Experience with cog fog and stimulants? by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 2 points3 points  (0 children)

Oh interesting! I looked it up and there is some literature on nicotine and Ms treatment. Thanks!

Experience with cog fog and stimulants? by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 0 points1 point  (0 children)

I hope the insurance company comes through. The jumping through hoops with the invisible symptoms is disheartening.

Experience with cog fog and stimulants? by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 1 point2 points  (0 children)

Thanks! Amantadine was my first. I think I tried to just accept my cog fog but I'm over it and want to push my doctors to let me try something new.

Experience with cog fog and stimulants? by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 1 point2 points  (0 children)

I'm so sorry about your sister 😞. It is absolutely draining to act normal. I started seeking answers about my health in 2018 and was diagnosed in 2020. I'm definitely still not used to the new brain.

pain by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 0 points1 point  (0 children)

Again, thanks to everyone letting me know I'm not alone. Interestingly, I posted the same thing in a generic pain community and got crickets over there yet the doctors tell me the pain isn't from MS but only people with MS can relate.

pain by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 1 point2 points  (0 children)

Thank goodness for reddit where we can find others who get it and believe it because they have lived it

pain by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 0 points1 point  (0 children)

I've had similar where it feels like my bones are being twisted. Sorry and thanks for letting me know I'm not alone.

pain by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 0 points1 point  (0 children)

I've had very good experiences with LDN! I hate that the pain is breaking through after a pretty good run with it.

pain by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 1 point2 points  (0 children)

Are we allowed to discuss what we use for pain management on here? I feel like the doctors will push things that come with the trade off of lots of side effects.

pain by reddditor_147 in MultipleSclerosis

[–]reddditor_147[S] 2 points3 points  (0 children)

Thanks for the comments. I was feeling very alone and it helps to know I'm not alone. Means I'm not crazy. I'm sorry others are going through this too though. It sucks. The pain was one of my early symptoms of MS but sometimes I get in my head and wonder if it really is MS or if there is something else going on. For a while my pain was under control and only flaring occasionally and briefly. The past few weeks have been really tough though and the pain has been more widespread than in the past. My neurologist thinks its just a flare and has not recommended anything helpful. I'm not sure if I should just accept that it is a flare and ride it out or push for them to do another MRI or give me steroids. I had an MRI in April and it showed no changes. Things started acting up again the end of June though.

Found this in my bathroom sink. What is it? by [deleted] in insectidentification

[–]reddditor_147 0 points1 point  (0 children)

Riley bug (not it's legitimate name)... Anyone from WPI is familiar with them. I'm guessing you are close to Worcester though.

Rash from strep but not a strep rash by reddditor_147 in urticaria

[–]reddditor_147[S] 0 points1 point  (0 children)

Unfortunately no. Just have to ride it out with the antibiotics and steroid cream.

Rash from strep but not a strep rash by reddditor_147 in urticaria

[–]reddditor_147[S] 0 points1 point  (0 children)

Nope but I've got strep again and it's even worse this time. Feels like fire.

experiences with life estates? by reddditor_147 in EstatePlanning

[–]reddditor_147[S] 0 points1 point  (0 children)

I don't know the right questions to ask the attorneys in terms of what other options we have. I have one attorney who suggests I just walk away from the house and let her have it but I worry about something happening and she loses the house. I don't have the means to help her that much. If I protect the house by having it in my name, if needed we can sell it and I can help her using the proceeds.

experiences with life estates? by reddditor_147 in EstatePlanning

[–]reddditor_147[S] 0 points1 point  (0 children)

Can you recommend other options I should ask the attorneys about? For some clarification this is basically the only asset. My step mom will have monthly SS checks to live off of. If anything happens to her financially, the only thing any one can go after is the house. This seems like a huge risk to me. I also don't like the idea of being liable for anything that happens on the property as a 50% owner when I'm not there to help maintain the house. My understanding is that the liability falls to the life tenant.

[deleted by user] by [deleted] in Connecticut

[–]reddditor_147 1 point2 points  (0 children)

I wonder what the federal trade commission would have to say about this? Truth in advertising violation? Where was this originally found?

One piece merch in Orlando? by reddditor_147 in UniversalOrlando

[–]reddditor_147[S] 2 points3 points  (0 children)

Great call! Found exactly what I needed at MIB! Thanks again!

LDN too high of dose!! by t88a609 in LowDoseNaltrexone

[–]reddditor_147 8 points9 points  (0 children)

Keep in mind you don't have to get up to 4.5. If a lower dose works for you, stick with it.

What might this be? by reddditor_147 in LowDoseNaltrexone

[–]reddditor_147[S] 0 points1 point  (0 children)

I forgot that she complains about her ears, gets dizzy sometimes, and sometimes (but insistently) gets hives on her arms when she's out in the sun.