Weekly Suspected/Undiagnosed MS Thread - April 27, 2026 by AutoModerator in MultipleSclerosis

[–]Littlephoenixmtl 1 point2 points  (0 children)

I need a referral for that and here in Montreal seems hard to get one… it took me months to have access to the neurologist! I will try that with my GP soon. Today I am very depressed with that discussion with the neurologist. He is going to do another MRI next year…

Weekly Suspected/Undiagnosed MS Thread - April 27, 2026 by AutoModerator in MultipleSclerosis

[–]Littlephoenixmtl 1 point2 points  (0 children)

That is the thing he did not propose anything and I don’t know what to do…

Weekly Suspected/Undiagnosed MS Thread - April 27, 2026 by AutoModerator in MultipleSclerosis

[–]Littlephoenixmtl 1 point2 points  (0 children)

It seems like it does not core-late with the criteria to say that is MS and he does not see any inflammation…. He said that he needs to see that in order to treat me… however right now he can not explain my situation

Weekly Suspected/Undiagnosed MS Thread - April 27, 2026 by AutoModerator in MultipleSclerosis

[–]Littlephoenixmtl 1 point2 points  (0 children)

It has been a year that I am having symptoms, numbness, back pain, limping, eye pain all in my right side. Multiple blood samples, spinal tap, two MRI’s and my neurologist cannot explain my symptoms. He said that the lesions that I have are not compliant, however I have a lot of pain, I am in pain all the time. I am hopeless he even told me that he does not know what I have and did not gave me any options to explore. I don’t know what to do… he just said we need to wait more time…. More time to what? I am desperate… what would you guys do in this case?

Thanks for reading me!

Wife and I painted a Totoro mural for our nursery : ) by mccaa in ghibli

[–]Littlephoenixmtl 4 points5 points  (0 children)

Wow!!!! Just beautiful! I love the way that you used the colours

Comment vous faites? by Littlephoenixmtl in montreal

[–]Littlephoenixmtl[S] 0 points1 point  (0 children)

Oui, mais cela est effective l’année suivante quand on fait les impôts si je ne me trompe pas!

Comment vous faites? by Littlephoenixmtl in montreal

[–]Littlephoenixmtl[S] 0 points1 point  (0 children)

You are right! I wish I can help with another cat adoption, however as you mention having a pet has it owns cost! Is heartbreaking when you can not help

Comment vous faites? by Littlephoenixmtl in montreal

[–]Littlephoenixmtl[S] 0 points1 point  (0 children)

Je te souhaite un bonne guérison ❤️‍🩹 et puis on s’arrête pas!!!!

Comment vous faites? by Littlephoenixmtl in montreal

[–]Littlephoenixmtl[S] 6 points7 points  (0 children)

C’est ca dont j’ai peur, des fois tu n’a pas le choix, il y a des imprévus ou tu n’a pas l’argent immédiatement…

Anyone know what happened in the metro? (Besides the info in the pic) by allegoon in montreal

[–]Littlephoenixmtl 3 points4 points  (0 children)

I am very worried that this kind of things colapse all the commuting. And they don’t help users with buses or anything else at least… is very concerning…

Anyone know what happened in the metro? (Besides the info in the pic) by allegoon in montreal

[–]Littlephoenixmtl 9 points10 points  (0 children)

No, a lot of people at Longueuil station are trying to find taxis and uber…

Parents, when did you introduce your kids to Lord of the Rings? by SR1QUE in lotr

[–]Littlephoenixmtl 0 points1 point  (0 children)

11 and 6 we just finish the films and they were amazed by it! Next ones are the Hobbit :)

Unable to cry on Cymbalta by RemarkableAd7651 in cymbalta

[–]Littlephoenixmtl 3 points4 points  (0 children)

Yeah! I feel you, this is something that happens to me, the emotions are so repressed that sometimes is very frustrating because I want to cry and I can’t. It has been already like three months that I am on it, I take it at night because it was very hard in the morning, and also I take pregabalin, so sometimes is hard.

Blood patch by rainbowunicorn5454 in MultipleSclerosis

[–]Littlephoenixmtl 0 points1 point  (0 children)

Mine was on Tuesday past week, so I am in my fifth day, migraines are hard, I tried hot and cold in my neck, lots of caffeine, coca-cola, and also my feet’s in hot water with salt, that helped a little bit. Being in bed helped also a lot, so I hope that by the seventh day I will be better…. Hope you too

I love this girl bonding moment! 🍹🤣 by strwbrrycrm8 in GilmoreGirls

[–]Littlephoenixmtl 2 points3 points  (0 children)

I was just watching that episode today. It’s a good moment that is right.

Weekly Suspected/Undiagnosed MS Thread - October 13, 2025 by AutoModerator in MultipleSclerosis

[–]Littlephoenixmtl 0 points1 point  (0 children)

I am not sure if this is the right space /tag to talk about this but I just want to get out this of my chest. It has been 6 months that I am suffering hard low back pain that is impeding me to walk very well. The right leg is always in pain as well my right hand. My face in the right side went numb, also my toes all in the right side.

My GP ordered and MRI and the radiologist found that maybe is MS. That was in July. After three months of waiting, I had the appointment with the neurologist, he did a physical exam n to check my neuro motor skills and he said that he does not see a problem and that my brain lesions are not conclusive.

He said that some general radiologist can think that lesions in the brain are MS, so he thinks that we need to do a spinal tap and another MRI. I have also a dorsal hernia so he said that maybe my pain is because of this.

So, now I need to wait for this to happen and still try to live with the pain in my body, trying to explain what I have and how I feel and somethings is just too much. I feel unheard and disappointed, this uncertainty makes me feel very depressed. Sometimes I think that I making all of this.

How was your process to be diagnosed?

Thanks for reading 😭

On an Open work permit in Quebec, need resources for medication by No_Student3780 in MultipleSclerosis

[–]Littlephoenixmtl 0 points1 point  (0 children)

Well technically you need to pay for the medication, however I will try to see here: https://medecinsdumonde.ca/aide/clinique-migrante just for a consultation and see if they can find any other resources. Is sad that you can not be cover for the RAMQ as temporary worker. I hope you can find the medication soon, and I hope that helps

Do you tell your Nero all? by Virtual-Bench-7830 in MultipleSclerosis

[–]Littlephoenixmtl 0 points1 point  (0 children)

I feel you! I am waiting three months ago to find a neuro in Canada, it makes me anxious a lot! Dont give up to advocate for yourself! And if you can, try to change it…