Hello!
I’m a 30 year old male living with my wife on a 3rd world country. We have no help from our families and we’ve been through some very difficult times, but we managed to get by. My wife had a severe case of depression and even tried to take her own life at a point.
Now things got a little better, even though we are in a tight financial situation. We both feel a lot better and we even managed to get off our meds (it’s nice to be able to save the money and get rid of the side-effects).
But, there is something weird that came as a consequence of all those bad times. Whenever I receive a text message from my wife, my heart races and my anxiety goes through the roof. It’s an irrational fear that the message will be bad news.
I don’t really know if there is such a thing as “text phobia”, but that’s how it feels (english is not my main language, so it’s kinda hard to explain). I alread mentioned this to my wife and I think it made her feel bad because she thinks it’s her fault. Of course I said it’s not her fault, but now I’m kinda afraid to bring this up again with her. We both are trying so hard to be strong for each other.
I wonder if anyone else had a similar problem and I would be very grateful if someone could give me some tips on how to work on this problem.
Thanks a lot and I hope you have a great day.
This is me. I’d just been diagnosed with a rare life threatening illness but I lived in a different city from my family and most of my friends. I was fielding calls constantly from my family, friends and my boss trying to explain what was happening to me, what the treatment was, when I’d be back to work. So many times I got a call to say I was neutropenic and needed to go to hospital ASAP. And then my brother attempted suicide. Single worse phone call I’ve ever received. After that I got panic attacks every time the phone rang. It kept getting worse, to the point that I couldn’t listen to voicemails even.
Now my phone is always on silent and most the time on do not disturb. I only answer phone calls from one person - my mum who lives 100 miles away. Even those calls cause panic if I’m not expecting them. I don’t have voicemail turned on. I can’t listen to voice memos. Video calling is even worse. My doctors now have my partners phone number because I simply can’t handle talking on the phone. I can text and I can email. But phone and video calls are completely off limits.
It’s been 15 years. 15 years I’ve lived like this. I was diagnosed with PTSD 18 months ago, just before I lost my mental health care. I have no help, no idea how to help myself. I’m sorry I don’t have anything helpful to add, I just haven’t come across people like me before. Plenty of people dislike the phone and avoid it, but they don’t break down in mess of tears and hyperventilation at the mere sound of a ringtone. I’m so embarrassed about it but I just can’t “get over it”.
Don’t be sorry, your reply actually helped. It’s good to know we’re not alone dealing with this kind of problem. And you should not feel embarassed, because the “get over it” mentality is toxic as fuck. Having PTSD is not your fault in any way.
Hey @HandOfDoom I answered a phone call today! I was expecting it (hospital stuff) and my pulse went through the roof when I saw it on the screen. All the usual happened, shaking, tears in my eyes, feeling like I was going to throw up. But I answered it - and I don’t think I would have done if you hadn’t have posted about your similar experience. Thank you 😊
That’s great! Thanks a lot for sharing this. I’m having a rough day and reading your reply made me smile. I’m happy my post could help you =)
I’m glad it raised a smile, but I’m sorry you’re having a rough day. Is your wife ok?
I was thinking a bit more about the steps I take with my mum so I can answer her calls, and if that could help you. We have a “code” for any phone calls that aren’t scheduled. She assumes I won’t answer so one missed call means she just wants to chat. Two missed calls means she was calling for a specific reason, she needs to speak with me about something but it’s not urgent urgent. Three missed calls means it’s an emergency - she absolutely needs to talk to me asap. She’s very good at not abusing the system so I answer the second call when I see it (my phone still doesn’t ring, even for her). Thankfully there’s only been a handful of true emergencies in 15 years.
I wondered if you and your wife could come up with a similar system - maybe using different messaging apps? Say normal, everyday messages go through WhatsApp but “I’m feeling bad” or “I need help” messages go through SMS. She wouldn’t even need to ask for help, using SMS would be enough to convey the message. Meanwhile you know that any message through WhatsApp is a nice normal (or even boring!) message.
I don’t know how practical that would be or if your wife would be willing to do it, or whether it’d even help, but I thought I’d mention it on the off chance. I’m wishing both of you the best.
Hey, we are feeling better now, thanks for asking :)
We’ll try different messaging apps if I can’t get better with some more time, that’s a good idea. Thanks again and I wish you the best too!
No need to be embarrassed. What you describe is more than enough to cause this type of response. I know it is different in different countries, but why can you not get help? Is it too expensive where you are? PTSD and these types of issues is treatable, so it is very likely that you will not suffer like this in the long term.
It’s a bit complicated. I live in the UK so healthcare is free - but the NHS is in a dire state at the moment. It’s so underfunded by the government it’s on its last legs. The diagnosis I mentioned before was lupus. I was desperately ill for the whole of my 20s, mentally and physically. When you’re deathly ill or suicidal a lot of the smaller complaints are deemed unimportant. And taken in the context of my other illnesses, not being able to speak on the phone was relatively insignificant. For the last few years I’ve been largely stable. Just as I felt ready to confront my phone issues, my psychiatrist retired and wasn’t replaced. For the last 10 years that man was my life raft, I saw him every 8 weeks. And then he was gone and they couldn’t afford to replace him fully. There’s a part time psychiatrist now but he only deals with the acutely mentally ill, and this doesn’t qualify. My depression has significantly worsened since then, but again, not to the point where I’m considered in need of emergency treatment.
18 months ago my family paid for me to see a private consultant for medical cannabis treatment - primarily to help my pain, but the effects on my mental health and sleep have also been really positive. It was the private consultant who diagnosed the PTSD. Medical cannabis is legal here, but only about 9 people in the whole country (I’m being literal here, no hyperbole) qualify for it on the NHS - mainly children with severe treatment resistant epilepsy. So in order to keep taking the medical cannabis which has improved my life so much, my family, friends, even neighbours have been chipping in so I can afford it, approx £150 a month. I can’t work due to my ill health, so I am completely reliant on my loved ones to pay for it. Nobody can afford for me to have private psychiatric treatment as well, and the NHS simply do not have the resources to treat me.
So that’s where I’m at. Even if I stopped the medical cannabis (and honestly that would be a ridiculous thing to do - I’ve managed to reduce 90% of my opioid intake, I sleep through the night, I actively want to live for the first time in over a decade…) I don’t think you can even get a single private consultation for £150, let alone be treated.
Sorry for my life story, it was a bit hard to explain without going into it. And thank you for the support.
That sounds like many complications for getting the help you need. I am glad people are supporting you, but it still seems very stressful.
If you ever get the chance to get further treatment. Maybe you can ask whether EMDR is useful in your case. For me it worked very well for my PTSD. I also think that, generally, it might require less treatments than other forms of therapy. So it might mean less of a financial burden. I am not a doctor, so I do not know what is best in your case, but you might ask about it.
Thank you 😊