- Home
- Share
- Forum
- General forums
- Living with Multiple Sclerosis
- Caring for one diagnosed with MS... What Should You Know?
Caring for one diagnosed with MS... What Should You Know?
- 26 views
- 1 support
- 3 comments
All comments
Lee__R
Community managerGood advisor
Lee__R
Community manager
Last activity on 04/03/2020 at 5:04 PM
Joined in 2018
1,338 comments posted | 84 in the Living with Multiple Sclerosis group
2 of their responses were helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Explorer
-
Friend
-
Top chef
@Niagia83 @Bbryant81 @LynndMS @suplkr1 @siemprelucha @meek58 @Samantha @Sillysarah8466 @Paulmarji977hooo.com @Emma2190 @MS_283 @broadwaylady @Kjess_srn @copa20 @maryam20 @Ms052018 @Tjw0673 @Areid79 @padres44 @Kelcrna @Baxter @Triciarie
Emma2190
Good advisor
Emma2190
Last activity on 07/04/2022 at 1:29 PM
Joined in 2018
94 comments posted | 70 in the Living with Multiple Sclerosis group
1 of their responses was helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Explorer
-
Friend
-
Newsfeeder
@Lee__R Hi, thanks for the tag and I will offer some input of my own. A caregiver or loved one should be understanding especially when it comes to the cognitive memory problems etc for the person with MS, because mistakes will happen and repetetion is normally a must with some re-teachings needed too. Basically patience and understanding is the most important things for a caregiver or loved one. It's also very helpful if they take part in appointments, research or anything regarding the person with MS, that way everyone can be on the same page and support will be stronger. Lastly, the other reason understanding and patience is needed for either, is because with MS there are mood swings that can mimic bi polar and depression is also worse especially if that person already has it. Everyone's different, so some may have mood swings, (like I do and depression) and some may not but still knowing this is important for the caregiver, loved one and family. Hope that answers things. ~Emma
See the signature
Just trying to get by..
copa20
Good advisor
copa20
Last activity on 09/02/2020 at 3:21 PM
Joined in 2018
21 comments posted | 19 in the Living with Multiple Sclerosis group
Rewards
-
Good Advisor
-
Contributor
-
Explorer
I agree @Emma2190 you hit some very good points!
Patience and a deep care for wanting to understand the symptoms and difficulties the disease presents... to not only understand the physical impact but also the mental aspect; to not only be there to help with the physical parts, but also the emotional and mental part (even if it is just watching a tv show with us... it means the world, trust me).
Give your opinion
Articles to discover...
11/18/2024 | News
Drugs and libido: Which treatments can affect your sexual desire?
11/08/2024 | Advice
11/04/2024 | News
02/20/2019 | Advice
Cigarettes VS e-cigarettes: an update on the consumption and pitfalls to avoid
03/11/2019 | News
04/15/2019 | Advice
02/14/2019 | Advice
Subscribe
You wish to be notified of new comments
You have been subscribed
Lee__R
Community managerGood advisor
Lee__R
Community manager
Last activity on 04/03/2020 at 5:04 PM
Joined in 2018
1,338 comments posted | 84 in the Living with Multiple Sclerosis group
2 of their responses were helpful to members
Rewards
Good Advisor
Contributor
Messenger
Explorer
Friend
Top chef
Multiple Sclerosis can be a debilitating disease and often times, those diagnosed with MS, lean on the shoulder of a loved one or a caregiver to help them with daily tasks; however, there is no one who knows better than how to properly help, care, and be there for someone with MS than a person diagnosed with the condition.
What do you feel is important for a caregiver to know?
What recommendations would you give to a caregiver?
How can one better be there emotionally and socially for one dealing with MS?