I have been waiting for support with my endometriosis for years myself.
I was recently told I have adenemyosis also (apologies for spelling check)
The twin to endometriosis too , besides Ibs copd and plenty more on my records I have been threw hell and I’m still near there now after so many tests , appointments and promises .
It’s ridiculous and so is p.ip and the support system .
I am like many who suffer and am on a constant rollercoaster waiting for a critical hysterectomy and doctors letting me down .
Apologies again but the fact it’s a invisible illness is alone a fight itself .
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Newjeff
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I sort of consider myself lucky that it’s only been a couple of years and coped the rest of the time with otc painkillers, when others have been going at this for years.
Where are you at with gynae/surgery?
If you’re applying for PIP or going to tribunal print off the info about the parliamentary discussion re endo, it might help.
I hope you don’t have to wait much longer for surgery 🤞
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