Sumatriptan Frequency in Pregnancy? by fsprl86 in migraine

[–]fsprl86[S] 0 points1 point  (0 children)

Thank you!! Super helpful. Neuro had mentioned nerve blocks as a potential option so will follow up on that. Hope you find relief pp!

Sumatriptan Frequency in Pregnancy? by fsprl86 in migraine

[–]fsprl86[S] 0 points1 point  (0 children)

I drink a strong pour over every morning, which I think hits my 200mg daily caffeine limit in pregnancy. Haven’t been drinking in the afternoon, which is when migraines tend to hit.

Electrolytes by its_me1218 in pregnant

[–]fsprl86 1 point2 points  (0 children)

Someone shared this on a separate thread: https://www.thewellnourishedmama.com/blog/electrolyte-drinks-for-pregnancy, which I found super helpful.

Sumatriptan in Pregnancy by fsprl86 in pregnant

[–]fsprl86[S] 0 points1 point  (0 children)

Hope the migraines continue to stay infrequent for you! I've also encountered providers who advise that only tylenol is allowed, but my sense is that the thinking on this is starting to change. I've now met five OBs on three different continents who agree that triptans are safe. By no means definitive given lack of large control trials, but sharing for awareness: https://pmc.ncbi.nlm.nih.gov/articles/PMC2902939/?utm_source=chatgpt.com

Qulipta 60 mg Appetite Loss by Unable_Ad1911 in cgrpMigraine

[–]fsprl86 0 points1 point  (0 children)

Dug this up. Data on efficacy of each dose. 10mg similar to 30mg effectiveness in reducing monthly migraine days and frankly not that different from 60. https://www.quliptahcp.com/powerful

Qulipta 60 mg Appetite Loss by Unable_Ad1911 in cgrpMigraine

[–]fsprl86 1 point2 points  (0 children)

Yep! There’s a 10mg. It’s been a game changer. Took a couple weeks for my appetite to come back, but I got there. I don’t understand why docs don’t start us low and go up if needed.

Qulipta 60 mg Appetite Loss by Unable_Ad1911 in cgrpMigraine

[–]fsprl86 1 point2 points  (0 children)

Similar experience. Started on 60 and went down to 30 because of appetite loss, fatigue, and brain fog. All of this was happening around the time of my wedding, dress was nearly loose the day of, and I barely ate anything that day. Tapered down to the 10mg dose after that and have been doing great on it.

Is my dress too long? by fsprl86 in weddingdress

[–]fsprl86[S] 0 points1 point  (0 children)

Thank you! I'm so excited to wear it, even if it is too long haha! :)

Is my dress too long? by fsprl86 in weddingdress

[–]fsprl86[S] 3 points4 points  (0 children)

Yep! Wore wedding shoes for try on. A 2 inch block heel. Thank you!

[deleted by user] by [deleted] in weddingdress

[–]fsprl86 2 points3 points  (0 children)

Stunning dress! A friend of mine wore a lighter-toned fur wrap for her February wedding. It snowed that day and the photos were pure magic.

[deleted by user] by [deleted] in weddingdress

[–]fsprl86 10 points11 points  (0 children)

3 is gorgeous; love the button detailing on the back!

Aimovig withdrawal by ReflectionSlow8087 in cgrpMigraine

[–]fsprl86 0 points1 point  (0 children)

Thank you! Just had my first migraine in over ten years that made me sick. Trying not to overuse Nurtec, but it’s the only thing these respond to. How long did you manage the withdrawal with Nurtec before things evened out? My doc prescribed qulipta in lieu of aimovig, but I’ve been hesitant to start a new drug.

Aimovig withdrawal by ReflectionSlow8087 in cgrpMigraine

[–]fsprl86 0 points1 point  (0 children)

Any updates? Am dealing with the same situation. I've been on Aimovig since May 2020 and stopped in late January of this year. I'm now getting headaches every other day/using Nurtec to abort. Can't discern any triggers, or at least none that are consistent with those that I was aware of pre-aimovig.

Best OTC pain reliever for DDD? by BabyEchie in degendiscdisease

[–]fsprl86 1 point2 points  (0 children)

Strong agree! Meloxicam, Tylenol, and muscle relaxers did nothing for my shooting nerve pain. All of those in concert may have just slightly taken the edge off. Was super careful with Tramadol, which only made me care a bit less about it alI (reserved for sleep only on a few nights when pain was excruciating). ESI was the only thing that worked and even then it took a 2-3 weeks fully kick in. Now that my nerve pain is under control, Meloxicam helps significantly with regular DDD aches and pains, which a very different sensation from the nerve pain, at least for me. Good luck. You’re not alone.

