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Daddy, Dad & Me
United Kingdom
เข้าร่วมเมื่อ 16 ม.ค. 2015
Hey!
We’re a same sex couple that started our adoption journey in 2018. We started our blog back as a way of documenting our journey but to share the highs and lows with everyone. Before we started on the road to adoption, we found very little info for same sex couples - and now we know of hundreds, all thanks to the blog!
2022 saw Sam diagnosed with Motor Neurone Disease and we’ve been sharing this journey too, to raise awareness of those who are diagnosed in the younger generations.
Always happy to hear from others, so feel free to subscribe, and pop us a DM, tweet or email.
J&S
We’re a same sex couple that started our adoption journey in 2018. We started our blog back as a way of documenting our journey but to share the highs and lows with everyone. Before we started on the road to adoption, we found very little info for same sex couples - and now we know of hundreds, all thanks to the blog!
2022 saw Sam diagnosed with Motor Neurone Disease and we’ve been sharing this journey too, to raise awareness of those who are diagnosed in the younger generations.
Always happy to hear from others, so feel free to subscribe, and pop us a DM, tweet or email.
J&S
#GlobalMNDAwarenessDay 21 June 2024 | Daddy, Dad & Me
This video may be upsetting for some people to watch but it shows the realities of living with Motor Neurone Disease. I have not edited the video because as some of you may know, it is not an illness that can be filtered. I had the pleasure of being asked to sit on the panel alongside others within the MND community and I hope this gives others a genuine insight into the trials and tribulations that are often encountered. Please do share, I really hope today has been an eye-opener for others and as a community that we are a force to be reckoned with. Much love, Sam X
Blog: www.daddydadandme.com
Facebook & Instagram: @DaddyDadandMe
Email: DaddyDadandMe@gmail.com
My Bucket List Instagram: @samandthebucketlist
TikTok: www.tiktok.com/@mndandme
#Adoption #UKAdoption #SameSexParents #DaddyDadandMe #MND #SamandTheBucketList
Blog: www.daddydadandme.com
Facebook & Instagram: @DaddyDadandMe
Email: DaddyDadandMe@gmail.com
My Bucket List Instagram: @samandthebucketlist
TikTok: www.tiktok.com/@mndandme
#Adoption #UKAdoption #SameSexParents #DaddyDadandMe #MND #SamandTheBucketList
มุมมอง: 224
วีดีโอ
Living with MND: 2 Years On | Daddy, Dad & Me
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Today marks the second anniversary of my diagnosis. It’s important for me to mark this as I don’t know how many of these I’ll get. Take a watch to find out what I’ve been up to. Blog: www.daddydadandme.com Facebook & Instagram: @DaddyDadandMe Email: DaddyDadandMe@gmail.com My Bucket List Instagram: @samandthebucketlist TikTok: www.tiktok.com/@Samandthebucketlist #Adoption #UKAdoption #SameSexPa...
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21 June 2023 ~ Global MND Awareness Day | Daddy, Dad & Me
มุมมอง 138ปีที่แล้ว
Wednesday, 21 June 2023 marks global MND awareness day, raising awareness of those are living with MND. The MND Association has launched a campaign for those within the MND community to openly share their stories in the #MNDOverMatter campaign. I believe in #MNDOverMatter, I’m going to campaign to give others like me, hope that there WILL be a world free of MND. Blog: www.daddydadandme.com Face...
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We've always wanted to go on a cruise, but never knew which was best to do. We heard that Disney were great to cruise with so we booked ourselves for a week to go and explore Mexico, Grand Cayman, Jamaica, and Disney's own private island, Castaway Cay. Here's a little vlog all about our adventure on board the Disney Fantasy... Blog: www.daddydadandme.com Facebook & Instagram: @DaddyDadandMe Ema...
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365 days later and I see my first anniversary following my diagnosis of MND on 5 March 2022. The last year has been a rollercoaster of emotions and I wanted to document my thoughts on this anniversary. I continue to spread awareness of this disease and to share that life is not over - it's for living! "To Live Will Be An Awfully Big Adventure" th-cam.com/video/lBfcLrZ7KzU/w-d-xo.html My GoFundM...
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We recently received a comment from a viewer regarding references being sought from ex partners, as part of the reference checking process. In this video, we explain more about why this information is required and why you need not worry about the reference being obtained. You may also want to watch… Stage 1 & 2 Assessment Process incl. Approval / Matching Panel th-cam.com/video/mRS8vtd6Umo/w-d-...
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It has been a year since our sleep anxiety vlog, in which we discussed sleep anxiety in adopted children. Following a recent request by a subscriber, here is a follow-up with discussion around sleep studies and practical tips which may help at bedtime. You may also wish to watch the video from last year which is linked below. Sleep Anxiety in Adopted Children th-cam.com/video/Ni0beqrg_aA/w-d-xo...
