crises. But now, the smallest changes in plans leave me angry, annoyed and miserable. Why?? With my sensible head on I know cars break down, it rains occasionally , my favourite TV is cancelled. But, New loony head just can't cope...

      in General Discussion about MS

    • I am just venting, not my ms but obviously family stress does affect it

      Dont read if you dont want to listen to a whinger.   I have spoke before about mum not accepting my ms and her ongoing age problems.   I am an only child, I visit once a week or more, She is 92. I do her washing, I do her online shopping, I do her wiltshire food online. I do her banking and post etc. She cant open tins or bottles anymore. She is registered blind. she is partially deaf. she cannot walk well, shuffles and uses a wheelie walker. She is borderline vascular dementia. She cannot use an ordinary oven or phone she just presses the button to get me. She is a bit incontinent urinary and i buy her pants. She insists on washing her own underwear and I have seen them hanging in the bathroom and they have allsorts of stains on them. I have told her wash them dry them and then I will put them through a proper wash, talking to myself there. The only good thing is she is in sheltered housing.   We had seen her on sunday, then she fell monday cannot get up when she falls. So she shuffled and shuffled on her bum she said she had probably worn holes in her knickers shuffling on the carpet. So she pressed my button on the phone, to go and get her off the floor. I said have you got your alarm button round your neck yes she said so I said press it they will get there quicker than us 60 mile away So she did and they sorted her quickly.   I keep bursting into tears because I dont know what to do , I was a bit nasty this morning telling her if she didnt sort her knicker hygiene out she will have to go and be looked after somewhere. We are taking her for a CT scan tomorrow. I dont think they will find anything, her BP is better than mine her heart rate better. I look fine with my MS so people expect more from me.   She does not have any carers coming in. She has a cleaner once a week. I feel more resentful and nasty than when I first started looking after her. Thank goodness I dont live with her, think I would do something really really nasty.   Thank you for anyone who has read this, you cant help no one can the memory clinic put her forward for a social service assesment to get some care. still waiting

      in General Discussion about MS

    • Stress Management

      Now, here's a good lesson that I picked up from Facebook :-   "Apparently: A psychologist walked around a room while teaching stress management to an audience. As she raised a glass of water, everyone expected they'd be asked the "half empty or half full" question. Instead, with a smile on her face, she enquired: "How heavy is this glass of water?"   Answers called out ranged from 8 oz. to 20 oz.   She replied, "The absolute weight doesn't matter. It depends on how long I hold it. If I hold it for a minute, it's not a problem. If I hold it for an hour, I'll have an ache in my arm. If I hold it for a day, my arm will feel numb and paralyzed. In each case, the weight of the glass doesn't change, but the longer I hold it, the heavier it becomes."   She continued, "The stresses and worries in life are like that glass of water. Think about them for a while and nothing happens. Think about them a bit longer and they begin to hurt. And if you think about them all day long, you will feel paralyzed – incapable of doing anything."   Remember to put the glass down."  

      in General Discussion about MS

    • Stress

      Ive had a really stressful and worrying weekend regarding my 19yr old son.Hopefully tomorrow alot of things will start to be sorted out.ive had woorsening of ms symptons i know stress can be a factor in this,is it possible for the stress to have a effect so quickly ? or just one of those things ? take care peeps,have a good day xx

      in General Discussion about MS

    • stress

      hi all i have posted a topic in the lounge but this is connected to that, my left eye is not seeing yet and i finished my steroids 12 days ago. should i be seeing yet? my other topic explains the stress i am having but could it delay my recovery? my eye is improved but nowhere near towhat it was before.  

      in General Discussion about MS

About Us

Founded in 2004, MS People UK is a community website and discussion forum by and for people with Multiple Sclerosis as well as for friends, families, supporters and those interested in this disabling condition.

If you’re newly diagnosed or want to ask about possible first symptoms, or if you’ve had Relapse Remit, Secondary or Primary Progressive MS for some time, a welcoming group of fellow MS sufferers is here to chat with you about MS symptoms, diagnosis and treatments.

The atmosphere is friendly whilst being compassionate, supportive and caring. Members also post about a variety of subjects not related to MS, as well as share jokes, talk about their hobbies, have fun, and more.


The MS People Forum is not responsible for advice or information supplied by members. We suggest you seek medical advice before trying anything.
×