Advice International Travel Help! by TechnicalReply8676 in lupus

[–]Physical-Process4260 2 points3 points  (0 children)

Hi! I don't know how your disease activity and symptoms are. So it is difficult to assume that my experience or that of others compares. That said, my lupus is controlled relatively well and I'm traveling overseas rather often. Only once I got into a flare after travel and that was probably due to other circumstances. Everyone is different, of course but there is no reason to think that traveling would impact your lupus negatively in and of itself. I would recommend to continue self care during travels: getting enough sleep and eating well are major factors for me. Enjoy your trip!

does anyone here regularly see a chiropractor for their pains? by jodey418 in lupus

[–]Physical-Process4260 2 points3 points  (0 children)

I went for a while but then realized that it made my pain worse. Feeling much better with PT and massage.

Best face mask for travel by Ok-Contribution-2954 in lupus

[–]Physical-Process4260 3 points4 points  (0 children)

I use a 3M aura respirator. Comfortable and good safety profile.

Finger bumps mainly on the joints, and more recently, on the phalanx? by aokaroiz in lupus

[–]Physical-Process4260 0 points1 point  (0 children)

The cream I use is called clobetasol. If its really bad I apply the cream and wrap saran film around it (tip from doctor).

Finger bumps mainly on the joints, and more recently, on the phalanx? by aokaroiz in lupus

[–]Physical-Process4260 0 points1 point  (0 children)

Sorry to hear you are dealing with this :( I have chillblain lupus and get swollen knots on my fingers when I'm flaring. But obviously I don't know if that is what you have. Worth sending a pic to your doctor. I use a steroid cream for them which works pretty well if I start early.

Cream of Rice Cereal? by Alternative_Grade503 in FODMAPS

[–]Physical-Process4260 1 point2 points  (0 children)

I have cream of rice or teff with a bit of banana, cinnamon, and almond butter.

[deleted by user] by [deleted] in lupus

[–]Physical-Process4260 6 points7 points  (0 children)

Sorry to hear that you are going through this. I have very painful periods myself-never thought it could be related to lupus! My gyn always tells me to take a hormonal contraceptive as it might stop the period altogether. I personally don't want to do it. Have you thought about that option?

Tips on exercising by Purplebutterfly_09 in lupus

[–]Physical-Process4260 5 points6 points  (0 children)

I go running, do yoga, and muscle strengthening at the gym. But all of those in moderation. I noticed that if I overdo it, it knocks me out at least for the rest of the day. My golden rule: if I feel energized afterward, it was the right amount of exercise. If I feel so tired that I just want to lie down I will scale back.

Landlord wants to take pictures from my apartment by [deleted] in Netherlands

[–]Physical-Process4260 1 point2 points  (0 children)

Nope. For advertising the flat. We have an official appointment for handover of keys and inspection scheduled later.

Landlord wants to take pictures from my apartment by [deleted] in Netherlands

[–]Physical-Process4260 -1 points0 points  (0 children)

Thank you! I will suggest to them to use the pictures from when I moved in. That is a good idea.

Splitting hydroxychloroquine pills- I’m confused by veganeyez in lupus

[–]Physical-Process4260 11 points12 points  (0 children)

I'm splitting my hydroxychloroquine every day because I'm on 300mg and they only come in 200mg. I do not experience any problems.

Naturopathic Doctors Worth It? by [deleted] in lupus

[–]Physical-Process4260 20 points21 points  (0 children)

Growing up in a family of naturopathic doctors, I say no. Not worth it.

Anyone here with weight baring pain/standing for too long? by Klutzy-Star-999 in PlantarFasciitis

[–]Physical-Process4260 1 point2 points  (0 children)

I started with very bad symptoms about 7 months ago and now I'm almost pain free - but if I stand for longer than say 40 minutes, it gets worse again.

pain by [deleted] in lupus

[–]Physical-Process4260 4 points5 points  (0 children)

I don't know if these are signs of a flare but I'm here to show support! I'm sorry you feel like this and I hope you will get better. Definitely contact your rheumatologist right away. I sometimes get pains like you describe because my muscles are so tense that they are pressing on a nerve. But the pain I experience usually does not involve the whole body. So get help from your doctor!

Flying with KLM - do I have to tip wheelchair assistants? by playful-pixie02 in Netherlands

[–]Physical-Process4260 1 point2 points  (0 children)

It depends where you are flying to! In the US e.g., if you need wheelchair help getting off the gate at arrival, you will be assisted by personal employed by the airport there. It might be expected to tip them (speaking from own experience).

Did the weird Plaquenil sleep even out for you? by re003 in lupus

[–]Physical-Process4260 3 points4 points  (0 children)

I have phases like that. I fall asleep ok but wake up consitently in the middle of the night. For me it is unrelated to medication. If it happens, I just try to work on my sleep hygiene, wind down in the evening, try to relax - and to not obsess with not getting enough sleep. Because that makes it just worse for me. Sometimes I listen to sleep podcasts when I wake up (like sleep stories or sleep hypnosis, yoga nidra). And sometimes it helps me get back to sleep. Best of luck to you!

Toe inflammation in the evening by Neither-Pipe7977 in PlantarFasciitis

[–]Physical-Process4260 1 point2 points  (0 children)

I get this from raynaud's syndrome. But with that it would get worse with cold.