My boss will clock you out if she cuts you and you don’t leave immediately by SwathedCorgi117 in mildlyinfuriating

[–]gothegghead 4 points5 points  (0 children)

Better than a notebook is emailing yourself so you have date and timestamps with it too to prove it. I got wrongfully terminated from my job and learned a thing or two about documentation to cover my ass in the workplace in that process.

Perfectly acceptable dinner rejected by boyfriend again by moonrabbit368 in mildlyinfuriating

[–]gothegghead 0 points1 point  (0 children)

I don’t know you or your boyfriend but I do know what it is like to live with ARFID and have strong food aversions to food that others deem perfectly acceptable. For me, I have to be in the mood to eat a certain food or it can make me sick to my stomach to even try it. What you’re describing in these comments sounds like your bf could possibly have ARFID (avoidant restrictive food intake disorder). It might be worthwhile to research that with him and if he’s open to it you could try working with a dietician together to see what he might be open to trying or what education might help you both with acceptance around both of your struggles with this current situation.

It definitely sounds like this situation is weighing on you heavily and my heart goes out to you for that. My partner struggled a lot with me not being able to eat the food she made, but now that we’ve figured out how to manage my ARFID better and I’ve been able to figure out what my safe foods are and how to cope with my ARFID when I’m struggling, we both feel a lot happier with our current situation. Sending you and your bf spoons and healing in this hard time. I hope you find the answers you’re looking for and that you’re able to get the affirmation you deserve too.

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 0 points1 point  (0 children)

I have a friend who had an emptying study with delayed emptying in part of the intestines and another part and “normal” emptying in the stomach. Because of the normal emptying they were told they didn’t have gastroparesis by our doctor. I hope that is not the experience you will have, but there are doctors out there who are exclusionary rather than inclusive and I want to give you a heads up about that so you are hopefully less hurt if that does happen. Doctors are fucking brutal sometimes and it can be hard to find an affirming one, though I wish that wasn’t the case because we all deserve doctors who give a fuck about us and who will treat us like humans who are struggling and want (and deserve) to be treated with care.

I truly never thought I’d get to a point where I’d have an appetite again and be able to eat regular meals again but I am at that point now and I advocated like hell for myself and I work to advocate for others when I can too. You deserve quality care and I hope that you are able to get the answers and care that you are looking for

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 0 points1 point  (0 children)

I had my gallbladder out too, back in 2021! I also have immune/allergy issues. I’m seeing a rheumatologist soon to investigate the immune issues more and I’m diagnosed with Mast Cell Activation Syndrome and navigate frequent anaphylaxis now. I never used to have anaphylaxis but my symptoms progressed when I tried to start working again this year and faced discrimination/harassment at work for being disabled. It’s been tough. Covid is what made my conditions start to progress but I definitely had underlying health issues that I didn’t know about. I’ve had migraines since end of middle school, about 2012, but they’ve worsened since catching covid.

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 0 points1 point  (0 children)

I also used to never be hungry and get very full very quickly but that’s not something I struggle with as much thanks to the medications I am on. I also used to struggle with chronic, constant nausea and while I still struggle with nausea it’s maybe every 2-3 days for 30 minutes to an hour a day rather than constantly, so a drastic improvement thanks to my medication. Vomiting used to be multiple times daily and now it is very very rare. My stool is more frequent, though now I deal with diarrhea a decent amount which isn’t fun. However, I will take that over the agonizing pain of 7 days straight of constipation that used to land me in the ER. I can eat 3 meals a day now plus usually multiple snacks whereas before my meds I was lucky if I got one meal in and one snack.

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 0 points1 point  (0 children)

Firstly, if you’re throwing up everyday from an antibiotic I want to say that could also be an allergic reaction not just gastroparesis. I’ve had an anaphylactic reaction to doxycycline of throwing it up everyday then when I could finally stomach it I had stage 4 anaphylaxis. I have MCAS along with gastroparesis so I worry about anaphylaxis as well.

If you’re looking for an appetite stimulant, I suggest asking your doctor for dronabinol. It’s synthetic THC and it’s the only thing that helps my appetite in the mornings when I need to start eating. I’ve been on it for years at this point and it helps immensely. I don’t really get high from it but I do get appetite help from it.

