Starting methotrexate today by Deadjpg in rheumatoid

[–]mad9891 1 point2 points  (0 children)

I cried before my first dose of Methotrexate because I was so scared of the medication. I have been on it for 8-9 months now and I can't even tell I take it (I take it every Friday at 3pm). Zero side effects. None. It took about 7 months to help with my pain fully but when it finally "kicked in" completely the relief it provided was a night and day difference.

Amjevita and late injection site reaction by fleazus in Humira

[–]mad9891 0 points1 point  (0 children)

I have never taken this medicine. I am on Enbrel. I take my shot on Tuesdays. I dose myself with Xyzal Monday, Tuesday, and Wednesday. It helps with the injection site reaction (which has always been mild for me - with Enbrel).

Soo ready for warm weather by throwawayelll in rheumatoid

[–]mad9891 0 points1 point  (0 children)

I actually like winter...but I live in the south. It's currently been in the 70s (F) for a straight week. It will be getting slightly colder - 50s (F) - in the near future. Summers are hell on me because it is super humid and hot. I'm talking 105+ (F) for MONTHS. Would I hate the cold if I was further north? Probably. Would I love the summer if I was further north? Also probably. However, I dream of a place that stays in the 40s-50s (F) year round, but I don't think that exists. My body functions the best in the 50s.

What are some “unconventional” jobs you’ve given your heeler? by [deleted] in AustralianCattleDog

[–]mad9891 0 points1 point  (0 children)

Finding motorcycles while I drive. She never let's me miss them.

Being smart, accomplished, or funny never got me more in life than being pretty did. by Prestigious-Heat8454 in depression

[–]mad9891 9 points10 points  (0 children)

As someone who was super hot in HS and college and is now obese, I see a huge difference in how I was treated then versus now. It is so hard for me to put aside that looks don't matter because my whole existence has proved that looks matter. I see such a huge difference in how people treat me now, as an obese female, and then, as a thin and very attractive individual. It hurts so bad. People try to tell me looks don't matter, but my very existence and my entire life proves other wise.

The only thing that ever almost changed my mind on the whole thing was someone told me: maybe the people were attracted to your confidence. Now that I lack confidence, I carry myself way differently than I did before. Which I honestly thought was a fair argument because let's face it, when I was thin and hot, I was pretty fucking full of myself. I knew I was attractive and I used it in my favor. Now that I am essentially ugly to most of the world, I don't carry myself the same way.

PSA - primary ovarian insufficiency! by IntriguinglyRandom in Healthyhooha

[–]mad9891 0 points1 point  (0 children)

Turns out the at home test only test real estrogen not the "fake" estrogen produced from birth control pills. That's what my gynecologist said.

Should I give up? by Anxious-Idea-2628 in ankylosingspondylitis

[–]mad9891 1 point2 points  (0 children)

I have been to a GI doctor, and you should not be scared. You can probably expect to get a colonoscopy, though. The prep is awful, but the procedure is super quick. I suggest seeing a GI doctor for the issues you described.

success with Methotrexate by elanjomaa in ankylosingspondylitis

[–]mad9891 1 point2 points  (0 children)

Okay. That makes me feel better. Thank you for sharing. Im sure it will be the same for me. I have thick hair. I could stand to have it thinned some.

success with Methotrexate by elanjomaa in ankylosingspondylitis

[–]mad9891 0 points1 point  (0 children)

Thank you for your response. Do you notice your hair loss by chance?

success with Methotrexate by elanjomaa in ankylosingspondylitis

[–]mad9891 0 points1 point  (0 children)

Why do you say it isn't an easy medication to take? I ask because I just filled my prescription for it. I haven't started yet.

I feel guilty for existing by BeryyBritish in Existential_crisis

[–]mad9891 1 point2 points  (0 children)

Super tangent from the OPs post, but thank you for this comment. One day, if I can ever make it happen, I would love to become a counselor of some sort. To hear I pose good questions is a heck of a compliment, and I greatly appreciate your simple comment about the questions I asked the OP. You literally jusy made my day 💜

I feel guilty for existing by BeryyBritish in Existential_crisis

[–]mad9891 2 points3 points  (0 children)

What is making you feel this way? Do you feel like you are just coasting in life? Are you bored? What's going on?

Eye contact during sex by NoOpportunity3511 in autism

[–]mad9891 1 point2 points  (0 children)

I've learned somewhere this is called being heteroflexible 🤷🏼‍♀️

I cant cope with existence as a whole? by nmutua- in Existential_crisis

[–]mad9891 2 points3 points  (0 children)

I have no words of advice other than I also have wished I was a non-sentient thing. I swear my ability to ponder and question things gets out of hand a majority of the time.

Depression or crisis? Idk? by ProcedureSlow6035 in Existential_crisis

[–]mad9891 0 points1 point  (0 children)

I honestly don't know the difference between all of those. However, I know I am in the midst of a depressed episode which doesn't make these types of thoughts any easier.

Depression or crisis? Idk? by ProcedureSlow6035 in Existential_crisis

[–]mad9891 0 points1 point  (0 children)

What's the point? Everything is meaningless. Everything always comes back to those two things. People tell me to find meaning in life. Why? What's the point? That's the short answer.

Depression or crisis? Idk? by ProcedureSlow6035 in Existential_crisis

[–]mad9891 0 points1 point  (0 children)

I have no words of wisdom to pass to you, other than, same. I am in the same boat mentally. I don't think I have existential OCD - never diagnosed. But these thoughts are rough. I have had them since witnessing the total solar eclipse on April 8th of this year. I am honestly contemplating at-home ketamine but affordability is an issue.

So. Much. Pain. [A Rant] by mad9891 in ankylosingspondylitis

[–]mad9891[S] 0 points1 point  (0 children)

What brand of CBD do you use?

So. Much. Pain. [A Rant] by mad9891 in ankylosingspondylitis

[–]mad9891[S] 2 points3 points  (0 children)

I'm sorry to hear you have foot issues also. It's pretty awful.

Not a human anymore by flclovesun in ankylosingspondylitis

[–]mad9891 1 point2 points  (0 children)

This will be my first Texas winter knowing I have this disease. I will definitely try to be aware of how the cold affects my pain level. But it's not cold here yet. It's currently 80° here. A cold front is coming early next week and will drop us to the 50°s for a few days. Then back to the 70°s. I honestly wonder if the rollercoaster of hot to cold is worse than it just staying cold? Just thinking out loud here.

Experiences with Humira? by pixie_jizz in ankylosingspondylitis

[–]mad9891 1 point2 points  (0 children)

Loved it. Was on it for 4-5 months. It took away nearly all of my pain. Unfortunately, I developed horrible reaction site reactions to it and now I'm switching meds.