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.
sharron

cognitive stimulation therapy

10 posts in this topic Last Reply

Recommended Posts

sharron

iam starting this next week,its a 8week course,4 hrs a week.doctors don't know if iam suffering from ms forgetfulness or early onset dementia.has anyone done this course ? was it helpful ? what iam to expect ? sorry for the bombardment of questions !! lol,take care everyone

Share this post


Link to post
Rama

Sorry Sharron - I have had no experience of this but I would be very interested to hear all about it.

 

Was the course recommended to you or do you have to be referred by a doctor?

 

Sorry - you come on looking for answers and I've got more questions for you. :what:

 

Gill x

Share this post


Link to post
sharron

hi jill, I was refered by my ms nurse,to a shrink saw him once he asked me questions like when is my kids bdays,didnt do very good at that,lol.then I got refered to a physcologist where I did a lot of different tests,didnt do very well at that either ! lol.then got refered to the memory service and this is were iam now !! one of the things I cant remember is conversations so iam very good at keeping secrets but cant pass on gossip !! lol. tc x

  • Like 1

Share this post


Link to post
Rama

Well I hope you see some improvement with these memory classes. After all what's the point in hearing a good bit of gossip if you can't share it!!

 

:whisper:

 

Gill x

  • Like 1

Share this post


Link to post
sharron

my point exactly !! lol,hope I do see some improvement. tc x

Share this post


Link to post
Carra

Hi Sharron. Could the memory problems be caused by medication you are taking? One of the reasons I stopped the Pregabalin was that my memory was badly effected by it. Im fine now that I've stopped it. I know that Gabapentin can cause this too. They must have considered that though surely? Good luck. X x

Share this post


Link to post
Mal

Hi Sharron. Could the memory problems be caused by medication you are taking? One of the reasons I stopped the Pregabalin was that my memory was badly effected by it. Im fine now that I've stopped it. I know that Gabapentin can cause this too. They must have considered that though surely? Good luck. X x

 

I think my memory has improved a little since i changed over from Gabapentin to Pregabalin ,

though i suppose drugs have different effects on people

 

Are you getting a lot of fatigue Sharron ? i know my memory is always at its worst

when i'm tired .

 

Mal x


Edited by Mal

Share this post


Link to post
sharron

Hi Sharron. Could the memory problems be caused by medication you are taking? One of the reasons I stopped the Pregabalin was that my memory was badly effected by it. Im fine now that I've stopped it. I know that Gabapentin can cause this too. They must have considered that though surely? Good luck. X x

hi carra,my problems with my memory started before I tried pregabalin now off it cause of other side effects,currently on gabentin seem fine with that. tc,x

Share this post


Link to post
sharron

mal and carra,iam sorry about putting replies and quotes in the wrong places !! lol,i couldn't remember how to do it ! lol. mal your point about memory and fatigue has got me thinking.i had a incident the other night that scared the hell out of me,i got up in the nite to go for a wee,which I do most nites,i stood at the bedroom door couldn't remember where I was,where the bathroom was.i was like this for about 10mins then it came back to me.i was scared,and angry with myself for not remembering.i hadn't been boozing,no new meds,no change of dose in my current meds,hahdnt taken illegal drugsand have been in my ground floor flat for about 3yrs ,so usually know the layout of my home.that was really scary.my usual memory probs are not remembering conversations,being on the phone is worse ! not remembering what was said to me 10 mins before,cant cross the roads by my self,as I have a tendancy to walk in front of traffic,especially buses ! lol.iam better with routine.sorry for the long post !!!!! tc x

Share this post


Link to post
sharron

mal ,ps ,how does your memory effect you ? tc ,xx

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

    • Advanced Hyperbaric Oxygen Therapy

      Hi everyone,   Has anyone experienced Advanced Hyperbaric Oxygen Therapy? I'm always on the look out for different therapies and I understand some MS centres offer this. I would be interested to hear your thoughts. Many thanks, Catherine

      in General Discussion about MS

    • Dorsal column stimulation for pain relief

      Hi all I get a lot of pain with my ms, have tried many drugs - gabapentin, amitriptyline, pregablin, duloxitine etc and nothing has helped. Finally convinced my neuro to refer me to a pain specialist back in September, and have an appointment in August.   Ive just received my copy of the referal letter and in it he suggests i may be a good candidate for a dorsal coloumn stimulator. Does anyone have any idea what this is? Im a bit scared to google it! Any input on this would be appreciated, its freaked me out a bit! Thank you Laura x

      in General Discussion about MS

    • Reiki Therapy

      ok. Had my first experience of Reiki today. For the uninitiated, this is the laying on of hands (although she held hands over me most of the time) in order to re-energise your aura (natural energy field). I went in looking to find a way to relax/ de-stress. Wasn't sure if/ what I believed but as a friend pointed out that simply the music, the calm, the candles, the music couldn't hurt, could it?? Couldn't argue with that. Other therapies didn't appeal given current condition - didn't want massage, wasn't up to yoga, can't meditate alone so Reiki won. Have to say it was not what I was expecting. Had a 30 min conversation before even starting where we discussed problems and she explained what would happen. Then wrapped warmly on a bed - no removal of any clothes - and we began. Almost instantly I began to experience different sensations round the body (not MS ones) sometimes warmth, sometimes cold, occasional twinges - not painful. Burning feeling inside, again tho I was very conscious of it, it was not painful in anyway. Then it was as if someone had hooked me up to a socket and a mild current ran thru me. She barely touched me but at one stage she put her hands under my head and told me to just rest on them. No massage, no movement. I had expected to find this uncomfortable but found it strangely comforting. It lasted 30 minutes but felt about 15 (no she hadn't switched the clock!) and tho I definitely didn't fall asleep, I felt when I sat up as if I had just woken up. We then chatted for another 30 mins about the experiience and I drank water. She warned me that experience was different every time; that I might be emotional or very tired later; that it was a good idea to have a quiet peaceful time afterwards (so don't do it before kids sleepover!). Since then I've been feeling I suppose pensive, thoughtful, slightly sad. A little tired too and without doubt not the nervy/ hyper character I've been these last few weeks. Having said that, coming down off steroids, so it could be just natural reaction to that. No idea what to think, folks, just wanted to let you know about it. It's hard to articulate but I feel it's been beneficial and I will definitely be returning next week. x Lottie

      in General Discussion about MS

    • Hyperbaric oxygen therapy

      Hi All, WellI had my first session of hyperbaric oxygen therapy ( HBOT) last night. Basically I sat in a small chamber while they compressed the chamber to the equivalent of being at a depth of 16 feet. Felt a bit like going up in a plane and I had to release the pressure in my ears every now and then by swallowing. Once we were at the correct pressure we put on masks and breathed in pure oxygen for an hour. I didn't feel any different after the session but I am assuming I will need to have several sessions before I see any benefit - assuming I see any benefit at all. The most disappointing thing was I couldn't take my kindle into the chamber - I was looking forward to a good read. So I'll need to take a magazine or a real book next time.   I was wondering if anyone else has tried HBOT and if they have seen any improvement in their symptoms as a result.   I have got to the stage that I am now willing to try anything.   Cazza - you said you had tried it - how did you find it? What a shame they closed it down.   Gill x

      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.
×