Sex and MS: Impact on Sex Lives, MS Sex Symptoms and Seeking support | Womanhood Ep 4

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Welcome to Episode 4 of our MS series, where we dive deep into the complexities of intimacy and sex when living with MS. In this episode ,our guests openly share personal experiences, discussing everything from dealing with numbness and fatigue to maintaining a fulfilling sex life despite the challenges.
🔍 Topics Covered:
Navigating numbness and fatigue
Overcoming communication barriers
The impact on libido and pleasure
Seeking support from healthcare professionals
Addressing societal norms and gender disparities
Empowering women to discuss sex openly
TV's role in normalizing conversations around intimacy
🔥 Our Guests
Roxy: / multiplesclerosisfashi...
Evie: / evie.orr
Emma: / solisyoga_hypnobirthing
Shereena: / reena.right.now
Katt: / deadliftsarebae
F Hoffmann-La Roche Ltd, Biogen, Merck, Novartis and Sandoz have provided financial support for the Womanhood project and have not had any involvement in the content.
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#MultipleSclerosis #Shiftms

Опубликовано:

21 окт 2024

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Комментарии : 8

@beeridgett 10 месяцев назад

Yes!! What women have to say is important. Our concerns are valid! Thank you

@desire1039 10 месяцев назад

I was hoping that you would all talk about worries about incontinence during sex. Worries about anything leaking out or coming out a little bit during any sexual moments. That is a huge worry for me. I was wondering if it’s also a worry for others, and what they do about that. Please touch on this conversation subject in the future if possible. Thank you for speaking about all of this stuff, because, you are right, I never find anything about women’s sexual dysfunctions in anything I watch or read.

@notasable 10 месяцев назад

@desire1039 it’s funny when you are put on the spot, that many topics and concerns get missed. This is most definitely a worry for me, it can be very distracting (wondering if thats just a feeling or if I actually need to pee) and that is not sexy.

@trevc12 10 месяцев назад

I great topic for discussion

@Defender78 6 месяцев назад

these gals are so energetic and expressive, they make a great team!

@clareeloise 10 месяцев назад

A few years ago I hadn’t put my lack of labido down to my diagnosis and medication, nor had a medical pro highlighted it as a side effect / symptom. I’d never connected the dots. You’re so right… do your own research and have open conversations with your partner. Another great topic!!

@willoubooby 10 месяцев назад

This is amazing just to hear other women talk about ms and sex I too have multiple sclerosis was diagnosed at 24/25 I'm now 31 and alot you all have spoken about is very helpful so I thankyou sp much ❤ and I prey for a cure!!! God bless you all and everyone ❤

@rogercookcouk 10 месяцев назад

Hi ladies! I have had MS since maybe 1997, been with Shift.MS since its conception (2009, I think) and do find this channel educational, in a 'selfish' way(?). However, I don't know if your know of www.youtube.com/@RenaMalikMD but she's a good source of related info. Roger Cook