S.p.d- Symphysis Pubis Dysfunction — Scope | Disability forum
If we become concerned about you or anyone else while using one of our services, we will act in line with our safeguarding policy and procedures. This may involve sharing this information with relevant authorities to ensure we comply with our policies and legal obligations.

Find out how to let us know if you're concerned about another member's safety.
Please read our updated community house rules and community guidelines.

S.p.d- Symphysis Pubis Dysfunction

Options
anniejewelss
anniejewelss Community member Posts: 2 Listener
 I have spd Symphysis Pubis Dysfunction, 
 spd (you only get it when you are pregant)I got it with my third child now 16, normal pregnancy with my first 2 , 
Getting spd was a shock , it was difficult getting it diagnosed took 2 doctor's visit ,  two hospital ones, I'm going to keep this very short, in case you get bored, but spd  cost me my fiancee , our house then I lost all my children(2006 when that happened) I lost everything , I got to  see a therapist , who told me you know I can't help, i can only listen, I never went again
, my story is huge, so much to tell , what spd has done to me, only plus  side is my son now lives with me since 2014 , 
hasn't help with the depression ECT, or the fact I can't do what I want to do , because the more I do the worst the pain will be,
I look at what needs doing, ie the house and just cry(because I can see what needs doing, I want to do it AND I CAN DO IT which what shocks most people but when I do and if I do, I'm in so much pain, a bit like child birth, you say your never going threw that again  ,it's hurts so much , but I guess to some you wonder why would you put yourself in so much pain if it hurts that much, well it's  yourself worth,people will think you are being lazy, or the fact you would  feel guilty someone else doing it , the fact that people can't see my disability doesn't help either, 
I lost some weight a few years back, and was told you must be feeling better now, 
NO I'M STILL DISABLED , 
In case I've scared some people, in 95% of the time spd goes away almost immediately after the birth, 
I even had a op, (didn't work,) 
One day i will write a book on my life , even though boring and simple as it is , I've not always been disabled but I do have a mind inside of me somewhere lol, yes despite now being disabled, I've got a brain that's works just fine 
Annie x(anniejewelss)


Comments

  • feir
    feir Community member Posts: 397 Pioneering
    Options
    Hi, i had 3 10lb babies, with the 3rd i got SPD and it was agony, going up and down stairs was impossible and they kept in my in for the last 2 weeks of my pregnancy as i was in so much pain and even then they delivered him 3 weeks early, i agree it's a very debilitating condition. I didn't even need to consider an operation afterwards as the pain went for me, sorry to hear yours didn't go and that an operation also didn't work. Chronic pain is awful to live with.

    I noticed with the next two after that i got it also but the 4th time i noticed that my babies head seemed to be going into my pelvis while i slept and this made it worse. I used the 'bandage' they gave me for the baby bump around my thighs instead to keep my legs closed while i slept (it was useless around my bump anyway) and put a cushion under my thighs to keep them raised at an angle while i slept as this also seemed to stop the babys head going down. This helped a lot and i was in a lot less pain. I thought i'd share that in case anyone with SPD during a pregnancy comes looking and it helps them.


  • Pippa_Alumni
    Pippa_Alumni Scope alumni Posts: 5,793 Disability Gamechanger
    Options
    Thank you for sharing your experience @anniejewelss, I hope today is as kind as possible to you.

Brightness

Complete our feedback form and tell us how we can make the community better.