I’M BACK! ~ #TakeoverMND | Daddy, Dad & Me
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After 10 long months, I am back! You may have seen from my video shared last March (linked below), about a change in my health. Following this, I took some time away to come to terms with the diagnosis and to live life to the fullest and tick off the bucket list! Here I am back in front of the camera ready to share my story, all the amazing opportunities available to me and to continue sharing ...
Book Review: The Strange & Curious Guide to Trauma - Sally Donovan | Daddy, Dad & Me
มุมมอง 1402 ปีที่แล้ว
We have been kindly gifted a copy of Sally Donovan’s new book, which is available for pre-order for a 21 March 2022 release date. Sally is an award winning author and is an adoptive parent herself. This book sees us discovering what trauma is, what it can do and how it affects it us. We get to meet Adrian Adrenalin, Courtney Cortisol and Amy Amygdala in the story and we discover what each of th...
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This was really hard to put together and as you’ll see, this is an emotional video from me. Please don’t watch if you think it’ll upset you - that is not my intention. The last few months have been hell and sadly with that comes some news which has rocked my world and that of my family and friends. Please be kind to yourself and those around you. Life, as we all know is so very fragile.
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You may soon be embarking on the family finding process, and you’ll soon be introduced to the world of Linkmaker. For many adopters, Linkmaker is the start of the family finding process and with that can come many complexities. Take a watch to hear more about what to expect. You may also want to watch; Linking... What Happens Once You're Approved to Adopt th-cam.com/video/ANqRx3rFOe8/w-d-xo.htm...
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It takes so much courage to be honest...we took a chikd who was 4 for long term fostering and I grieved the loss of our life ...I so get u❤
Really appreciate ur honesty
All the love and good wishes ❤
Bravo Sam, congrats on the 2 year milestone and on living life to the full. I’m just 9 months in and it’s great to see people can get through the terror/depression to lead a life which still has joy. Keep up the good work and here’s to a cure for us ASAP!!
Well done babe! Thanks for sharing
💞💞💞
Hi! Do you know if it's a legal requirement to have 10 years of medical history in UK to be able to adopt? Thanks!
I don't know your name, but thankyou for being vocal about MND & your journey. Where are you based? I'm in Devon. I went to a Solstice Event this evening in aid of Macmillan Cancer, but there, I started talking about MND. Keep up the fight! Sharon
Thank you for this, its so refreshing and honest, brave and hopeful. To even be able to see some goodness in all this shows the type of person you are. Your right MND does not define you, fingers crossed you have plenty of time left to do some more wonderful things, and live your life. Your legacy is huge already.
I am feeling like this right now and this video really helps! We had a LO placed 5 months ago, I feel such grief for my old life and feel horrible about it. I wasn’t expecting it. I love my child but I doubt myself and whether I’m cut out for this!?
Hi thank you so much for your honest post. We start our introductions on Monday. Pretty much can relate to what you covered especially around the attachment to foster carer. She done such great job of building secure attachment that I think it be so hard on our AS 19 months. We are lucky we have had a chemistry meet and 2 play dates and another booked over weekend but little man hasn’t a clue and adores his carer. Thanks for taking time to share your experiences. I check out your other videos. We’re not 2 mums or 2 dads but I’m sure issues are similar with anyone going through process ❤
Hey. Thanks for your video! Just starting stage 1. For the workbook, how much info do I need to put in. Like say about you. Is it a general overview of likes and hobbies etc or long winded pages or writing? Don't want there to be not enough if it's needed! Thanks x
Thank you for sharing! I agree 💯 that family/friends are priceless. I tell my wife all the time, I did not realize how much I loved her until this diagnosis.
You’re so inspiring Sam. We’re in this together 💪🏻
Yes we are!!
Thanks for the video, very informative. My partner and I have just started stage 2 today! Excited but also nervous. Were you asked to give ex references? I feel it's irrelevant as my relationships didn't end so well and I didn't have children with them.
This is really helpful thank you for taking the time to record this video! :)
you're most welcome!
Wow what a list! We are at the start of our adoption process atm, and this is a very weird list! (ceremonial swords I mean!)
. well done for sharing 👏
🧡💙
Welcome back! Marvellous to see and hear from you. Hugs from Spain
Thank you so much!
I have Als myself. Stay strong mentally and physically. The will to live needs to be stronger than the will not to. Go live my friend.
Hi, I didn't know about this so if opting out of the competitive matching wouldn't that make the waiting time for your child so much longer.?
I'll pop a video up to explain more!
Thank you so much for sharing....this is helping me a lot!
I'm gay. How do you plan on providing a female influence in his life. I know single mum's do a fabulous job without a man I'm not saying they don't and I'm asking because I wonder what I might do to ensure he understands how to treat women properly or she can discuss feminine issues that I would not know about. I seriously don't even know what goes on with girls I need a book. Just a general question I am honestly fact finding working out how I can do it. Or maybe I lack imagination but I would love to know others thoughts there seems very little advice out there. Love to the family.
