#keep - Shift.ms

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@Eltel

Last reply

A lot of you guys are talking about dating with MS, it’s now been 6years since my last relationship, I miss the banter , the fun , the hugging , the intimacy with a woman. So due to the lack of activity in my sex life I’ve decided to become a Muslim. My Muslim name will be “Seldom Bin Laidon”. Having MS is not exciting or easy to live with but we have to keep going and hoping life might get a little better for us , we have to keep smiling guys

First posted on the Shift.ms app

1

@Keith71

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Hi there everyone just a quick note I had a fall the other week and I have a hairline fracture of my left hip and I have been in hospital for two weeks and now I have to have rehab and get my hip working again so far not going very good but I’ll keep trying

First posted on the Shift.ms app

13

@MSshef17

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Has anyone tried using neurotrophic vitamins to help regrow myelin? I keep seee these ads for it and I did some research. There is some truth behind it and I was wondering which brand you were taking? Seems like the OTC drugstore/grocery store synthetic vitamins don’t do the job like the natural ones. Any thoughts??

First posted on the Shift.ms app

2

@HappyLady42

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New Here : Hello all , I’m Miss Mary . I been diagnosed since 2011 , it’s been rough , but I’m making it. I work out everyday for an hour to keep me grounded I also implemented Nutrition meals . I start with slim fast shake with an apple and I have berries for lunch with dinner I have glazed salmon with fresh lemon to end meal

First posted on the Shift.ms app

9

@Taras

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Hi everyone. God bless you all. Please let me know if you hear about Ubiquinol. I'm getting it tomorrow I ll keep you updated.

First posted on the Shift.ms app

2

@Randyadams

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I can't get sleep. Nerve pain is bad. And my insomnia has been hard. Anybody up for talking. I need a friend. My ms is really acting up. My body especially my legs keep on going stiff. . My caregiver is sound asleep. And doesn't understand what I am going through. Please help.

Jurupa Valley, United States

First posted on the Shift.ms app

3

@Glamluvs5H8MS

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True story really. I am going to stay with my oldest son, here home my other son is overwhelmed, he doesn’t feel comfortable being too far from me🥹 his other siblings have minimized what he seeing maximally! We talk and I do understand his feelings, they are valid! So I’m me meeting my 2 granddaughters who are both under 4 so I am excited yet I have zero income😫 my flight and thing were gifted to me. I’m am grateful for that. I wanted to get to meet my granddaughters before anything else happens. I have hired counsel to assist me in obtaining Disability, I apply a few times and was denied. I can’t even afford my medication. Not looking for sympathy, I guess, just wanted to be more clear, I ABSOLUTELY hate MS and what it’s done to my confidence, yeah I don’t trust myself,& I before this all I was actually looking forward to turning 50! Yeah made it to 50 but I don’t like how I feel and how unsure I am now about the things I was MOST confident about doing, not so much these days and it makes me ANGRY cuz I didn’t plan this nor have the resources to live with this confidently. Praying for a steady body to keep doing what it HAS been doing for 49 years!! Health care is NOT caring these days and I can only say, timing has been my lack for some time now. I digress have a awesome MS’n day everyone. 💜🫶🏾🤟🏾💪🏾🤞🏾✌🏾

Fort Worth, United States

First posted on the Shift.ms app

9

@NeuroPulse

EditedLast reply

Alot of yall might agree with me but uh…“MS is the only roommate I never invited… and somehow it keeps changing the thermostat, moving my stuff, and turning off the lights.” 😂

First posted on the Shift.ms app

11

@Angelwings79

EditedLast reply

Fighting to keep my independence

New symptoms have been coming on thick and fast. 8 conditions all overlapping MS. In 2.5years my life has changed drastically. 80% cognitive, but coping better as im not going crazy and assessment confirmed cognitive decline. Now my mobility! I've fought this since 2015 pre diagnosis doing little th...

First posted on the Shift.ms app

5

@kala21

EditedLast reply

I’m experiencing neuropathic nerve pain in my legs and feet 😔 Its so mentally draining I’m finding it hard to cope with because I got to stay active to keep my mind sane and because I can’t do that right now I’m not coping at all. I’m having bad thoughts and I don’t normally get this low or depressed. How do you all manage this?

Aberdare, United Kingdom

First posted on the Shift.ms app

9

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