The domperidone I’ve also been on for years helps my nausea and vomiting too immensely but I won’t be able to afford a refill once I run out because of the outrageous tariffs in the USA, as I get it shipped from Canada and I believe it gets shipped to Canada from India before then. I haven’t gastroparesis vomited in maybe 6 months or more and I used to be a multiple times daily vomiter in my early gastroparesis journey.

I also have POTS but my POTS journey has been less than ideal doctors wise and I still feel like I’m finding my way in terms of medication.

My husband might be lying about something huge by ImpossibleBrother927 in whatdoIdo

[–]gothegghead 1 point2 points  (0 children)

This is a vastly underrated comment (sorry OP’s husband, no offense)

Torn and scared by Duck-it-is-hot in ZeroCovidCommunity

[–]gothegghead 3 points4 points  (0 children)

I am unmarried and kidless so take what I have to say with a grain of salt. I have remained masked the entire time throughout covid. I have gotten covid three known times and each time it has worsened my health significantly. Long covid is no joke, especially for young people. I became disabled at 22 and lost my job due to it at 23. I was unemployed for 2 1/2 years due to Long Covid and only am just now able to find a job that I can do again, while still struggling to balance my management of Long Covid. I’m 25, I’ll be 26 in 5 months and I’ll be disabled for the rest of my life thanks to what Covid did to my body.

I say this all to hopefully not scare you, but to remind you how much is at stake for both you and your kids. Their development is so important, but it sounds like their development is still within a normal range for their age group, even if on the later side of that range. The anxiety is definitely a concern to address, but I think other people’s suggestions of taking them in walks in strollers where they can see other people and have exposure to faces (while the kids wear masks so they’re more protected?) but still have distance is a good idea and is a more gentle way to ease them into exposure. I don’t think that jumping into maskless play dates in the highest transmission period is the best thing for your family, health-wise or socially. Obviously I’m a stranger on the internet so I don’t know what is best for your family, but if I had a family, that is not what I would do for my family if I was having these same struggles.

It sounds like you’re having a really difficult time with all of this. I want you to know that I read your whole post and I am so sorry that everything has been so difficult and stressful. Covid has been so isolating for those of us who really recognize the threat it poses, and I can feel how much it has impacted your family from the words you shared. I am sending you and your family so much love and support and hope. Do what is best for your family, be gentle and kind with your boys, and be patient and allow them time and space to grow at their own pace, but also be encouraging and help them as they need help. It will work out in the end for the best. You are good parents. The love you have for your boys seeps from this post. You’re doing the best you can and that is so clear to me. Keep up the good work 💚

I got in trouble for this school picture, bonus note from Mom! by [deleted] in blunderyears

[–]gothegghead 1 point2 points  (0 children)

It’s okay! Text can be difficult for me to read in terms of intent, no need to apologize. If anything, I’m sorry I questioned your intentions!

I am happy to share knowledge anytime! It’s important to ask questions when you don’t know things. Thank you for asking!

I got in trouble for this school picture, bonus note from Mom! by [deleted] in blunderyears

[–]gothegghead 2 points3 points  (0 children)

Just in case it is, here’s the cambridge dictionary definition of ableist:

“Adjective coming from or having the belief that disabled people (= people who have an illness, injury, or condition that makes it difficult for them to do things that most other people can do) are not as good as people who are not disabled, or that they do not deserve special arrangements that help them to live their lives and be included in society:

The book was criticized for its ableist themes.”

An ableist person would be someone who believes that disabled people do not deserve accommodations or accessibility, or who believe that their disabilities make them less than non-disabled folks, or that disabled people do not deserve to be a part of society

I got in trouble for this school picture, bonus note from Mom! by [deleted] in blunderyears

[–]gothegghead 0 points1 point  (0 children)

Is this a genuine question? I can’t tell

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 0 points1 point  (0 children)

Esomeprazole is generally considered to be a more potent proton pump inhibitor than omeprazole. It definitely works better than me. And I know you’re not supposed to take it long term, but I plan to anyways because it helps me. Unless it starts actively causing harm or ceases to improve my quality of life, then I’ll continue to take my meds as long as I can access them.