Support networks. He has lots of females in our support network that would be able, and already provide that support to him. Hope that helps.
So brave of you to do this video! My heart goes out to you. I hope you can achieve as much as you want to while you can. Sending love and strength to you. Xx
Hi, you mentioned that it had to be a couple. Did they give you any additional information as to why single adopters weren’t being looked at?
It depends, they should usually state why though
Sending u so much love and prayers, your a beautiful and amazing person! Don't give up xxx
Thank you so much for doing this video. We’ve had our first meeting with our agency, they told us there didn’t seem to be anything that would prevent us starting the application process then came back a few days later to say they wouldn’t be starting the process because of x,y & z. Childcare experience being the main thing. You have explained the reasoning perfectly & now it makes sense! 🙏
My heart aches for your precious and beautiful family , we’ve followed you quietly for so long on your journey and will continue sending you so much love x
Never ever give up, respect for you, our hearts and love goes to you in your battle, but never ever give up, miracles do happen
I have so much respect for you, Sam, for sharing. You are so right about the things that really matter,
The most normal reaction to say in this time is " I'm sorry", but I don't want to say this. The reason why is because I'm going through similar situations as yourself. 12 years ago I got diagnosed with a type of muscular dystrophy, I am now in a wheelchair and on oxygen at home. I got told I would have 10 years max but ive already beaten this and the one thing I hated the most is people saying "I'm sorry". I would always tell people, please don't be sorry, atleast now I know and I know know more than ever that I need to enjoy life to the fullest. I need to live everyday as if it is my last because I don't know if I will wake in the morning. These first few days, weeks and possibly months will be the hardest for sure, but please, if there's one bit of advice that I can give you, it's to tell the people you love, that you love them, multiple times a day, ALWAYS go to sleep at peace with your family and tomorrow when you wake up, enjoy every minute but know "time doing nothing is never wasted" (book by james norbury, big panda and tiny dragon -highly recommend reading). Just being with your family is doing something 💛
Sending love and hugs to you all xxx
Sending you and your family lots of love 💙
I am so sorry to hear this. It can’t have been easy to share. ❤️
So, so sorry to hear this mate. Hope this disease hits you as slowly as possible. As I hope you have many year's to live normally as possible 🙏
I am so sorry for you and your family ❤️
I’m so so sorry to hear this! Live life to the max xx
Virtual hug 🤗 you have provided me with so much knowledge insight and resources praying for the best for you and your family
I'm so sorry xx 🧡
Thank you for this :)
Are you adopting? I am a muslim as well today I got approved with my husband as adopters
Thank you this was super useful to hear. We are going through stage 1 right now! Thanks for your honesty and hope your family are doing well
so helpful thanks so much! your honesty has really helped prepare me, as its coming up in a month! eek!
Thank you for this! Can you speak a little bit more about the actual profiles you're shown as adopters? I'm a bit unclear on how you can look at a short profile and make any kind of decision! I suppose you can't really say what drew you to your son's profile without divulging his personal info, but if there's something more general that you can talk about I'd love to hear it!
Of course - watch this space!
How long was the process for you from the moment you were approved to family find to when you found your son's profile? I imagine it was quite short, if you didn't see many profiles before him. Did you feel any sort of pressure, internally or externally, to find a suitable match as soon as you could?
Hi Emma, thanks for watching. From approval to when we found Little Man's profile was only a few few months, so quite quick in the scheme of things. Then from profile to matching panel was approx. 4/5 months. In total we had considered probably 10/15 profiles. Didn't feel any pressure, just knew something had to feel right about it all.
This was really interesting, thank you! I've not heard anyone mention the birthday thing before.
You're so welcome!
I'm looking forward to the process because I've been researching on and off for 6 years, but I'm only 26 and not financially or emotionally in a place to be a parent yet. I can imagine it's hard to find a balance between proudly telling relevant people your child is adopted, but also not making your child feel like "adopted" follows them everywhere and makes them an outsider. Thank you for the info!
Thank you so much for sharing! We have our first bump into this morning! ❤️
Do you know of any transgender/non-binary adoptive parents? LGB folks are pretty accepted in most adoption circles now, but we still don't hear/see much (I haven't seen anything) about transgender/non-binary adoptive parents.
No, sorry I've not heard of any.
I've struggled to find resources on this unfortunately! But there must be some out there, maybe just less visible :)
I hope they aren't discriminatory based on BMI because it's been proven as an outdated and inaccurate way to assess health (not to mention the countless "healthy" BMI folks who have unhealthy lifestyles), but maybe BMI will be fairly irrelevant if the other health checks are decent. I do wonder if weight was a deciding factor in the GP being more thorough with your health and not your husband's, but it shouldn't have been. Besides, with the prevalence of eating disorders, I'd have thought it would have been more important that potential adopters had a good relationship with food, rather than repeated dieting or seeing some body types as better than others (since many of us with eating disorders gained it partially from how those around us spoke about food/weight when we were young). Thank you for sharing this info! :)