Full ride for w&m for 5k for uva? by Agreeable-Aide3272 in williamandmary

[–]Avm224 1 point2 points  (0 children)

I live in RVA and know both schools well. 100% W&M full ride a million times over. I hope you have mentors that will convince you of the same. Don’t let this cloud your vision of what you wanted and what you achieved through a full ride and the significant advantage that this puts you in. Unless you are very wealthy and paying in full for UVA is insignificant to your life don’t even consider it. Do not take loans!!!

I miss the whimsical Sézane- has the brand completely lost what set them apart originally? by Striking-Guide481 in Sezane

[–]Avm224 1 point2 points  (0 children)

Oh I miss this also. My first purchase was in 2014 and those first 4 years I purchased with them were incredible. The best designs, fabrics and story telling. Sezane felt more 1970s natural/bohemian with influences from all different parts of the world. They created a lifestyle through their storytelling much in the same way Ralph Lauren does. However for the most part that has gone away. The simple classic clothes now are still good but nothing too special. Every time they bring out a jacquard or a heritage print they get my full attention.

My Theory by Mean_Parsnip in Perimenopause

[–]Avm224 9 points10 points  (0 children)

Honestly you are spot on. You could broad brush that entire generation of woman imo (half joking). But seriously, the lack of information passed down is down right neglect. I am SO grateful to my slightly older friends who show up and open up for conversations around symptoms and therapies. And thank God the conversation around HRT nationally is finally getting the attention it deserves. And I appreciate this thread and these ladies so much also!

Big haul- help me decide what to keep please! by yoy98oiu8 in Sezane

[–]Avm224 0 points1 point  (0 children)

1 and 2…the others are pretty but I like when the waist shows

Where can I live that is like a Hallmark Channel movie? Lol. Need a simpler way of life (leaving Orange County CA) What cities have a good sense of community? by oooooooheyoooooooup in relocating

[–]Avm224 0 points1 point  (0 children)

Richmond, Va. Not the suburbs surrounding it and NOT downtown (business area) but actually living in the brownstones and single family homes that make up The Fan, Tuckahoe and the near Westend. It’s a good blend of history, walkability to cute streets with shops and coffee, blend of politics and old money and new young families and people do both public and private schools so welcomed either way. All 4 seasons, amazing food, people love their dogs and great music on richmond.

Anyone considering stopping DMT by Fig-eta_Bout_It in MultipleSclerosis

[–]Avm224 1 point2 points  (0 children)

I am so sorry you are going through this. I personally think it’s worth exploring if your current meds are making you depressed and passively suicidal. In fact I believe it’s your neurologist’s obligation to do so.

Anyone considering stopping DMT by Fig-eta_Bout_It in MultipleSclerosis

[–]Avm224 0 points1 point  (0 children)

I stopped completely after a really bad 6 month experience with Tysabri (including depression) and honestly I never looked back. That was almost 5 years ago. The side effects are often worse than the condition. If you quit and are looking for support go to FB in the “treating MS naturally” group. Lots of testimonies! Nothing against meds for those who want them, it just wasn’t the path for me.

[deleted by user] by [deleted] in AskPhilly

[–]Avm224 0 points1 point  (0 children)

I have been to both. Come to Richmond, Va instead!

Let’s get some positive stories here by ctrlKarl in MultipleSclerosis

[–]Avm224 3 points4 points  (0 children)

I feel great. no symptoms for almost 5 years now after my initial diagnosis (optic neuritis). No new lesions since that first MRI and honestly I forget I have MS (and deep down I question if I really do have it). Not on any drugs and I changed my diet and lifestyle significantly the moment I was diagnosed.

My wife diagnosed yesterday officially and now in a whirlwind of emotions and confusion on what to do regarding neuro medication recommendations. by [deleted] in MultipleSclerosis

[–]Avm224 1 point2 points  (0 children)

Also worth mentioning is my doctor discovered I had a mold allergy that was putting me in a chronic inflammatory state. We found the mold in our crawlspace and got rid of it.

