@la.vida.de.veronica: Common!! It’s one of those days where I sit here and just can’t take no for an answer. We need to stand up and figure this out together! So enlighten me please! #multiplesclerosis #autoimmunedisease #ms
How does gapapentin works for you? Do you take it at night or during the day? I take it at night and I think is defeated the purpose! I’m all alone no support, I wish you well in this fuc*** journey
2026-09-10 10:52:02
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Marie 💫🌠☪️ :
I'm on Duloxine, which is Cymbalta.. I'm taking 65mg but Busy, at Dr. says 65 in the morning and 65 at night. I'm waiting for the break down like a mucha Sucker
2026-09-11 01:43:05
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Jess :
Girl… be CAREFUL with Cymbalta. That med worked for me until it didn’t. First med I was on that ever gave me withdrawals. Like I said, be careful with that one. WEEN off if you ever go off of it.
2026-09-10 02:12:58
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gabys_conspiracies 🫰🏽🧡♿️ :
Last year I saw a research article saying vitamin B1 helps with brain fog but if I know I have to be productive that day. I just take my ADHD medication and it turns my brain on so I can focus. If I don’t take it then I’m just a bum all day.
2026-09-09 20:51:37
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gabys_conspiracies 🫰🏽🧡♿️ :
It’s the nasty side effects too. I haven’t taken my Wellbutrin for my depression. I guess anxiety for years because somewhere I heard that it shrinks our brain even more! I just take my medication at night and supplements, and I just take them and knock myself out to sleep. I have day supplement as well, but I don’t take them every day because again it’s just so many pills. Mostly supplements the big ones I take them at night. Just hang in there, girl! ♿️✊🏽🧡
2026-09-09 20:48:56
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Gov’t 🧀 & Other Fables :
I was diagnosed with MS in March of 2020 (I know.🙃), and I refused DMT. Instead I did the Wahl’s protocol which is a protocol created by an MD with MS. It includes a diet, stress reduction suggestions, exercise recommendations, etc. I slipped off of in the last year ish due to focus on another health issue. In June I had a high level of stress due to a family issue and had a serious relapse that left me paralyzed on the left leg and arm. I didn’t respond to the high dose steroids, and the new lesions actually got larger. I had to do something called plasmapheris in the hospital in attempt to help me recover and stop the relapse. After more than six weeks in the hospital and neuro rehab, I left on a walker. Now I’m working my way to a cane and hopefully no aide. I believe that had I stayed strict with the protocol and really focused more on managing stress that I could have prevented this new lesion and relapse. I’m going on a DMT at least for a while to stabilize myself and hopefully have no new lesions. During this time I’m still going to do the protocol because I believe you have to do both. There is also a book and protocol called Overcoming MS that’s written by an Australian doctor with MS. It’s similar to the Wahl’s Protocol. Also there’s MS Hope based in Canada. I believe what you said that this can’t be what our lives are. There have to be more solutions!
2026-09-10 04:26:26
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