u/Eternalhusk

Seeing if anyone here has gone through it and has answers. I became homeless due to circumstances and due to my health im going to be put in a temporary council house till a more permanent solution comes along. Now these places i know can vary in time and with shortages i could be here for a long time. Im happy as its a good place with a garden for my dog.

So has anyone got experiences of times and my main question is internet. Can you get a contract if your living there?

Relationship breakdown

So I was diagnosed last year in january, it was fast and had no time to process it and then had a stem cell transplant.

Im still immuno compromised and behind on vaccinations as ive had just flu and covid due to continued tretament and top ups for the transplant.

I just got one a couple weeks ago and im of course that risk of gvhd gets closer evwrytime.

On top of all this i just split from my partner after they said it was too much and they said they have to focus on them. So im now homeless with nothing.

The kicker my partner messaged saying ahe was upset as filling out forms is hard as she has to update things and im litterly homeless with nothing desperately trying to find somewhere safe while also being high risk.

I feel like leukeima has ruined everything as its just got worse and worse.

So I was diagnosed last year in january, it was fast and had no time to process it and then had a stem cell transplant.

Im still immuno compromised and behind on vaccinations as ive had just flu and covid due to continued tretament and top ups for the transplant.

I just got one a couple weeks ago and im of course that risk of gvhd gets closer evwrytime.

On top of all this i just split from my partner after they said it was too much and they said they have to focus on them. So im now homeless with nothing.

The kicker my partner messaged saying ahe was upset as filling out forms is hard as she has to update things and im litterly homeless with nothing desperately trying to find somewhere safe while also being high risk.

I feel like leukeima has ruined everything as its just got worse and worse.

Feeling so tired of it all. Partner decided to end our relationship today after I got back from sounding fathers day with my son.

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So I had to move in last year as I was diagnosed with leukemia and had to have support and lost everything. Things have been hard my mental health got worse and she felt distant. We argue alot now over things as it got so tense as i felt ahe seen me as a burden and issue all the time and she seen that as me attacking her.

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Today I had a panic attack when seeing my son and wasnt doing great. I rang her and she was more interested in drinking and other things. This upset me especially the drinking as it triggers my trauma. She just said 'I can do wat i want' then said i was projecting on her.

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Then I left to walk as I was feeling overwhelmed and it helped then after back and forths its over.

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Im now in homeless place for thw night with nothing unsure of the future while still receiving treatment and feel like everything is a mess.

I feel at my lowest and so alone

My circumstances have changed and I will be homeless. What are people's experiences of calling them and do they sort it out?

I have mental health issues and on top of that fought leukemia last year to the point I got a stem cell transplant. Im still in treatment no and immuno compromised. Will they be able to helo me?

So I passed my one year mark of stem cell transplant, and ill be honest im struggling to see the milestone.

Ive tried to be ok but since I was diagnosed its made me feel more alone and scared than ever.

When i was initially diagnosed people did the old sorry to hear do you need anything. But then after a few weeks all gone. I have zero friends now as noone cared to text or anything. My family is hear from very rarely with month gaps. My partner is my only support and she is mentally burnt out with it all yet she has a support network who has constantly been there checking and continues. And it hurts as i want help amd ask for it yet no one shows up. The drs ect are aware how much im struggling yet nothing has changed.

Im still receiving my dli top ups as my chimerism isnt where it needs to be. And had my mrd done this past week so thats on my mind.

Im lost in the whole thinking of when does it gwt better? I fought aml leukemia and im really struggling to see the light and im trying to hard to see it.