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

The Emotional Issues Of MS

12 posts in this topic Last Reply

Recommended Posts

Sluggish
Marina

Contributed by Marcus, via the mailing list.

 

http://www.healthtalk.com/multiplesclerosi...22604/index.cfm

 

passage from said website

 

Anger, frustration, despair - emotions so consuming that if left unchecked can overwhelm and destroy a person, a family or a community. Dealing with a chronic illness may cause depression and anxiety too. In this program, we'll explore the range of emotional issues people with MS experience and examine ways to acknowledge these feelings in order to deal with the pain they evoke.

My query is that - would it be possible to put a UK version on your website? MS is universal but discussion of emotions on a more UK based interpretation would (in my mind) be a bit easier to associate with.

 

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

 

If anyone would like to take up this subject of the emotional issues of MS, please feel free to discuss it.


Marina

(belated DX in June '05, SPMS)

Share this post


Link to post
crispy

Hi all,

 

I have written about this before on certain other MS forums, so apologies if anyone has heard it all before.

 

My original scrawls were based more on a question than on a statement - at that time I didn't understand why my emotions were so easily brought to the fore. That question was answered by somebody with more of an understanding of the medical side of MS, and it seems there is a name for it. My brain being fairly addled these days, it left my head at almost the moment it entered it, so if anyone knows of the term, please respond here.

 

I first noticed the effect while watching Miss Saigon in the West End about six years ago. Anyone who has seen the show will know that there are sad sections in it, particularly when Kim shoots herself, but the effect it had onme was unreal. I knew what was going to happen, I had seen the show four times before, yet my sobbing was loud and uncontrollable. It would have been bad enough for a lady in that position, but for me, it was just too much :no:

 

From that time on, I never went to see a show again. I have similar attacks at home, usually alone fortunately, over crazy things like Home & Away, Neighbours and even EastEnders, but it's out of my hands - I just have to learn to cope.

 

Some people it seems, have laughing fits, caused by the same MS problem, but I don't have to worry about those. This past week has seen quite a lot of the emotional outbursts, as those who know me here will understand, but for those who have not experienced this little addition to the other problems, I hope this may help you to understand, if and when they do occur.

 

All the best,

Chris P :crutch:


................................ :dog: ........................................

All the best,

Chris P

Share this post


Link to post
ddgorgeous

Chris,

 

It sounds like Smokey is a great loss, I hope you manage to get through it all and are coping.

 

I am sorry to hear about your own experiences with your own emotions and can sympathise a bit.

 

I have noticed over the last couple of years occasionally laughing uncontrollably over the smallest thing. I do not know why it happens, or when to expect this, it can be the most innocent thing that can set me off. (I first noticd it 3 years ago) I read about this and that it had been noted as happening in some people, but was not aware there was a name given to it. I am/have been too embarrassed to mention it to my GP or family, although I am sure my family suspect a bit (they think I am nuts anyway so I get away with it to an extent), but think it is something my GP should be aware is happening. As it has not been one of the most important items to dicuss during any very brief consultation it has never been mentioned. I should possibly think about bringing it up when I next see him. If you ever come across a name for this, or any details, please pass them on.

 

Look after yourself,

 

Ron


ppms, dx 2001

Share this post


Link to post
crispy

Hi Ron,

 

Thanks for your thoughts.

 

I found the article that I read and the condition is called Emotional Lability - it is part of the cognitive problems associated with some forms of MS. I believe a drug called Neurodex is being tested in the US for use in MS.

 

Chris P :crutch:


................................ :dog: ........................................

All the best,

Chris P

Share this post


Link to post
ddgorgeous

Hi Chris,

 

Thank you for your information on Emotional Liability. I will look into it all more now and probably write to my GP before bringing it up during a consultation with him.

 

I actually find him a lot more helpful when I write to him and just drop a letter in by hand with the receptionist than making an appointment where an appointment is possibly not needed. It also means that any notes I bring to an appointment are usually covered in more depth and I receive much better response than otherwise. I write to him frequently to request copies of items held in my file etc and he has always been very halpful when using this approach. I do not know if anyone else uses this kind of appraoch, but it appears to work very well for me so far.

