u/TheTousler

Hi all,

I actually own this book (Strudels, Noodles, & Dumpings" by Anja Dunk), but I have a friend who admires it each time they come over. I'd like to get them a copy as a gift, but it seems impossible to find an unused copy for a book published only in 2018.

Has anyone seen a new copy at a local bookstore?

I really don't want to get them a pre-owned version, both because it is a gift and because they have an allergic/immune condition and dislike used books for health reasons.

Thanks for any leads

Does anyone know if the recipes in this cookbook are authentic, or if they are just the author's modern inventions using Russian ingredients and techniques? I am no expert.

Some are obviously traditional Russian recipes (Vatrushki, Blini, Pelmeni, etc.) but I am not sure about others (Braised Duck with Turnips, Veal Stew with Cherries, etc).

Here are a list of the recipes (ingredients shown but you can't see the actual directions)

https://www.eatyourbooks.com/library/recipes?q=192953%20%22Beyond%20the%20North%20Wind%22&sort=book_id%20desc

I know it somewhat pales in comparison to other things we deal with - this condition has nearly taken my life on more than one occasion. But I feel genuine anguish over the thought that I will never eat so many things again. Cooking used to be one of my favorite hobbies and I still have a shelf of cookbooks, which only brings me sadness now.

I grieve the food-related experiences I'll never have, too. The idea that I will never be able to travel and try exotic foods from other cuisines or try a random restaurant. That I will never again be able to have a have a cocktail with my friends or toast with champagne on NYE.

Food is such an important part of the human experience. It all feels like too much sometimes.

I hope in the future there is a real cure for all of us.

My mother is in her mid sixties and the skin on her arms is very thin and fragile. However, she is not physically frail and always has wounds on her arms from carrying boxes, etc. because she is still fairly active.

She has never liked long sleeves and her arms are pretty sun-damaged as well.

Is there anything that can be done? Most of what I've read is just to use sun protection and keep them well moisturized. Curious if there is anything that can reverse a bit of the damage or thicken the skin a bit so it is less prone to tearing.

I feel a bit overwhelmed by all the options. Is there a type of neurofeedback that is scientifically best supported? I was considering trying LENS neurofeedback since there is one near me, but I don't know if this would be best. Any advice?

For reference, I have a dysregulated nervous system related to a chronic illness.

What are your plans for Midsummer this year?

Any special traditions in your family? Any unique customs local to your area?

Does anyone have either of these cookbooks by by Eva Helbæk Tram & Nicolai Tram? I'm interested, because I love outdoor cooking, but I am always a bit skeptical of cookbooks written by michelin star chefs.

Are the recipes actually practical or are they overly "Chef-y", with uncommon ingredients and techniques?

For context, I have POTS and a very severe case of MCAS (the worst most of my doctors have ever seen). I have previously lived in mold but I don't think I am right now (multiple inspectors did not find anything). My health did not improve noticeably upon moving out of mold and tossing most of my stuff.

However, many of my doctors insist I must have an ongoing trigger to have this level of mast cell reactivity. I don't know what it would be, though. I have already cut as many things out as I possibly can.

Personally, I don't believe the urine mycotoxin tests are very accurate at all. Is there a different test that will tell me for sure whether I am currently exposed or whether there are still mycotoxins within my body?

Has anyone tried and found them helpful for reducing reactivity?

Since MCAS is a neuroimmune condition, it would make sense that anything that helps regulate the nervous system could be beneficial.

I have been dealing with this for about 8 years and my situation has become quite dire. I've already worked with all the mcas specialists in my area and I can't even get stable. I react to literally every possible treatment.

Are there any doctors or facilities who can help with a severe refractory case of MCAS? I am willing to travel. Unfortunately, I have spent my life savings and cannot afford to pay thousands to see any more private pay doctors, so it would have to be someone who accepts insurance (unless their rates are reasonable).

I would like to politely ask that this not turn into a discussion about mold, Lyme, or nervous system regulation programs. I have been dealing with this for quite a while and I have explored all of those avenues.

Thanks!

I have been dealing with this for about 8 years and my situation has become quite dire. I've already worked with all the mcas specialists in my area and I can't even get stable. I react to literally every possible treatment.

Are there any doctors or facilities who can help with a severe refractory case of MCAS? I am willing to travel. Unfortunately, I have spent my life savings and cannot afford to pay thousands to see any more private pay doctors, so it would have to be someone who accepts insurance (unless their rates are reasonable).

I would like to politely ask that this not turn into a discussion about mold, Lyme, or nervous system regulation programs. I have been dealing with this for quite a while and I have explored all of those avenues.

Thanks!

I can't eat fish, fish oil, algae, or flaxseed. How do I get omega-3s? I know chia has some, but that's ALA rather than EPA and DHA.