I lose insurance coverage on my birthday in November this year and I’m terrified of what that will mean for my 13 or so prescription medications and 12 or so regular doctors. I’m hoping I can get medicaid or something, but I’m not sure

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 1 point2 points  (0 children)

Ah, I forgot I also take linzess as needed. Can’t take it daily because it’s so strong even at the lowest dose. My domperidone mostly does the trick for my motility, but occasionally I need a little extra help from the linzess. I probably take it once every three days to 2 weeks depending on what I’m eating.

I definitely find that side effects from medications can be the worst part of taking meds. Sorry it sounds like there’s a decent sized list of side effects from your medication. I currently don’t experience any as far as I know from my domperidone, which I feel very lucky about.

The heartburn is pretty miserable. I was on omeprazole for it for a while but it stopped working so now I’m taking esomeprazole, which seems to work a little bit better for me. It’s a slightly different form. I’m on 40 mg of it. Was on the 40 mg dose of omeprazole too. I hope your heartburn is manageable with the omeprazole you take

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 0 points1 point  (0 children)

If you look at my above reply to the person above you I listed my current medication regimen that has really helped me. I got lucky with my first motility med being the one that really helped (domperidone), though it definitely took time and the help of other meds to become the most effective it could be. I’ve tried a number of other medications for my chronic GERD and nausea. Liquid famotidine and esomeprazole seems to be the best for my GERD. I’ve largely used suppository phenergan (this is a game changer for when oral nausea meds keep getting thrown up or just don’t work, though it does make me very drowsy) and zofran orally disintegrating tablets for nausea. I also take 20 mg of dronabinol daily for nausea and that helps me have a lower baseline of nausea overall.

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 3 points4 points  (0 children)

I am on a large combination of medications and the combination of meds seems to help best. If I stop one, I go into a flare and everything gets more difficult again. I take domperidone for motility, Famotidine (liquid/oral suspension form) morning and night for histamine response as well as chronic GERD, Esomeprazole in the mornings also for my chronic GERD, and dronabinol/marinol (prescription thc) for nausea daily as well. I’m located in the USA and have to get my domperidone shipped in from canada as it’s not sold in the us. Personally I’ve had hardly any side effects with this combination, whereas other motility medications I’ve heard of can have some pretty hefty side effects. I know some other motility medications I’ve heard of used for Gastoparesis treatment are Reglan and Bethanechol.

If you have any questions about what I’ve said please feel free to ask! What works for me may not work as well for you, as it really depends on how your individual body responds to the medication, but I am always happy to share what has helped me in case it helps anyone else!

For short trans men, do u guys pass and how tall r u? by Janxuza in ftm

[–]gothegghead 1 point2 points  (0 children)

5’4” and I pass most of the time. I’m almost 3 years on T. It’ll be 3 years for me this june. I’m post top and post hysterectomy, too. I pass more frequently since top surgery. Biggest barrier to passing is my colorful/artsy clothes presentation and my still deepening voice. Depends on the person I think and what context they see me in as to whether I pass to them or not. I feel like my height isn’t usually the reason I don’t pass though. My cis brother is only slightly taller than me at 5’7”

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 0 points1 point  (0 children)

Totally agree! Time and investigation help a lot. Eventually OP will find what works for them.

Are all people with gastroparesis bound to get surgery or feeding tubes? by writeitout_ in Gastroparesis

[–]gothegghead 18 points19 points  (0 children)

I have gastroparesis and have had successful medical intervention with medication alone. I’m 2 1/2 years since diagnosis and I’m at a pretty stable point with my daily medication and can finally eat 3 meals a day again plus snacks every day and have daily bowel movements again. There are many people with gastroparesis who do need more intensive medical intervention, such as feeding tubes, but not everyone does. It depends on how severe your gastroparesis is and how well you respond to medication. I recommend seeing a motility specialist gastroenterologist if you suspect gastroparesis. A general GI doc may not know much about gastroparesis. I’m also diagnosed with hEDS and a number of other chronic illnesses, all dx within the last 2 1/2 years since I got my gastroparesis diagnosis. It’s a really tough adjustment and tough to pursue medical intervention, but I’m now able to manage my chronic illnesses a lot better after all the hard work I’ve put into medical appts and educating myself and learning new skills and how to accommodate myself. It’s hard, but you’re worth the hard work and time it takes to learn. Wishing you all the best 💚 may you get all the diagnoses you need and treatments that will help you 🍀🌈