 

All the ebst,

 

Ron :crutch:


ppms, dx 2001

Share this post


Link to post
crispy

Hi Ron,

 

I seem to have missed this one yesterday, so I'll make good now :tabletalk:

Thank you for your information on Emotional Liability.

If you are doing a search on the Internet for this, please note that it is 'Lability' rather than liability.

 

I agree with your point of writing to your GP, I adopted the same policy when trying to obtain LDN, and sent through a lot of information together with a letter, several days before my appointment. When I got there, he had even managed to read it all, and knew what I was talking about :D

 

Chris P :crutch:


................................ :dog: ........................................

All the best,

Chris P

Share this post


Link to post
Ellie

:crying: Hi All

 

I have wandered back on to the forum which I have not used since before I went on hols. Have been too busy trying to deal with all the accumulated emails. Interested oin the mails on emotional lability. I seem to have gone the other way. I feel SAD but can seldom cry, and Im sure I do not laugh as much as I did. I know I have a sense of humour, at least Marina says I have ! but no, I do not laugh like I used to. I dont cry at "weepies" I too was moved by Miss Saigon but did not show it. It may be due to drugs, As well as MS I had a heart attack in March this years so now I take eight pills wwhen I get up in the morning, and another three when I go to bed, perhaps they are killing off my reactions, but no matter how sad I feel I seldom cry or laugh like I used to. I dont like it much, but there you go, Id give anything for a good howl :tabletalk: Even a good belly laugh would help, lol. Anyone got any ideas. I feel like a moron :crutch:

Luv

Ellie

Share this post


Link to post
crispy

Hi Ellie,

 

It's good to have you back on the forum :yes:

 

I can't offer any ideas on why you seem to be affected emotionally in the reverse form to mine, but it could always be the pills, as you suggest. Much as I hate the uncontrolled outbursts, I think I'd much rather that, than nothing at all :crutch:

 

I think I may try to do a little more research into the subject :tabletalk:

 

Keep smiling,

Chris P :tabletalk:


................................ :dog: ........................................

All the best,

Chris P

Share this post


Link to post
Ellie

Hi Chris

 

I tend to agree with you, I dont like being "switched off" I think Jim probably prefers it this way, more like to stop me crying, he hates that, just cannot handle it, and does not seem to mind if I do not laugh lol, I just dont like ME very much, perhaps it is depression :crying: :crutch::tabletalk: Oh well, may be it is old age.

 

Luv

Ellie

Share this post


Link to post
crispy

Hi Ellie,

 

I just dont like ME very much, perhaps it is depression

Hey, if you don't like you, what chance is there for anyone else? Keep smiling :yes:

 

I've been out today, there's a novelty all by itself, but now I'm back, I'll do a little digging.

Now, what's all this about old age? I straight way went to look at your profile, to see what you thought old age was, but guess what - no details filled in :no:

 

All the very best :D

Chris P :crutch:


................................ :dog: ........................................

All the best,

Chris P

Share this post


Link to post
Hodge

Hi all

 

I know I have an article somewhere about "Emotional Lability" and will have to dig it out. I have been feeling really emotional and very tearful recently over silly little things i.e. programmes on TV, even some of the adverts for goodness sake. I've always been a strong independent sort of person and this just isn't like me at all.

 

I know I've been getting really frustrated because I can no longer manage or I really struggle to do certain things but I don't feel "down" at all and I still have a good sense of humour and enjoy a good laugh with friends.

 

My husband isn't well at the moment and today I thought I would try and help him in the garden by doing a little weeding and cutting back some of the plants. I just didn't think that I would find this so difficult to do and it made me realise how weak and useless I've become over the past couple of years. Not only was I absolutely exhausted within 30 mins I became very angry and the tears were not faraway.

 

I realise I'm having short term memory problems. difficulty with concentration, finding the right words and often talking "double dutch" when having a conversation. I find I'm worrying over little things throughout the day and I'm unable to get to sleep until the early hours which again worries me as I know how useless I will be the following day. It seems like a vicious circle. I'm going through the menopause as well which doesn't help so can only hope everything will settle down soon.

 

I'm sorry if this is a bit garbled. It's been a very long day.

 

Hope you are all keeping reasonably well.

 

Sue :rolleyes:

Share this post


Link to post
crispy

Hi Sue,

 

I hope you have a better day today.

