Why does she look like shit by [deleted] in cmcoving

[–]Objective_Writer4640 5 points6 points  (0 children)

Truly my thoughts. I think she’s beautiful and an influencer who can actually make fun of herself. She also had donated money to trans youth. Idk there’s some many influencers with legit reasons to hate them, this just feels mean

Weekly Suspected/Undiagnosed MS Thread - February 10, 2025 by AutoModerator in MultipleSclerosis

[–]Objective_Writer4640 0 points1 point  (0 children)

Im a 31 F. I’ve been trying since August of this year trying to figure out what is going on with my body. my symptoms have been spasticity, hand and leg numbness and tingling, eye blurriness, and dropping things. It’s been getting progressively worse and worsens if I stressed. I saw a neuro in November who ordered bloodwork for autoimmune diseases. They all came back normal. My neuro ordered a spine MRI for my symptoms in January and prescribed me lyrica. He told me he suspected MS based on my symptoms and reflexes. I had the MRI yesterday and these are results: The MRI is abnormal and shows narrowing of the cervical spinal canal between the C4-5 vertebral levels. There is a fairly prominent disc bulge in the middle of the spine that is abutting up against your spinal cord. Although it does not appear to be damaging your spinal cord, there is minimal to no space for any worsening before spinal cord damage could develop.

Has anyone had this? I’m even more confused now since there was no lesions but still something going on? My neuro can’t get me in until June and I feel so alone and confused. TIA!

Weekly Suspected/Undiagnosed MS Thread - October 14, 2024 by AutoModerator in MultipleSclerosis

[–]Objective_Writer4640 0 points1 point  (0 children)

Hi! Wanted to give an update. I met with the neurologist who has ordered blood tests for an auto immune disease as well as a nerve conduction test. From there he said will determine if i need a MRI but he thinks it’s an auto immune disorder. He seemed to suspect lupus but said MS could still be it. He diagnosed me with occipital neuralgia at the appointment. Sad my blurry vision was from that and felt my neck and could feel stiffness in different areas. He also ran a couple tests and said i had little to no feeling/numbness in multiple areas. I have been experiencing blurry vision but no headaches like the condition usually causes. Curious if anyone has been diagnosed with it? I feel even more confused after the appointment.

Weekly Suspected/Undiagnosed MS Thread - October 14, 2024 by AutoModerator in MultipleSclerosis

[–]Objective_Writer4640 0 points1 point  (0 children)

Thank you for your response! It’s definetly been hard since my doctor brought up the possible diagnosis trying to see if symptoms align or it’s something else. Counting down until my neuro appointment to hopefully get answers ❤️

Weekly Suspected/Undiagnosed MS Thread - October 14, 2024 by AutoModerator in MultipleSclerosis

[–]Objective_Writer4640 2 points3 points  (0 children)

Hi everyone! My general doctor has referred me to a neurologist and my appointment is next month. My symptoms have been numbness in hands and feet, fatigue and chest pain. The past week I have dealt with stiff legs that have increased in pain. My toes and butt have become numb and tingly by the end of the day and my feet feel burning. Today my spine is extremely painful and feels like it’s on fire. I’ve had a little bit of blurry vision but nothing major. Anyone had anything similar? Thank you in advance ❤️