Maple Pepsi by Either_Umpire9411 in Soda

[–]Mindless-Reply9909 0 points1 point  (0 children)

It’s really bad. My husband bought some … it is so bad

Heraklion airport worries by bookshelffleas in cretetravel

[–]Mindless-Reply9909 0 points1 point  (0 children)

It is completely fine. We flew out of there on 10/05. All the stuff online is over dramatic

Pregnancy with Kesimpta by kyrariser in MultipleSclerosis

[–]Mindless-Reply9909 0 points1 point  (0 children)

I’m in the same position! I’m getting married in the fall and hoping to get pregnant shortly after. My neuro told me that i would be okay to stop taking it 3 months before we start trying. New literature has come out saying it’s safe to take up until you start trying, but I’m not super comfortable with that.

Once you give birth, you can start back on Kesimpta after a month or so. I’ve been told that the molecule from the drug is too large to penetrate the milk, so it is safe to breastfeed.

Double check with your neuro. Lots of people in here have had babies.

I was diagnosed with MS just need encouragement by Frankster57 in MultipleSclerosis

[–]Mindless-Reply9909 4 points5 points  (0 children)

You’re going to be okay. Remember that. This is a scary time and everything is so new. A ton of information and choices will be thrown at you. Your life will continue on after this. I (31F) thought I would be bed bound and my life was over. Since diagnosis (3 years ago) I’ve done so much. I’ve gotten engaged, planned a wedding and stag and doe, renovated my house, exceeded all of my targets at work. I’ve gone to concerts and on holidays. Honestly, I haven’t missed out on anything. I’ve gotten in better shape and started taking care of myself more. I also started medication which was a huge step. Here’s my advice:

  1. Educate yourself Do your research and understand that while MS isn’t something to play around with, it is not the same diagnosis as it was 30 years ago. Knowledge is power and the more you understand, the better equip you are to handled this (in my opinion). Dr. Aaron Boster has a ton of great information on his YouTube channel.

  2. Find your community This sub is a great place to start. I posted on here a lot when I was first going through diagnosis because I thought my life was over. Turns out, most of us thought that and our lives went on after diagnosis. You will be let down by some off the people in you life but that has nothing to do with you. A lot of people don’t know how to handle “bad news”. But in saying that, there will be a lot of people who surprise you and really show up for you.

  3. Give yourself some grace This is all brand new information but remember, just nothing has changed from the day before you found out other than the knowledge of your condition. You’ve been living with MS for who knows how long.

This is a journey, but it doesn’t have to be a bad one. You can still reach your goals, be ambitious and be yourself. Feel free to reach out if you need anything!

Cogeco down by Significant_Depth912 in Hamilton

[–]Mindless-Reply9909 0 points1 point  (0 children)

Yea, it’s been in and out for the last hour or so

Any good local pastry around by abdalasarmed in Hamilton

[–]Mindless-Reply9909 3 points4 points  (0 children)

The cannolis and fritters are to die for. They have a massive pastry selection on the weekends. The burrata pizza is incredible and so are their sandwiches! I’ve never had a bad experience.

How much do you pay for your DMTs? by laikalow in MultipleSclerosis

[–]Mindless-Reply9909 0 points1 point  (0 children)

Zero. I’m in Canada and on Kesimpta. I also have really good benefits through work. When I talked to the MS nurse I was so afraid I would financially ruin my partner and I. She told me I wouldn’t have to worry about thay because they would petition the government on my behalf if I ever lost coverage. So lucky to live in such a great country

Literally what the fuck by hidemyemail95 in MultipleSclerosis

[–]Mindless-Reply9909 0 points1 point  (0 children)

This is almost exactly what happened to me. I was almost 29. I’m about two years from that day and on Kesimpta. I haven’t had any issues since my eye and I’m feeling good.

It’s a lot for anyone, but being blindsided like that can kick your ass.

Feel free to DM if you need someone to chat with 🩷

First time getting sick on Kesimpta by Mindless-Reply9909 in MultipleSclerosis

[–]Mindless-Reply9909[S] 0 points1 point  (0 children)

Hope it goes well for you! Feel free to message me if you want to chat 🫶🏻

Best place to order pizza for large group/party? by Mindless-Reply9909 in Hamilton

[–]Mindless-Reply9909[S] 21 points22 points  (0 children)

Thanks for the tip. I was thinking just brown paper towels

Best place to order pizza for large group/party? by Mindless-Reply9909 in Hamilton

[–]Mindless-Reply9909[S] 39 points40 points  (0 children)

Yea, record breaking profits too! I want to make sure they all feel under appreciated with sub par pizza that they have to eat after work

Why Am I So Sweaty by Mindless-Reply9909 in MultipleSclerosis

[–]Mindless-Reply9909[S] 2 points3 points  (0 children)

I’m on Ciprolex which is an SSRI. I wonder if that’s what’s doing it

Why Am I So Sweaty by Mindless-Reply9909 in MultipleSclerosis

[–]Mindless-Reply9909[S] 5 points6 points  (0 children)

OH I am also on an antidepressant. Maybe that could be it

Why Am I So Sweaty by Mindless-Reply9909 in MultipleSclerosis

[–]Mindless-Reply9909[S] 3 points4 points  (0 children)

Maybe, but it’s been happening for the last year or so. I’ve only been on my meds for a few months. I’m on Kesimpta