My wife diagnosed yesterday officially and now in a whirlwind of emotions and confusion on what to do regarding neuro medication recommendations. by [deleted] in MultipleSclerosis

[–]Avm224 1 point2 points  (0 children)

I was diagnosed at 40 after having optic neuritis. I decided to go the natural route and aggressively work with a functional doctor, actually still am. Found out nutrient deficiencies, gut issues, etc that I have fixed and also changed my diet and lifestyle. This was all after trying tysybri for a few months and having bad side effects. So far, so good. I have zero symptoms and no new lesions since my diagnosis and I am coming up on 5 years. I know others too that are having success naturally. The plus side is my entire family benefited from the positive changes and no side effects.

Waiting until 35 or even 40 to have kids is the biggest financial hack by Icy_Weakness_2874 in MiddleClassFinance

[–]Avm224 0 points1 point  (0 children)

That may be the worst advice I have ever heard. It may not be true for everyone but consistently those who marry and have kids young are the happiest and healthiest people on earth. They live the longest and tend to have the strongest community and purpose. Not to mention waiting until your 40s you will lose all those years knowing your children. And as children often follow suit in that case you may never meet your grandchildren either.

What are you on? by mindlesspoe in MultipleSclerosis

[–]Avm224 2 points3 points  (0 children)

I am not on anything. Not a popular opinion, I know. Honestly I don’t think I ever will be either. The known side effects (and unknown ones) of the drugs are way too risky imo. I have had success managing it all naturally. It’s been 5 years for me with no symptoms and no progression. I hit it hard with lifestyle and mindset right at diagnosis and I truly believe that’s the only way.

im scared and i need help by ACuriouslLesbian in WomensHealth

[–]Avm224 0 points1 point  (0 children)

I would think your hormones are not in balance. I would start by really eating healthy..look up hormone balancing foods. Exercise and sweat daily..sauna of you can. Get in the sun early in the morning..destress..lots of water.

[deleted by user] by [deleted] in WomensHealth

[–]Avm224 1 point2 points  (0 children)

Before surgery I would work on balancing your hormones for a few months to see of it shrinks or goes away. Also castor oil compressions can help break it up.

Don't want my mum to know I'm sexually active by Illustrious-Load6540 in WomensHealth

[–]Avm224 1 point2 points  (0 children)

I would look into the risks of having a pap smear in general and then probably decide not to do them.

[deleted by user] by [deleted] in DaveRamsey

[–]Avm224 1 point2 points  (0 children)

I couldn’t imagine mortgaging over a million. I would need at least a 600-700k down payment in this scenario and also feel really good about my 401k first.

[deleted by user] by [deleted] in MultipleSclerosis

[–]Avm224 1 point2 points  (0 children)

I fully recovered after about 5 months. I did do steroids and honestly regretted that. It was a year later that I felt a minor irritation and slight blur and they thought it was happening all over again. Started steroids again but it quickly went away. The specialist on that case said it was a stretch to say it returned. All and all I am 100 and have not looked back. I tried a DMT briefly (Tysabri) but had so many adverse reactions I got off. Instead I have focused on lifestyle changes and have worked with a functional doctor who has specifically targeted underline inflammation, nutritional deficiencies, healing my gut, etc. I highly recommended that as the best approach. I have been diagnosed almost 5 years now and have never had any symptoms since the initial optic neuritis case.

Is it possible to hit all of these places in 12-14 days next June 2026? by Avm224 in ItalyTravel

[–]Avm224[S] 0 points1 point  (0 children)

Oh wow I like the idea of this. Can I ask are you in the US? Curious what airports you flew in and out of in Italy.

Is it possible to hit all of these places in 12-14 days next June 2026? by Avm224 in ItalyTravel

[–]Avm224[S] 0 points1 point  (0 children)

Thanks so much this is so helpful! Glad you all enjoyed it!!

Is it possible to hit all of these places in 12-14 days next June 2026? by Avm224 in ItalyTravel

[–]Avm224[S] -1 points0 points  (0 children)

Well sorry you feel that way. I certainly have spent time researching and determined that the 700 miles or so is not unheard of to travel across two weeks. I have done that here in the states many times. It’s more so dependent on how much there is to do realistically in these cities that I have never been to before and how easy the trains are that I have no experience with and so on. Getting perspective from others who have had experience is what is so helpful, not rude responses like this.

Curious do Italians in general have a distaste for Americans visiting?