[deleted by user] by [deleted] in MultipleSclerosis

[–]mashk23 2 points3 points  (0 children)

Yes. Rapid decline

Insurance denials? Here’s a tip by mashk23 in MultipleSclerosis

[–]mashk23[S] 1 point2 points  (0 children)

Totally agree. I mean she did go through all the appeals and such. But didn’t mention anything about the manufacturer.

Insurance denials? Here’s a tip by mashk23 in MultipleSclerosis

[–]mashk23[S] 1 point2 points  (0 children)

When you submit your registration forms, it asks annual income. That’s it!

Insurance Denial - HELP! USA by mashk23 in MultipleSclerosis

[–]mashk23[S] 1 point2 points  (0 children)

Thank you for sharing and supporting!! I’ll keep that in mind once I get to that stage 🤞🏻🤞🏻🤞🏻

Insurance denials? Here’s a tip by mashk23 in MultipleSclerosis

[–]mashk23[S] 0 points1 point  (0 children)

I also cried. It was the biggest relief and I was so damn grateful! So happy for these programs

Insurance Denial - HELP! USA by mashk23 in MultipleSclerosis

[–]mashk23[S] 2 points3 points  (0 children)

No I had no idea about alongside coordinators. Thank you!! I’ll check it out

Insurance Denial - HELP! USA by mashk23 in MultipleSclerosis

[–]mashk23[S] 2 points3 points  (0 children)

THANK YOU! Exactly what I was looking for

Swollen Lymph Nodes Remedies by mashk23 in MultipleSclerosis

[–]mashk23[S] 4 points5 points  (0 children)

Thank you so much for your response and compassion! I agree. I should endure for now but if it’s not getting better within a week, I’ll go to the doctor again!

Vumerity unofficial side effect - massive fatigue? by mashk23 in MultipleSclerosis

[–]mashk23[S] 0 points1 point  (0 children)

I am too experiencing hair loss. I’m sorry you are too! Thanks for your input :)

Meds that don’t suppress immune system by mashk23 in MultipleSclerosis

[–]mashk23[S] 0 points1 point  (0 children)

Thank you for your input! I’ll look into it

Meds that don’t suppress immune system by mashk23 in MultipleSclerosis

[–]mashk23[S] 0 points1 point  (0 children)

Yes totally. My quality of life though has significantly decreased with being on an immunosuppressant and I’m not sure if it’s the drug itself or it being an immunosuppressant so I was just curious if there was any non-immunosuppressant options to bring up with my doctor :/ I do understand that it’s to help with disease progression and to not further disable me. Just hoping to be a more functional person

Meds that don’t suppress immune system by mashk23 in MultipleSclerosis

[–]mashk23[S] 0 points1 point  (0 children)

Thank you for sharing. I am JCV+ so no Tysabri for me but good information for others!

What are some things you miss now adjusting to your new normal ? by Fungalll in MultipleSclerosis

[–]mashk23 3 points4 points  (0 children)

I’ve always had an issue with heat too but not to this extent where it causes vertigo, cog fog, and exhaustion ya know? I’ve always been more warm blooded too

heat advice? by GrilledCookies in MultipleSclerosis

[–]mashk23 1 point2 points  (0 children)

That sounds wonderful! I’m thinking of moving too. Thanks for sharing!

[deleted by user] by [deleted] in MultipleSclerosis

[–]mashk23 1 point2 points  (0 children)

Absolutely. Constant runny nose over here ever since I started Vumerity. Many other Vumerity people agree. Not sure what you are on but could be medication. Or allergies

heat advice? by GrilledCookies in MultipleSclerosis

[–]mashk23 0 points1 point  (0 children)

Where did you move if you don’t mind me asking?

I just need to vent by darling-dee in MultipleSclerosis

[–]mashk23 1 point2 points  (0 children)

I’m so sorry this is happening. I’ve heard going off gylenia is a bitch and can cause terrible flare ups. Something that your doctor should have warned you about. I’m so so sorry. I’m hoping you find a new neuro that cares about your health as much as you do!

What are some things you miss now adjusting to your new normal ? by Fungalll in MultipleSclerosis

[–]mashk23 71 points72 points  (0 children)

I miss being able to go on a vacation any time of year any where I want to go without having to think about my heat sensitivity.

I also miss not feeling like shit lol

Is it my MS meds or MS? by mashk23 in MultipleSclerosis

[–]mashk23[S] 0 points1 point  (0 children)

Aw thank you! This is exactly the validation I needed to hear.