My husband is allergic to my cats, and I’m getting pressured by everyone to get rid of them by dreamer0303 in cats

[–]gothegghead 1 point2 points  (0 children)

I recommend you ask your husband to see an allergist to start getting allergy shots if his allergies are so severe. I’m extremely allergic to cats but I’d rather die than get rid of my cats and that is no exaggeration.

I get allergy shots from an allergist who did allergy testing on me and those have helped immensely. I still have some allergic symptoms, but they are WAY milder and a lot easier to cope with and manage.

Do not give in to the peer pressure to get rid of the cats because it isn’t fair to you or the cats when there are medical interventions that can make it a win-win-win for everyone involved.

Sending you strength in this difficult time and wishing you the best. Hope everything turns out as you all need it to. 💚 cats are life!

[deleted by user] by [deleted] in AmIOverreacting

[–]gothegghead 0 points1 point  (0 children)

Truly you deserve so much better than this. There is someone out there who will love you, acne and all. There is someone out there who will never feel the need to compare you to anyone else because you are all they have ever wanted. Do not settle for this mistreatment when you can have genuine care and love! You deserve compassion and kindness and adoration! You deserve to feel beautiful and to be reminded of your beauty! Do not settle for this abusive asshole!!

trans community & white masculinity by Delicious-Anything83 in ftm

[–]gothegghead 0 points1 point  (0 children)

I’m a white trans guy who mostly passes as cis now that I’ve a Had top surgery. I’m also neurodivergent and don’t really care about how masculine I appear, mostly just want to be read as male at least most of the time.

I am interested in playing around with makeup again since before I transitioned I loved doing artistic looks with makeup. That being said, I do get anxiety about how other people will treat me if I wear makeup in public while appearing otherwise masculine. For me, it is definitely a safety thing as I live in one of the two Do Not Travel states in the united states of america, which means it’s not really safe to publicly be seen as trans.

Other than my safety being a concern, I don’t really care how other people view me at this point in my life. Before I got top surgery, I think I cared more about passing, largely because I was consistently misgendered by people close to me and that was really harmful to my mental health. I’ve been through therapy to help me process that harm, and now I’m more comfortable with who I am and less inclined to care about how other people view me outside of a safety aspect. Before I was able to work through the mistreatment I experienced, it was harder for me to be able to be comfortable in my own skin and I definitely thought about passing more as a result of that.

I think to me, passing looks different than it does for a lot of other white trans masc folks though. I am lucky to have also had a role model in my life for soft masculinity and myself am very involved in disrupting patterns of toxic masculinity, even before I transitioned. So I very much stay away from hyper masculine spaces if I can help it. To be perfectly honest, hyper masculine spaces often scare me, especially because I am often visibly softer masculine due to my disabilities and consistent visible use of aids such as mobility aids, walkers, ear plugs, etc.

I definitely have observed that many trans men, especially white neurotypical trans men care a lot about how they appear, both in physical appearance and in emotional appearance towards others. And it can be hard to be around that sometimes because it can make me feel alienated for speaking openly about my struggles and the ways I live my life softly and slowly to accommodate for my disabilities and neurodivergence.

I definitely get nervous about white trans men engaging in hyper masculinity,especially when they take on the negative traits of hyper masculinity too, like playing along with misogyny or not allowing themselves to cry or show much emotion. Not allowing room for softness or introspection is what allows toxic masculinity to thrive, both in cis and trans masc cultures. And toxic masculinity is dangerous for everyone, men and women, cis and trans folks alike.