 

I eventually found my article in the May/June edition of New Pathways magazine - Do you get that mag?

 

Keep on smiling,

Chris P :rolleyes:


................................ :dog: ........................................

All the best,

Chris P

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

    • Cognitive and Memory Issues Have Got Worse

      Hi everyone Just to clarify. I saw a neurologist back in the early 90s as my GP suspected I had a problem with my central nervous system but the Neurologist, without pursuing any investigations, told me all of my symptoms were down to anxiety.   Since then I have never managed to convince any GP to refer me to anyone else about my continuing symptoms so I am self-diagnosed. I have finally managed to get referred to a memory clinic and am also waiting for the results of a head scan that happened in June. The referrals were not connected to any mention of M.S. as I asked due to deterioration in my cognitive functioning which wasn't great anyway.   A privately funded clinical psychologist picked up on all of these issues + ADD and Dyslexia but NHS doctors dismissed the report and continued to put things down to anxiety, which thankfully I don't suffer with.

      in General Discussion about MS

    • Eyesight issues

      A little over three weeks ago I started having pain in my left eye when moving it (looking to the sides or up/down) and after around a week my vision started to get worse in that eye. The pain lasted for two weeks and has now gone, but the vision is still bad. Everything is duller, colours less vibrant, it sort of looks like the world has gone misty and I can't see properly. Just sitting here at my computer, if I close my good eye I can't read what I'm typing without sticking my face very close to the screen.   I had optic neuritis a couple of years ago and was worried it could be that again so told my nurse who bumped up my appointment with the eye department and I went in yesterday. They did the basic eye test reading the chart, which I couldn't read as well as usual but it wasn't too bad (I always find the chart is misleading about my eyes because it's lit up and so high contrast I see it a lot better then I do things in the normal world). I also had the field of vision test and a scan of my eyes.   At the end she told me my vision was better then 100% and she didn't need to see me again until May next year. I told her I can't see properly from that eye but she just kept telling me there's nothing wrong with the eye and not to worry.   When I asked about why it's bad she said maybe a headache, a memory of my past optic neuritis or maybe early optic neuritis that isn't showing signs yet. I assume by headache she meant migraine, but from what I've read it doesn't sound like that's the case. I don't know what she meant by memory. And if it could be optic neuritis in the early stages wouldn't they want to see me again to confirm it?   I'll be seeing my neuro soon for other test results so I guess I'll wait and ask him about it as he's always been very helpful.   Have any of you had similar eye issues and what did it turn out to be?

      in General Discussion about MS

    • Emotional numbness

      Has anybody or is anybody feeling emotionally numb. Apparently comes under Cognition symptoms/depression/clinical depression and as no 2 people are a like in the symptoms was just wondering if thse are common

      in General Discussion about MS

    • DVLA issues

      Hi guys,   I don't hold a full driving licence, just a provisional. After my diagnosis way back in feb I dug it out and sent it off to declare my dx, also to change my address and surname (better late than never!) as I suddenly realised how much i need to be able to drive as it will give me so much more independence. I filled it all out and got a letter back to say they needed my dr's details etc, sent off in march. Got a letter today (yes today 10m on!) saying they still had not made contact with my neuro, could I chase him up and get back to them? I have changed neuro's in this time and according to my nurse, current neuro is off until January (nice life for sum huh?!). So what do I do now? Just wait or try the old neuro again? Would he still count as my doctor? Why do we always end up having to organise things?!   All advice welcome, thanks Lx

      in General Discussion about MS

    • Memory issues

      Hello everyone   I am doing a university course at the moment in psychology which is all very interesting and i'm enjoying it a lot. I have declared my disability to the university and they have been really helpful in making sure i'm catered for, giving extensions etc.   However I am finding it really hard to remember what I read, I seem to have a very short concentration span and my memory is well, useless (putting it mildly). I also struggle with spelling, I'm forever getting letters the wrong way round and just can't recall the right words at all sometimes.....thank goodness for spell checkers and the internet!   I really do feel my cognitive abilities are fading fast and I would really like to find a way to adapt. So I wondered if anyone else suffered with the same and if so how they manage?   All thoughts welcomed :-)   Laura

      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.
×