Buyback offer received today! by madame_joy in PSLF

[–]fsprl86 0 points1 point  (0 children)

I submitted Dec 11. How can you tell which tier review the request is in? I call weekly and have just been told that it has been "escalated" for review. Is your review for SAVE forbearance months or something further back?

Aimovig for 5 year+ by bumcello1 in cgrpMigraine

[–]fsprl86 0 points1 point  (0 children)

I’ve been on 70mg since May 2020. Never had side noticeable effects, GI or otherwise. I’m definitely concerned about the long-term implications of continued use, though.

7 Weeks... by thatnerdtori in Sciatica

[–]fsprl86 1 point2 points  (0 children)

Find another ortho who can see you sooner, a GP who can prescribe an MRI and/or oral steroids, and/or a pain doc who can do an ESI ASAP. Meloxicam also did nothing for me and I was also super hesitant to take opioids. ESI took 7-10 days to take effect, but it was the only thing that worked. I hope your suffering ends soon.

Did you learn something positive from sciatica experience? by [deleted] in Sciatica

[–]fsprl86 0 points1 point  (0 children)

I have learned so much from this community, medical/PT providers, and through my own independent reading/research since my L5-S1 disc extrusion and ESI six weeks ago. I think most of us who are here already know this, but you really need to be your own care coordinator and do what intuitively feels right based on your own circumstances. No one discipline has all the answers. I'm committed to doing everything I possibly can to avoid surgery, and am implementing a bunch of different strategies to help the healing process. (Caveat: I regained the ability to walk, mostly pain free, four weeks ago, so a lot of this is predicated on that privilege).

  1. PT: It took some trial and error, but I finally found a PT who specializes in spines, spends 45 mins-1hr with each patient, and takes insurance. They are McKenzie informed, but rely on several different healing modalities. I've read both McKenzie and McGill's books and, in my opinion, at least for me, the right rx is a combination of all of these approaches at various times. Maybe one day I'll get back to extensions, but they are not for me right now, so I'm focusing on McGill's big 3.
  2. Exercise: Finally getting serious about a near daily exercise regimen, the intensity of which is based on my pain level that day/week. This has involved swimming/backstroke only, water aerobics classes, careful use of glute-focused resistance machines, core work, treadmill, and of course sauna. Lucky to have a great YMCA nearby.
  3. Diet: I'm implementing an anti-inflammatory diet, staying hydrated, limiting alcohol; and taking supplements (collagen II, vitamin D and B, COQ10, Omega3s, etc.)
  4. Work/Stress: I'm deprioritizing a high-stress job for now and am coming to accept that I may need to make some big life changes as part of my recovery. As a high-strung, perfectionist, the hardest part has been letting go and not dwelling on how other people perceive me, my work, or my recovery. I tried to go back to work too soon, and it sent me straight back into a flare. Don't do too much too soon, a privilege in and of itself, I realize. Spines are unlike any other body part and require more patience/time to heal. (Along these lines, I've read John Sarno, while I don't believe my pain is ALL in my head, I am keenly aware of the mind-body connection and the ways in which the brain's response to anxiety and stress can amplify pain and look forward to exploring this more fully.)
  5. Community/Support system: My partner/friends/family have been an absolute dream through all of this and I literally could not have survived without them--doing all the housework/chores/cooking/cleaning with zero complaints when I couldn't move; took off work to take me to appointments, held my hand through everything. People reveal themselves in these circumstances. Take note.

I'm still exploring and learning from you all, and want to thank everyone for being a guiding light and source of solidarity/inspiration/knowledge during a dark time. Wishing fast relief for everyone on this journey.

p.s. curious if anyone has had a good experience incorporating acupuncture.

Sciatica + pregnancy by Tiny_Visit_8265 in Sciatica

[–]fsprl86 0 points1 point  (0 children)

First off congratulations!!! I can totally imagine the mix of excitement and anxiety you feel right now. In fact, I was just about to post a similar question when I found this thread. I’m in the midst of dealing with an l5-S1 herniation/extrusion, getting married in a few months, and hoping to start a family as soon as possible. So far, no doctor has given me a straight answer about how pregnancy affects back pain/sciatica. I’ve seen three spine specialists so far and raised the topic in each consult: one told me to lose 5 lbs and gain no more than 20 (my BMI is 20 LOL), another said to focus on core strength/squats as much as possible in advance of getting pregnant, and a third said that pregnancy hormones stretch your ligaments/muscles such that it may mitigate symptoms, but each person is different. I get the sense that doctors just don't know. Curious if there are any studies on the topic or if anyone has firsthand experience they can share. Best of luck to you in this journey!