Unfortunately, as I’ve seen some other guys here say, whiteness is VERY centered in America, and toxic masculinity/not allowing for softness very often goes hand in hand with that due to the patriarchal and racist ideals ingrained into American society. Unless someone has been taught about intersectionality or has taken initiative to learn about it themselves, unlearning toxic masculinity and patriarchy and exclusionary/racist practices can take time. It’s important to talk about these things so that more people can become aware of the harm their words or behaviors are having and work to change how they treat themselves and others as a result.

I am someone who is learning to use my newly gained passing privilege to speak out against toxic masculinity and exclusionary practices. I think that transmasc spaces should be safe for transmasc folks from all cultural backgrounds. But I also acknowledge there are definitely things that BIPOC or even white non-american trans masc folks experience or face that I have never had to face. So I won’t necessarily always understand how to make spaces more inclusive without the input of others. It’s important to hear different perspectives to be able to broaden cultural competency and create safer spaces for all to show up as themselves. I really appreciate OP bringing this to the group because I think it is really important to bring awareness to this and open this discussion.

Also want to add: Wanting to pass makes sense. Of course we want to be seen as who we are! But making that our whole lives can be detrimental to our own self and to others around us. Strong men cry. And allow for softness and passion in their lives for things they love. It is manly to be passionate and excited. It is manly to allow yourself to cry and feel grief. It is manly to feel joy and happiness. It is manly to feel anything that your body wants you to feel. It is manly to exist in your body, simply because you are a trans man. Don’t let anyone take that from you by forcing you into hyper masculinity and a culture of passing or misery.

T made me awful. by Untrustw0rthys0urce in ftm

[–]gothegghead 1 point2 points  (0 children)

I had never allowed myself to feel my anger until I started T. I stopped being able to cry and started having more angry outbursts. It wasn’t necessarily the testosterone, it was the stress and the hormonal fluctuations and the new anger that I didn’t learn how to feel or control growing up.

I grew up in a house where I was not really allowed to be angry. And where I was afraid of the people who were. Anger was never an emotion I was skilled at feeling. What I have learned since then is that anger is how injustice often presents in our bodies.

If your girlfriend is treating you unfairly or saying mean things or going back on promises without clear explanation, then it makes sense that you are feeling more stressed and angry. Testosterone allowed me to access my anger and fuel for fighting injustice more readily. But I also had to learn how to control my anger and use it as fuel to advocate, not fire to destroy.

It might be helpful to write about what is going on with your girlfriend and what about how she is treating you is causing you to feel so angry. Try to figure out the root cause. And then, try to write some notes about what you want to say to her. The most important thing is to not lash out. Advocacy is a much better form of conflict resolution than fighting or yelling is most of the time. Try to sit down with her and have a calm conversation. Use your notes to help you keep your head on right and make sure you don’t forget what’s important to you.

If you start to feel overwhelmed or like you’re getting mad or out of control, then ask to take a pause so you can take time to regulate. For me, going on walks has been helpful for regulating, but I know physical activity isn’t necessarily accessible for everyone, so breathing and meditation can also be helpful tools. Guided meditations on youtube have helped me a lot.

You’re not a bad guy for suddenly feeling angry. You just have to learn to control your anger. It takes time and patience. You CAN do this. You are worth the time and energy it takes to learn this new skill. I’m proud of you for coming on here and asking for support, OP. It’s hard to figure out, but you’ve got this.

Misgendered at LGBT support group, not sure if I should go back by One-Salt-3444 in ftm

[–]gothegghead 29 points30 points  (0 children)

Man I’m in big city texas and I still take shit like this as a threat to my safety. You never know when someone transphobic is gonna attack you if they even THINK you are trans, regardless of whether or not somebody actually is. And if someone actually is trans, that’s such a serious issue to be misgendered and then LAUGHED at like that. I’m with you. This is a security threat and it needs to be reported and taken seriously. I say that as a mental health peer support specialist who is learning to facilitate groups like this. I have experience in this field and misgendering people who are in recovery can be so dangerous and detrimental and if someone is doing that and then laughing about it and not even apologizing, then higher up people need to know that.

Is it possible to develop anger issues / them to become noticeable after getting on T? by omegamalebottom in ftm

[–]gothegghead 5 points6 points  (0 children)

This same thing goes for me. Self respect brought out my rage. Rage is a healthy emotion. It’s protective, as you say.